Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Ek, Novak"'
Autor:
William C. Nichols, RT Swank, JD Ballew, KA Cooney, K. L. Mohlke, M Reddington, EK Novak, ME Bruck, A Yang, David Ginsburg
Publikováno v:
Blood. 83:3225-3231
An animal model for human type I von Willebrand disease (vWD) has been previously described in the inbred mouse strain RIIIS/J. Murine vWD is characterized by a prolonged bleeding time, normal von Willebrand factor (vWF) multimer distribution, autoso
Publikováno v:
Blood. 81:2626-2635
Gunmetal (gm/gm) is a recessively inherited mouse pigment dilution mutant that has high mortality and poor reproductive rates. In these studies, several hematologic defects were found associated with the mutation, including prolonged bleeding times,
Publikováno v:
Blood. 78:2036-2044
Several inherited human syndromes have combined platelet, auditory, and/or pigment abnormalities. In the mouse the pallid pigment mutant has abnormalities of the otoliths of the inner ear together with a bleeding abnormality caused by platelet storag
Autor:
Zhen L, Jiang S, Feng L, Na, Bright, Andrew Peden, Ab, Seymour, Ek, Novak, Elliott R, Mb, Gorin, Ms, Robinson, Rt, Swank
Publikováno v:
Europe PubMed Central
The pearl mouse is a model for Hermansky Pudlak Syndrome (HPS), whose symptoms include hypopigmentation, lysosomal abnormalities, and prolonged bleeding due to platelet storage pool deficiency (SPD). The gene for pearl has recently been identified as
Publikováno v:
Blood. 76(11)
Mice of the RIIIS/J inbred strain have prolonged bleeding times (greater than 15 minutes) after experimental injury when compared with normal C57BL/6J mice (1.8 minutes) and other strains of mice. The prolonged bleeding time was accompanied by normal
Publikováno v:
Blood. 69:1300-1306
Mepacrine uptake into platelets and bone marrow megakaryocytes was analyzed to further characterize the dense granule defects in a group of seven mouse pigment mutants that have characteristics of platelet storage pool disease (SPD). In contrast to o
Publikováno v:
Blood. 66(5)
Two human diseases of platelet storage pool deficiency (SPD), Hermansky- Pudlak syndrome and Chediak-Higashi syndrome, are recessively inherited disorders characterized by hypopigmentation, prolonged bleeding, and normal platelet counts accompanied b
Publikováno v:
Blood. 57(1)
The mouse pigment mutant pale ear, ep/ep, which has a defect in kidney lysosomal enzyme secretion, had prolonged bleeding on experimental injury. Platelet counts and platelet protein did not differ from normal. There was, however, a deficiency in the
Autor:
Guo X; Department of Cell Biology, New York University School of Medicine, New York, NY 10016, USA., Tu L, Gumper I, Plesken H, Novak EK, Chintala S, Swank RT, Pastores G, Torres P, Izumi T, Sun TT, Sabatini DD, Kreibich G
Publikováno v:
Traffic (Copenhagen, Denmark) [Traffic] 2009 Sep; Vol. 10 (9), pp. 1350-61. Date of Electronic Publication: 2009 May 26.
Autor:
Chintala S; Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, NY, USA. sreenivasulu.chintala@roswellpark.org, Novak EK, Spernyak JA, Mazurchuk R, Torres G, Patel S, Busch K, Meeder BA, Horowitz JM, Vaughan MM, Swank RT
Publikováno v:
Brain research [Brain Res] 2009 Apr 17; Vol. 1266, pp. 18-28. Date of Electronic Publication: 2009 Feb 27.