Characterization of hemostasis in mice lacking the novel thrombosis susceptibility gene Slc44a2.
Sign Up to like & getrecommendations! Published in 2018 at "Thrombosis research"
DOI: 10.1016/j.thromres.2018.09.057
Abstract: INTRODUCTION Recent genome wide association studies (GWAS) identified a novel susceptibility locus for thrombosis, harbouring the SLC44A2 gene which encodes the Solute Carrier Family 44 Member 2 protein (SLC44A2). Thus far, SLC44A2 has not been… read more here.
Keywords: mice lacking; mice; slc44a2; gene ... See more keywords
Lack of the human choline transporter‐like protein SLC44A2 causes hearing impairment and a rare red blood phenotype
Sign Up to like & getrecommendations! Published in 2023 at "EMBO Molecular Medicine"
DOI: 10.15252/emmm.202216320
Abstract: Blood phenotypes are defined by the presence or absence of specific blood group antigens at the red blood cell (RBC) surface, due to genetic polymorphisms among individuals. The recent development of genomic and proteomic approaches… read more here.
Keywords: choline transporter; red blood; slc44a2; transporter like ... See more keywords