المؤلفون: Fernanda Bueno Barbosa, Milena Simioni, Cláudia Emília Vieira Wiezel, Fábio Rossi Torres, Miriam Coelho Molck, Melvin M Bonilla, Tânia Kawasaki de Araujo, Eduardo Antônio Donadi, Vera Lúcia Gil-da-Silva-Lopes, Bernardo Lemos, Aguinaldo Luiz Simões

المصدر: PLoS ONE, Vol 13, Iss 11, p e0206683 (2018)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/03becdc2e13043aba5cf02ae137b9926

المؤلفون: Cláudia Emília Vieira Wiezel, Maria do Carmo Tomitão Canas, Aguinaldo Luiz Simões

المصدر: Genetics and Molecular Biology, Vol 26, Iss 2, Pp 115-119 (2003)

مصطلحات موضوعية: segregation distortion, Spinocerebellar ataxia type 1, Machado-Joseph disease, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572003000200002; https://doaj.org/toc/1415-4757; https://doaj.org/toc/1678-4685

URL الوصول: https://doaj.org/article/54300abe36e443aead5befab799e4222

المؤلفون: Luzitano Brandão Ferreira, Celso Teixeira Mendes-Junior, Cláudia Emília Vieira Wiezel, Marcelo Rizzatti Luizon, Aguinaldo Luiz Simões

المصدر: Genetics and Molecular Biology, Vol 29, Iss 4, Pp 605-607 (2006)

مصطلحات موضوعية: Brazil, Mulatto, White, Y-STR, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000400004; https://doaj.org/toc/1415-4757; https://doaj.org/toc/1678-4685

URL الوصول: https://doaj.org/article/3c52503941bb44fe844a74b60fe97f22

المؤلفون: Maria Luisa de Barros Rodrigues, Juliet Figueiredo Gonçalves Maciel, Cláudia Emília Vieira Wiezel, Igor Caetano Dias Alcarás, Ana Maria Barbosa Pessotti, Aguinaldo Luiz Simões

المصدر: Genética na Escola. 17:139-149

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3344802813b08ca90033088822ab63ad
https://doi.org/10.55838/1980-3540.ge.2022.435

المؤلفون: Fernanda Fernandes Souza, Juliana Doblas Massaro, Ana de Lourdes Candolo Martinelli, Andreza Correa Teixeira, Aguinaldo Luiz Simões, Wagner Narciso de Campos, Cláudia Emília Vieira Wiezel, Celso T. Mendes-Junior, Eduardo Luiz Rachid Cançado, Eduardo Antônio Donadi

المصدر: World Journal of Hepatology

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Hepatocellular carcinoma, Hfe gene, digestive system, 03 medical and health sciences, 0302 clinical medicine, medicine, Allele, Alleles, Genetics, Hepatology, business.industry, digestive, oral, and skin physiology, Haplotype, nutritional and metabolic diseases, Hepatitis C, Case Control Study, medicine.disease, Hemochromatosis hereditary, Haplotypes, 030220 oncology & carcinogenesis, Hereditary hemochromatosis, 030211 gastroenterology & hepatology, HFE gene, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ae8aeb25efdf32f2b221e691a2b8a97
https://doi.org/10.4254/wjh.v11.i2.186

المؤلفون: C. C. F. Andrade, Mateus Spinelli da Silva, Lídia Renata Zanão, Leonardo Arduino Marano, Erick C. Castelli, N. C. A. Fracasso, Edilene Santos de Andrade, Celso T. Mendes-Junior, Aguinaldo Luiz Simões, Cláudia Emília Vieira Wiezel, Eduardo Antônio Donadi

المساهمون: Universidade de São Paulo (USP), Universidade Estadual Paulista (Unesp)

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP

مصطلحات موضوعية: 0301 basic medicine, SLC45A2, Tyrosinase, Single-nucleotide polymorphism, Skin Pigmentation, Biology, Melanosis, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Human Genome Project, SNP, Humans, 030216 legal & forensic medicine, OLHO, Allele, 1000 Genomes Project, Hair Color, Gene, Alleles, Genetics, Eye Color, Pigmentation, Haplotype, Issues, ethics and legal aspects, 030104 developmental biology, Haplotypes, biology.protein, sense organs, Polymorphism, Restriction Fragment Length, Brazil, SNPs

