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Gene Mutations and Polymorphisms of TP53 and FHIT in Chronic Esophagitis and Esophageal Carcinoma

Fedossi Silveira, Aparecida Perpetuo; Manoel-Caetano, Fernanda da Silva; Aoki, Sergio; Tomonari Yamasaki, Lilian Hiromi; Rahal, Paula; Silva, Ana Elizabete (Int Inst Anticancer Research, 2014)

Band 3tambaú: A De Novo Mutation In The Ae1 Gene Associated With Hereditary Spherocytosis. Implications For Anion Exchange And Insertion Into The Red Blood Cell Membrane.

Lima, Paulo Roberto Moura; Baratti, Mariana Ozello; Chiattone, Maria Lúcia; Costa, Fernando Ferreira; Saad, Sara Teresinha Olalla (2005)

Avaliação das características demográficas, clínicas e polimorfismo genético como fatores de risco para o prolapso pélvico em mulheres brasileiras

Martins, Karina de Falco (Universidade Federal de São Paulo (UNIFESP), 2010-05-26)

Objective: To verify the possible association between the presence of the polymorphism in exon 31 of COL3A1 gene and the occurrence of genital prolapse in a sample of the population. Methods: case-control study involving ...

Eleven Novel Mutations In The Factor Viii Gene From Brazilian Hemophilia A Patients.

Arruda, V R; Pieneman, W C; Reitsma, P H; Deutz-Terlouw, P P; Annichino-Bizzacchi, J M; Briët, E; Costa, F F (1995)

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Cuperman, Thais; Fernandes, Stephanie A; Lourenço, Naila C; Yamamoto, Lydia U; Silva, Helga C; Pavanello, Rita C; Yamamoto, Guilherme L; Zatz, Mayana; Oliveira, Acary S; Vainzof, Mariz (2014-08-01)

Abstract Background Central core disease is a congenital myopathy, characterized by presence of central core-like areas in muscle fibers. Patients have ...

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Cuperman, Thais; Fernandes, Stephanie A; Lourenço, Naila C; Yamamoto, Lydia U; Silva, Helga C; Pavanello, Rita C; Yamamoto, Guilherme L; Zatz, Mayana; Oliveira, Acary S; Vainzof, Mariz (2014-08-01)

Abstract Background Central core disease is a congenital myopathy, characterized by presence of central core-like areas in muscle fibers. Patients have ...

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Gene Mutations and Polymorphisms of TP53 and FHIT in Chronic Esophagitis and Esophageal Carcinoma

Band 3tambaú: A De Novo Mutation In The Ae1 Gene Associated With Hereditary Spherocytosis. Implications For Anion Exchange And Insertion Into The Red Blood Cell Membrane.

Avaliação das características demográficas, clínicas e polimorfismo genético como fatores de risco para o prolapso pélvico em mulheres brasileiras

Eleven Novel Mutations In The Factor Viii Gene From Brazilian Hemophilia A Patients.

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Lack Of Mutations Of Exon 2 Of The Men1 Gene In Endocrine And Nonendocrine Sporadic Tumors.

Restriction fragment length polymorphism (RFLP) in Exon 2 of the BoLA-DRB3 gene in South American cattle

Detecção de mutações no gene da anquirina eritroide em pacientes portadores de esferocitose hereditaria

Myostatin (GDF8) single nucleotide polymorphisms in Nellore cattle

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Gene Mutations and Polymorphisms of TP53 and FHIT in Chronic Esophagitis and Esophageal Carcinoma

Band 3tambaú: A De Novo Mutation In The Ae1 Gene Associated With Hereditary Spherocytosis. Implications For Anion Exchange And Insertion Into The Red Blood Cell Membrane.

Avaliação das características demográficas, clínicas e polimorfismo genético como fatores de risco para o prolapso pélvico em mulheres brasileiras

Eleven Novel Mutations In The Factor Viii Gene From Brazilian Hemophilia A Patients.

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report

Lack Of Mutations Of Exon 2 Of The Men1 Gene In Endocrine And Nonendocrine Sporadic Tumors.

Restriction fragment length polymorphism (RFLP) in Exon 2 of the BoLA-DRB3 gene in South American cattle

Detecção de mutações no gene da anquirina eritroide em pacientes portadores de esferocitose hereditaria

Myostatin (GDF8) single nucleotide polymorphisms in Nellore cattle