skip to main content
Idioma:
Mostrar Somente
Refinado por: assunto: Mutação Genética remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Exomic sequencing of four rare central nervous system tumor types
Exomic sequencing of four rare central nervous system tumor types
Material Type:
Artigo 		Adicionar ao Meu Espaço

Exomic sequencing of four rare central nervous system tumor types

Chetan Bettegowda Nishant Agrawal; Yuchen Jiao; Yuxuan Wang; Laura D Wood; Fausto J Rodriguez; Ralph H Hruban; Gary L Gallia; Zev A Binder; Calle J Riggins; Vafi Salmasi; Gregory J Riggins; Zachary J Reitman; Ahmed Rasheed; Stephen Keir; Sueli Mieko Oba Shinjo; Suely Kazue Nagahashi Marie; Roger McLendon; George Jallo; Bert Vogelstein; Darell Bigner; Hai Yan; Kenneth W Kinzler; Nickolas Papadopoulos

Oncotarget New York v.4, n.4, p. 572-583, 2013

New York 2013

Item não circula. Consulte sua biblioteca.(Acessar)

2
Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with FAnconi anaemia
Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with FAnconi anaemia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with FAnconi anaemia

David Enrique Aguilar Rodriguez Carmen Silvia Passos Lima; Gustavo Jacob Lourenço; Maria Estela Figueiredo; Jorge David Aivazoglou Carneiro; Luiz Gonzaga Tone; Juan Clinton Llerena Júnior; Raquel Alves Toscano; Sílvia Brandalise; Walter Pinto Júnior; Fernando Ferreira Costa; Carmem Sílvia Bertuzzo

Genetics and molecular biology Ribeirão Preto v. 28, n. 2, p. 205-209, 2005

Ribeirão Preto 2005

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1496168 )(Acessar)

3
Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with FAnconi anaemia
Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with FAnconi anaemia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Molecular analysis of the most prevalent mutations of the FANCA and FANCC genes in Brazilian patients with FAnconi anaemia

David Enrique Aguilar Rodriguez Carmen Silvia Passos Lima; Gustavo Jacob Lourenço; Maria Estela Figueiredo; Jorge David Aivazoglou Carneiro; Luiz Gonzaga Tone; Juan Clinton Llerena Júnior; Raquel Alves Toscano; Sílvia Brandalise; Walter Pinto Júnior; Fernando Ferreira Costa; Carmem Sílvia Bertuzzo

Genetics and molecular biology Ribeirão Preto v. 28, n. 2, p. 205-209, 2005

Ribeirão Preto 2005

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1496168 )(Acessar)

4
Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma
Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma

Chetan Bettegowda Nishant Agrawal; Yuchen Jiao; Mark Sausen; Laura D Wood; Ralph H Hruban; Fausto J Rodriguez; Daniel P Cahill; Roger McLendon; Gregory Riggins; Victor E Velculescu; Sueli Mieko Oba-Shinjo; Suely Kazue Nagahashi Marie; Bert Vogelstein; Darell Bigner; Hai Yan; Nickolas Papadopoulos; Kenneth W Kinzler

Science Washington v. 333, p. 1453-1455, 2011

Washington 2011

Acesso online. A biblioteca também possui exemplares impressos.

5
Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma
Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma

Chetan Bettegowda Nishant Agrawal; Yuchen Jiao; Mark Sausen; Laura D Wood; Ralph H Hruban; Fausto J Rodriguez; Daniel P Cahill; Roger McLendon; Gregory Riggins; Victor E Velculescu; Sueli Mieko Oba-Shinjo; Suely Kazue Nagahashi Marie; Bert Vogelstein; Darell Bigner; Hai Yan; Nickolas Papadopoulos; Kenneth W Kinzler

Science Washington v. 333, p. 1453-1455, 2011

Washington 2011

Acesso online. A biblioteca também possui exemplares impressos.

