Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice.

Autor: Geng X; Cardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA., Chen L; Cardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA., Srinivasan RS; Cardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA., Kylat RJ; Department of Pediatrics, University of Arizona-Tucson, Tucson, AZ, USA., Witte MH; Department of Surgery, University of Arizona-Tucson, Tucson, AZ, USA., Erickson RJ; Department of Pediatrics, University of Arizona-Tucson, Tucson, AZ, USA.

Publikováno v: Lymphology [Lymphology] 2022; Vol. 55 (3), pp. 129-134.