glutamic acid and Ciliary Dyskinesia

glutamic acid has been researched along with Ciliary Dyskinesia in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Attié-Bitach, T; Barbot, C; Bielas, SL; Boltshauser, E; Brancati, F; Castroviejo, IP; Cluckey, A; Doherty, DA; Glass, IA; Gleeson, JG; Hildebrandt, F; Iannicelli, M; Ikegami, K; Johnson, CA; Lee, JE; Lee, JH; Logan, CV; Louie, CM; Marsh, SE; Merriman, B; Nelson, SF; Olvera, J; Rapin, I; Raynes, HR; Schlossman, AM; Schroth, J; Setou, M; Silhavy, JL; Valente, EM; Zaki, MS	1

Other Studies

1 other study(ies) available for glutamic acid and Ciliary Dyskinesia

Article	Year
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium. Nature genetics, 2012, Jan-15, Volume: 44, Issue:2 Topics: Animals; Centrosome; Cerebellar Diseases; Chromosome Mapping; Cilia; Ciliary Motility Disorders; Eye Abnormalities; Female; Genetic Loci; Glutamic Acid; Humans; Male; Mice; Mutation; Peptide Synthases; Polycystic Kidney Diseases; Polymorphism, Single Nucleotide; Protein Processing, Post-Translational; Proteins; Syndrome; Tubulin	2012

Article

Year

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium.

Nature genetics, 2012, Jan-15, Volume: 44, Issue:2

Topics: Animals; Centrosome; Cerebellar Diseases; Chromosome Mapping; Cilia; Ciliary Motility Disorders; Eye Abnormalities; Female; Genetic Loci; Glutamic Acid; Humans; Male; Mice; Mutation; Peptide Synthases; Polycystic Kidney Diseases; Polymorphism, Single Nucleotide; Protein Processing, Post-Translational; Proteins; Syndrome; Tubulin

2012