132 related articles for article (PubMed ID: 38858683)
1. PCYT1A deficiency disturbs fatty acid metabolism and induces ferroptosis in the mouse retina.
Wang K; Xu H; Zou R; Zeng G; Yuan Y; Zhu X; Zhao X; Li J; Zhang L
BMC Biol; 2024 Jun; 22(1):134. PubMed ID: 38858683
[TBL] [Abstract][Full Text] [Related]
2. Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy.
Testa F; Filippelli M; Brunetti-Pierri R; Di Fruscio G; Di Iorio V; Pizzo M; Torella A; Barillari MR; Nigro V; Brunetti-Pierri N; Simonelli F; Banfi S
Eur J Hum Genet; 2017 May; 25(5):651-655. PubMed ID: 28272537
[TBL] [Abstract][Full Text] [Related]
3. Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease.
Payne F; Lim K; Girousse A; Brown RJ; Kory N; Robbins A; Xue Y; Sleigh A; Cochran E; Adams C; Dev Borman A; Russel-Jones D; Gorden P; Semple RK; Saudek V; O'Rahilly S; Walther TC; Barroso I; Savage DB
Proc Natl Acad Sci U S A; 2014 Jun; 111(24):8901-6. PubMed ID: 24889630
[TBL] [Abstract][Full Text] [Related]
4.
Andrejeva G; Gowan S; Lin G; Wong Te Fong AL; Shamsaei E; Parkes HG; Mui J; Raynaud FI; Asad Y; Vizcay-Barrena G; Nikitorowicz-Buniak J; Valenti M; Howell L; Fleck RA; Martin LA; Kirkin V; Leach MO; Chung YL
Autophagy; 2020 Jun; 16(6):1044-1060. PubMed ID: 31517566
[TBL] [Abstract][Full Text] [Related]
5. PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress.
Haider A; Wei YC; Lim K; Barbosa AD; Liu CH; Weber U; Mlodzik M; Oras K; Collier S; Hussain MM; Dong L; Patel S; Alvarez-Guaita A; Saudek V; Jenkins BJ; Koulman A; Dymond MK; Hardie RC; Siniossoglou S; Savage DB
Dev Cell; 2018 May; 45(4):481-495.e8. PubMed ID: 29754800
[TBL] [Abstract][Full Text] [Related]
6. Prohibitin 2 deficiency in photoreceptors leads to progressive retinal degeneration and facilitated Müller glia engulfing microglia debris.
Zuo H; Han W; Wu K; Yang H; Song H; Zhang Z; Lai Y; Pan Z; Li W; Zhao L
Exp Eye Res; 2024 Jul; 244():109935. PubMed ID: 38763352
[TBL] [Abstract][Full Text] [Related]
7. Disease-linked mutations in the phosphatidylcholine regulatory enzyme CCTα impair enzymatic activity and fold stability.
Cornell RB; Taneva SG; Dennis MK; Tse R; Dhillon RK; Lee J
J Biol Chem; 2019 Feb; 294(5):1490-1501. PubMed ID: 30559292
[TBL] [Abstract][Full Text] [Related]
8. Early embryonic lethality in mice with targeted deletion of the CTP:phosphocholine cytidylyltransferase alpha gene (Pcyt1a).
Wang L; Magdaleno S; Tabas I; Jackowski S
Mol Cell Biol; 2005 Apr; 25(8):3357-63. PubMed ID: 15798219
[TBL] [Abstract][Full Text] [Related]
9. PCYT1A suppresses proliferation and migration via inhibiting mTORC1 pathway in lung adenocarcinoma.
Yu J; Wu C; Wu Q; Huang J; Fu W; Xie X; Li W; Tang W; Xu C; Jin G
Biochem Biophys Res Commun; 2020 Aug; 529(2):353-361. PubMed ID: 32703435
[TBL] [Abstract][Full Text] [Related]
10. Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy.
