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Life Sciences
Cell Biology
Ana Carolina Lima CAMARGO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Júlia Nicoliello Pereira De CASTRO; Thiago Adalton Rosa RODRIGUES et al.
2023.
Comparative transcriptome analysis of endothelial colony-forming cells from hbsc and hbss patients with sickle cell retinopathy.
In:
26th human genome meeting ? hugo.
Brasil.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Ana Carolina Lima CAMARGO; Júlia Nicoliello Pereira De CASTRO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Thiago Adalton Rosa RODRIGUES et al.
2023.
Identification of potential transcription factors and micrornas associated with proliferative sickle cell retinopathy in hbsc and hbss patients using in silico analyses.
In:
X-meeting / bsb 2023.
Brasil.
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Life Sciences
Cell Biology
Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Mirta Tomie ITO; Ana Carolina Lima CAMARGO; Souza B B et al.
2023.
In-silico comparison of potentially secreted proteins from endothelial colony-forming cells in ischemic stroke and sickle cell anemia.
In:
X-meeting / bsb 2023.
Brasil.
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Health Sciences
Medicine (miscellaneous)
Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Ana Carolina Lima CAMARGO; Mirta Tomie ITO; Souza B B et al.
2023.
Prediction of regulatory factors of differentially expressed genes in sickle cell anemia and ischemic stroke.
In:
26th human genome meeting ? hugo.
Brasil.
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Health Sciences
Infectious Diseases
Thiago Adalton Rosa RODRIGUES; Yuri De Carvalho Oiamore SILVA; Júlia Nicoliello Pereira De CASTRO; Ana Carolina Lima CAMARGO; Souza B B et al.
2023.
Association variants at the afap1 (rs4619890); and tmco1 (rs2814471) as a risk factor for primary open-angle glaucoma development in a brazilian cohort.
In:
26th human genome meeting ? hugo.
Brasil.
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Life Sciences
Neuroscience (miscellaneous)
Thiago Adalton Rosa RODRIGUES; Souza B B; Victor De Haidar E BERTOZZO; Júlia Nicoliello Pereira De CASTRO; Ana Carolina Lima CAMARGO et al.
2023.
Associação da variante rs7137828 (atxn2) com o desenvolvimento de gpaa e aumento da relação escavação/disco vertical em uma amostra da população brasileira.
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Simpósio de pós-graduação em oftalmologia - 11ª. jornada paulista de oftalmologia;.
Brasil.
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Life Sciences
Genetics
Ana Vitória Volpato JENSEN; Thiago Adalton Rosa RODRIGUES; Ana Carolina Lima CAMARGO; Ana Rafaela Carvalho MONTE; Gabrielle Maria Giovanna Da Silva GONÇALVES et al.
2023.
Evaluation of rs7426380 in the efemp1 gene as a risk factor for primary open-angle glaucoma development in a brazilian cohort.
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26th human genome meeting ? hugo.
Brasil.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Thiago Adalton Rosa RODRIGUES; Souza B B; Victor De Haidar E BERTOZZO; Júlia Nicoliello Pereira De CASTRO et al.
2022.
Association of variants in the foxc1 ; atxn2 and txnrd2 genes with primary open angle glaucoma in a brazilian population.
In:
Arvo annual meeting.
Estados Unidos.
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Life Sciences
Cell Biology
Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Ana Carolina Lima CAMARGO; Mirta Tomie ITO; Souza B B et al.
2022.
Transcriptomic analysis of circulating endothelial colony-forming cells in patients with sickle cell anemia and ischemic stroke.
In:
American society of human genetics annual meeting.
Estados Unidos.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Ana Carolina Lima CAMARGO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Júlia Nicoliello Pereira De CASTRO; Thiago Adalton Rosa RODRIGUES et al.
2022.
Identification of fzd3 and sema3a as potentially secreted proteins involved in proliferative sickle cell retinopathy.
In:
American society of human genetics annual meeting.
Estados Unidos.
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Life Sciences
Cell Biology
Júlia Nicoliello Pereira De CASTRO; Costa Sueli MS; Mirta Tomie ITO; Ana Carolina Lima CAMARGO; Souza B B et al.
2022.
Transcriptomic-based secretome analysis of circulating endothelial colony-forming cells in patients with ischemic stroke and sickle cell anemia.
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Iii escola paranaense de bioinformática 2022.
Brasil.
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Life Sciences
Developmental Biology
Ana Carolina Lima CAMARGO; Victor De Haidar E BERTOZZO; Costa Sueli MS; Júlia Nicoliello Pereira De CASTRO; Thiago Adalton Rosa RODRIGUES et al.
2022.
Identification of mirnas associated with pathological angiogenesis in in proliferative sickle cell retinopathy.
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Iii escola paranaense de bioinformática 2022.
Brasil.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Manoel Vinicius Rocha ARAKI; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO et al.
2021.
Association of abca1 rs2472493 and gas7 rs9913911 variants with poag in a brazilian population.
In:
Association for research in visual and ophthalmology annual meeting.
Estados Unidos.
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Life Sciences
Neuroscience (miscellaneous)
Victor De Haidar E BERTOZZO; Sueli Matilde Da Silva COSTA; Souza B B; Cruz P R S; Marina Gonçalves Monteiro VITURINO et al.
2021.
Candidate genes involved in sickle cell retinopathy.
In:
66th brazilian congress of genetics.
Brasil.
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Life Sciences
Genetics
Rodrigues Thiago Adalton ROSA; Souza B B; Victor De Haidar E BERTOZZO; Júlia Nicoliello Pereira De CASTRO; Costa VP et al.
2021.
Evaluation of genetic variants associated with primary open angle glaucoma in a brazilian population.
In:
66th brazilian congress of genetics.
