[HTML][HTML] A molecular ensemble in the rER for procollagen maturation
Y Ishikawa, HP Bächinger - Biochimica et Biophysica Acta (BBA)-Molecular …, 2013 - Elsevier
Extracellular matrix (ECM) proteins create structural frameworks in tissues such as bone,
skin, tendon and cartilage etc. These connective tissues play important roles in the …
skin, tendon and cartilage etc. These connective tissues play important roles in the …
[HTML][HTML] The endoplasmic reticulum and junctional membrane communication during calcium signaling
AKM Lam, A Galione - Biochimica et Biophysica Acta (BBA)-Molecular Cell …, 2013 - Elsevier
The endoplasmic reticulum is a major organelle in all eukaryotic cells which performs
multiple functions including protein and lipid synthesis and sorting, drug metabolism, and Ca …
multiple functions including protein and lipid synthesis and sorting, drug metabolism, and Ca …
A deletion mutation in TMEM 38 B associated with autosomal recessive Osteogenesis imperfecta
M Volodarsky, B Markus, I Cohen… - Human …, 2013 - Wiley Online Library
Autosomal recessive osteogenesis imperfecta (OI) was diagnosed in three unrelated I sraeli
B edouin consanguineous families. Fractures were evident in all cases in infancy. Genome …
B edouin consanguineous families. Fractures were evident in all cases in infancy. Genome …
Tissue specificity in the nuclear envelope supports its functional complexity
Nuclear envelope links to inherited disease gave the conundrum of how mutations in near-
ubiquitous proteins can yield many distinct pathologies, each focused in different tissues …
ubiquitous proteins can yield many distinct pathologies, each focused in different tissues …
Genome wide association study of age at menarche in the Japanese population
Age at menarche (AAM) is a complex trait involving both genetic and environmental factors.
To identify the genetic factors associated with AAM, we conducted a large-scale meta …
To identify the genetic factors associated with AAM, we conducted a large-scale meta …
TRIC-B channels display labile gating: evidence from the TRIC-A knockout mouse model
E Venturi, A Matyjaszkiewicz, SJ Pitt… - … -European Journal of …, 2013 - Springer
Sarcoplasmic/endoplasmic reticulum (SR) and nuclear membranes contain two related
cation channels named TRIC-A and TRIC-B. In many tissues, both subtypes are co …
cation channels named TRIC-A and TRIC-B. In many tissues, both subtypes are co …
TRIC channels supporting efficient Ca2+ release from intracellular stores
E Venturi, R Sitsapesan, D Yamazaki… - Pflügers Archiv-European …, 2013 - Springer
Trimeric intracellular cation-selective (TRIC) channel subtypes, namely TRIC-A and TRIC-B,
are derived from distinct genes and distributed throughout the sarco/endoplasmic reticulum …
are derived from distinct genes and distributed throughout the sarco/endoplasmic reticulum …
Sarcoplasmic reticulum K+ (TRIC) channel does not carry essential countercurrent during Ca2+ release
T Guo, A Nani, S Shonts, M Perryman, H Chen… - Biophysical journal, 2013 - cell.com
The charge translocation associated with sarcoplasmic reticulum (SR) Ca 2+ efflux is
compensated for by a simultaneous SR K+ influx. This influx is essential because, with no …
compensated for by a simultaneous SR K+ influx. This influx is essential because, with no …
Facilitated hyperpolarization signaling in vascular smooth muscle-overexpressing TRIC-A channels
S Tao, D Yamazaki, S Komazaki, C Zhao, T Iida… - Journal of Biological …, 2013 - ASBMB
The TRIC channel subtypes, namely TRIC-A and TRIC-B, are intracellular monovalent
cation-specific channels and likely mediate counterion movements to support efficient Ca 2+ …
cation-specific channels and likely mediate counterion movements to support efficient Ca 2+ …
Молекулярно-генетические основы несовершенного остеогенеза
ДД Надыршина, РИ Хусаинова… - Медицинская …, 2013 - elibrary.ru
Несовершенный остеогенез (НО)(МКБ-10-Q78. 0-незавершённый остеогенез)-
тяжёлое, клинически и генетически гетерогенное наследственное заболевание …
тяжёлое, клинически и генетически гетерогенное наследственное заболевание …