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Refinado por: Biblioteca: FMRP - Fac. Medicina de Ribeirão Preto remover
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1
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]

Anna M. Aalbers Rodrigo Tocantins Calado; Neal S Young; C. Michel Zwaan; Sachiko Kajigaya; André Baruchel; Karin Geleijns; Valerie de Haas; Gertjan J. L Kaspers; Dirk Reinhardt; Jan Trka; Taco W Kuijpers; Rob Pieters; Vincent H. J. van der Velden; Marry M. van den Heuvel-Eibrink

British Journal of Haematology West Sussex v. 160, n. 4, p. 559-561, 2013

West Sussex 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2400034 Estantes Deslizantes )(Acessar)

2
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]

Anna M. Aalbers Rodrigo Tocantins Calado; Neal S Young; C. Michel Zwaan; Sachiko Kajigaya; André Baruchel; Karin Geleijns; Valerie de Haas; Gertjan J. L Kaspers; Dirk Reinhardt; Jan Trka; Taco W Kuijpers; Rob Pieters; Vincent H. J. van der Velden; Marry M. van den Heuvel-Eibrink

British Journal of Haematology West Sussex v. 160, n. 4, p. 559-561, 2013

West Sussex 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2400034 Estantes Deslizantes )(Acessar)

3
Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia
Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia

Anna M. Aalbers Rodrigo Tocantins Calado; Neal S Young; Christian M Zwaan; Colin O Wu; Sachiko Kajigaya; Eva A Coenen; André Baruchel; Karin Geleijns; Valerie de Haas; Gertjan J. L Kaspers; Taco W Kuijpers; Dirk Reinhardt; Jan Trka; Martin Zimmermann; Rob Pieters; Vincent H. J van der Velden; Marry M van den Heuvel-Eibrink; Annual Meeting of the American Society of Hematology (ASH) (54. 2012 Atlanta)

Blood Washington v. 120, n. 21, res. 1482, 2012

Washington 2012

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2329856 estantes deslizantes )(Acessar)

4
Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis
Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis
Material Type:
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Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis

Raquel M. Alves-Paiva Adeline Bertola; Jichun Chen; Danielle Townsley; Bogdan Dumitriu; Sachiko Kajigaya; Neal S Young; Bin Gao; Rodrigo Tocantins Calado; Meeting on Telomeres and Telomerase (2013 Cold Spring Harbor)

Abstracts Cold Spring Harbor, 2013

Cold Spring Harbor 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2429964 Estantes Deslizantes )(Acessar)

5
Constitutional telomerase mutations are genetic risk factors for cirrhosis
Constitutional telomerase mutations are genetic risk factors for cirrhosis
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Constitutional telomerase mutations are genetic risk factors for cirrhosis

Rodrigo Tocantins Calado Jennifer Brudno; Paulomi Mehta; Joseph J Kovacs; Colin Wu; Marco Antonio Zago; Stephen J Chanock; Thomas D Boyer; Neal S Young

Hepatology Hoboken v. 53, n. 5, p. 1600-1607, 2011

Hoboken 2011

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2280755 Estantes Deslizantes )(Acessar)

6
Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia

Rodrigo Tocantins Calado Joshua A Regal; Mark Hills; William T Yewdell; Leandro F Dalmazzo; Marco Antonio Zago; Peter M Lansdorp; Donna Hogge; Stephen J Chanock; Elihu H Estey; Roberto Passetto Falcao; Neal S Young

Proceedings of the National Academy of Sciences Wahington v. 106, n. 4, p. 1187-1192, 2009

Washington 2009

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1814408 estantes deslizantes )(Acessar)

7
Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia

Rodrigo Tocantins Calado Joshua A Regal; Mark Hills; William T Yewdell; Leandro F Dalmazzo; Marco Antonio Zago; Peter M Lansdorp; Donna Hogge; Stephen J Chanock; Elihu H Estey; Roberto Passetto Falcao; Neal S Young

Proceedings of the National Academy of Sciences Wahington v. 106, n. 4, p. 1187-1192, 2009

Washington 2009

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1814408 estantes deslizantes )(Acessar)

8
Normal pituitary hypertrophy as a frequent cause of pituitary incidentaloma a follow-up study
Normal pituitary hypertrophy as a frequent cause of pituitary incidentaloma a follow-up study
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Normal pituitary hypertrophy as a frequent cause of pituitary incidentaloma a follow-up study

Philipe Chanson France Daujat; Jacques Young; Ângela Delete Bellucci; Michèle Kujas; Dominique Doyon; Gilbert Schaison

Journal of Clinical Endocrinology and Metabolism Springfield v. 86, n. 7, p. 3009-3015, 2001

Springfield 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1327244 )(Acessar)

9
Normal pituitary hypertrophy as a frequent cause of pituitary incidentaloma a follow-up study
Normal pituitary hypertrophy as a frequent cause of pituitary incidentaloma a follow-up study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Normal pituitary hypertrophy as a frequent cause of pituitary incidentaloma a follow-up study

Philipe Chanson France Daujat; Jacques Young; Ângela Delete Bellucci; Michèle Kujas; Dominique Doyon; Gilbert Schaison

Journal of Clinical Endocrinology and Metabolism Springfield v. 86, n. 7, p. 3009-3015, 2001

Springfield 2001

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1327244 )(Acessar)

10
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits
Material Type:
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Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits

Avik Choudhuri Eirini Trompouki; Brian J Abraham; Leandro Machado Colli; Kian Hong Kock; William Mallard; Min-Lee Yang; Divya S Vinjamur; Alireza Ghamari; Audrey Sporrij; Karen Hoi; Barbara Hummel; Sonja Boatman; Victoria Chan; Sierra Tseng; Satish K Nandakumar; Song Yang; Asher Lichtig; Michael Superdock; Seraj N Grimes; Teresa V Bowman; Yi Zhou; Shinichiro Takahashi; Roby Joehanes; Alan B Cantor; Daniel E Bauer; Santhi K Ganesh; John Rinn; Paul S Albert; Martha L Bulyk; Stephen J Chanock; Richard A Young; Leonard I Zon

Nature Genetics New York v. 52, n. 12, p. 1333-1345, 2020

New York 2020

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3016014 Acervo Digital )(Acessar)

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Deste Autor:

  1. Young, N
  2. Calado, R
  3. Kajigaya, S
  4. Townsley, D
  5. Gutierrez-Rodrigues, F

Neste Assunto:

  1. Telômero
  2. Neoplasias
  3. Expressão Gênica
  4. Crianças
  5. Mutação Genética

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

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