Page last updated: 2024-08-21

ethylnitrosourea and Congenital X-Linked Retinoschisis

ethylnitrosourea has been researched along with Congenital X-Linked Retinoschisis 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	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Dalke, C; Favor, J; Goldowitz, D; Graw, J; Jablonski, MM; Lu, L; Manly, KF; Pardue, MT; Pretsch, W; Rinchik, EM; Wang, X; Williams, RW	1

Other Studies

1 other study(ies) available for ethylnitrosourea and Congenital X-Linked Retinoschisis

Article	Year
An ENU-induced mutation in Rs1h causes disruption of retinal structure and function. Molecular vision, 2005, Jul-27, Volume: 11 Topics: Alkylating Agents; Animals; Base Sequence; Cell Adhesion Molecules; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Electroretinography; Ethylnitrosourea; Eye Proteins; Female; Immunoenzyme Techniques; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation; Retina; Retinoschisis	2005

Article

Year

An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.

Molecular vision, 2005, Jul-27, Volume: 11

Topics: Alkylating Agents; Animals; Base Sequence; Cell Adhesion Molecules; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Electroretinography; Ethylnitrosourea; Eye Proteins; Female; Immunoenzyme Techniques; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation; Retina; Retinoschisis

2005