نتایج جستجو برای: ins 1 cells

تعداد نتایج: 3783999  

Journal: :The Journal of biological chemistry 1991
T Balla S S Sim T Iida K Y Choi K J Catt S G Rhee

The proposed Ca(2+)-signaling actions of inositol 1,3,4,5-tetrakisphosphate (Ins(1,3,4,5)P4), formed by phosphorylation of the primary Ca(2+)-mobilizing messenger, inositol 1,4,5-trisphosphate (Ins(1,4,5)P3), were analyzed in NIH 3T3 and CCL39 fibroblasts transfected with rat brain Ins(1,4,5)P3 3-kinase. In such kinase-transfected cells, the conversion of Ins(1,4,5)P3 to Ins(1,3,4,5)P4 during a...

Journal: :The Biochemical journal 2001
M S Nash K W Young G B Willars R A Challiss S R Nahorski

The pleckstrin homology domain of phospholipase Cdelta1 (PH(PLCdelta)) binds Ins(1,4,5)P(3) and PtdIns(4,5)P(2) specifically, and can be used to detect changes in Ins(1,4,5)P(3) in single cells. A fusion construct of PH(PLCdelta) and enhanced green fluorescent protein (EGFP-PH(PLCdelta)) associates with the plasma membrane due to its association with PtdIns(4,5)P(2). However, PH(PLCdelta) has g...

Journal: :Blood 1953
N L PETRAKIS

photometry, a relationiship betweens nucleic acids and protein synthesis has l)een demonstrated, particularly with respect to rihonsucleic acid amid the myeloma plasma cell.’ . 2 Recently au important correlations between the chromosome usumber anid the 1)NA contenst of the cell nsucleus has been established.38 Th cellular DNA appears to be coisfined to the chromosomes, amid this quantity of DN...

2008
L Susick R Veluthakal M V Suresh T Hadden A Kowluru

Histone (de)acetylases control gene transcription via modification of the chromatin structure. Herein, we investigated potential roles for histone deacetylation (or hypoacetylation) in interleukin-1 (IL-1 )-mediated inducible nitric oxide synthase (iNOS) and nitric oxide (NO) release in insulin-secreting INS 832/13 (INS) cells. Western blot analysis suggested localization of members of Class 1 ...

Journal: :The Korean Journal of Physiology and Pharmacology 2011

Journal: :The Biochemical journal 1994
P M Smith D V Gallacher

The tumour-promoting agent thapsigargin has been shown to inhibit the microsomal Ca(2+)-ATPase and cause Ca2+ mobilization in a variety of cell types including exocrine acinar cells [Bird, Obie and Putney (1992) J. Biol. Chem. 267, 18382-18386]. When applied to acutely isolated lacrimal acinar cells, thapsigargin caused a slow biphasic activation of both the Ca(2+)-dependent K+ and Cl- currents...

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