skip to main content
Idioma:
Mostrar Somente
Refinado por: Biblioteca: FMRP - Fac. Medicina de Ribeirão Preto remover assunto: Mutação Genética remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Somatic mutations of calreticulin in a Brazilian cohort of patients with myeloproliferative neoplasms. [Carta]
Somatic mutations of calreticulin in a Brazilian cohort of patients with myeloproliferative neoplasms. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Somatic mutations of calreticulin in a Brazilian cohort of patients with myeloproliferative neoplasms. [Carta]

João Agostinho Machado Neto Paula de Melo Campos; Dulcinéia Martins de Albuquerque; Fernando Ferreira Costa; Irene Lorand-Metze; Sara Terezinha Olalla Saad; Fabiola Traina

Revista Brasileira de Hematologia e Hemoterapia São Paulo v. 37, n.3, p. 211-214, 2015

São Paulo 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2765832 Estantes Deslizantes )(Acessar)

2
IRS2 associates with JAK2 and may be involved in cell proliferation pathways in chronic myeloproliferative neoplasms
IRS2 associates with JAK2 and may be involved in cell proliferation pathways in chronic myeloproliferative neoplasms
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

IRS2 associates with JAK2 and may be involved in cell proliferation pathways in chronic myeloproliferative neoplasms

Paula de Melo Campos João Agostinho Machado Neto; Adriana Silva Santos Duarte; Rafaela Mendonça; Irene Lorand-Metze; Fernando Ferreira Costa; Sara Teresinha Ollala Saad; Fabíola Traina; Annual Meeting and Exposition of American Society of Hematology (ASH) (55. 2013 New Orleans)

Abstracts, Program and Personal Scheduler New Orleans, 2013

New Orleans 2013

Acesso online. A biblioteca também possui exemplares impressos.

3
Ten-eleven-translocation 2 (TET2) is downregulated in myelodysplastic syndromes
Ten-eleven-translocation 2 (TET2) is downregulated in myelodysplastic syndromes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Ten-eleven-translocation 2 (TET2) is downregulated in myelodysplastic syndromes

Renata Scopim-Ribeiro João Agostinho Machado Neto; Paula de Melo Campos; Cleide Aparecida Moreira Silva; Patricia Favaro; Irene Lorand-Metze; Fernando Ferreira Costa; Sara Teresinha Olalla Saad; Fabiola Traina

European Journal of Haematology Malden v. 94, n. 5, p. 413-418, 2015

Malden 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2714505 Estantes Deslizantes )(Acessar)

4
IRS2 silencing increases apoptosis and potentiates the effects of ruxolitinib in JAK2V617F-positive myeloproliferative neoplasms
IRS2 silencing increases apoptosis and potentiates the effects of ruxolitinib in JAK2V617F-positive myeloproliferative neoplasms
Material Type:
Artigo 		Adicionar ao Meu Espaço

IRS2 silencing increases apoptosis and potentiates the effects of ruxolitinib in JAK2V617F-positive myeloproliferative neoplasms

Paula de Melo Campos João Agostinho Machado Neto; Christopher A Eide; Samantha L Savage; Renata Scopim-Ribeiro; Adriana da Silva Souza Duarte; Patrícia Favaro; Irene Lorand-Metze; Fernando F Costa; Cristina E Tognon; Brian J Druker; Sara T. Olalla Saad; Fabiola Traina

Oncotarget Albany v. 7, n. 6, p. 6948-6959, 2016

Albany 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2849600 Estantes Deslizantes )(Acessar)

5
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)

6
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)

7
Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation
Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Enteroendocrine connections in congenital isolated GH deficiency due to a GHRH receptor gene mutation

Alécia A. Oliveira Santos Roberto Salvatori; Mônica Cristina Nogueira; Ana Carolina Bueno de Queiroz Arruda; Cynthia S Barros-Oliveira; Ângela Cristina Gomes Borges Leal; Cindi Guimarães Marinho; Nayra Prata Damascena; Djane A Oliveira; Manuela A Melo; Carla Raquel Pereira Oliveira; Flavia O. da Costa; Jéssica S. S. dos Santos; Paula F. C Santos; Viviane C Campos; Elenilde Gomes Santos; Enaldo Vieira de Melo; Meirielly L. A Barbosa; Ivina E. S Rocha; Margaret de Castro; Manuel Herminio de Aguiar Oliveira

