نتایج جستجو برای: src family kinase

تعداد نتایج: 637862  

Journal: :Cancer research 2009
Banibrata Sen Babita Saigal Nila Parikh Gary Gallick Faye M Johnson

Locoregional and distant recurrence remains common and usually fatal for patients with advanced head and neck squamous cell carcinoma (HNSCC). One promising molecular target in HNSCC is the Src family kinases (SFK). SFKs can affect cellular proliferation and survival by activating the signal transducer and activator of transcription (STAT) family of transcription factors, especially STAT3. Surp...

Journal: :The Journal of biological chemistry 2002
Karen K Cook Debra A Fadool

The Shaker family K(+) channel protein, Kv1.3, is tyrosine phosphorylated by v-Src kinase at Tyr(137) and Tyr(449) to modulate current magnitude and kinetic properties. Despite two proline rich sequences and these phosphotyrosines contained in the carboxyl and amino terminals of the channel, v-Src kinase fails to co-immunoprecipitate with Kv1.3 as expressed in HEK 293 cells, indicating a lack o...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2005
Mahito Sato Keiko Kawai-Kowase Hiroko Sato Yuko Oyama Hiroyoshi Kanai Yoshio Ohyama Tatsuo Suga Toshitaka Maeno Yasuhiro Aoki Junichi Tamura Hironosuke Sakamoto Ryozo Nagai Masahiko Kurabayashi

OBJECTIVE Transforming growth factor-beta1 (TGF-beta1) controls the expression of numerous genes, including smooth muscle cell (SMC)-specific genes and extracellular matrix protein genes. Here we investigated whether c-Src plays a role in TGF-beta1 signaling in mouse embryonic fibroblast C3H10T1/2 cells. METHODS AND RESULTS TGF-beta1 induction of the SMC contractile protein SM22alpha gene exp...

Journal: :The Journal of biological chemistry 2009
Jianmin Sun Malin Pedersen Lars Rönnstrand

The receptor tyrosine kinase c-Kit plays a critical role in hematopoiesis, and gain-of-function mutations of the receptor are frequently seen in several malignancies, including acute myeloid leukemia, gastrointestinal stromal tumors, and testicular carcinoma. The most common mutation of c-Kit in these disorders is a substitution of the aspartic acid residue in position 816 to a valine (D816V), ...

Journal: :journal of reports in pharmaceutical sciences 0
alireza aliabadi department of medicinal chemistry, faculty of pharmacy, kermanshah university of medical sciences, kermanshah 67145-1673, iran alireza foroumadi maliheh safavi susan kaboudian ardestani

the development and discovery of new anticancer agents is one of the main goals in medicinal chemistry. the conventional anticancer drugs are concomitant with high incidence of unpleasant side effects like severe gastrointestinal side effects and bone marrow suppression. in recent years, various selective anticancer agents have been emerged like dasatinib. the exact mechanism of dasatinib is th...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Francesca Bianchi Alessandra Magnifico Clelia Olgiati Nicola Zanesi Yuri Pekarsky Elda Tagliabue Carlo Maria Croce Sylvie Ménard Manuela Campiglio

The tumor suppressor gene FHIT is inactivated by genetic and epigenetic changes in the majority of common human cancers. The human Fhit protein undergoes phosphorylation on tyrosine residue 114 by Src and related kinases both in vitro and in vivo. Src is a key cytoplasmic tyrosine kinase downstream to several growth factor receptors, including those of the EGF receptor family, which are overexp...

Journal: :The European respiratory journal 2013
Joanne A Groeneveldt Steven J M Gans Harm J Bogaard Anton Vonk-Noordegraaf

We read with interest the article ‘‘Src tyrosine kinase is crucial for potassium channel function in human pulmonary arteries’’ by NAGARAJ et al. [1]. The authors elegantly demonstrated that in physiological conditions, a low pulmonary vascular tone is maintained by Src family tyrosine kinase (SrcTK) and that inhibition of SrcTK will lead to vasoconstriction of pulmonary resistance arteries and...

2016
Brant M. Wagener Nicole A. Marjon Eric R. Prossnitz Adriano Marchese

Arrestins were originally described as proteins recruited to ligand-activated, phosphorylated G protein-coupled receptors (GPCRs) to attenuate G protein-mediated signaling. It was later revealed that arrestins also mediate GPCR internalization and recruit a number of signaling proteins including, but not limited to, Src family kinases, ERK1/2, and JNK3. GPCR-arrestin binding and trafficking con...

Journal: :Molecular pharmacology 2005
Malcolm A Meyn Steven J Schreiner Teodora Pene Dumitrescu Gerard J Nau Thomas E Smithgall

Self-renewal and differentiation of embryonic stem (ES) cells are regulated by cytokines and growth factors through tyrosine kinase-dependent signaling pathways. In murine ES cells, signals for self-renewal are generated by the leukemia inhibitory factor (LIF). LIF and other growth factors are linked to the activation of the Src family of cytoplasmic protein-tyrosine kinases (SFKs), which consi...

Journal: :Blood 1995
N Sharfe H K Dadi C M Roifman

The interleukin-7 (IL-7) receptor is expressed throughout T-cell differentiation and, although lacking a tyrosine kinase domain, mediates tyrosine phosphorylation in T cells. We have identified IL-7-induced activation of three cyoplasmic tyrosine kinases in T cells, Jak1, Jak3, and the src-like kinase p56lck. Many members of the cytokine receptor superfamily activate the Jak protein tyrosine ki...

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