Swanson KD - Search Results

1

Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia.

Kratz CP, Niemeyer CM, Thomas C, Bauhuber S, Matejas V, Bergsträsser E, Flotho C, Flores NJ, Haas O, Hasle H, van den Heuvel-Eibrink MM, Kucherlapati RS, Lang P, Roberts AE, Starý J, Strahm B, Swanson KD, Trebo M, Zecca M, Neel B, Locatelli F, Loh ML, Zenker M. Kratz CP, et al. Among authors: swanson kd. Leukemia. 2007 May;21(5):1108-9. doi: 10.1038/sj.leu.2404620. Epub 2007 Feb 22. Leukemia. 2007. PMID: 17315019 No abstract available.

2

Germline gain-of-function mutations in SOS1 cause Noonan syndrome.

Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS. Roberts AE, et al. Among authors: swanson kd. Nat Genet. 2007 Jan;39(1):70-4. doi: 10.1038/ng1926. Epub 2006 Dec 3. Nat Genet. 2007. PMID: 17143285

3

PTPN11 (Shp2) mutations in LEOPARD syndrome have dominant negative, not activating, effects.

Kontaridis MI, Swanson KD, David FS, Barford D, Neel BG. Kontaridis MI, et al. Among authors: swanson kd. J Biol Chem. 2006 Mar 10;281(10):6785-92. doi: 10.1074/jbc.M513068200. Epub 2005 Dec 23. J Biol Chem. 2006. PMID: 16377799 Free article.

4

SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients.

Swanson KD, Winter JM, Reis M, Bentires-Alj M, Greulich H, Grewal R, Hruban RH, Yeo CJ, Yassin Y, Iartchouk O, Montgomery K, Whitman SP, Caligiuri MA, Loh ML, Gilliland DG, Look AT, Kucherlapati R, Kern SE, Meyerson M, Neel BG. Swanson KD, et al. Genes Chromosomes Cancer. 2008 Mar;47(3):253-9. doi: 10.1002/gcc.20527. Genes Chromosomes Cancer. 2008. PMID: 18064648

5

Regulation of in vitro and in vivo immune functions by the cytosolic adaptor protein SKAP-HOM.

Togni M, Swanson KD, Reimann S, Kliche S, Pearce AC, Simeoni L, Reinhold D, Wienands J, Neel BG, Schraven B, Gerber A. Togni M, et al. Among authors: swanson kd. Mol Cell Biol. 2005 Sep;25(18):8052-63. doi: 10.1128/MCB.25.18.8052-8063.2005. Mol Cell Biol. 2005. PMID: 16135797 Free PMC article.

6

SHPS-1 is a scaffold for assembling distinct adhesion-regulated multi-protein complexes in macrophages.

Timms JF, Swanson KD, Marie-Cardine A, Raab M, Rudd CE, Schraven B, Neel BG. Timms JF, et al. Among authors: swanson kd. Curr Biol. 1999 Aug 26;9(16):927-30. doi: 10.1016/s0960-9822(99)80401-1. Curr Biol. 1999. PMID: 10469599 Free article.

7

Phosphatase-dependent and -independent functions of Shp2 in neural crest cells underlie LEOPARD syndrome pathogenesis.

Stewart RA, Sanda T, Widlund HR, Zhu S, Swanson KD, Hurley AD, Bentires-Alj M, Fisher DE, Kontaridis MI, Look AT, Neel BG. Stewart RA, et al. Among authors: swanson kd. Dev Cell. 2010 May 18;18(5):750-62. doi: 10.1016/j.devcel.2010.03.009. Dev Cell. 2010. PMID: 20493809 Free PMC article.

8

Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangement.

Alenghat FJ, Baca QJ, Rubin NT, Pao LI, Matozaki T, Lowell CA, Golan DE, Neel BG, Swanson KD. Alenghat FJ, et al. Among authors: swanson kd. J Cell Sci. 2012 Nov 15;125(Pt 22):5535-45. doi: 10.1242/jcs.111260. Epub 2012 Sep 12. J Cell Sci. 2012. PMID: 22976304 Free PMC article.

9

The Skap-hom dimerization and PH domains comprise a 3'-phosphoinositide-gated molecular switch.

Swanson KD, Tang Y, Ceccarelli DF, Poy F, Sliwa JP, Neel BG, Eck MJ. Swanson KD, et al. Mol Cell. 2008 Nov 21;32(4):564-75. doi: 10.1016/j.molcel.2008.09.022. Mol Cell. 2008. PMID: 19026786 Free PMC article.

10

ADAP is required for normal alphaIIbbeta3 activation by VWF/GP Ib-IX-V and other agonists.

Kasirer-Friede A, Moran B, Nagrampa-Orje J, Swanson K, Ruggeri ZM, Schraven B, Neel BG, Koretzky G, Shattil SJ. Kasirer-Friede A, et al. Blood. 2007 Feb 1;109(3):1018-25. doi: 10.1182/blood-2006-05-022301. Epub 2006 Sep 26. Blood. 2007. PMID: 17003372 Free PMC article.

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