6
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil
Material Type:
Artigo 		Adicionar ao Meu Espaço

WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil

Giovanny Rebouças Pinto France Keiko Nascimento Yoshioka; Carlos Afonso Clara; Marcelo José dos Santos; José Reynaldo Walther de Almeida; Rommel Rodríguez Burbano; Juan A Rey; Cacilda Casartelli

Journal of Neuro-Oncology New York v. 90, n. 3, p. 253-258, 2008

New York 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1714398 )(Acessar)

7
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil
Material Type:
Artigo 		Adicionar ao Meu Espaço

WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil

Giovanny Rebouças Pinto France Keiko Nascimento Yoshioka; Carlos Afonso Clara; Marcelo José dos Santos; José Reynaldo Walther de Almeida; Rommel Rodríguez Burbano; Juan A Rey; Cacilda Casartelli

Journal of Neuro-Oncology New York v. 90, n. 3, p. 253-258, 2008

New York 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1714398 )(Acessar)

8
Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas
Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas
Material Type:
Artigo 		Adicionar ao Meu Espaço

Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas

Yuchen Jiao Patrick J Killela; Zachary J Reitman; B. Ahmed Rasheed; Christopher M Heaphy; Roeland F. de Wilde; Fausto J Rodriguez; Sergio Rosemberg; Sueli Meiko Oba-Shinjo; Suely Kazue Nagahashi Marie; Chetan Bettegowda; Nishant Agrawal; Eric Lipp; Christopher Pirozzi; Giselle Lopez; Yiping He; Henry Friedman; Allan H Friedman; Gregory J Riggins; Matthias Holdhoff; Peter Burger; Roger McLendon; Darell D Bigner; Bert Vogelstein; Alan K Meeker; Kenneth W Kinzler; Nickolas Papadopoulos; Luis A DiazJr.; Hai Yan

Oncotarget Albany (US) v. 3, n. 7, p. 709-722, 2012

Albany US 2012

Acesso online. A biblioteca também possui exemplares impressos.

9
Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance
Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance
Material Type:
Artigo 		Adicionar ao Meu Espaço

Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance

Carmen Oleaga Quintas Edgar Borges de Oliveira Júnior; Jérémie Rosain; Franck Rapaport; Caroline Deswarte; Antoine Guérin; Sairaj Munavar Sajjath; Yu Jerry Zhou; Stéphane Marot; Claire Lozano; Lidia Branco; Nuria Fernández Hidalgo; Dukhee Betty Lew; Anne Sophiehttps Brunel; Caroline Thomas; Elise Launay; Andrés Augusto Arias; Alexis Cuffel; Vanesa Cunill Monjo; Anna-Lena Neehus; Laura Marques; Manon Roynard; Marcela Moncada Vélez; Bengü Gerçeker; Roger Colobran; Marie-Gabrielle Vigué; Gabriela Lopez Herrera; Laura Berron Ruiz; Nora Hilda Segura Méndez; Patricia O’Farrill Romanillos; Tom Le Voyer; Anne Puel; Christine Bellanné Chantelot; Kacy A Ramirez; Lazaro Lorenzo Diaz; Noé Ramirez Alejo; Rebeca Pérez de Diego; Antonio Condino Neto; Fethi Mellouli; Carlos Rodriguez Gallego; Torsten Witte; José Franco Restrepo; Mariana Jobim; Stéphanie Boisson Dupuis; Eric Jeziorski; Claire Fieschi; Guillaume Vogt; Jean Donadieu; Marlène Pasquet; Julia Vasconcelos; Fatma Omur Ardeniz; Mónica Martínez Gallo; Regis A Campos; Luiz Fernando Jobim; Rubén Martínez Barricarte; Kang Liu; Aurélie Cobat; Laurent Abel; Jean-Laurent Casanova; Jacinta Bustamante

Journal of Clinical Immunology New York 19 p., 2021

New York 2021

Item não circula. Consulte sua biblioteca.(Acessar)

Personalize Seus Resultados

  1. Editar

Refine Search Results

Mostrar Somente

  1. Disponível na Biblioteca (7)
  2. Recursos Online (3)

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Papadopoulos, N
  2. McLendon, R
  3. Yan, H
  4. Agrawal, N
  5. Bigner, D

Neste Assunto:

  1. Prognóstico
  2. Anemia
  3. Genes
  4. Biomarcadores
  5. Neoplasias Cerebrais (Patologia)

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

Buscando em bases de dados remotas. Favor aguardar.