Kahr WH - Search Results

1

Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet alpha-granule biogenesis.

Lo B, Li L, Gissen P, Christensen H, McKiernan PJ, Ye C, Abdelhaleem M, Hayes JA, Williams MD, Chitayat D, Kahr WH. Lo B, et al. Among authors: kahr wh. Blood. 2005 Dec 15;106(13):4159-66. doi: 10.1182/blood-2005-04-1356. Epub 2005 Aug 25. Blood. 2005. PMID: 16123220 Free article.

2

Liver biopsy complicated by hemorrhage in a patient with ARC syndrome.

Hayes JA, Kahr WH, Lo B, Macpherson BA. Hayes JA, et al. Among authors: kahr wh. Paediatr Anaesth. 2004 Nov;14(11):960-3. doi: 10.1111/j.1460-9592.2004.01301.x. Paediatr Anaesth. 2004. PMID: 15500499

3

Fibrinogen is required for maintenance of platelet intracellular and cell-surface P-selectin expression.

Yang H, Lang S, Zhai Z, Li L, Kahr WH, Chen P, Brkić J, Spring CM, Flick MJ, Degen JL, Freedman J, Ni H. Yang H, et al. Among authors: kahr wh. Blood. 2009 Jul 9;114(2):425-36. doi: 10.1182/blood-2008-03-145821. Epub 2009 Mar 30. Blood. 2009. PMID: 19332769 Free article.

4

Granules and thrombus formation.

Kahr WH. Kahr WH. Blood. 2009 Jul 30;114(5):932-3. doi: 10.1182/blood-2009-05-220665. Blood. 2009. PMID: 19643993 Free article. No abstract available.

5

Platelet-associated complement factor H in healthy persons and patients with atypical HUS.

Licht C, Pluthero FG, Li L, Christensen H, Habbig S, Hoppe B, Geary DF, Zipfel PF, Kahr WH. Licht C, et al. Among authors: kahr wh. Blood. 2009 Nov 12;114(20):4538-45. doi: 10.1182/blood-2009-03-205096. Epub 2009 Aug 24. Blood. 2009. PMID: 19704120 Free article.

6

Megakaryocyte and platelet abnormalities in a patient with a W33C mutation in the conserved SH3-like domain of myosin heavy chain IIA.

Kahr WH, Savoia A, Pluthero FG, Li L, Christensen H, De Rocco D, Traivaree C, Butchart SE, Curtin J, Stollar EJ, Forman-Kay JD, Blanchette VS. Kahr WH, et al. Thromb Haemost. 2009 Dec;102(6):1241-50. doi: 10.1160/TH09-02-0119. Thromb Haemost. 2009. PMID: 19967157

7

Anucleate platelets generate progeny.

Schwertz H, Köster S, Kahr WH, Michetti N, Kraemer BF, Weitz DA, Blaylock RC, Kraiss LW, Greinacher A, Zimmerman GA, Weyrich AS. Schwertz H, et al. Among authors: kahr wh. Blood. 2010 May 6;115(18):3801-9. doi: 10.1182/blood-2009-08-239558. Epub 2010 Jan 19. Blood. 2010. PMID: 20086251 Free PMC article.

8

Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy).

Hartley JL, Zachos NC, Dawood B, Donowitz M, Forman J, Pollitt RJ, Morgan NV, Tee L, Gissen P, Kahr WH, Knisely AS, Watson S, Chitayat D, Booth IW, Protheroe S, Murphy S, de Vries E, Kelly DA, Maher ER. Hartley JL, et al. Among authors: kahr wh. Gastroenterology. 2010 Jun;138(7):2388-98, 2398.e1-2. doi: 10.1053/j.gastro.2010.02.010. Epub 2010 Feb 20. Gastroenterology. 2010. PMID: 20176027 Free PMC article.

9

Complement halts angiogenesis gone wild.

Kahr WH. Kahr WH. Blood. 2010 Nov 25;116(22):4393-4. doi: 10.1182/blood-2010-08-297648. Blood. 2010. PMID: 21109626 Free article. No abstract available.

10

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome.

Kahr WH, Hinckley J, Li L, Schwertz H, Christensen H, Rowley JW, Pluthero FG, Urban D, Fabbro S, Nixon B, Gadzinski R, Storck M, Wang K, Ryu GY, Jobe SM, Schutte BC, Moseley J, Loughran NB, Parkinson J, Weyrich AS, Di Paola J. Kahr WH, et al. Nat Genet. 2011 Jul 17;43(8):738-40. doi: 10.1038/ng.884. Nat Genet. 2011. PMID: 21765413 Free PMC article.

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