Mor-Cohen R - Search Results

1

Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3).

Peretz H, Rosenberg N, Landau M, Usher S, Nelson EJ, Mor-Cohen R, French DL, Mitchell BW, Nair SC, Chandy M, Coller BS, Srivastava A, Seligsohn U. Peretz H, et al. Hum Mutat. 2006 Apr;27(4):359-69. doi: 10.1002/humu.20304. Hum Mutat. 2006. PMID: 16463284

2

Disulfide bond disruption by a beta 3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active alpha IIb beta 3.

Mor-Cohen R, Rosenberg N, Peretz H, Landau M, Coller BS, Awidi A, Seligsohn U. Mor-Cohen R, et al. Thromb Haemost. 2007 Dec;98(6):1257-65. Thromb Haemost. 2007. PMID: 18064323

3

A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.

Rosenberg N, Hauschner H, Peretz H, Mor-Cohen R, Landau M, Shenkman B, Kenet G, Coller BS, Awidi AA, Seligsohn U. Rosenberg N, et al. J Thromb Haemost. 2005 Dec;3(12):2764-72. doi: 10.1111/j.1538-7836.2005.01618.x. J Thromb Haemost. 2005. PMID: 16359514 Free PMC article.

4

Specific cysteines in beta3 are involved in disulfide bond exchange-dependent and -independent activation of alphaIIbbeta3.

Mor-Cohen R, Rosenberg N, Landau M, Lahav J, Seligsohn U. Mor-Cohen R, et al. J Biol Chem. 2008 Jul 11;283(28):19235-44. doi: 10.1074/jbc.M802399200. Epub 2008 May 5. J Biol Chem. 2008. PMID: 18458089 Free article.

5

Unique disulfide bonds in epidermal growth factor (EGF) domains of β3 affect structure and function of αIIbβ3 and αvβ3 integrins in different manner.

Mor-Cohen R, Rosenberg N, Einav Y, Zelzion E, Landau M, Mansour W, Averbukh Y, Seligsohn U. Mor-Cohen R, et al. J Biol Chem. 2012 Mar 16;287(12):8879-91. doi: 10.1074/jbc.M111.311043. Epub 2012 Feb 3. J Biol Chem. 2012. PMID: 22308022 Free PMC article.

6

Disulfide bond exchanges in integrins αIIbβ3 and αvβ3 are required for activation and post-ligation signaling during clot retraction.

Mor-Cohen R, Rosenberg N, Averbukh Y, Seligsohn U, Lahav J. Mor-Cohen R, et al. Thromb Res. 2014 May;133(5):826-36. doi: 10.1016/j.thromres.2014.02.001. Epub 2014 Feb 7. Thromb Res. 2014. PMID: 24560420

7

Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome.

Hauschner H, Mor-Cohen R, Messineo S, Mansour W, Seligsohn U, Savoia A, Rosenberg N. Hauschner H, et al. Among authors: mor cohen r. Blood Coagul Fibrinolysis. 2015 Apr;26(3):302-8. doi: 10.1097/MBC.0000000000000241. Blood Coagul Fibrinolysis. 2015. PMID: 25806962

8

A mutation in the β3 cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of αIIb β3 to an active state.

Hauschner H, Mor-Cohen R, Seligsohn U, Rosenberg N. Hauschner H, et al. J Thromb Haemost. 2012 Feb;10(2):289-97. doi: 10.1111/j.1538-7836.2011.04577.x. J Thromb Haemost. 2012. PMID: 22136613 Free article.

9

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.

Peretz H, Salomon O, Mor-Cohen R, Usher S, Zucker M, Zivelin A, Seligsohn U. Peretz H, et al. J Thromb Haemost. 2013 Apr;11(4):724-30. doi: 10.1111/jth.12137. J Thromb Haemost. 2013. PMID: 23332144 Free article.

10

A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients.

Mor-Cohen R, Zivelin A, Rosenberg N, Goldberg I, Seligsohn U. Mor-Cohen R, et al. Hepatol Res. 2005 Feb;31(2):104-11. doi: 10.1016/j.hepres.2004.11.010. Hepatol Res. 2005. PMID: 15777714

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