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phosphatidylcholines and Amaurosis, Leber Congenital

phosphatidylcholines has been researched along with Amaurosis, Leber Congenital in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, AR1

Other Studies

1 other study(ies) available for phosphatidylcholines and Amaurosis, Leber Congenital

ArticleYear
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice.
    Proceedings of the National Academy of Sciences of the United States of America, 2010, Aug-31, Volume: 107, Issue:35

    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