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Refinado por: autor: Montenegro, L remover assunto: Reação Em Cadeia Por Polimerase remover
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1
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
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Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3

Ana Paula Abreu Andrew Dauber; Delanie B Macedo; Sekoni D Noel; Vinicius N Brito; John C Gill; Priscilla Cukier; Iain R Thompson; Victor M Navarro; Priscila C Gagliardi; Tânia Rodrigues; Cristiane Kochi; Carlos Alberto Longui; Dominique Beckers; Francis de Zegher; Luciana R Montenegro; Berenice B Mendonca; Rona S Carroll; Joel N Hirschhorn; Ana Claudia Latronico; Ursula B Kaiser

The New England Journal of Medicine Boston v. 368, n. 26, p. 2467-2475, 2013

Boston 2013

Localização: FM - Fac. Medicina    (BCSEP 297 2013 )(Acessar)

2
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
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Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty

Andrew Dauber Marina Cunha-Silva; Delanie B Macedo; Vinicius N Brito; Ana Paula Abreu; Stephanie A Roberts; Luciana R Montenegro; Melissa Andrew; Andrew Kirby; Matthew T Weirauch; Guillaume Labilloy; Danielle S Bessa; Rona S Carroll; Dakota C Jacobs; Patrick E Chappell; Berenice B Mendonca; David Haig; Ursula B Kaiser; Ana Claudia Latronico

Journal of clinical endocrinology and metabolism Springfield v. 102, n. 5, p. 1557-1567, 2017

Springfield 2017

Localização: FM - Fac. Medicina    (BCSEP 130 2017 )(Acessar)

3
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
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Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome

Luciana Ribeiro Montenegro Leticia F. G Silveira; Cintia Tusset; Margaret de Castro; Beatriz R Versiani; Ana Claudia Latronico; Berenice Bilharinho Mendonca; Ericka B Trarbach

Fertility and Sterility New York v.100, n.3, p. 854-859, 2013

New York 2013

Localização: FM - Fac. Medicina    (BCSEP 167 2013 ) e outros locais(Acessar)

4
Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line
Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line
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Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line

Tamaya C. Ribeiro Luciana Montenegro; Alexander A Jorge; Miriam Y Nishi; 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-496, 2012

Chevy Chase 2012

Acesso online

5
Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line
Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line
Material Type:
Artigo 		Adicionar ao Meu Espaço

Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line

Tamaya C. Ribeiro Luciana Montenegro; Alexander A Jorge; Miriam Y Nishi; 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-496, 2012

Chevy Chase 2012

Acesso online

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