Skip to Main Content

Paper Details

Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease.
Proc Natl Acad Sci U S A
8
2021
Cas9, Jeune syndrome, Sensenbrenner syndrome, Skeletal ciliopathies, TTC30A, TTC30A/B, Ttc30a, Ttc30a/b transcripts, Xenopus tropicalis, cartilage defects, chondrocytes, ciliary chondrodysplasia, ciliary chondrodysplasia loci, ciliopathies, cystic kidney disease, cystic kidneys, disease genes, ift172, ift80, limb deformities, limb malformations, loci, mouse, nephronophthisis, nephronophthisis-like disease, osteocytes, patients, polycystic kidney disease, polydactyly, renal cysts, short rib polydactyly syndrome, skeletal, skeletal and renal ciliopathy, skeletal ciliopathy, ttc30a, tubulin
Author NameAffiliation
Friedhelm HildebrandtBoston Children's Hospital, Harvard Medical School
Anna K??ttgenInstitute of Genetic Epidemiology, Medical Center - University of Freiburg
Anna K??ttgenInstitute of Genetic Epidemiology, Medical Center - University of Freiburg
  • 1 - 3

Datasets

Release 1.2