MicroRNA 132-3p Is Upregulated in Laron Syndrome Patients and Controls Longevity Gene Expression

Autor: Danielle Yaron-Saminsky, Karthik Nagaraj, Rive Sarfstein, Zvi Laron, Metsada Pasmanik-Chor, Haim Werner

Publikováno v: International Journal of Molecular Sciences, Vol 22, Iss 21, p 11861 (2021)

The growth hormone (GH)–insulin-like growth factor-1 (IGF1) endocrine axis is a central player in normal growth and metabolism as well as in a number of pathologies, including cancer. The GH–IGF1 hormonal system, in addition, has emerged as a maj

Externí odkaz: https://doaj.org/article/eeb9cb2ea6f449418f83d63753f81694

A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency

Autor: M J E Walenkamp, J.M. Wit

Publikováno v: European Journal of Endocrinology, 181(6), C29-C33. BioScientifica Ltd.
Walenkamp, M J E & Wit, J M 2019, ' A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency ', European Journal of Endocrinology, vol. 181, no. 6, pp. C29-C33 . https://doi.org/10.1530/EJE-19-0801
European Journal of Endocrinology, 181(6), C29-C33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d54764a163ea0f3bcaa389ac9be20f7
https://hdl.handle.net/1887/3195451

Insulin-Like Growth Factor 1 in the Cardiovascular System

Autor: José Luis González-Guerra, Inma Castilla-Cortázar, Gabriel A. Aguirre, Luis Espinosa

Publikováno v: Reviews of Physiology, Biochemistry and Pharmacology, Vol. 175 ISBN: 9783319952871

Non-communicable diseases, such as cardiovascular diseases, are the leading cause of mortality worldwide. For this reason, a tremendous effort is being made worldwide to effectively circumvent these afflictions, where insulin-like growth factor 1 (IG

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::85718ba8a48c9a997d27c1f996273dfc
https://doi.org/10.1007/112_2017_8

Novel compound heterozygous mutation in ASXL3 causing bainbridge-ropers syndrome and primary IGF1 deficiency: Expanding phenotype

Autor: Dinesh Giri, Astrid Weber, Paul S. McNamara, Mohammed Didi, Matthew Peak, Senthil Senniappan, Brian F. Flanagan

Publikováno v: Endocrine Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7473467e8d2dbfbe720da09727d18c18
https://doi.org/10.1530/endoabs.45.p65

GH treated children with IGF1 deficiency and excluded GH insensitivity despite normal GH secretion may attain similar final height as children with GH deficiency

Autor: Renata Stawerska, Andrzej Lewiński, Joanna Smyczyńska, Maciej Hilczer

Publikováno v: Endocrine Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::68282704ac21c0e268a062943f230215
https://doi.org/10.1530/endoabs.32.p791