Brasil.
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Life Sciences
Genetics
Vasconcellos J P C; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Francisco Carenzi Da SILVA; Mônica ALVES et al.
2020.
Association of sall1 rs1362756 and six1/six6 rs33912345 variants with poag in a brazilian population.
In:
Association for reserach in vision and ophthalmology annual meeting.
Estados Unidos.
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Health Sciences
Pharmacology (medical)
Mônica Barbosa De MELO; Marina Gonçalves Monteiro VITURINO; Neto Jamil M; Alicia B ROQUE; Gessica F S BORGES et al.
2020.
Analysis of cfb (r32q - rs641153) and cfh (rs1410996) variants as risk factors for age-related macular degeneration in a brazilian population.
In:
Association for research in vision and ophthalmology annual meeting.
Estados Unidos.
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Life Sciences
Parasitology
R PINTO; F GOMES; A MARTINI; Daniel BORGES; E BARBOSA et al.
2020.
Quality of life in keratoconus: evaluation with keratoconus outcomes specific questionnaire (korq).
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Association for research in vision and ophthalmology annual meeting.
Estados Unidos.
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Health Sciences
Medicine (miscellaneous)
E BARBOSA; A ELOY; A F BARBOSA; C TAVARES; R PINTO et al.
2020.
Meibomian gland dysfunction and ocular surface findings in rosacea patients.
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Association for research in visual and ophthalmology annual meeting.
Estados Unidos.
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Life Sciences
Genetics
Marcelo Luís OCCHIUTTO; Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO et al.
2020.
Associação dos polimorfismos do gene apoe com glaucoma primário de ângulo aberto em uma amostra da população brasileira.
In:
64º congresso brasileiro de oftalmologia.
Brasil.
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Life Sciences
Genetics
Manoel Vinicius Rocha ARAKI; Yuri De Carvalho Oiamore SILVA; Thiago Adalton Rosa RODRIGUES; Flavia Fialho BAJANO; Rui Barroso SCHIMITI et al.
2020.
Associação das variantes abca1 (rs2472493) e gas7 (rs9913911) com gpaa em uma população brasileira.
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64º congresso brasileiro de oftalmologia.
Brasil.
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Health Sciences
Genetics (clinical)
Gislene Pereira GIL; Galina ANANINA; Mariana MASCHIETTO; Sheila Soares LIMA; Sueli Matilde Da Silva COSTA et al.
2019.
Altered dna methylation profile in placentas from pregnant women with sickle cell disease.
In:
69th american society of human genetics annual meeting.
Estados Unidos.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Gislene Pereira GIL; Ananina GALINA; Mariana MASCHIETTO; Baptista Letícia C; Da Silva Costa Sueli MATILDE et al.
2019.
Dna methylation profile in placentas of sickle cell anemia women.
In:
International federation of placenta associations meeting; 2019.
Estados Unidos.
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Life Sciences
Genetics
P V SVIDNICKI; Melo M B; José Paulo Cabral De VASCONCELLOS; Ss RONG; A LARSON et al.
2019.
Apex 1 as a new candidate gene for glaucoma.
In:
Arvo annual meeting.
Estados Unidos.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Sueli Matilde Da Silva COSTA; Mirta Tomie ITO; Souza B B; Pedro Rodrigues Sousa Da CRUZ; Marina Gonçalves Monteiro VITURINO et al.
2018.
Identification of candidate genes involved in proliferative sickle cell retinopathy by rnaseq.
In:
Association for research in vision and ophthalmology annual meeting.
Estados Unidos.
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Health Sciences
Medicine (miscellaneous)
Mônica Barbosa De MELO; Mirta Tomie ITO; Sueli Matilde Da Silva COSTA; Baptista Letícia C; Gabriela Queila De Carvalho SIQUEIRA et al.
2018.
Gene expression analysis of endothelial cells from sickle cell anemia patients and its relation with stroke.
In:
68th american society of human genetics annual meeting.
Estados Unidos.
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Health Sciences
Genetics (clinical)
Baptista Letícia C; Costa Maria LAURA; Souza B B; Costa F F; Mônica Barbosa De MELO.
2018.
Transcriptome of placentas from two pregnancies of a patient with sickle cell disease.
In:
International congress of genetics.
Brasil.
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Life Sciences
Genetics
Jhonathan Aa FERNÁNDEZ; Sueli M Da Silva COSTA; Ana C CARNEIRO; Raquel A LAURIA; Bruno B SOUZA et al.
2017.
Novel compound heterozygous mutations in ush2a gene associated with usher syndrome type ii.
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Xvii workshop de genética; realizado em botucatu - sp.
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Life Sciences
Genetics
Vasconcellos J P C; Souza B B; Jamil Miguel NETO; Ricardo Yuji ABE; Rui Barroso SCHIMITI et al.
2017.
Snp rs11024102 in plekha7 as a risk factor for pacg development in a brazilian population.
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World glaucoma congress 2017.
Holanda.
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Life Sciences
Molecular Biology
Gabriela Queila De Carvalho SIQUEIRA; Souza B B; Murilo Guimarães BORGES; Mirta Tomie ITO; Ananina GALINA et al.
2017.
Exome sequencing of extreme phenotypes identifies potential novel genes as modifiers of leg ulcer in sickle cell anemia.
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American society of human genetics 67th annual meeting.
Brasil.
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Health Sciences
Genetics (clinical)
Baptista Letícia C; Maria Laura COSTA; Surita Fernanda G; Parpinelli Mary A; Souza B B et al.
2017.
Analysis of placenta transcriptome in patients with hemoglobin sc disease.
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11th annual conference - academy for sickle cell and thalassemia - ascat.
Brasil.
