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

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 trafficking adaptor 1 and 2 (PHET...

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Detalles Bibliográficos
Autores principales: Ates, Kristin M., Wang, Tong, Moreland, Trevor, Veeranan-Karmegam, Rajalakshmi, Ma, Manxiu, Jeter, Chelsi, Anand, Priya, Wenzel, Wolfgang, Kim, Hyung-Goo, Wolfe, Lynne A., Stephen, Joshi, Adams, David R., Markello, Thomas, Tifft, Cynthia J., Settlage, Robert, Gahl, William A., Gonsalvez, Graydon B., Malicdan, May Christine, Flanagan-Steet, Heather, Pan, Y. Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272357/
https://www.ncbi.nlm.nih.gov/pubmed/32152089
http://dx.doi.org/10.1242/dmm.041913

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272357/
https://www.ncbi.nlm.nih.gov/pubmed/32152089
http://dx.doi.org/10.1242/dmm.041913

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