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Refinado por: assunto: Mutação Genética remover
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11
Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1
Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1

Rodrigo A. Toledo Delmar M Lourenço Junior; Flavia L Coutinho; Elisangela Quedas; Ivone Mackowiack; Marcel Cerqueira César Machado; Fabio Montenegro; Malebranche B. C Cunha-Neto; Bernardo Liberman; Maria A. A Pereira; Pedro H. S Correa; S. P. A Toledo (Sérgio Pereira de Almeida)

Clinical Endocrinology Oxford v. 67, p. 377-384, 2007

Oxford 2007

Localização: FM - Fac. Medicina    (FM BCSEP 2007 001 )(Acessar)

12
Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions
Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Characterization of Clinical and laboratorial findings in patients with isolated exercise intolerance due to multiple MTDNA deletions

Cláudia Ferreira da Rosa Sobreira E. H. T Carvalho; Sílvia Helena Andrião Escarso; F. O Toledo; K. B. B Trindade; F. H. Z Reis; Wilson Marques Júnior; International Meeting of Mitochondrial Pathology (EUROMIT) (10. 2017 Cologne)

Abstracts Cologne, 2017

Cologne 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2922006 Estantes Deslizantes )(Acessar)

13
MKRN3 mutations in central precocious puberty a systematic review and meta-analysis
MKRN3 mutations in central precocious puberty a systematic review and meta-analysis
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MKRN3 mutations in central precocious puberty a systematic review and meta-analysis

Luciana Pinto Valadares Cinthia Gabriel Meireles; Isabela Porto De Toledo; Renata Santarem de Oliveira; Luiz Claudio Goncalves de Castro; Ana Paula Abreu; Rona S Carroll; Ana Claudia Latronico Xavier; Ursula B Kaiser; Eliete Neves Silva Guerra

Journal of the endocrine society v. 3, n. 5, p. 979-995, 2019

Washington 2019

Acesso online. A biblioteca também possui exemplares impressos.

14
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations

Viviane Cristina Longuini Delmar M Lourenço Júnior; Tomoko Sekiya; Osorio Meirelles; Tatiana D Goncalves; Flavia L Coutinho; Guilherme Francisco; Luciana H Osaki; Roger Chammas; Venâncio Avancini Ferreira Alves; Sheila A. C Siqueira; David Schlesinger; Michel Naslavsky; Mayana Zatz; Yeda Aparecida de Oliveira Duarte; Maria Lucia Lebrão; Patrícia Gama; Misu Lee; Sara Molatore; Maria Adelaide A Pereira; Raquel S Jallad; Marcello D Bronstein; Malebranche B Cunha-Neto; Bernardo Liberman; Maria Candida B. V Fragoso; Sergio Pereira de Almeida Toledo; Natalia S Pellegata; Rodrigo A Toledo

European Journal of Endocrinology Woodlands on-line, Jun. 2014

Woodlands 2014

Localização: EE - Escola de Enfermagem    (DUARTE, Y. A. de O. doc 111 ) e outros locais(Acessar)

15
Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS
Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS
Material Type:
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Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS

Nishant Agrawal Yuchen Jiao; Mark Sausen; Rebecca Leary; Chetan Bettegowda; Nicholas J Roberts; Sheetal Bhan; Allen S Ho; Zubair Khan; Justin Bishop; William H Westra; Laura D Wood; Ralph H Hruban; Ralph P Tufano; Bruce Robinson; Henning Dralle; Sergio Pereira Almeida Toledo; Rodrigo A Toledo; Luc G T Morris; Ronald A Ghossein; James A Fagin; Timothy A Chan; Victor E Velculescu; Bert Vogelstein; Kenneth W Kinzler; Nickolas Papadopoulos; Barry D Nelkin; Douglas W Ball

The Journal of Clinical Endocrinology & Metabolism Springfield v. 98, n. 2, p. E364-E369, 2013

Springfield 2013

Localização: FM - Fac. Medicina    (BCSEP 054 2013 )(Acessar)

16
Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with carney complex caused by the novel nonsense mutation p.Y21X
Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with carney complex caused by the novel nonsense mutation p.Y21X
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with carney complex caused by the novel nonsense mutation p.Y21X

Madson Q. Almeida Luciana Pinto Brito; Sorahia Domenice; Marcia Helena Soares Costa; Emilia Modolo Pinto; Cynthia A. Toledo Osório; Ana Claudia Latronico; Berenice Bilharinho de Mendonça; Maria Candida B. V Fragoso