The Journal of Clinical Endocrinology & Metabolism Cary v. 104, n. 7, p. 2777-2784, 2019

Cary 2019

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3005185 Estantes Deslizantes )(Acessar)

8
Hemizygous deletion of FGFR1 gene identified in a patient with congenital normosmic isolated hypogonadotropic hypogonadism by ligation-dependent probe amplification analysis
Hemizygous deletion of FGFR1 gene identified in a patient with congenital normosmic isolated hypogonadotropic hypogonadism by ligation-dependent probe amplification analysis
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Hemizygous deletion of FGFR1 gene identified in a patient with congenital normosmic isolated hypogonadotropic hypogonadism by ligation-dependent probe amplification analysis

M. G. Teles E. B Trarbach; E. M. F Costa; A. P Abreu; G Guerra Júnior; M. T. M Batista; Margaret de Castro; Berenice Bilharinho de Mendonça; Annual Meeting of the Endocrine Society (90. 2008 San Francisco)

Program and Abstracts Book San Francisco, 2008

San Francisco 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1682883 ) e outros locais(Acessar)

9
Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2
Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2

A. P. Abreu E. B Trarbach; Margaret de Castro; E. M. F Costa; B Versiani; G Guerra Júnior; M. T. M Baptista; H. M Garmes; Berenice Bilharinho de Mendonça; A. C Latronico; Annual Meeting of the Endocrine Society (90. 2008 San Francisco)

Program and Abstracts Book San Francisco, 2008

San Francisco 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1682900 ) e outros locais(Acessar)

10
Nucleocapsid (N) gene mutations of SARS-CoV-2 can affect real-time RT-PCR diagnostic and impact false-negative results
Nucleocapsid (N) gene mutations of SARS-CoV-2 can affect real-time RT-PCR diagnostic and impact false-negative results
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nucleocapsid (N) gene mutations of SARS-CoV-2 can affect real-time RT-PCR diagnostic and impact false-negative results

Jessika Cristina Chagas Lesbon Mirele Daiana Poleti; Elisângela Chicaroni de Mattos Oliveira; Jose Salvatore Leister Patane; Luan Gaspar Clemente; Vincent Louis Viala; Gabriela Ribeiro; Marta Giovanetti; Luiz Carlos Junior Alcantara; Loyze Paola Oliveira de Lima; Antonio Jorge Martins; Cláudia Renata dos Santos Barros; Elaine Cristina Marqueze; Jardelina de Souza Todão Bernardino; Débora Botequio Moretti; Ricardo Augusto Brassaloti; Raquel L. R. C Cassano; Pilar Drummond Sampaio Correa Mariani; Svetoslav Nanev Slavov; Rafael Bezerra dos Santos; Evandra Strazza Rodrigues; Elaine Vieira Santos; Josiane Serrano Borges; Debora Glenda Lima de La Roque; João Paulo Kitajima; Bibiana Santos; Patricia Akemi Assato; Felipe Allan da Silva Costa; Cecilia Artico Banho; Lívia Sacchetto; Marilia Mazzi Moraes; Melissa Palmieri; Fabiana Erica Vilanova da Silva; Rejane Maria Tommasini Grotto; João A Souza Neto; Mauricio Lacerda Nogueira; Luiz Lehman Coutinho; Rodrigo Tocatins Caldo; Raul Machado-Neto; Dimas Tadeu Covas; Simone Kashima; Maria Carolina Elias; Sandra Coccuzzo Sampaio; Heidge Fukumasu

Viruses Basel v. 13, art. 2474, p. 1-9, 2021

Basel 2021

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3059969 Acervo Digital ) e outros locais(Acessar)

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (2)

Data de Publicação 

De até
Refinar
  1. Antes de2008  (4)
  2. 2008Até2012  (4)
  3. 2013Até2015  (4)
  4. 2016Até2020  (3)
  5. Após 2020  (3)
  6. Mais opções open sub menu

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Costa, F
  2. Traina, F
  3. Ramalho, L
  4. Teixeira, A
  5. Martinelli, A

Neste Assunto:

  1. Neoplasias
  2. Reação Em Cadeia Por Polimerase
  3. Hepatite C
  4. Covid-19
  5. Anemia

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

Buscando em bases de dados remotas. Favor aguardar.