✦ LIBER ✦

Characterisation of adiponectin multimers and the IGF axis in humans with a heterozygote mutation in the tyrosine kinase domain of the insulin receptor gene

✍ Scribed by Hojlund, K.; Beck-Nielsen, H.; Flyvbjerg, A.; Frystyk, J.

Book ID: 118237833
Publisher: Bioscientifica
Year: 2012
Tongue: English
Weight: 168 KB
Volume: 166
Category: Article
ISSN: 0804-4643
DOI: 10.1530/eje-11-0790

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Analysis of the insulin receptor gene ty

Analysis of the insulin receptor gene tyrosine kinase domain in obese patients with hyperandrogenism, insulin resistance and acanthosis nigricans (type C insulin resistance)

✍ Globerman, H; Karnieli, E 📂 Article 📅 1998 🏛 Nature Publishing Group 🌐 English ⚖ 288 KB

A Common Mutation in the Tyrosine Kinase

A Common Mutation in the Tyrosine Kinase Domain of the Fibroblast Growth Factor Receptor 3 Gene in Two Japanese Patients with Hypochondroplasia

✍ Hiroshi KITOH; Yasukazu YAMADA; Haruko GOTO; Nobuaki OGASAWARA; Hiroshi NOGAMI 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 428 KB

Functional properties of a heterozygous

Functional properties of a heterozygous mutation (Arg1174 → Gln) in the tyrosine kinase domain of the insulin receptor from a Type A insulin resistant patient

✍ W. Moritz; E.R. Froesch; M. Böni-Schnetzler 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 545 KB

Gene structure of the human receptor tyr

Gene structure of the human receptor tyrosine kinase RON and mutation analysis in lung cancer samples

✍ Debora Angeloni; Alla Danilkovitch-Miagkova; Sergey V. Ivanov; Richard Breathnac 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 277 KB 👁 1 views

SSCP analysis of the tyrosine kinase dom

SSCP analysis of the tyrosine kinase domain of the insulin receptor gene: Polymorphisms detected in South African black and white subjects

✍ Vanessa R. Panz,Paul Ruff,Barry I. Joffe,Mary-Anne Kedda… 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 38 KB

Novel mutation in the tyrosine kinase do

Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndrome

✍ Andreas Zankl; Gudrun Jaeger; Luisa Bonafé; Eugen Boltshauser; Andrea Superti-Fu 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 60 KB 👁 2 views