๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Distinct Properties of CPVT Mutations Located in the Central Domain of Human RyR2

โœ Scribed by Blayney, Lynda; Nomikos, Michail; Beck, Konrad; D'Cruz, Leon; McDonald, Ewan; Griffiths, Julia; Lai, F. Anthony


Book ID
122026736
Publisher
Biophysical Society
Year
2010
Tongue
English
Weight
37 KB
Volume
98
Category
Article
ISSN
0006-3495

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Variable pathogenic potentials of mutati
โœ Bertrand Goudeau; Fernando Rodrigues-Lima; Dirk Fischer; Monique Casteras-Simon; ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 395 KB

Mutations in the desmin gene have been recognized as a cause of desminopathy, a familial or sporadic disorder characterized by skeletal muscle weakness, often associated with cardiomyopathy or respiratory insufficiency. Distinctive histopathologic features include aberrant intracytoplasmic accumulat

Somatic mutations of the ERBB4 kinase do
โœ Young Hwa Soung; Jong Woo Lee; Su Young Kim; Young Pil Wang; Keon Hyun Jo; Seok ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 155 KB ๐Ÿ‘ 1 views

The EGFR family consists of 4 receptor tyrosine kinases, EGFR (ERBB1), ERBB2 (HER2), ERBB3 (HER3) and ERBB4 (HER4). Recent reports revealed that the kinase domains of both EGFR (ERBB1) and ERBB2 gene were somatically mutated in human cancers, raising the possibility that the other ERBB members posse