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Health Sciences
Medicine (miscellaneous)
Mirta Tomie ITO; Sueli Matilde Da Silva COSTA; Albuquerque Dulcinéia M; Baptista Letícia C; Gabriela Queila De Carvalho SIQUEIRA et al.
2017.
Gene expression analysis of endothelial cells with stroke in sickle cell patients.
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Genética 2017 - brazilian-international congress of genetics.
Brasil.
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Life Sciences
Genetics
Milena Atique TACLA; Camila ZANGALLI; Souza B B; Stancato D; Ananina G et al.
2017.
Evaluation of genetic polymorphisms in the determination of optic disc parameters and circumpapillary retinal nerve fi ber layer thickness in normal individuals in a sample of the brazilian population.
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67nd annual meeting of american society of human genetics (ashg).
Estados Unidos.
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Life Sciences
Cell Biology
Mônica Barbosa De MELO; Leticia De Carvalho BAPTISTA; Regiane FERREIRA; Fernanda SURITA; Dulcineia Martins ALBUQUERQUE et al.
2016.
Expression profile of inflammatory genes in placenta from sickle cell disease patients.
In:
13th international congress of human genetics.
Brasil.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Melo M B; Caique MARTINS; Oliveira MB; Costa Sueli M Da S; José Paulo Cabral De VASCONCELLOS.
2016.
Analysis of the col8a2 and slc4a11 genes and of the tgc intronic expansion in the tcf4 gene in families with fuchs endothelial corneal distrophy (fecd).
In:
66nd annual meeting of american society of human genetics meeting (ashg).
Estados Unidos.
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Health Sciences
Infectious Diseases
Mariana B OLIVEIRA; Vasconcellos J P C; Costa Vital P; Mônica Barbosa De MELO.
2015.
Elevated il1-beta level in plasma is associated with primary open angle glaucoma in a brazilian population.
In:
Arvo 2015 annual meting.
Estados Unidos.
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Life Sciences
Cell Biology
Pedro Rodrigues Sousa Da CRUZ; Galina ANANINA; Marcos André BEZERRA; Wagner M AVELAR; A C Amato FILHO et al.
2015.
Characterizing brazilian sickle cell anemia patients.
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American society of human genetics 65th annual meting.
Brasil.
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Health Sciences
Immunology and Allergy
Paulo Vinícius SVIDNICKI; Vasconcellos J P C; Helber D Teles CALDEIRA; Mariana B OLIVEIRA; Hugo Freire NUNES et al.
2015.
Exome sequencing analysis in a primary open angle glaucoma brazilian family.
In:
American society of human genetics 65th annual meting.
Estados Unidos.
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Life Sciences
Cell Biology
Hugo Freire NUNES; Vasconcellos J P C; Iscia Teresinha Lopes CENDES; Benilton De Sá CARVALHO; Murilo Guimarães BORGES et al.
2015.
Whole exome sequencing in a family with primary open angle glaucoma.
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American society of human genetics 65th annual meting.
Estados Unidos.
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Life Sciences
Neurology
Souza B B; José Paulo Cabral De VASCONCELLOS; Benilton De Sá CARVALHO; Murilo G BORGES; Lopes Cendes I et al.
2015.
Whole exome sequencing in a family with early onset primary angle-closure glaucoma.
In:
American society of human genetics 65th annual meting.
Estados Unidos.
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Social Sciences & Humanities
Psychology (miscellaneous)
Mônica Barbosa De MELO; G ANANINA; M A BEZERRA; A S ARAUJO; P R S CRUZ et al.
2014.
High degree of admixture in an urban brazilian population.
In:
American society of human genetics 64th annual meeting.
Estados Unidos.
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Life Sciences
Genetics
Medina Flávio MACCORD; Augusto Lopes Alves Da MOTTA; Walter Y TAKAHASHI; Pedro Carlos CARRICONDO; Mario Martins Dos Santos MOTTA et al.
2014.
Association of the y402h polymorphism of cfh gene with response of exudative amd to intravitreal vegf inhibitors in the brazilian population.
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Arvo 2014 annual meeting.
Estados Unidos.
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Health Sciences
Immunology and Allergy
Mariana B OLIVEIRA; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Mônica Barbosa De MELO.
2014.
Inflammatory cytokines in aqueous humor and plasma are associated with primary open angle glaucoma in a brazilian population.
In:
Arvo 2014 annual meting.
Estados Unidos.
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Health Sciences
Genetics (clinical)
Ana Luiza ARAÚJO; Eugênio Santana De FIGUEIREDO; Pedro Rodrigues Sousa Da CRUZ; Bruno Batista De SOUZA; Carlos Eduardo Leite ARIETA et al.
2014.
Identification of structural alterations in the cx50 gene in patients with congenital cataracts.
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American society of human genetics 64th annual meeting.
Estados Unidos.
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Life Sciences
Animal Science and Zoology
Leticia De Carvalho BAPTISTA; Regiane FERREIRA; Fernanda SURITA; Mary Angela PARPINELLI; Kleber Y FERTRIN et al.
2014.
Alteração na expressão de genes relacionados à inflamação na placenta de paciente com anemia falciforme.
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Congresso brasileiro de hematologia; hemoterapia e terapia celular - hemo 2014.
Brasil.
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Life Sciences
Genetics
Leticia De Carvalho BAPTISTA; Fertrin K Y; Regiane FERREIRA; Carolina LANARO; Dulcineia Martins ALBUQUERQUE et al.
2014.
Hyperexpression of inflammatory genes in placental tissue in patients with hemoglobin sc disease.
In:
56th ash annual meeting.
Estados Unidos.
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Health Sciences
Radiology, Nuclear Medicine and Imaging
José Paulo Cabral De VASCONCELLOS; P V SVIDNICKI; Braghini Carolina AYUMI; Melo M B.