Yamamoto GL; Baratela WA; Almeida TF; Lazar M; Afonso CL; Oyamada MK; Suzuki L; Oliveira LA; Ramos ES; Kim CA; Passos-Bueno MR; Bertola DR
Am J Hum Genet; 2014 Jan; 94(1):113-9. PubMed ID: 24387991
[TBL] [Abstract][Full Text] [Related]
11. Cellular and Molecular Mechanisms of Pathogenesis Underlying Inherited Retinal Dystrophies.
Manley A; Meshkat BI; Jablonski MM; Hollingsworth TJ
Biomolecules; 2023 Feb; 13(2):. PubMed ID: 36830640
[TBL] [Abstract][Full Text] [Related]
12. Notch Inhibition Promotes Regeneration and Immunosuppression Supports Cone Survival in a Zebrafish Model of Inherited Retinal Dystrophy.
Fogerty J; Song P; Boyd P; Grabinski SE; Hoang T; Reich A; Cianciolo LT; Blackshaw S; Mumm JS; Hyde DR; Perkins BD
J Neurosci; 2022 Jun; 42(26):5144-5158. PubMed ID: 35672150
[TBL] [Abstract][Full Text] [Related]
13. Gene Therapy in Hereditary Retinal Dystrophies: The Usefulness of Diagnostic Tools in Candidate Patient Selections.
Malvasi M; Casillo L; Avogaro F; Abbouda A; Vingolo EM
Int J Mol Sci; 2023 Sep; 24(18):. PubMed ID: 37762059
[TBL] [Abstract][Full Text] [Related]
14. Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
Quinn PM; Mulder AA; Henrique Alves C; Desrosiers M; de Vries SI; Klooster J; Dalkara D; Koster AJ; Jost CR; Wijnholds J
Hum Mol Genet; 2019 Jan; 28(1):105-123. PubMed ID: 30239717
[TBL] [Abstract][Full Text] [Related]
15. PRCD is concentrated at the base of photoreceptor outer segments and is involved in outer segment disc formation.
Allon G; Mann I; Remez L; Sehn E; Rizel L; Nevet MJ; Perlman I; Wolfrum U; Ben-Yosef T
Hum Mol Genet; 2019 Dec; 28(24):4078-4088. PubMed ID: 31628458
[TBL] [Abstract][Full Text] [Related]
16. MYC is a positive regulator of choline metabolism and impedes mitophagy-dependent necroptosis in diffuse large B-cell lymphoma.
Xiong J; Wang L; Fei XC; Jiang XF; Zheng Z; Zhao Y; Wang CF; Li B; Chen SJ; Janin A; Gale RP; Zhao WL
Blood Cancer J; 2017 Jul; 7(7):e0. PubMed ID: 28686226
[TBL] [Abstract][Full Text] [Related]
17. Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice.
Eblimit A; Agrawal SA; Thomas K; Anastassov IA; Abulikemu T; Moayedi Y; Mardon G; Chen R
Exp Eye Res; 2018 Jan; 166():120-130. PubMed ID: 29100828
[TBL] [Abstract][Full Text] [Related]
18. Gene therapy for inherited retinal diseases: progress and possibilities.
Hu ML; Edwards TL; O'Hare F; Hickey DG; Wang JH; Liu Z; Ayton LN
Clin Exp Optom; 2021 May; 104(4):444-454. PubMed ID: 33689657
[TBL] [Abstract][Full Text] [Related]
19. The m
Yang Y; Jiang X; Chen J; Liu L; Liu G; Sun K; Liu W; Zhu X; Guan Q
J Genet Genomics; 2024 Feb; 51(2):208-221. PubMed ID: 38157933
[TBL] [Abstract][Full Text] [Related]
20. Lysophosphatidylcholine acyltransferase 1 controls mitochondrial reactive oxygen species generation and survival of retinal photoreceptor cells.
Nagata K; Hishikawa D; Sagara H; Saito M; Watanabe S; Shimizu T; Shindou H
J Biol Chem; 2022 Jun; 298(6):101958. PubMed ID: 35452679
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]