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::889d627037b74d8b4746e43b14f26b45

المؤلفون: Marcelo R. Luizon, Aguinaldo Luiz Simões, Cláudia Emília Vieira Wiezel, Sandra Mara Bispo Sousa, Yara Costa Netto Muniz, Celso T. Mendes-Junior, Lenize M.W. Santos

المصدر: American Journal of Human Biology. 25:313-317

مصطلحات موضوعية: education.field_of_study, Amazon rainforest, Genetic genealogy, Amazonian, Haplotype, Population, Zoology, Analysis of molecular variance, Geography, Anthropology, Genetics, Y linkage, Microsatellite, Anatomy, education, Ecology, Evolution, Behavior and Systematics, Demography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::39cc571631ac5297a8fb57c9c949c1aa
https://doi.org/10.1002/ajhb.22361

المؤلفون: Aguinaldo Luiz Simões, Luzitano Brandão Ferreira, Cláudia Emília Vieira Wiezel, Yara Costa Netto Muniz, Celso T. Mendes-Junior

المصدر: Annals of Human Biology. 35:104-111

مصطلحات موضوعية: Genetic Markers, Aging, Urban Population, Physiology, Epidemiology, Black People, Pilot Projects, White People, Gene Frequency, Population Groups, Genetic variation, Ethnicity, Genetics, Tandem Repeat Sequence, Humans, Allele frequency, Afro brazilians, Public Health, Environmental and Occupational Health, Genetic Variation, Genomics, Phenotype, Geography, Tandem Repeat Sequences, Genetic marker, Indians, North American, Str loci, Brazil, Demography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70b184663d4dd3dbadd89bf29e361483
https://doi.org/10.1080/03014460701782256

المؤلفون: Sandra Mara Bispo Sousa, Ana Lúcia Pimentel, Aguinaldo Luiz Simões, Cláudia Emília Vieira Wiezel, Marcelo R. Luizon, Luzitano Brandão Ferreira, Maria Izabel O. Heckmann, Maria do Carmo Tomitão Canas, Yara Costa Netto Muniz, Celso T. Mendes-Junior

المصدر: Journal of Forensic Sciences. 52:495-497

مصطلحات موضوعية: Geography, Haplotype, Genetics, Tandem Repeat Sequence, Y chromosome, Archaeology, Genealogy, Pathology and Forensic Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0c10b787e5f0ac8221f75c556d07ba24
https://doi.org/10.1111/j.1556-4029.2006.00372.x

المؤلفون: Yara Costa Netto Muniz, Marcelo R. Luizon, Aguinaldo Luiz Simões, Doralina Guimarães Brum, Cristiane Franklin Rocha, Elizabeth Regina Comini-Frota, Celso T. Mendes-Junior, Enedina Maria Lobato de Oliveira, Marco Aurélio Lana-Peixoto, Eduardo Antônio Donadi, Damacio Ramón Kaimen-Maciel, Roberta Martins da Silva Costa, Denis Bernardi Bichuetti, Alberto Alan Gabbai, Cláudia Emília Vieira Wiezel, Denise Sisterolli Diniz, Amilton Antunes Barreira, Maria Lucia Brito, Antonio Carlos dos Santos

المساهمون: Universidade de São Paulo (USP), Universidade Estadual Paulista (Unesp), Universidade Federal de Minas Gerais (UFMG), Hospital da Restauração, Universidade Federal de São Paulo (UNIFESP), Universidade Federal de Goiás (UFG), Universidade Estadual de Londrina (UEL)

المصدر: PLoS ONE, Vol 8, Iss 3, p e58925 (2013)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
PLoS ONE