2014.
New mutations in the myoc gene in patients with juvenile open-angle glaucoma.
In:
American society of human genetics 64nd annual meeting; 2014; san diego.
Estados Unidos.
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Life Sciences
Neurology
Mônica Barbosa De MELO; Daniela Prescila Dezidério SACCONI; Galina ANANINA; Fábio Endo HIRATA; Priscila Hae Hyun RIM et al.
2013.
Contribution of cfh y402h polymorphism and cfhr3/cfhr1 deletion to age-related macular degeneration in brazil.
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Arvo 2013 annual meeting.
Estados Unidos.
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Life Sciences
Neurology
Monica MELO; Pedro R CRUZ; Galina ANANINA; Sergio A Pereira FILHO; Rodrigo P LIRA et al.
2013.
Analysis of pedf levels and pedf gene promoter polymorphisms (-790t>c; -358g>a) in a cohort of brazilian patients with and without sickle cell retinopathy.
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Asia-arvo 2013.
Índia.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Bruno B L SOUZA; Mariana B L OLIVEIRA; Vital P COSTA; Monica MEIO.
2013.
Asb10 gene variants in primary open angle glaucoma brazilian patients.
In:
Asia-arvo 2013.
Índia.
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Life Sciences
Genetics
Galina ANANINA; Farid MENAA; Marcos André BEZERRA; Aderson S ARAÚJO; Pedro Rodrigues Sousa Da CRUZ et al.
2012.
Copy number variations in a cohort of brazilian sickle cell anemia patients with and without cerebrovascular accident.
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American society of human genetics 62nd annual meeting.
Estados Unidos.
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Health Sciences
Genetics (clinical)
Mônica Barbosa De MELO; Gislene Pereira GIL; Galina ANANINA; Mariana B OLIVEIRA; Márcio José Da SILVA et al.
2012.
Polymorphism in the hmox-1 gene is associated with high levels of hbf in brazilian patients with sickle cell anemia.
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American society of human genetics 62nd annual meeting.
Estados Unidos.
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Life Sciences
Neuroscience (miscellaneous)
Pedro Rodrigues Sousa Da CRUZ; Tânia R ZACCARIOTTO; Fábio Nero MITSUUSHI; Sérgio A Pereira FILHO; Rodrigo P C LIRA et al.
2012.
Soluble icam-1 levels are associated to a protective prognosis in sickle cell retinopathy.
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American society of human genetics 62nd annual meeting.
Estados Unidos.
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Life Sciences
Genetics
Oliveira MB; José Paulo Cabral De VASCONCELLOS; Costa VP; Melo Mônica B.
2012.
Association between il1a; il1b and tnfa polymorphisms and glaucoma in a brazilian population.
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American society of human genetics 62nd annual meeting.
Estados Unidos.
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Life Sciences
Genetics
Hugo F NUNES; Mariana Borges OLIVEIRA; José Paulo Cabral De VASCONCELLOS; Vital P COSTA; Mônica Barbosa MELO.
2012.
Investigation of rs4236601 and rs4977756 snps in a primary open angle glaucoma brazilian population.
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American society of human genetics 62nd annual meeting; 2012; san francisco.
Estados Unidos.
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Health Sciences
Immunology and Allergy
Melo Mônica B; Pedro Rodrigues Sousa Da CRUZ; Zaccarioto TR; Mitsuusci FN; Pereira Filho SA et al.
2012.
Angiopoietin-2 may play a role as protective factor in sickle cell retinopathy.
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Annual meeting of the association for research in vision and ophthalmology (arvo).
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Bibiana A SANTOS; Rodrigo SECOLIN; Fabio R TORRES; Carolina A BRAGHINI et al.
2012.
Investigation of candidate loci for primary open angle glaucoma in a brazilian family through snp array.
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Annual meeting of the association for research in vision and ophthalmology (arvo).
Estados Unidos.
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Life Sciences
Genetics
Fábio E HIRATA; Priscila Hae Hyun RIM; Andréa Mara Simões TORIGOE; Enzo A FULCO; Anderson TAVARES et al.
2011.
Loc387715/arms2 polymorphism analysis in brazilian patients with age-related macular degeneration.
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2011 association for research in vision and ophthalmology annual meeting.
Estados Unidos.
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Health Sciences
Genetics (clinical)
Mônica Barbosa De MELO; Gislene Pereira GIL; Galina ANANINA; Mariana B OLIVEIRA; Márcio José Da SILVA et al.
2011.
Analysis of the polymorphism -930 a/g (rs9932581) in the cyba gene in pediatric patients with sickle cell anemia.
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12th international congress of human genetics/61st annual meeting of the american society of human genetics.
Estados Unidos.
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Health Sciences
Medicine (miscellaneous)
Farid MENAA; Marcos André BEZERRA; Aderson S ARAÚJO; Galina ANANINA; Pedro Rodrigues Sousa Da CRUZ et al.
2011.
Evaluating genomic copy number variations in a brazilian population of adult sickle cell anemia patients with and without stroke complication.
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12th international congress of human genetics/61st annual meeting of the american society of human genetics.
Estados Unidos.
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Life Sciences
Genetics
Braghini CA; José Paulo Cabral De VASCONCELLOS; Stancato D; Silva MJ; Tavares A et al.
2011.
Cyp1b1 as a modifier gene for two brazilian families with juvenile-onset open angle glaucoma harboring the c433r mutation in the myoc gene.
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European human genetics conference 2011.
Holanda.
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Life Sciences
Genetics
Ananina G; José Paulo Cabral De VASCONCELLOS; Vicentini R; Menaa BOUZID; Costa FF et al.
2011.
