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Showing 1-12 of 12 results for "M5691" within Papers
MAGI-1, a candidate stereociliary scaffolding protein, associates with the tip-link component cadherin 23
Xu Z, et al.
The Journal of Neuroscience, 28(44), 11269-11276 (2008)
Jie Ni et al.
The Journal of biological chemistry, 291(47), 24406-24417 (2016-10-21)
MAGI-1 is a multidomain cytosolic scaffolding protein that in the kidney is specifically located at the podocyte slit diaphragm, a specialized junction that is universally injured in proteinuric diseases. There it interacts with several essential molecules, including nephrin and neph1
Binding of PDZ proteins to HPV E6 proteins does neither correlate with epidemiological risk classification nor with the immortalization of foreskin keratinocytes
Muench P, et al.
Virology, 387(2), 380-387 (2009)
Kedar Ghimire et al.
Cells, 8(5) (2019-05-01)
Fluid shear stress stimulates endothelial nitric oxide synthase (eNOS) activation and nitric oxide (NO) production through multiple kinases, including protein kinase A (PKA), AMP-activated protein kinase (AMPK), AKT and Ca2+/calmodulin-dependent protein kinase II (CaMKII). Membrane-associated guanylate kinase (MAGUK) with inverted
Peter Muench et al.
Virology, 387(2), 380-387 (2009-03-17)
There is compelling evidence that high-risk human papillomaviruses (HPV) can cause cervical cancer. Strikingly, HPV16 and 18 account for approximately 70% of all cervical cancers, whereas phylogenetically related types are found at much lower frequencies. Most likely, differences in the
MAGI-1: A Widely Expressed, Alternatively Spliced Tight Junction Protein
Dobrosotskaya IY, et al.
Biochemical and Biophysical Research Communications, 270(3), 903-909 (2000)
MAGI-1: A Widely Expressed, Alternatively Spliced Tight Junction Protein
Laura RP, et al.
Experimental Cell Research, 275(2), 155-170 (2002)
Begoña Alday-Parejo et al.
Cell adhesion & migration, 15(1), 126-139 (2021-04-08)
MAGI1 is an intracellular adaptor protein that stabilizes cell junctions and regulates epithelial and endothelial integrity. Here, we report that that in endothelial cells MAGI1 colocalizes with paxillin, β3-integrin, talin 1, tensin 3 and α-4-actinin at mature focal adhesions and
Shuqin Jia et al.
Chinese journal of cancer research = Chung-kuo yen cheng yen chiu, 29(1), 25-35 (2017-04-05)
To explore the association of membrane-associated guanylate kinase inverted 1 (MAGI1) with gastric cancer (GC) and the related molecular mechanisms. The reverse transcription-polymerase chain reaction (RT-PCR) and immunohistochemistry (IHC) were utilized to measure the MAGI1 expression level in GC tissues.
Jun-Ichi Abe et al.
JCI insight, 4(7) (2019-04-05)
The possible association between the membrane-associated guanylate kinase with inverted domain structure-1 (MAGI1) and inflammation has been suggested, but the molecular mechanisms underlying this link, especially during atherogenesis, remain unclear. In endothelial cells (ECs) exposed to disturbed flow (d-flow), p90
Janine Wörthmüller et al.
Cells, 12(15) (2023-08-11)
MAGI1 acts as a tumor suppressor in estrogen receptor-positive (ER+) breast cancer (BC), and its loss correlates with a more aggressive phenotype. To identify the pathways and events affected by MAGI1 loss, we deleted the MAGI1 gene in the ER+
E6AP-dependent degradation of DLG4/PSD95 by high-risk human papillomavirus type 18 E6 protein
Handa K, et al.
Journal of Virology, 81(3), 1379-1389 (2007)
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