Functional characterization of a novel insulin receptor mutation contributing to Rabson-Mendenhall syndrome.
about
Sequencing analysis of insulin receptor defects and detection of two novel mutations in INSR geneSevere insulin resistance alters metabolism in mesenchymal progenitor cells.Successful rhIGF1 treatment for over 5 years in a patient with severe insulin resistance due to homozygous insulin receptor mutation.Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidenceTranscriptional signature of lymphoblastoid cell lines of BRCA1, BRCA2 and non-BRCA1/2 high risk breast cancer families.
P2860
Functional characterization of a novel insulin receptor mutation contributing to Rabson-Mendenhall syndrome.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Functional characterization of ...... to Rabson-Mendenhall syndrome.
@en
type
label
Functional characterization of ...... to Rabson-Mendenhall syndrome.
@en
prefLabel
Functional characterization of ...... to Rabson-Mendenhall syndrome.
@en
P2093
P2860
P1476
Functional characterization of ...... to Rabson-Mendenhall syndrome
@en
P2093
P2860
P356
10.1111/J.1365-2265.2006.02678.X
P577
2007-01-01T00:00:00Z