Genomic variation in a brazilian population.
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12th international congress of human genetics; 61st annual meeting of the american society of human genetics.
Canadá.
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Life Sciences
Genetics
Priscila Hae Hyun RIM; Fábio E HIRATA; Andréa Mara Simões TORIGOE; Luís Alberto MAGNA; Mônica Barbosa De MELO et al.
2010.
Genética e prevenção da cegueira: estudo dos fatores de risco que influenciam o desenvolvimento da degeneração macular relacionada à idade em uma população brasileira.
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Xxii congresso brasileiro de genética médica.
Brasil.
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Life Sciences
Genetics
Carolina Ayumi BRAGHINI; Mônica Barbosa De MELO.
2010.
Avaliação dos genes myoc e cyp1b1 em famílias portadoras de glaucoma primário de ângulo aberto.
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Xviii congresso interno de iniciação científica da unicamp.
Brasil.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Jayter Silva De PAULA; Mariana Borges OLIVEIRA; Renata PELLEGRINO; Gislene Pereira GIL et al.
2010.
Copy number variation analysis of a primary open angle glaucoma brazilian familiy.
In:
2010 association for research in vision and ophthalmology (arvo) annual meeting.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Tanno T; Miranda PMAD; Callefo F; Sartorato EL et al.
2010.
Coexistence of glaucomatous phenotype and mitochondrial mutation in a three generation brazilian family.
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Annual meeting of the association for research in vision and ophthalmology (arvo).
Estados Unidos.
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Life Sciences
Neuroscience (miscellaneous)
Pedro Rodrigues Sousa Da CRUZ; Maria De Fátima SONATI; Fernando Ferreira COSTA; Gislene Pereira GIL; Anderson TAVARES et al.
2009.
Analysis of the role of pedf gene polymorphisms in the sickle cell retinopathy.
In:
55o congresso brasileiro de genética.
Brasil.
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Life Sciences
Neuroscience (miscellaneous)
Pedro Rodrigues Sousa Da CRUZ; Anderson TAVARES; Mônica Barbosa De MELO.
2009.
Análise do papel de polimorfismos nos genes vegf e pedf na retinopatia falciforme.
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Xvii congresso interno de iniciação científica da unicamp.
Brasil.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Carolina Ayumi BRAGHINI; Anderson TAVARES; Sérgio Ricardo Elias Pião JR; Gislene Pereira GIL et al.
2009.
Mutation in the myoc gene; c.1187_1188inscccaga; segregates with juvenile open angle glaucoma in a brazilian family.
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2009 annual meeting of the association for research in vision and ophthalmology (arvo).
Estados Unidos.
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Health Sciences
Infectious Diseases
Mônica Barbosa De MELO; Maurício Della PAOLERA; Cristiano Caixeta UMBELINO; Niro KASAHARA; Mylene Neves ROCHA et al.
2008.
Molecular analysis of the cyp1b1 gene in congenital glaucoma brazilian patients.
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Association for research in vision and ophthalmology (arvo) 2008 annual meeting.
Estados Unidos.
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Life Sciences
Genetics
Niro KASAHARA; Cristiano Caixeta UMBELINO; José Paulo Cabral De VASCONCELLOS; Murilo Resende MELO; Maurício Della PAOLERA et al.
2008.
Mt.1gene promotersingle nucleotide polymorphism in brazilian patients with primary open angle glaucoma.
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Association for research in vision and ophthalmology (arvo) 2008 annual meeting.
Estados Unidos.
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Life Sciences
Genetics
Enyr Saran ARCIERI; Rafael Saran ARCIERI; Emerson Soares De Souza FRANÇA; Fernanda Caroline SOARDI; Fernanda L CALAIS et al.
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Análise molecular do gene pax6 em pacientes com aniridia.
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Xviii congresso brasileiro de prevenção da cegueira e reabilitação visual.
Brasil.
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Life Sciences
Genetics
Alessandro SANTANA; Mauro WAISWOL; Enyr Saran ARCIERI; Flávio RICHETI; José Paulo Cabral De VASCONCELLOS et al.
2008.
Mutation (tyr56stop) in thegamma d-crystallin gene causing autosomal dominant congenital cataract in a brazilian family.
In:
Association for research in vision and ophthalmology (arvo) 2008 annual meeting.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Ricardo REIS; C STEFANI; Anderson TAVARES; Carolina Ayumi BRAGHINI et al.
2008.
Genotype/phenotype correlation in two brazilian families harboring the cys433arg mutation in the myoc gene.
In:
58ª annual meeting of the american society of human genetics (ashg).
Estados Unidos.
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Life Sciences
Developmental Biology
José Paulo Cabral De VASCONCELLOS; Anderson TAVARES; Iscia Teresinha Lopes CENDES; Cláudia Vianna Maurer MORELLI; Rodrigo SECOLIN et al.
2007.
Analysis of candidate loci in primary open angle glaucoma families.
In:
57ª annual meeting of the american society of human genetics (ashg).
Estados Unidos.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Alessandro SANTANA; Mauro WAISWOL; Enyr Saran ARCIERI; Flávio RICHETI et al.
2007.
New mutation in the alpha-a crystallin gene causing autosomal dominant congenital cataract.
In:
Association for research in vision and ophthalmology (arvo) 2007 annual meeting.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Cristiano Caixeta UMBELINO; Maurício Della PAOLERA; Niro KASAHARA; Mylene Neves ROCHA et al.
2007.
Optineurin gene evaluation in primary open angle glaucoma brazilian patients.
In:
Annual meeting of the association for research in vision and ophthalmology (arvo).
Estados Unidos.
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Life Sciences
Genetics
Flavio RICHETI; Renata Maria De NORONHA; R T L WAETGE; Luis Eduardo Procópio CALLIARI; Osías Francisco De SOUZA et al.
