Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Sarah E. Arnold"'
Autor:
Emily L Rivard, Andrew G Ludwig, Prajal H Patel, Anna Grandchamp, Sarah E Arnold, Alina Berger, Emilie M Scott, Brendan J Kelly, Grace C Mascha, Erich Bornberg-Bauer, Geoffrey D Findlay
Publikováno v:
PLoS Genetics, Vol 17, Iss 9, p e1009787 (2021)
Comparative genomics has enabled the identification of genes that potentially evolved de novo from non-coding sequences. Many such genes are expressed in male reproductive tissues, but their functions remain poorly understood. To address this, we con
Externí odkaz:
https://doaj.org/article/914a8daee7114d5e9ee0eb6c73a363ec
Publikováno v:
eJHaem. 2:485-487
Autor:
Anna Grandchamp, Emilie M. Scott, Geoffrey D. Findlay, Prajal H. Patel, Erich Bornberg-Bauer, Emily L Rivard, Grace C. Mascha, Sarah E. Arnold, Andrew G. Ludwig, Brendan J Kelly, Alina Berger
Comparative genomics has enabled the identification of genes that potentially evolved de novo from non-coding sequences. Many such genes are expressed in male reproductive tissues, but their functions remain poorly understood. To address this, we con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70300ea601512a4c40290f133fdec4ae
https://doi.org/10.1101/2021.06.10.447990
https://doi.org/10.1101/2021.06.10.447990
Autor:
Ty Achtermann, Laura Carrel, Fang Chen, M. Elaine Eyster, Sarah E. Arnold-Croop, Yuhuan Cheng, Dajiang J. Liu
Publikováno v:
Haemophilia. 27
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
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
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
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
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
Publikováno v:
Journal of Health Politics, Policy & Law. Oct2022, Vol. 47 Issue 5, p555-581. 27p. 5 Charts, 3 Graphs.