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1257-1263, 2008

Rio de Janeiro 2008

Localização: FM - Fac. Medicina    (FM BCSEP 126 2008 )(Acessar)

17
Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with carney complex caused by the novel nonsense mutation p.Y21X
Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with carney complex caused by the novel nonsense mutation p.Y21X
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with carney complex caused by the novel nonsense mutation p.Y21X

Madson Q. Almeida Luciana Pinto Brito; Sorahia Domenice; Marcia Helena Soares Costa; Emilia Modolo Pinto; Cynthia A. Toledo Osório; Ana Claudia Latronico; Berenice Bilharinho de Mendonça; Maria Candida B. V Fragoso

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1257-1263, 2008

Rio de Janeiro 2008

Localização: FM - Fac. Medicina    (FM BCSEP 126 2008 )(Acessar)

18
p27 variant and corticotropinoma susceptibility a genetic and in vitro study
p27 variant and corticotropinoma susceptibility a genetic and in vitro study
Material Type:
Artigo 		Adicionar ao Meu Espaço

p27 variant and corticotropinoma susceptibility a genetic and in vitro study

Tomoko Sekiya Marcello Delano Bronstein; Katiuscia Benfini; Viviane Cristina Longuini; Raquel Soares Jallad; Marcio Cardoso Machado; Tatiana Denk Gonçalves; Luciana Harumi Osaki; Leonardo Higashi; Jose Viana Junior; Claudio Kater; Misu Lee; Sara Molatore; Guilherme Francisco; Roger Chammas; Michel Naslavsky; David Schlesinger; Patrícia Gama; Yeda Aparecida de Oliveira Duarte; Maria Lúcia Lebrão; Mayana Zatz; Osorio Meirelles; Bernardo Liberman; Maria Candida Barisson Villares Fragoso; Sergio Pereira de Almeida Toledo; Natalia S Pellegata; Rodrigo de Almeida Toledo

Endocrine-Related Cancer Woodlands v. 21, n. 3, p. 395-404, 2014

Woodlands 2014

Item não circula. Consulte sua biblioteca.(Acessar)

19
A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas
A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas
Material Type:
Artigo 		Adicionar ao Meu Espaço

A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas

Patricia L. M. Dahia Ken N Ross; Matthew E Wright; César Y Hayashida; Sandro Santagata; Marta Barontini; Andrew L Kung; Gabriela Sanso; James F Powers; Arthur S Tischler; Richard Hodin; Shannon Heitritter; Francis Moore; Robert Dluhy; Julie Ann Sosa; I. Tolgay Ocal; Diana E Benn; Deborah J Marsh; Bruce G Robinson; Katherine Schneider; Judy Garber; Seth M Arum; Márta Korbonits; Ashley Grossman; Pascal Pigny; S. P. A Toledo (Sérgio Pereira de Almeida); Vania Nosé; Cheng Li; Charles D Stiles

PLOS Genetics San Francisco v. 1, n. 1, p. 72-80, July, 2005

San Francisco 2005

Localização: FM - Fac. Medicina    (FM BCSEP 250 2005 )(Acessar)

20
A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas
A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas
Material Type:
Artigo 		Adicionar ao Meu Espaço

A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas

Patricia L. M. Dahia Ken N Ross; Matthew E Wright; César Y Hayashida; Sandro Santagata; Marta Barontini; Andrew L Kung; Gabriela Sanso; James F Powers; Arthur S Tischler; Richard Hodin; Shannon Heitritter; Francis Moore; Robert Dluhy; Julie Ann Sosa; I. Tolgay Ocal; Diana E Benn; Deborah J Marsh; Bruce G Robinson; Katherine Schneider; Judy Garber; Seth M Arum; Márta Korbonits; Ashley Grossman; Pascal Pigny; S. P. A Toledo (Sérgio Pereira de Almeida); Vania Nosé; Cheng Li; Charles D Stiles

PLOS Genetics San Francisco v. 1, n. 1, p. 72-80, July, 2005

San Francisco 2005

Localização: FM - Fac. Medicina    (FM BCSEP 250 2005 )(Acessar)

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Deste Autor:

  1. Toledo, S
  2. Toledo, R
  3. Liberman, B
  4. Fragoso, M
  5. Longuini, V

Neste Assunto:

  1. Neoplasia Endócrina Múltipla
  2. Brasileiros
  3. Doenças Hereditárias
  4. Adenoma
  5. Neoplasias (Patologia;Genétgica)

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

Buscando em bases de dados remotas. Favor aguardar.