Award

DK088767

Funder: National Institute of Diabetes and Digestive and Kidney Diseases

Funded outputs count: 4

Funder award ID: DK088767

OpenAlex ID: G2645988016

Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies ImplicateZIC3andFOXF1in Human VATER/VACTERL Association

2015 · Alina C. Hilger, Jan Halbritter, et al. · Human Mutation · 55

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

2015 · Asaf Vivante, Marc-Jens Kleppa, et al. · The American Journal of Human Genetics · 92

Nephronophthisis-Associated CEP164 Regulates Cell Cycle Progression, Apoptosis and Epithelial-to-Mesenchymal Transition

2014 · Gisela G. Slaats, Amiya K. Ghosh, et al. · PLoS Genetics · 70

Autosomal Dominant Mutation in the Signal Peptide of Renin in a Kindred With Anemia, Hyperuricemia, and CKD

2011 · Bodo B. Beck, Howard Trachtman, et al. · American Journal of Kidney Diseases · 32