مصطلحات موضوعية: Male, Pediatrics, Epidemiology, genotype, Prevalence, myelooptic neuropathy, multiple sclerosis, population genetic parameters, Gene Frequency, single nucleotide polymorphism, Genotype, Ethnicity, indel mutation, African American, European American, Genetics, Multidisciplinary, adult, Neuromyelitis Optica, Middle Aged, female, Neurology, Genetic Epidemiology, American Indian, Medicine, Female, Brazil, gene insertion, Research Article, Adult, Genetic Markers, medicine.medical_specialty, ESCLEROSE MÚLTIPLA (GENÉTICA), Multiple Sclerosis, bone marrow, Genetic genealogy, Science, Single-nucleotide polymorphism, Ancestry-informative marker, ancestry informative marker, gene frequency, Biology, Autoimmune Diseases, Young Adult, male, geographic distribution, medicine, Humans, controlled study, human, genealogy, Allele frequency, Genetic Association Studies, Neuromyelitis optica, Population Biology, Multiple sclerosis, high risk population, Human Genetics, medicine.disease, Demyelinating Disorders, major clinical study, human tissue, Biomarker Epidemiology, plesiomorphy, Clinical Immunology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1caea26a2b9351e5163b741b35f91cde
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23527051/?tool=EBI

المؤلفون: Eduardo Magalhães Rego, L. C. O. de Oliveira, Juliana Doblas Massaro, Cláudia Emília Vieira Wiezel, Yara Costa Netto Muniz, Celso T. Mendes-Junior, Aguinaldo Luiz Simões

المصدر: Haemophilia.

مصطلحات موضوعية: Genetics, education.field_of_study, Linkage disequilibrium, Population, Haemophilia A, Haplotype, Hematology, General Medicine, Biology, medicine.disease, Haemophilia, Genetic marker, IKBKG, medicine, Microsatellite, education, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8f170e87d66843ae7a2b7a8bafda896a
https://doi.org/10.1111/j.1365-2516.2011.02592.x

المؤلفون: Luzitano Brandão Ferreira, Sandra Mara Bispo Sousa, Aguinaldo Luiz Simões, Dulce Maria Sucena da Rocha, Maria de Nazaré Klautau-Guimarães, Cláudia Emília Vieira Wiezel, G. G. B. L. Ribeiro, Maria do Carmo Tomitão Canas, Juliana Nardelli-Costa, Reginaldo Ramos De Lima, Silviene Fabiana de Oliveira

المصدر: American journal of human biology : the official journal of the Human Biology Council. 21(3)

مصطلحات موضوعية: Male, media_common.quotation_subject, Ethnic group, Black People, Polymorphism, Single Nucleotide, White People, Gene flow, Gene Frequency, Genetics, Hum, Ethnicity, Humans, Ecology, Evolution, Behavior and Systematics, media_common, Chromosomes, Human, Y, Constitution, Haplotype, Founder Effect, Geography, Haplotypes, Anthropology, Microsatellite, Anatomy, geographic locations, Brazil, Demography, Microsatellite Repeats

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::689fc881d7e7a4dc473c057f5e5d2ce2
https://pubmed.ncbi.nlm.nih.gov/19189414

المؤلفون: Cláudia Emília Vieira Wiezel, J. A. C Scuoteguazza, Aguinaldo Luiz Simões, Celso T. Mendes-Junior, R. C Miziara, Reinaldo Azoubel

المصدر: International Journal of Morphology. 26

مصطلحات موضوعية: Gynecology, Dental anomalies, medicine.medical_specialty, business.industry, Medicine, Brazilian population, Anatomy, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3bcb5bb83fc57df4273c355dbc997883
https://doi.org/10.4067/s0717-95022008000200025

المؤلفون: Celso Teixeira Mendes, Luzitano Brandão Ferreira, Cláudia Emília Vieira Wiezel, Aguinaldo Luiz Simões, Marcelo R. Luizon

المصدر: American journal of human biology : the official journal of the Human Biology Council. 18(5)

مصطلحات موضوعية: Male, education.field_of_study, Population, Quantitative Trait Loci, Racial Groups, UPGMA, Sample (statistics), Biology, Genetics, Population, Tandem Repeat Sequences, Anthropology, Genetics, Hum, Humans, Brazilian population, Female, Anatomy, Allele, education, Ecology, Evolution, Behavior and Systematics, Brazil, Arithmetic mean, Demography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91ed3bb18c22982787ae395c649525e5
https://pubmed.ncbi.nlm.nih.gov/16917899

