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Items: 1 to 20 of 105

1.

L718P mutation in the membrane-proximal cytoplasmic tail of beta 3 promotes abnormal alpha IIb beta 3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype.

Jayo A, Conde I, Lastres P, Martínez C, Rivera J, Vicente V, González-Manchón C.

Haematologica. 2010 Jul;95(7):1158-66. doi: 10.3324/haematol.2009.018572. Epub 2010 Jan 15.

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Serine 752 in the cytoplasmic domain of the beta 3 integrin subunit is not required for alpha v beta 3 postreceptor signaling events.

Kieffer N, Melchior C, Guinet JM, Michels S, Gouon V, Bron N.

Cell Adhes Commun. 1996 Jul;4(1):25-39.

PMID:
8870971
7.

Missense mutations in the beta(3) subunit have a different impact on the expression and function between alpha(IIb)beta(3) and alpha(v)beta(3).

Tadokoro S, Tomiyama Y, Honda S, Kashiwagi H, Kosugi S, Shiraga M, Kiyoi T, Kurata Y, Matsuzawa Y.

Blood. 2002 Feb 1;99(3):931-8.

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A novel Phe171Cys mutation in integrin alpha causes Glanzmann thrombasthenia by abrogating alphabeta complex formation.

Rosenberg N, Landau M, Luboshitz J, Rechavi G, Seligsohn U.

J Thromb Haemost. 2004 Jul;2(7):1167-75.

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Cooperative role of the membrane-proximal and -distal residues of the integrin beta3 cytoplasmic domain in regulation of talin-mediated alpha IIb beta3 activation.

Hato T, Yamanouchi J, Tamura T, Yakushijin Y, Sakai I, Yasukawa M.

J Biol Chem. 2008 Feb 29;283(9):5662-8. doi: 10.1074/jbc.M707246200. Epub 2008 Jan 2.

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A Glanzmann thrombasthenia-like phenotype caused by a defect in inside-out signaling through the integrin alpha(IIb)beta3.

Tomiyama Y, Shiraga M, Kinoshita S, Ambo H, Kurata Y, Matsuzawa Y, Kunicki TJ.

Thromb Haemost. 1998 Nov;80(5):735-42.

PMID:
9843164
17.

Detection of integrin alpha IIbbeta 3 clustering in living cells.

Buensuceso C, de Virgilio M, Shattil SJ.

J Biol Chem. 2003 Apr 25;278(17):15217-24. Epub 2003 Feb 20.

18.

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.

J Thromb Haemost. 2012 Feb;10(2):289-97. doi: 10.1111/j.1538-7836.2011.04577.x.

19.

Overexpression of the partially activated alpha(IIb)beta3D723H integrin salt bridge mutant downregulates RhoA activity and induces microtubule-dependent proplatelet-like extensions in Chinese hamster ovary cells.

Schaffner-Reckinger E, Salsmann A, Debili N, Bellis J, De Mey J, Vainchenker W, Ouwehand WH, Kieffer N.

J Thromb Haemost. 2009 Jul;7(7):1207-17. doi: 10.1111/j.1538-7836.2009.03494.x. Epub 2009 May 22.

20.

A novel Pro126His beta propeller mutation in integrin alphaIIb causes Glanzmann thrombasthenia by impairing progression of pro-alphaIIbbeta3 from endoplasmic reticulum to Golgi.

Shen WZ, Ding QL, Jin PP, Wang XF, Jiang YZ, Li SM, Wang HL.

Blood Cells Mol Dis. 2009 Jan-Feb;42(1):44-50. doi: 10.1016/j.bcmd.2008.08.005. Epub 2008 Oct 30.

PMID:
18976939
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