Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sarah E. Arnold-Croop"'
Publikováno v:
eJHaem. 2:485-487
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::731f8a84374f3dc39d8bc0285425b33e
https://doi.org/10.1002/jha2.267
https://doi.org/10.1002/jha2.267
Autor:
Ty Achtermann, Laura Carrel, Fang Chen, M. Elaine Eyster, Sarah E. Arnold-Croop, Yuhuan Cheng, Dajiang J. Liu
Publikováno v:
Haemophilia. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::883869230b635823417e849812e56352
https://doi.org/10.1111/hae.14348
https://doi.org/10.1111/hae.14348
Autor:
Laura Carrel, M. Elaine Eyster, Elizabeth A. Weidman, Peter H. Cygan, Sarah E. Arnold-Croop, Dajiang J. Liu, Fang Chen
Publikováno v:
Thrombosis research. 193
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4999c06a8acb8507a9e887446f4c752b
https://pubmed.ncbi.nlm.nih.gov/32521332
https://pubmed.ncbi.nlm.nih.gov/32521332
Publikováno v:
Blood. 136:11-11
INTRODUCTION: Dehydrated hereditary stomatocytosis (DHSt) is an autosomal dominant red blood cell membrane disorder characterized by hemolytic anemia and splenomegaly. DHSt has an estimated incidence of 1:50,000 births, and the degree of anemia varie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a32edaf89e54cb8dac29bc2cfdcb72b3
https://doi.org/10.1182/blood-2020-137481
https://doi.org/10.1182/blood-2020-137481
Autor:
Elizabeth A. Weidman, Peter H. Cygan, Laura Carrel, Fang Chen, Sarah E. Arnold-Croop, Dajiang J. Liu, M. Elaine Eyster
Publikováno v:
Blood. 134:1125-1125
Introduction: While Factor VIII (FVIII) activity correlates with phenotype in most Hemophilia A (HA) males, the study of rare individuals with discrepant bleeding phenotypes can provide insight into F8 genotype-bleeding phenotype relationships, refin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a15e999178677044dd1b89f85e5a62d9
https://doi.org/10.1182/blood-2019-126026
https://doi.org/10.1182/blood-2019-126026
Publikováno v:
Mammalian Genome. 22:572-582
X Chromosome inactivation (XCI) silences one copy of most X-linked genes in female mammals. Notably, human and mouse differ strikingly in the number and organization of the genes that escape XCI. While on the human X Chromosome (Chr) escape genes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f36e32f0cbdbaf970c1ee411b49790d9
https://doi.org/10.1007/s00335-011-9350-6
https://doi.org/10.1007/s00335-011-9350-6
Elevated Von Willebrand Factor May Abrogate Bleeding Phenotype in a Male with a Non-Null F8 Mutation
Publikováno v:
Blood. 132:3787-3787
Introduction: Although FVIII activity (FVIII:C) correlates with phenotype in most Hemophilia A males, some have bleeding phenotypes milder than predicted by FVIII:C. Analysis of these individuals may provide additional insight into the relationship b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::198cf286d90e5886a6047c705e29eec5
https://doi.org/10.1182/blood-2018-99-116905
https://doi.org/10.1182/blood-2018-99-116905