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Refinado por: assunto: Mutação Genética remover
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1
Novel CYP3A4 gene mutations contribution to the pharmacogenetic profile of hypercholesterolemic individuals treated with atorvastin
Novel CYP3A4 gene mutations contribution to the pharmacogenetic profile of hypercholesterolemic individuals treated with atorvastin
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Novel CYP3A4 gene mutations contribution to the pharmacogenetic profile of hypercholesterolemic individuals treated with atorvastin

S. Cavali I Moretti; L Matsumoto; L Salazar; M Hiroyuki; Neusa Assumpta Forti; J Diament; M Chiara; A Faludi; R Dominguez; Congress of the European Atherosclerosis Society (74. 2004 Seville , Spain)

Atherosclerosis Amsterdam v. 5, n. 1, p. 112, res. M.484, 2004

Amsterdam 2004

Item não circula. Consulte sua biblioteca.(Acessar)

2
Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia
Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia

Luís Antônio Salazar Mario Hiroyuki Hirata; Rosario Dominguez Crespo Hirata

Clinical Chemistry and Laboratory Medicine Berlin v. 40, n. 5, p. 441-445, 2002

Berlin 2002

Item não circula. Consulte sua biblioteca.(Acessar)

3
Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia
Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia

Luís Antônio Salazar Mario Hiroyuki Hirata; Rosario Dominguez Crespo Hirata

Clinical Chemistry and Laboratory Medicine Berlin v. 40, n. 5, p. 441-445, 2002

Berlin 2002

Item não circula. Consulte sua biblioteca.(Acessar)

4
Molecular basis of familial hypercholesterolemia in Brazil Identification of nine novel LDLR gene mutations
Molecular basis of familial hypercholesterolemia in Brazil Identification of nine novel LDLR gene mutations
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Molecular basis of familial hypercholesterolemia in Brazil Identification of nine novel LDLR gene mutations

Luís Antônio Salazar Mario Hiroyuki Hirata; Selma Andrea Cavalli; Edna Regina Nakandakare; Neusa Assumpta Forti; Jayme Diament; S Giannini; Marcelo Chiara Bertolami; Rosario Dominguez Crespo Hirata; Congress of the European Atherosclerosis Society (73. 2002 Salzburg)

Atherosclerosis Clare v. 3/2 , supls., p. 200 res. 621, 2002

Clare 2002

Item não circula. Consulte sua biblioteca.(Acessar)

5
Genetic characterization of patients with familial hypercholesterolemia from Brazil a broad spectrum of mutations in the LDLR gene
Genetic characterization of patients with familial hypercholesterolemia from Brazil a broad spectrum of mutations in the LDLR gene
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Genetic characterization of patients with familial hypercholesterolemia from Brazil a broad spectrum of mutations in the LDLR gene

Luís Antônio Salazar Mario Hiroyuki Hirata; Selma Andréa Cavalli; Edna Regina Nakandakare; Neusa Assumpta Forti; Jayme Diament; Marcelo Chiara Bertolami; Rosario Dominguez Crespo Hirata; Semana Farmacêutica de Ciência e Tecnologia da FCF-USP (7. 2002 São Paulo); Seminário de Pós-Graduação (17. 2002 São Paulo); Reunião de Iniciação Científica (10. 2002 São Paulo); Semana Universitária Paulista de Farmácia e Bioquímica (37. 2002 São Paulo)

Revista Brasileira de Ciências Farmacêuticas São Paulo v. 38, supl. 1 , p. 21 res. ACT38, 2002

São Paulo Faculdade de Ciências Farmacêuticas - USP 2002

Item não circula. Consulte sua biblioteca.(Acessar)

6
Corrigendum to NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss
Corrigendum to NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss
Material Type:
Artigo 		Adicionar ao Meu Espaço

Corrigendum to NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

Rodrigo Salazar da Silva Vitor Lima Goes Dantas; Leandro Ucela Alves; Ana Carla Batissoco; Jeanne Oiticica; Elizabeth A Lawrence; Abdelwahab Kawafi; Yishi Yang; Fernanda Stávale Nicastro; Beatriz Caiuby Novaes; Chrissy Hammond; Érika Kague; Regina Celia Mingroni Netto

Human Molecular Genetics Oxford v. 31, n. 1, p156, Jan. 2022

Oxford 2022

Item não circula. Consulte sua biblioteca.(Acessar)

7
NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss
NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss
Material Type:
Artigo 		Adicionar ao Meu Espaço

NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

Rodrigo Salazar da Silva Vitor Lima Goes Dantas; Leandro Ucela Alves; Ana Carla Batissoco; Jeanne Oiticica; Elizabeth A Lawrence; Abdelwahab Kawafi; Yishi Yang; Fernanda Stávale Nicastro; Beatriz Caiuby Novaes; Chrissy Hammond; Érika Kague; Regina Celia Mingroni Netto

Human Molecular Genetics Oxford, United Kingdom v.29, n.2, p.3691–3705, 2020

Oxford, United Kingdom 2020

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Salazar, L
  2. Hirata, M
  3. Hirata, R
  4. Diament, J
  5. Forti, N

Neste Assunto:

  1. Hipercolesterolemia
  2. Bioquímica
  3. Surdez
  4. Hipercolesterolemia (Avaliação)
  5. Doenças Cardiovasculares (Avaliação)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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