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PRKCSH functions as a chaperone-like molecule, which prevents endoplasmic reticulum-associated degradation of TRPP2.
PI3K may have a role in nuclear PLD1 regulation; pertussis toxin induced a decrease of LPA-stimulated nuclear PLD1 activity, suggesting that heterotrimeric G(i)/G(0) protein involvement in intranuclear PLD1 regulation(phospholipase D (show PLD ELISA Kits)-1)
acetylcholine induces phosphorylation of PLD1 in porcine tracheal smooth muscle.
The results indicate that PKC (show FYN ELISA Kits) could be the final target and an integrator molecule of different signaling pathways triggered by angiotensin II (Ang II), which could explain the sustained activation of Na(+)-ATPase (show DNAH8 ELISA Kits) by Ang II (show AGT ELISA Kits).
Polycystic liver disease is recessive at the cellular level, and loss of functional PRKCSH is an important step in cystogenesis.
The induction of autophagy by hepatocystin deficiency is mediated through mammalian target of rapamycin (mTOR (show FRAP1 ELISA Kits)).
Results provide evidence that mutations at the coding PRKCSH GAG repeat are a target of MSI (show MSI1 ELISA Kits) and are selectively associated with the MSI (show MSI1 ELISA Kits)-H phenotype in gastric carcinomas.
The common SNPs tested in DDOST (show DDOST ELISA Kits), PRKCSH and LGALS3 (show LGALS3 ELISA Kits) do not seem to be associated with diabetic micro- or macrovascular complications or with type 1 diabetes in Finnish patients.
identified a total of 26 novel mutations in PRKCSH (n = 14) and SEC63 (show SEC63 ELISA Kits) (n = 12), including four splice site mutations, eight insertions/ deletions, six non-sense mutations, and eight missense mutations
Our results suggest that PRKCSH gene is not a major genetic cause of PCLD and there may be at least another locus responsible for the disease in Taiwan.
germline mutations in PRKCSH as the probable cause of autosomal dominant polycystic liver disease
role of hepatocystin in carbohydrate processing and quality control of newly synthesized glycoproteins in the endoplasmic reticulum
results identify 80K-H as a new player involved in GLUT4 vesicle transport and identify a link between a kinase involved in the insulin signalling cascade, PKCzeta, and a known component of the GLUT4 vesicle trafficking pathway, munc18c
TRIM67 regulates Ras signaling via degradation of 80K-H, leading to neural differentiation including neuritogenesis.
Data demonstrate the presence of a binding site on the 3'-untranslated region of NR1 mRNA for AnxA2 and show the regulation of NR1 mRNA by AnxA2, GIIbeta and a third NR1 mRNA-binding protein, which is yet to be identified.
80K-H is a Ca(2 (show CA2 ELISA Kits)+) sensor controlling TRPV5 (show TRPV5 ELISA Kits) channel activity
80K-H is a novel regulator of IP3R1 (show ITPR1 ELISA Kits) activity, and it may contribute to neuronal functions.
This study is the first to report that VASAP-60 is up-regulated in granulosa cells of dominant follicles, to document the primary structure of the VASAP-60 gene and the YY1 (show YY1 ELISA Kits) binding to promoter may act as a positive transcriptional regulator.
This gene encodes the beta-subunit of glucosidase II, an N-linked glycan-processing enzyme in the endoplasmic reticulum (ER). This protein is an acidic phospho-protein known to be a substrate for protein kinase C. Mutations in this gene have been associated with the autosomal dominant polycystic liver disease (PCLD). Alternatively spliced transcript variants encoding distinct isoforms have been observed.
glucosidase 2 subunit beta
, protein kinase C substrate 80K-H
, phospholipase D1, phosphatidylcholine-specific
, phospholipase D1
, AGE-binding receptor 2
, glucosidase II subunit beta
, glucosidase II, beta subunit
, protein kinase C substrate 60.1 kDa protein heavy chain
, protein kinase C substrate, 80 Kda protein
, alpha glucosidase II, beta-subunit
, carbohydrate processing enzyme of the endoplasmic reticulum
, glucosidase II beta-subunit
, 80K-H protein
, vacuolar system associated protein-60
, vacuolar system-associated protein 60