2006.
Avaliação dos polimorfismos c-106t e (ac)n no gene alr2 e suscetibilidade ao desenvolvimento de retinopatia diabética em pacientes com diabetes tipo 1.
In:
World ophthalmology congress.
Brasil.
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Life Sciences
Genetics
Cristiano Caixeta UMBELINO; José Paulo Cabral De VASCONCELLOS; Maurício Della PAOLERA; Niro KASAHARA; Geraldo Viecente De ALMEIDA et al.
2006.
Investigação das alterações e50k e t34t no exon 4 do gene optn em pacientes com glaucoma primário de ângulo aberto.
In:
World ophthalmology congress.
Brasil.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Aglair Veridiana CELESTINO; Anderson TAVARES; Cíntia Moura ARCANJOLETO; Bianca KNEIPP et al.
2006.
Analysis of opa1 gene polymorphisms in brazilian patients with primary open angle glaucoma.
In:
Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Life Sciences
Neurology
Mônica Barbosa De MELO; Flávio RICHETI; Renata Maria NORONHA; Ricardo Temudo Lessa WAETGE; Luís Eduardo Procópio CALLIARI et al.
2006.
Ac(n) and c(-106)t polymorphisms of the aldose reductase gene and susceptibility to diabetic retinopathy in brazilian patients with type 1 diabetes mellitus.
In:
Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Health Sciences
Medicine (miscellaneous)
Vânia P A WOBETO; E T ROSIM; Mônica Barbosa De MELO; Ricardo Temudo Lessa WAETGE; Luís Eduardo Procópio CALLIARI et al.
2005.
Polimorfismo da haptoglobina e retinopatia diabética.
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Congresso brasileiro de patologia clínica/ medicina laboratorial.
Brasil.
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Social Sciences & Humanities
Psychology (miscellaneous)
Carlos Alberto LONGUI; Cristiane KOCHI; Mônica Barbosa De MELO; Murilo Rezende MELO; Lilian MARTELO et al.
2005.
Parental origin of x chromosome: influence on height determination in patients with turner syndrome and normal control boys.
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European society for paediatric endocrinology (espe) / 7th joint meeting in collaboration with apeg; appes; jspe and slep.
Estados Unidos.
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Life Sciences
Genetics
Cintia Moura ARCANJOALETO; ANDERSONTAVARES; Aglair CELESTINO; José Paulo Cabral De VASCONCELLOS.
2005.
Avaliação de polimorfismos no gene opa1 em pacientes brasileiros com glaucoma primário de ângulo aberto.
In:
Vii congresso aberto aos estudantes de biologia.
Brasil.
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Life Sciences
Genetics
Wenner CELLA; José Paulo Cabral De VASCONCELLOS; Monica Barbosa De MELO; Bianca KNEIPP; Vital Paulino COSTA.
2005.
Aspectos genéticos da síndrome de axenfeld-rieger: descrição de novas mutações nos genes foxc1 e gja1 em pacientes brasileiros.
In:
Xxxiii congresso brasileiro de oftalmologia.
Brasil.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Monica Barbosa De MELO; Wenner CELLA; Bianca KNEIPP; Mylene Neves ROCHA et al.
2005.
Mutation screening of foxc1 and pitx2 genes in brazilian patients with axenfeld-rieger malformations.
In:
Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Monica Barbosa De MELO; Wener CELLA; Bianca KNEIPP; Mylene Neves ROCHA et al.
2005.
Axenfeld-rieger syndrome: coexistence of mutations in the foxc1 and gja1 genes.
In:
Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Rui Barroso SCHIMITI; Vital Paulino COSTA; Norisvaldo César BRESSANIM; Fernando Ferreira COSTA et al.
2004.
Pro59his: a novel mutation inthe gja1 gene in a brazilian family with oculodentodigitaldysplasia.
In:
Association for research in vision and ophthalmology.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Wener CELLA; Mônica Barbosa De MELO; Bianca KNEIPP; Vital Paulino COSTA.
2004.
Síndrome de axenfeld-rieger: associação à mutação no gene da conexina 43 humana (gja1)?.
In:
Xix reunião anual da federação de sociedades de biologia experimental - fesbe.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Vital Paulino COSTA; Norisvaldo César BRESSANIM; Rui Barroso SCHIMITI; José Paulo Cabral De VASCONCELLOS.
2004.
Nova mutação no gene da conexina 43 (gja1) em uma família com displasia óculo-dento-digital.
In:
Xix reunião anual da federação de sociedades de biologia experimental - fesbe.
Brasil.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Rui Barroso SCHIMITI; Norisvaldo César BRESSANIM; Mônica Barbosa De MELO; Vital Paulino COSTA.
2003.
Descrição de uma família com síndrome de displasia óculo-dento- digital e glaucoma.
In:
Xxxi congresso brasileiro de oftalmologia.
Brasil.
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Health Sciences
Genetics (clinical)
Wenner CELLA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Dulcinéia ALBUQUERQUE; Vital Paulino COSTA.
2003.
Rastreamento de mutações no gene pitx2 em pacientes com anomalia e síndrome de axenfeld-rieger.
In:
Xxxii congresso brasileiro de oftalmologia.
Brasil.
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Life Sciences
Genetics
Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI et al.
2002.
Polymorphism of glutathione s-transferase mu1 (gstm1) gene in multiple myeloma.
In:
7th meeting of the european hematology association.
Itália.
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Health Sciences
Medicine (miscellaneous)
Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Mônica Barbosa De MELO; Irene Lorand METZE; Cármino Antônio De SOUZA et al.
2002.
Predictive role of p53 deletion for short survival in patients with multiple myeloma.
