phosphatidylcholines has been researched along with Amaurosis, Leber Congenital in 1 studies
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 | Studies |
---|---|
Bakeri, HA; Bhattacharya, SS; Branham, KE; Brooks, MJ; Campos, MM; Chang, B; Feathers, KL; Friedman, JS; Heckenlively, JR; Hurd, RE; Koenekoop, RK; Krauth, DS; Liu, C; Lopez, I; Maubaret, C; Rodriguez, IR; Shaw, M; Swaroop, A; Thomas, GE; Thompson, DA; Waseem, NH; Webster, AR | 1 |
1 other study(ies) available for phosphatidylcholines and Amaurosis, Leber Congenital
Article | Year |
---|---|
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice.
Topics: 1-Acylglycerophosphocholine O-Acyltransferase; Animals; Base Sequence; Blotting, Northern; Chromatography, High Pressure Liquid; Chromosome Mapping; DNA Mutational Analysis; Humans; Immunoblotting; Leber Congenital Amaurosis; Lipids; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Inbred Strains; Mice, Mutant Strains; Microscopy, Electron, Transmission; Phosphatidylcholines; Photoreceptor Cells, Vertebrate; Retinal Degeneration; Retinitis Pigmentosa; Reverse Transcriptase Polymerase Chain Reaction | 2010 |