نتایج جستجو برای: مدل pip

تعداد نتایج: 122445  

Journal: :The Journal of Cell Biology 2004
Rabiya Tuma

Tucker, and Edwin Chapman (University of Wisconsin, Madison, WI) find that PIP 2 is a plasma membrane dock for synaptotagmin-1 (syt), a transmembrane protein localized in secretory vesicle membranes, when calcium is absent. This dock may ensure speedy and directed fusion in response to calcium influx. The syt dock has two calcium-binding domains in its cytoplasmic region, called C 2 A and C 2 B...

Journal: :The Journal of biological chemistry 1990
M C Pike M E Bruck C Arndt C S Lee

Chemoattractant receptor-mediated hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) by phospholipase C is instrumental for leukocyte activation. Previous studies have demonstrated that chemoattractant treatment of intact polymorphonuclear leukocytes (PMN) causes a transient decrease in PIP2 due to phospholipase C activation, followed by an increase in cellular PIP2 levels. The present ...

Journal: :Archives of facial plastic surgery 2007
Clinton D Humphrey Terence E McIff Kevin J Sykes Terance T Tsue J David Kriet

BACKGROUND Static facial suspension (SFS) continues to play a role for rehabilitation in patients with facial paralysis. We perform SFS almost exclusively with a suture technique in our practice. Monofilament polypropylene suture (Prolene) is commonly used for SFS, but we have witnessed occasional failure and some stretching with this material. The purpose of this study was to establish and com...

Journal: :Current Biology 2000
Katherine Hinchliffe

The phospholipid phosphatidylinositol (4,5) bisphosphate (PIP(2)) has recently been shown to act downstream of the small G proteins Rac and Arf. Different effectors may be employed in each case, suggesting that PIP(2) has multiple signalling roles.

Journal: :The Programming Historian 2013

Journal: :The Journal of Cell Biology 2004
Rabiya Tuma

Tucker, and Edwin Chapman (University of Wisconsin, Madison, WI) find that PIP 2 is a plasma membrane dock for synaptotagmin-1 (syt), a transmembrane protein localized in secretory vesicle membranes, when calcium is absent. This dock may ensure speedy and directed fusion in response to calcium influx. The syt dock has two calcium-binding domains in its cytoplasmic region, called C 2 A and C 2 B...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
M A Ortiz J Light R A Maki N Assa-Munt

The PU.1 interaction partner (Pip) is a member of the interferon regulatory factor family that regulates gene expression through heterodimerization with the ETS transcription factor PU.1. Binding of Pip alone to DNA is weak, and usually it is recruited by phosphorylated PU.1 to form a strong ternary complex with specific DNA sequences. An approach combining sequence homology analysis, secondary...

2015
Barbara Clyne Susan M. Smith Carmel M. Hughes Fiona Boland Janine A. Cooper Tom Fahey

BACKGROUND Potentially inappropriate prescribing (PIP) is common in older people in primary care and can result in increased morbidity, adverse drug events and hospitalisations. We previously demonstrated the success of a multifaceted intervention in decreasing PIP in primary care in a cluster randomised controlled trial (RCT). OBJECTIVE We sought to determine whether the improvement in PIP i...

2017
Wen Wang Linxin Wu Chaobin Zhang Li Sun

BACKGROUND Propofol injection pain (PIP) has been adequately studied during the past decades. However, patients' opinion on this problem and the incidence of patients' recall of this brief discomfort are still unknown. Thus, we conducted this study to know the patients' perspectives on PIP and provide useful information about the incidence of recall of PIP under our routine general anesthesia. ...

2009
J Gabrielsson AR Green

Pharmacodynamics (PD) examines the relationship between drug concentration and onset, intensity and duration of the pharmacological effect. Pharmacokinetics (PK) is the science of the time course of drugs in the organism. The quantitative pharmacological approach focuses on concentration-response and response-time relationships with special emphasis on the proposed impact of the drug on the dis...

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