In:
7th meeting of the european hematology association.
Itália.
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Life Sciences
Cancer Research
Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Mônica Barbosa De MELO; Irene Lorand METZE; Cármino Antônio De SOUZA et al.
2002.
P53 gene deletion as a prognostic factor in multiple myeloma.
In:
44th annual meeting of the american society of hematology.
Estados Unidos.
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Health Sciences
Immunology and Allergy
Carmen Silvia Passos LIMA; Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI et al.
2002.
A polymorphism in endostatin; an angiogenesis inhibitor on multiple myeloma.
In:
48o congresso nacional de genética.
Brasil.
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Life Sciences
Genetics
Manoela Marques ORTEGA; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO; Irene Lorand METZE; Fernando Ferreira COSTA et al.
2001.
P53 gene mutations are rare in brazilian patients with multiple myeloma.
In:
47o congresso nacional de genética.
Brasil.
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Life Sciences
Clinical Biochemistry
Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Carmen Sílvia Passos LIMA.
2001.
Glutathione s-transferase m1 and t1 polymorphisms: no influence for the risk of multiple myeloma in brazilian patients.
In:
Xviii congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Health Sciences
Medicine (miscellaneous)
Manoela Marques ORTEGA; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO; Irene Lorand METZE; Fernando Ferreira COSTA et al.
2001.
Low frequency of p53 gene mutations in brazilian patients with multiple myeloma.
In:
Xviii congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Life Sciences
Genetics
Edson SHITARA; Mônica Barbosa De MELO; Fernando Ferreira COSTA.
2001.
Freqüência de mutações do oncogene n-ras; codons 12; 13 em pacientes com mieloma múltiplo.
In:
Xviii congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Simone Bordignon De JORGE; Mônica Barbosa De MELO; Edna Maria KIMURA; Fernando Ferreira COSTA; Maria De Fátima SONATI.
2001.
Optimization of single-strand conformation polymorphism-sscp for screening mutations in fragments of human alpha-globin genes.
In:
Xviii congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Life Sciences
Agricultural and Biological Sciences (miscellaneous)
Mônica Barbosa De MELO; Silvana BORDIN; Adriana Silva Santos DUARTE; André VETTORE; Edson Luís KEMPER et al.
2001.
Molecular characterization of hemoglobin alpha-d chains of geochelone carbonaria and geochelone denticulata lans turtles.
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Xviii congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Health Sciences
Genetics (clinical)
Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; M T TEORI; Fernando Ferreira COSTA et al.
2001.
High frequency of glutathione s-transferase mu1 (gstm1) null genotype in brazilian patients with advanced multiple myeloma.
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43 annual meeting of the american society of hematology.
Estados Unidos.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Rui SCHMITI; Fernando Ferreira COSTA; Vital Paulino COSTA.
2001.
Phenotype/genotype correlation in a family pedigree with the cys433arg mutation in the myoc gene.
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3rd international glaucoma symposium - igs.
República Tcheca.
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Life Sciences
Genetics
Vital Paulino COSTA; José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Rui SCHMITI; Fernando Ferrreira COSTA.
2001.
Phenotype/genotype correlation in a family with poag harboring the cys433arg mutation in the myoc gene.
In:
Xxiii congresso panamericano de oftalmologia.
Argentina.
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Life Sciences
Genetics
Stoilov I; Costa Vital P; José Paulo Cabral De VASCONCELLOS; Melo Mônica B; A J BETINJANE et al.
2001.
Mutation screening of the cyp1b1 gene and phenotype-genotype correlation in primary congenital glaucoma cases from brazil.
In:
Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Health Sciences
Medicine (miscellaneous)
Manoela Marques ORTEGA; Hélvia NASCIMENTO; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Carmen Sílvia Passos LIMA.
2000.
Polimorfismos dos genes mu1 e theta 1 do sistema da glutationa s-transferase em pacientes com mieloma múltiplo.
In:
46º congresso nacional de genética.
Brasil.
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Life Sciences
Genetics
Mônica Barbosa De MELO; José Paulo Cabral De VASCONCELLOS; Vital Paulino COSTA; Rui SCHIMITI; Fernando Ferreira COSTA.
2000.
Estudo da mutação cys433arg em família com glaucoma primário de ângulo aberto.
In:
46º congresso nacional de genética.
Brasil.
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Health Sciences
Genetics (clinical)
Carmen Sílvia Passos LIMA; Valder Roberval ARRUDA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al.
2000.
Increased risk for acute myeloid leukemia in individuals with glutathione s-transferase mu1 (gstm1) and theta (gstt1) gene defects.
In:
28th world congress of the international society of hematology.
Canadá.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Silvana BORDIN; Fernando Lopes ALBERTO; Vanessa G CRESPI; Adriana Silva Santos DUARTE; Daniela Sanchez BASSÈRES et al.
1998.
Dnase i hypersensitive site 3'to the beta globin gene cluster contains a taa insertion specific for beta s-benin haplotype.
In:
Ish-eha combined haematology congress.
Holanda.
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Life Sciences
Genetics
Daniela Sanchez BASSÈRES; Dilmara Lopes VICENTIM; Silvana BORDIN; Mônica Barbosa De MELO; Fernando Ferreira COSTA et al.
1998.
Beta-spectrin santa barbara: a novel frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis.
In:
Ish-eha combined haematology congress.
Holanda.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Silvana BORDIN; Daniela Sanchez BASSÈRES; Sara Teresinha Ollala SAAD; Irene Lorand METZE et al.
1998.
Mutações no gene p53 em pacientes com leucemia mielóide aguda.
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Vii international congress of the world apheresis association - waa e xxiii congresso brasileiro de hematologia e hemoterapia (hemo 98).
