phosphatidylcholines has been researched along with Pigmentary Retinopathy in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cornell, RB; Dennis, MK; Dhillon, RK; Lee, J; Taneva, SG; Tse, R | 1 |
| Blout, C; Cho, SY; Cho, TJ; Doheny, KF; Hetrick, KN; Hoover-Fong, J; Jin, DK; Jurgens, J; Kim, OH; Kim, SJ; Kitoh, H; Ling, H; Modaff, P; Moser, A; Park, WY; Pauli, RM; Sobreira, N; Valle, D | 1 |
| Wong, CK | 1 |
| 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 |
| Fujiwara, H | 1 |
| Mitchell, JE; Swartz, JG | 1 |
6 other study(ies) available for phosphatidylcholines and Pigmentary Retinopathy
| Article | Year |
|---|---|
Disease-linked mutations in the phosphatidylcholine regulatory enzyme CCTα impair enzymatic activity and fold stability.
Topics: Animals; Catalysis; Catalytic Domain; Chlorocebus aethiops; Choline-Phosphate Cytidylyltransferase; COS Cells; Crystallography, X-Ray; Humans; Lipodystrophy; Mutation; Osteochondrodysplasias; Phosphatidylcholines; Protein Binding; Protein Folding; Protein Stability; Retinal Dystrophies; Retinitis Pigmentosa | 2019 |
Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.
Topics: Alleles; Child, Preschool; Choline-Phosphate Cytidylyltransferase; Female; Humans; Infant; Male; Middle Aged; Mutation, Missense; Osteochondrodysplasias; Pedigree; Phosphatidylcholines; Retinitis Pigmentosa | 2014 |
Novel mutations in PCYT1A are responsible for spondylometaphyseal dysplasia with cone-rod dystrophy.
Topics: Choline-Phosphate Cytidylyltransferase; Female; Humans; Male; Mutation, Missense; Osteochondrodysplasias; Phosphatidylcholines; Retinitis Pigmentosa | 2014 |
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 |
[Biochemical studies on retinitis pigmentosa. 2. Study on plasma lipids of retinitis pigmentosa by thin layer chromatography].
Topics: Adolescent; Adult; Child; Cholesterol; Chromatography, Thin Layer; Fatty Acids; Humans; Lipids; Metabolic Diseases; Middle Aged; Phosphatidylcholines; Phosphatidylethanolamines; Retinitis Pigmentosa | 1966 |
Biosynthesis of retinal phospholipids: incorporation of radioactivity from labeled phosphorylcholine and cytidine diphosphate choline.
Topics: Adenosine Triphosphate; Animals; Carbon Isotopes; Choline; Chromatography; Coenzyme A; Cytosine Nucleotides; Glycerides; Lysophosphatidylcholines; Magnesium; Microsomes; Mitochondria; Paper; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Phosphoric Acids; Photoreceptor Cells; Rats; Retina; Retinitis Pigmentosa; Sphingomyelins; Transferases | 1970 |