Page last updated: 2024-09-04

cyc 202 and Eye Abnormalities

cyc 202 has been researched along with Eye Abnormalities 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
Alkanderi, S; Filby, A; Henry, C; Miles, CG; Molinari, E; Ramsbottom, SA; Saunier, S; Sayer, JA; Srivastava, S; White, K	1

Other Studies

1 other study(ies) available for cyc 202 and Eye Abnormalities

Article	Year
A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies. Human molecular genetics, 2017, 12-01, Volume: 26, Issue:23 Topics: Abnormalities, Multiple; Antigens, Neoplasm; Cell Cycle Proteins; Cerebellum; Child; Child, Preschool; Cilia; Ciliopathies; Cyclin-Dependent Kinase 5; Cytoskeletal Proteins; Epithelial Cells; Eye Abnormalities; Humans; Kidney Diseases, Cystic; Kidney Failure, Chronic; Male; Morpholines; Mutation; Neoplasm Proteins; Pedigree; Polycystic Kidney Diseases; Primary Cell Culture; Purines; Retina; Roscovitine; Signal Transduction	2017

Article

Year

A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies.

Human molecular genetics, 2017, 12-01, Volume: 26, Issue:23

Topics: Abnormalities, Multiple; Antigens, Neoplasm; Cell Cycle Proteins; Cerebellum; Child; Child, Preschool; Cilia; Ciliopathies; Cyclin-Dependent Kinase 5; Cytoskeletal Proteins; Epithelial Cells; Eye Abnormalities; Humans; Kidney Diseases, Cystic; Kidney Failure, Chronic; Male; Morpholines; Mutation; Neoplasm Proteins; Pedigree; Polycystic Kidney Diseases; Primary Cell Culture; Purines; Retina; Roscovitine; Signal Transduction

2017