Brasil.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Vital Paulino COSTA; Newton Kara JOSÉ; Fernando Ferreira COSTA.
1998.
Mutações no gene tigr (trabecular meshwork-induced glucocorticoid response protein) em uma população com glaucoma juvenil e glaucoma primário de ângulo aberto.
In:
Xiii congresso brasileiro de prevenção da cegueira e reabilitação visual.
Brasil.
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Life Sciences
Genetics
José Paulo Cabral De VASCONCELLOS; Mônica Barbosa De MELO; Vital Paulino COSTA; Fernando Ferreira COSTA; Silvana BORDIN et al.
1998.
Mutations in the tigr gene in a brazilian population with juvenile glaucoma.
In:
Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Silvana BORDIN; Vanessa G CRESPI; Daniela Sanchez BASSÈRES; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO et al.
1997.
Different rates of recombination among polymorphic short tandem repeats of the beta-globin gene cluster in beta s chromosomes.
In:
Xxxix annual meeting of the american society of hematology.
Estados Unidos.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Valder Roberval ARRUDA; Carmen Sílvia Passos LIMA; Carlos Roberto Escrivão GRIGNOLI; Mônica Barbosa De MELO; Irene Lorand METZE et al.
1997.
High prevalence of the glutathione s-transferase (gst) null genotype in acute myeloblastic leukemia.
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Xxxix annual meeting of the american society of hematology.
Estados Unidos.
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Life Sciences
Genetics
Daniela Sanchez BASSÈRES; Alessandra C TAVARES; Silvana BORDIN; Dilmara Lopes VICENTIM; Mônica Barbosa De MELO et al.
1997.
Novel beta-spectrin variants associated with hereditary spherocytosis in brazil.
In:
Xxxix annual meeting of the american society of hematology.
Estados Unidos.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Silvana BORDIN; Vanessa G CRESPI; Daniela Sanchez BASSÈRES; Adriana Silva Santos DUARTE; Mônica Barbosa De MELO et al.
1997.
Caracterização molecular das regiões polimórficas de repetição do complexo da globina beta por pcr-sscp.
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Xvi congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Life Sciences
Genetics
Fernando Ferreira COSTA; Mônica Barbosa De MELO; Sara Teresinha Ollala SAAD; Nilofer Nina AHMAD.
1997.
P53 and rb1 gene mutations in brazilian patients with acute myeloid leukemia.
In:
Xiv meeting of the international society of haematology - european and african division.
Suécia.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Sara Teresinha Ollala SAAD; Nilofer Nina AHMAD; Fernando Ferreira COSTA.
1997.
Mutações nos genes supressores de tumores p53 e rb1 em pacientes com leucemia mielóide aguda (lma).
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Xii reunião anual da federação de sociedades de biologia experimental - fesbe.
Brasil.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Fernando Ferreira COSTA; Nilofer Nina AHMAD.
1996.
Conformation sensitive gel electrophoresis (csge) for rapid screening of the retinoblastoma (rb1) gene.
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Annual meeting of the association for research in vision and ophthalmology.
Estados Unidos.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Nilofer Nina AHMAD; Jerry A SHIELDS; Larry A DONOSO.
1996.
Conformation sensitive gel electrophoresis (csge) for rapid detection of mutations in the rb1 gene.
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48th annual conference - wills eye hospital.
Estados Unidos.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Carmen Sílvia Passos LIMA; Irene Lorand METZE; Sara Teresinha Ollala SAAD; Fernando Ferreira COSTA.
1994.
Mutações no proto-oncogene n-ras em pacientes com leucemia mielóide aguda (lma) estão associadas a mau prognóstico.
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Xxi congresso brasileiro de hematologia e hemoterapia.
Brasil.
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Health Sciences
Genetics (clinical)
N A BERGAMO; Claudia S RAINHO; Mônica Barbosa De MELO; A MEDEIROS; Sílvia R ROGATTO.
1994.
Alterações citogenéticas e do oncogene k-ras em leiomiomas uterinos.
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Ii congresso latinoamericano de genética.
México.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Mônica Vannucci NUNES; Mônica Barbosa De MELO; Fernando Ferreira COSTA; Marileila Varella GARCIA.
1994.
Método simples de extração de dna a partir de preparações cromossômicas para citogenética.
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Ix reunião da federação de sociedades de biologia experimental - fesbe.
Brasil.
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Life Sciences
Genetics
Mônica Barbosa De MELO; Irene Lorand METZE; Fernando Ferreira COSTA.
1992.
N-ras mutations in patients with acute leukemia.
In:
Xx congresso brasileiro de hematologia.
Brasil.
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Life Sciences
Neurology
Mônica Barbosa De MELO; Sandra Cecília Botelho COSTA; Irene Lorand METZE; Fernando Ferreira COSTA.
1992.
Mutações do oncogene n-ras em pacientes com leucemia aguda.
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Vii reunião anual da federação de sociedades de biologia experimental.
Brasil.
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Health Sciences
Medicine (miscellaneous)
Mônica Barbosa De MELO; Tereza Sueko Ide SALES; Irene Lorand METZE; Fernando Ferreira COSTA.
1991.
Dna isolado de esfregaços usados na rotina hematológica pode ser utilizado para detecção de alterações genéticas moleculares pela reação em cadeia da polimerase (pcr).
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Xiii congresso nacional do colégio brasileiro de hematologia.
Brasil.
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Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Mônica Barbosa De MELO; Tereza Sueko Ide SALES; Irene Lorand METZE; Fernando Ferreira COSTA.
1991.
Dna isolado de esfregaços usados na rotina hematológica pode ser utilizado para detecção de alterações genéticas moleculares pela pcr.
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Xxxvii congresso nacional de genética.
Brasil.
