The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4John A. Sayer, Friedhelm Hildebrandt, Massimo Attanasio et al.|Nature Genetics|2006Cited by 573
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary DyskinesiaChristina Austin‐Tse, Friedhelm Hildebrandt, Jan Halbritter et al.|The American Journal of Human Genetics|2013Cited by 201
Candidate lung tumor susceptibility genes identified through whole-genome association analyses in inbred micePengyuan Liu, Ming You, Yian Wang et al.|Nature Genetics|2006Cited by 82
Inhibitory effect of ETB receptor on Na+–K+ ATPase activity by extracellular Ca2+ entry and Ca2+ release from the endoplasmic reticulum in renal proximal tubule cellsYan Liu, Chunyu Zeng|Hypertension Research|2009Cited by 21