Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
第一作者:
Paul L,Auer
第一单位:
1] School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin, USA. [2] Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
作者:
医学主题词
成年人(Adult);老年人(Aged);趋化作用(Chemotaxis);女(雌)性(Female);移码突变(Frameshift Mutation);全基因组关联研究(Genome-Wide Association Study);基因型(Genotype);血细胞比容(Hematocrit);血细胞生成(Hematopoiesis);血红蛋白类(Hemoglobins);人类(Humans);Janus激酶2(Janus Kinase 2);白细胞计数(Leukocyte Count);男(雄)性(Male);中年人(Middle Aged);突变, 误义(Mutation, Missense);中性粒细胞减少(Neutropenia);系谱(Pedigree);血小板计数(Platelet Count);受体, 白细胞介素8B(Receptors, Interleukin-8B)
DOI
10.1038/ng.2962
PMID
24777453
发布时间
2024-06-10
基金项目
RC2 HL102926/HL/NHLBI NIH HHS/United States
P01 CA053996/CA/NCI NIH HHS/United States
HHSN268201100046C/HL/NHLBI NIH HHS/United States
HHSN268201100003C/WH/WHI NIH HHS/United States
RC2 HL102924/HL/NHLBI NIH HHS/United States
UC2 HL102924/HL/NHLBI NIH HHS/United States
U01 HG005152/HG/NHGRI NIH HHS/United States
HHSN268201100001C/WH/WHI NIH HHS/United States
R25 CA094880/CA/NCI NIH HHS/United States
U01 CA137088/CA/NCI NIH HHS/United States
HHSN268201100002C/WH/WHI NIH HHS/United States
P01 AI061093/AI/NIAID NIH HHS/United States
RC2 HL102925/HL/NHLBI NIH HHS/United States
HHSN268201100004C/WH/WHI NIH HHS/United States
R21 HL121422/HL/NHLBI NIH HHS/United States
- 浏览29
Nature genetics
629-34页
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