المؤلفون: Cláudia Emília Vieira Wiezel, Aguinaldo Luiz Simões, Luzitano Brandão Ferreira, Celso T. Mendes-Junior, Marcelo R. Luizon

المصدر: Genetics and Molecular Biology v.29 n.4 2006
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 29, Iss 4, Pp 605-607 (2006)
Genetics and Molecular Biology, Volume: 29, Issue: 4, Pages: 605-607, Published: 2006

مصطلحات موضوعية: Genetics, lcsh:QH426-470, Haplotype, Ethnic group, White, Biology, White (mutation), lcsh:Genetics, Mulatto, Microsatellite, Y-STR, Brazilian population, Molecular Biology, Allele frequency, Historical record, Brazil, Demography

وصف الملف: text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d646737d069ef28f2b1c493642dedf9
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000400004

المؤلفون: N. C. A. Fracasso, C. C. F. Andrade, Lídia Renata Zanão, M. S. Silva, Aguinaldo Luiz Simões, Edilene Santos de Andrade, Eduardo Antônio Donadi, Celso T. Mendes-Junior, Cláudia Emília Vieira Wiezel, Leonardo Arduino Marano

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

مصطلحات موضوعية: Genetics, SLC45A2, MELANINAS, Tyrosinase, Single-nucleotide polymorphism, Biology, Pathology and Forensic Medicine, Genotype, biology.protein, SNP, sense organs, Allele, Gene, Melanosome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::224f1a8dd10e82c047a39d5be4378a49
https://doi.org/10.1016/j.fsigss.2013.10.174

المؤلفون: Aguinaldo Luiz Simões, Maria do Carmo Tomitão Canas, Cláudia Emília Vieira Wiezel

المصدر: Genetics and Molecular Biology, Volume: 26, Issue: 2, Pages: 115-119, Published: 2003
Genetics and Molecular Biology, Vol 26, Iss 2, Pp 115-119 (2003)
Genetics and Molecular Biology v.26 n.2 2003
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG

مصطلحات موضوعية: Genetics, Spinocerebellar Ataxia Type 1, education.field_of_study, MJD - Machado-Joseph disease, congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, Machado-Joseph disease, Population, Locus (genetics), Biology, lcsh:Genetics, Dynamic mutation, Spinocerebellar ataxia type 1, segregation distortion, education, Trinucleotide repeat expansion, Molecular Biology, Gene, Allele frequency

وصف الملف: text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11a2be251eff174e1184fef81078117a
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572003000200002&lng=en&tlng=en

المؤلفون: Nalu T. A. Peres, Eduardo Antônio Donadi, N. M. M. Rossi, Celso T. Mendes-Junior, Erick C. Castelli, Cláudia Emília Vieira Wiezel, Aguinaldo Luiz Simões

المصدر: Tissue Antigens. 70:349-350

مصطلحات موضوعية: Molecular Sequence Data, Population, Immunology, Fixed allele, Human leukocyte antigen, Biology, Polymorphism, Single Nucleotide, Biochemistry, HLA Antigens, HLA-G, Genetics, Humans, Immunology and Allergy, Allele, Transversion, Allele frequency, Alleles, HLA-G Antigens, Base Sequence, Histocompatibility Antigens Class I, General Medicine, C957T, Null allele, Molecular biology, Brazil

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b54b212272cd021ce025f2f6573f83eb
https://doi.org/10.1111/j.1399-0039.2007.00902.x

المؤلفون: Cláudia Emília Vieira Wiezel, Geraldo Aleixo da Silva Passos Júnior, Renata Camacho Miziara, Aguinaldo Luiz Simões

المصدر: Revista Brasileira Multidisciplinar-ReBraM; v. 11 n. 1: janeiro/junho; 213-221
Revista Brasileira Multidisciplinar
Universidade de Araraquara (UNIARA)
instacron:UNIARA

مصطلحات موضوعية: Distrofia Miotônica, Computer Networks and Communications, Hardware and Architecture, Expansão da Repetição, Distúrbio de Segregação, Software

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85a50f25609067282dfd647c3d61bacd
https://doi.org/10.25061/2527-2675/rebram/2007.v11i1.242