skip to main content
Idioma:
Mostrar Somente
Refinado por: autor: Passos-Bueno, M remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Global analysis of gene expression in inherited human craniosinostosis
Global analysis of gene expression in inherited human craniosinostosis
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Global analysis of gene expression in inherited human craniosinostosis

T. S. Zorick A. Y Fernandes; P Turma; Hamilton Matsushita; Silvio Antonio Zanini; A Palhares; Maria Rita Passos-Bueno; Annual Meeting of the American Society of Human Genetics (51. 2001 San Diego)

American Journal of Human Genetics Chicago v. 69, n. 4, suppl., p. 454, oct. 2001

Chicago 2001

Item não circula. Consulte sua biblioteca.(Acessar)

2
Estudo funcional do colágeno tipo XVIII
Estudo funcional do colágeno tipo XVIII
Material Type:
Tese de Doutorado 		Adicionar ao Meu Espaço

Estudo funcional do colágeno tipo XVIII

Oscar Takeo Suzuki Maria Rita Passos-Bueno

2006

Localização: IB - Instituto de Biociências    (D-1219 )(Acessar)

3
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Further evidence for a fourth gene causing X-linked pure spastic paraplegia

A. Starling P Rocco; F Cambi; G. M Hobson; Maria Rita Passos-Bueno; Mayana Zatz

American Journal of Medical Genetics v. 111, p. 152-156, 2002

New York 2002

Item não circula. Consulte sua biblioteca.(Acessar)

4
RAB23 mutations in carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity
RAB23 mutations in carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity
Material Type:
Artigo 		Adicionar ao Meu Espaço

RAB23 mutations in carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity

Dagan Jenkins Dominik Seelow; Fernanda Sarquis Jehee; Chad A Perlyn; Luís Garcia Alonso NAC; Daniela Franco Bueno; Dian Donnai; Dragana Josifiova; Irene M. J Mathijssen; Jenny E. V Morton; Karen Helene Orstavik; Elizabeth Sweeney; Steven A Wall; Jeffrey L Marsh; Peter Nürnberg; Maria Rita Passos-Bueno; Andrew O. M Wilkie

American Journal of Human Genetics v. 80, n. 6, p. 1162-1170, jun. 2007

Baltimore 2007

Item não circula. Consulte sua biblioteca.(Acessar)

5
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Further evidence for a fourth gene causing X-linked pure spastic paraplegia

A. Starling P Rocco; F Cambi; G. M Hobson; Maria Rita Passos-Bueno; Mayana Zatz

American Journal of Medical Genetics v. 111, p. 152-156, 2002

New York 2002

Item não circula. Consulte sua biblioteca.(Acessar)

6
RAB23 mutations in carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity
RAB23 mutations in carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity
Material Type:
Artigo 		Adicionar ao Meu Espaço

RAB23 mutations in carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity

Dagan Jenkins Dominik Seelow; Fernanda Sarquis Jehee; Chad A Perlyn; Luís Garcia Alonso NAC; Daniela Franco Bueno; Dian Donnai; Dragana Josifiova; Irene M. J Mathijssen; Jenny E. V Morton; Karen Helene Orstavik; Elizabeth Sweeney; Steven A Wall; Jeffrey L Marsh; Peter Nürnberg; Maria Rita Passos-Bueno; Andrew O. M Wilkie

American Journal of Human Genetics v. 80, n. 6, p. 1162-1170, jun. 2007

Baltimore 2007

Item não circula. Consulte sua biblioteca.(Acessar)

7
A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

R. D. Fanganiello V. E Kimonis; R Nitrini; C. C Côrte; Maria Rita Passos-Bueno

Brazilian Journal of Medical and Biological Research Ribeirao Preto, SP v. 44, n. 4, p. 374-380, 2011

Ribeirao Preto, SP 2011

Localização: FM - Fac. Medicina    (BCSEP 020 2011 )(Acessar)

8
A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

R. D. Fanganiello V. E Kimonis; R Nitrini; C. C Côrte; Maria Rita Passos-Bueno

Brazilian Journal of Medical and Biological Research Ribeirao Preto, SP v. 44, n. 4, p. 374-380, 2011

Ribeirao Preto, SP 2011

Localização: FM - Fac. Medicina    (BCSEP 020 2011 )(Acessar)

9
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population
Material Type:
Artigo 		Adicionar ao Meu Espaço

IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population

Luciano A. Brito Camila F. S Bassi; Cibele Masotti; Carolina Malcher; Kátia M Rocha; David Schlesinger; Daniela F Bueno; Lucas A Cruz; Ligia K Barbara; Débora R Bertola; Diogo Meyer; Diogo Franco; Nivaldo Alonso; Maria Rita Passos-Bueno

American journal of medical genetics part. A Hoboken v. 158A, n. 9, p. 2170\20132175, 2012

Hoboken 2012

Localização: FM - Fac. Medicina    (BCSEP 063 2012 )(Acessar)

10
Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer
Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer
Material Type:
Artigo 		Adicionar ao Meu Espaço

Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer

Gabriel Bandeira Katia Rocha; Monize Lazar; Suzana Ezquina; Guilherme Yamamoto; Monica Varela; Vanessa Takahashi; Meire Aguena; Thomaz Gollop; Mayana Zatz; Maria Rita Passos-Bueno; Ana Cristina Victorino Krepischi; Oswaldo Keith Okamoto

Breast Cancer Kudan-kita v. 28, n. 2, p. 346-354, Mar. 2021

Kudan-kita 2021

Item não circula. Consulte sua biblioteca.(Acessar)

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Disponível na Biblioteca (4)

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Passos-Bueno, M
  2. Bueno, D
  3. Zatz, M
  4. Orstavik, K
  5. Côrte, C

Neste Assunto:

  1. Doenças Hereditárias
  2. Genética Médica
  3. Mutação Genética
  4. Doenças Ósseas
  5. Malformações

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

Buscando em bases de dados remotas. Favor aguardar.