Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line (2012)
- Authors:
- USP affiliated authors: MONTENEGRO, LUCIANA RIBEIRO - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- Subjects: EXPRESSÃO GÊNICA; NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS; REAÇÃO EM CADEIA POR POLIMERASE; WESTERN BLOTTING; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Publisher place: Chevy Chase
- Date published: 2012
- Source:
- Título do periódico: Endocrine Reviews
- ISSN: 0163-769X
- Volume/Número/Paginação/Ano: v. 33, 03_meetingAbstracts, Res. SUN-496, 2012
- Conference titles: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo
-
ABNT
RIBEIRO, Tamaya C. et al. Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496. Acesso em: 12 maio 2024. -
APA
Ribeiro, T. C., Montenegro, L., Jorge, A. A., Nishi, M. Y., Latronico, A. C., & Mendonca, B. B. (2012). Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496 -
NLM
Ribeiro TC, Montenegro L, Jorge AA, Nishi MY, Latronico AC, Mendonca BB. Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 maio 12 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496 -
Vancouver
Ribeiro TC, Montenegro L, Jorge AA, Nishi MY, Latronico AC, Mendonca BB. Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 maio 12 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496 - Clinical and Genetic Characterization of Familial Central Precocious Puberty
- Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth
- Loss-of-function mutations in a gene cause central precocius puberty
- Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region
- Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development
- Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty
- High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic
- Pathogenic variants inTNRC6Bcause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
- Analysis of FGFR4 Locus amplification in pediatric and adult sporadic adrenocortical tumors
- The role of fibroblast growth factor receptor 4 overexpression and gene amplification as prognostic markers in pediatric and adult adrenocortical tumors [Carta]
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