Deficiency in the endocytic adaptor proteins PHETA1/2 impair renal and craniofacial development

Deficiency in the endocytic adaptor proteins PHETA1/2 impair renal and craniofacial development

<p dir="ltr">A critical barrier in the treatment of endosomal and lysosomal diseases is the lack of understanding of the in vivo functions of the putative causative genes. We addressed this by investigating a key pair of endocytic adaptor proteins, PH domain containing endocytic traf...

Full description

Saved in:
Bibliographic Details
Main Author: Kristin M. Ates (18949450) (author)
Other Authors: Tong Wang (87696) (author), Trevor Moreland (18949453) (author), Rajalakshmi Veeranan-Karmegam (10707960) (author), Manxiu Ma (8347386) (author), Chelsi Jeter (18949456) (author), Priya Anand (6838310) (author), Wolfgang Wenzel (25116) (author), Hyung-Goo Kim (728597) (author), Lynne A. Wolfe (18949459) (author), Joshi A. Stephen (18949462) (author), David R. Adams (2135944) (author), Thomas Markello (202566) (author), Cynthia J. Tifft (8981177) (author), Robert Settlage (751097) (author), William A. Gahl (169534) (author), Graydon B. Gonsalvez (10707963) (author), May Christine Malicdan (5229317) (author), Heather Flanagan-Steet (18949465) (author), Y. Albert Pan (8347389) (author)
Published: 2020
Subjects:
Biological sciences
Biochemistry and cell biology
Genetics
Biomedical and clinical sciences
Neurosciences
PHETA1
IPIP27A
OCRL
Endocytosis
Undiagnosed disease
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items