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Resultados de 1 a 10 de 15  para Produção Intelectual da USP

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1
Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function
Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function

Ana Paula Abreu Sekoni D Noel; Shuyun Xu; Rona S Carroll; Ana Claudia Latronico; Ursula B Kaiser

Molecular Endocrinology Baltimore v. 26, n. 8, p. 1417-1427, 2012

Baltimore 2012

Localização: FM - Fac. Medicina    (BCSEP 227 2012 )(Acessar)

2
TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood
TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood

E. Gianetti C Tusset; S Noel; M.G Au; A. A Dwyer; V. A Hughes; Abreu, A. P.; Carrol, J.; Trarbach, E.; Silveira, L. F. G.; Costa, E. M. F; Mendonça, B. B.; Castro, Margaret de; Lofrano, A.; Hall, J. E.; Bolu, E.; Ozata, M.; Quinton, R.; Amory, J. K.; Stewart, S. E.; Arlt, W.; Cole, T. R.; Crowley, W. F.; Kaiser, B. B.; Latronico, S. B.; Seminara, S. B.; Annual Meeting and Expo of the Endocrine Society (ENDO) (92. 2010 San Diego)

Advance Program San Diego 2010

San Diego 2010

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1834336 estantes deslizantes ) e outros locais(Acessar)

3
A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2 New Insights into the Effects of PROKR2 Heterozygous Mutations
A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2 New Insights into the Effects of PROKR2 Heterozygous Mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2 New Insights into the Effects of PROKR2 Heterozygous Mutations

Ana Paula Abreu Shuvun Xu; Sekomi D Noel; Rona S Carroll; Ursula B Kaiser; Ana C Latronico; ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo 94 2012 Houston, Texas

Endocrine Reviews Chevy Chase v. 33, 03_meetingAbstracts, Res. SAT-687, 2012

Chevy Chase 2012

Acesso online. A biblioteca também possui exemplares impressos.

4
TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients
TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients
Material Type:
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TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients

Sekoni D. Noel Ana Paula Abreu; Shuyun Xu; Titilayo Muyide; Elena Gianetti; Cintia Tusset; Jessica Carroll; Ana Claudia Latronico; Stephanie B Seminara; Rona S Carroll; Ursula B Kaiser

The FASEB journal Bethesda v. 28, n. 4, p. 1924-1937, 2014

Bethesda 2014

Acesso online. A biblioteca também possui exemplares impressos.

5
Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders
Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders

Cintia Tusset Sekoni Noel; Leticia Silveira; Ericka Trarbach; Elena Gianetti; Stephanie Seminara; Ursula Kaiser; Ana C Latronico; Berenice B Mendonca; ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo 94 2012 Houston, Texas

Endocrine Reviews Chevy Chase v. 33, 03_meetingAbstracts, Res. SUN-619, 2012

Chevy Chase 2012

Acesso online. A biblioteca também possui exemplares impressos.

6
Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders
Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders

Cintia Tusset Sekoni D Noel; Ericka B Trarbach; Letícia F G Silveira; Alexander Augusto de Lima Jorge; Vinicius N Brito; Priscila Cukier; Stephanie B Seminara; Berenice Bilharinho de Mendonça; Ursula B Kaiser; Ana Claudia Latronico Xavier

Arquivos Brasileiros de Endocrinologia & Metabologia São Paulo v. 56, n. 9, p. 646-652, 2012

São Paulo 2012

Localização: FM - Fac. Medicina    (BCSEP 422 2012 )(Acessar)

7
Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders
Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutational Analysis of Neurokinin B and Its Receptor in Patients with Idiopathic Central Pubertal Disorders

Cintia Tusset Sekoni Noel; Leticia Silveira; Ericka Trarbach; Elena Gianetti; Stephanie Seminara; Ursula Kaiser; Ana C Latronico; Berenice B Mendonca; ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo 94 2012 Houston, Texas

Endocrine Reviews Chevy Chase v. 33, 03_meetingAbstracts, Res. SUN-619, 2012

Chevy Chase 2012

Acesso online. A biblioteca também possui exemplares impressos.

8
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism

M. G. Teles E. B Trarbach; S. D Noel; G Guerra Junior; D Beneduzzi; S. D Bianco; Alexander A. L Jorge; A Mukherjee; M. T Baptista; E. M Costa; M. de Castro; B. B Mendonça; U. B Kaiser; A. C Latronico

European Journal of Endocrinology Bristol v. 163, n. 1, p. 29-34, 2010

Bristol 2010

Localização: FM - Fac. Medicina    (BCBIB )(Acessar)

9
Mutations of the KISS1 gene in disorders of puberty
Mutations of the KISS1 gene in disorders of puberty
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations of the KISS1 gene in disorders of puberty

L. G. Silveira S. D Noel; A. P Silveira-Neto; A. P Abreu; V. N Brito; M. G Santos; S. D. C Bianco; W Kuohung; S Xu; M Gryngarten; M. E Escobar; I. J. P Arnhold; B. B Mendonca; U. B Kaiser; A. C Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 5, p. 2276-2280, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

10
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism

M. G. Teles E. B Trarbach; S. D Noel; G Guerra Junior; D Beneduzzi; S. D Bianco; Alexander A. L Jorge; A Mukherjee; M. T Baptista; E. M Costa; M. de Castro; B. B Mendonça; U. B Kaiser; A. C Latronico

European Journal of Endocrinology Bristol v. 163, n. 1, p. 29-34, 2010

Bristol 2010

Localização: FM - Fac. Medicina    (BCBIB )(Acessar)

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Deste Autor:

  1. Noel, S
  2. Kaiser, U
  3. Latronico, A
  4. Abreu, A
  5. Trarbach, E

Neste Assunto:

  1. Mutação Genética
  2. Fenótipos
  3. Hipogonadismo
  4. Genes (Análise)
  5. Puberdade Precoce

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

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