Cavet M - Search Results

1

Na(+)/H(+) exchanger 3 is in large complexes in the center of the apical surface of proximal tubule-derived OK cells.

Akhter S, Kovbasnjuk O, Li X, Cavet M, Noel J, Arpin M, Hubbard AL, Donowitz M. Akhter S, et al. Among authors: cavet m. Am J Physiol Cell Physiol. 2002 Sep;283(3):C927-40. doi: 10.1152/ajpcell.00613.2001. Am J Physiol Cell Physiol. 2002. PMID: 12176749 Free article.

2

Na(+)/H(+) exchangers (NHE1-3) have similar turnover numbers but different percentages on the cell surface.

Cavet ME, Akhter S, de Medina FS, Donowitz M, Tse CM. Cavet ME, et al. Am J Physiol. 1999 Dec;277(6):C1111-21. doi: 10.1152/ajpcell.1999.277.6.C1111. Am J Physiol. 1999. PMID: 10600762

3

C-terminal domains of Na(+)/H(+) exchanger isoform 3 are involved in the basal and serum-stimulated membrane trafficking of the exchanger.

Akhter S, Cavet ME, Tse CM, Donowitz M. Akhter S, et al. Among authors: cavet me. Biochemistry. 2000 Feb 29;39(8):1990-2000. doi: 10.1021/bi991739s. Biochemistry. 2000. PMID: 10684649

4

Half-lives of plasma membrane Na(+)/H(+) exchangers NHE1-3: plasma membrane NHE2 has a rapid rate of degradation.

Cavet ME, Akhter S, Murtazina R, Sanchez de Medina F, Tse CM, Donowitz M. Cavet ME, et al. Am J Physiol Cell Physiol. 2001 Dec;281(6):C2039-48. doi: 10.1152/ajpcell.2001.281.6.C2039. Am J Physiol Cell Physiol. 2001. PMID: 11698263 Free article.

5

Constitutively active phosphatidylinositol 3-kinase and AKT are sufficient to stimulate the epithelial Na+/H+ exchanger 3.

Lee-Kwon W, Johns DC, Cha B, Cavet M, Park J, Tsichlis P, Donowitz M. Lee-Kwon W, et al. Among authors: cavet m. J Biol Chem. 2001 Aug 17;276(33):31296-304. doi: 10.1074/jbc.M103900200. Epub 2001 May 25. J Biol Chem. 2001. PMID: 11375999 Free article.

6

Short-term regulation of NHE3 by EGF and protein kinase C but not protein kinase A involves vesicle trafficking in epithelial cells and fibroblasts.

Donowitz M, Janecki A, Akhter S, Cavet ME, Sanchez F, Lamprecht G, Zizak M, Kwon WL, Khurana S, Yun CH, Tse CM. Donowitz M, et al. Among authors: cavet me. Ann N Y Acad Sci. 2000;915:30-42. doi: 10.1111/j.1749-6632.2000.tb05221.x. Ann N Y Acad Sci. 2000. PMID: 11193592 Review.

7

cGMP inhibition of Na+/H+ antiporter 3 (NHE3) requires PDZ domain adapter NHERF2, a broad specificity protein kinase G-anchoring protein.

Cha B, Kim JH, Hut H, Hogema BM, Nadarja J, Zizak M, Cavet M, Lee-Kwon W, Lohmann SM, Smolenski A, Tse CM, Yun C, de Jonge HR, Donowitz M. Cha B, et al. Among authors: cavet m. J Biol Chem. 2005 Apr 29;280(17):16642-50. doi: 10.1074/jbc.M500505200. Epub 2005 Feb 18. J Biol Chem. 2005. PMID: 15722341 Free article.

8

Na(+)/H(+) exchanger NHE3 has 11 membrane spanning domains and a cleaved signal peptide: topology analysis using in vitro transcription/translation.

Zizak M, Cavet ME, Bayle D, Tse CM, Hallen S, Sachs G, Donowitz M. Zizak M, et al. Among authors: cavet me. Biochemistry. 2000 Jul 11;39(27):8102-12. doi: 10.1021/bi000870t. Biochemistry. 2000. PMID: 10891093

9

14-3-3beta is a p90 ribosomal S6 kinase (RSK) isoform 1-binding protein that negatively regulates RSK kinase activity.

Cavet ME, Lehoux S, Berk BC. Cavet ME, et al. J Biol Chem. 2003 May 16;278(20):18376-83. doi: 10.1074/jbc.M208475200. Epub 2003 Mar 4. J Biol Chem. 2003. PMID: 12618428 Free article.

10

14-3-3beta binds to big mitogen-activated protein kinase 1 (BMK1/ERK5) and regulates BMK1 function.

Zheng Q, Yin G, Yan C, Cavet M, Berk BC. Zheng Q, et al. Among authors: cavet m. J Biol Chem. 2004 Mar 5;279(10):8787-91. doi: 10.1074/jbc.M310212200. Epub 2003 Dec 16. J Biol Chem. 2004. PMID: 14679215 Free article.

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