197 related articles for article (PubMed ID: 30221923)
1. The Spastic Paraplegia-Associated Phospholipase DDHD1 Is a Primary Brain Phosphatidylinositol Lipase.
Inloes JM; Jing H; Cravatt BF
Biochemistry; 2018 Oct; 57(39):5759-5767. PubMed ID: 30221923
[TBL] [Abstract][Full Text] [Related]
2. Generation of lysophosphatidylinositol by DDHD domain containing 1 (DDHD1): Possible involvement of phospholipase D/phosphatidic acid in the activation of DDHD1.
Yamashita A; Kumazawa T; Koga H; Suzuki N; Oka S; Sugiura T
Biochim Biophys Acta; 2010 Jul; 1801(7):711-20. PubMed ID: 20359546
[TBL] [Abstract][Full Text] [Related]
3. Oleic Acid-Containing Phosphatidylinositol Is a Blood Biomarker Candidate for SPG28.
Morikawa T; Takahashi M; Izumi Y; Bamba T; Moriyama K; Hattori G; Fujioka R; Miura S; Shibata H
Biomedicines; 2023 Apr; 11(4):. PubMed ID: 37189713
[TBL] [Abstract][Full Text] [Related]
4. Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia.
Morikawa T; Ohishi H; Kosaka K; Shimojo T; Nagano A; Taniguchi I; Fujioka R; Moriyama K; Unoki M; Takahashi M; Nakao M; Izumi Y; Bamba T; Sasaki H; Miura S; Shibata H
Biosci Rep; 2021 Feb; 41(2):. PubMed ID: 33600578
[TBL] [Abstract][Full Text] [Related]
5. Phosphorylation of human phospholipase A1 DDHD1 at newly identified phosphosites affects its subcellular localization.
Matsumoto N; Nemoto-Sasaki Y; Oka S; Arai S; Wada I; Yamashita A
J Biol Chem; 2021 Jul; 297(1):100851. PubMed ID: 34089703
[TBL] [Abstract][Full Text] [Related]
6. Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation.
Dard R; Meyniel C; Touitou V; Stevanin G; Lamari F; Durr A; Ewenczyk C; Mochel F
Eur J Med Genet; 2017 Dec; 60(12):639-642. PubMed ID: 28818478
[TBL] [Abstract][Full Text] [Related]
7. Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis.
Maruyama T; Baba T; Maemoto Y; Hara-Miyauchi C; Hasegawa-Ogawa M; Okano HJ; Enda Y; Matsumoto K; Arimitsu N; Nakao K; Hamamoto H; Sekimizu K; Ohto-Nakanishi T; Nakanishi H; Tokuyama T; Yanagi S; Tagaya M; Tani K
Cell Death Dis; 2018 Jul; 9(8):797. PubMed ID: 30038238
[TBL] [Abstract][Full Text] [Related]
8. A novel frameshift mutation of DDHD1 in a Japanese patient with autosomal recessive spastic paraplegia.
Miura S; Morikawa T; Fujioka R; Kosaka K; Yamada K; Hattori G; Motomura M; Taniwaki T; Shibata H
Eur J Med Genet; 2016 Aug; 59(8):413-6. PubMed ID: 27216551
[TBL] [Abstract][Full Text] [Related]
9. Expression of Lysophosphatidylinositol Signaling-relevant Molecules in Colorectal Cancer.
Kitamura C; Sonoda H; Anzai H; Nagai Y; Abe S; Yokoyama Y; Ishii H; Kishikawa J; Emoto S; Murono K; Sasaki K; Kawai K; Nozawa H; Ishihara S
Anticancer Res; 2021 May; 41(5):2349-2355. PubMed ID: 33952459
[TBL] [Abstract][Full Text] [Related]
10. Current Knowledge on Mammalian Phospholipase A
Yaginuma S; Kawana H; Aoki J
Molecules; 2022 Apr; 27(8):. PubMed ID: 35458682
[TBL] [Abstract][Full Text] [Related]
11. Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations.
Liguori R; Giannoccaro MP; Arnoldi A; Citterio A; Tonon C; Lodi R; Bresolin N; Bassi MT
J Neurol; 2014 Sep; 261(9):1789-93. PubMed ID: 24989667
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28.
Mignarri A; Rubegni A; Tessa A; Stefanucci S; Malandrini A; Cardaioli E; Meschini MC; Stromillo ML; Doccini S; Federico A; Santorelli FM; Dotti MT
J Neurol Sci; 2016 Mar; 362():287-91. PubMed ID: 26944165
[TBL] [Abstract][Full Text] [Related]
13. The actions and metabolism of lysophosphatidylinositol, an endogenous agonist for GPR55.
Yamashita A; Oka S; Tanikawa T; Hayashi Y; Nemoto-Sasaki Y; Sugiura T
Prostaglandins Other Lipid Mediat; 2013 Dec; 107():103-16. PubMed ID: 23714700
[TBL] [Abstract][Full Text] [Related]
14. Functional Contribution of the Spastic Paraplegia-Related Triglyceride Hydrolase DDHD2 to the Formation and Content of Lipid Droplets.
Inloes JM; Kiosses WB; Wang H; Walther TC; Farese RV; Cravatt BF
Biochemistry; 2018 Feb; 57(5):827-838. PubMed ID: 29278326
[TBL] [Abstract][Full Text] [Related]
15. Phosphorylation and subcellular localization of human phospholipase A1, DDHD1/PA-PLA1.
Yamashita A; Matsumoto N; Nemoto-Sasaki Y; Oka S; Arai S; Wada I
Methods Enzymol; 2022; 675():235-273. PubMed ID: 36220272
[TBL] [Abstract][Full Text] [Related]
16. The hereditary spastic paraplegia-related enzyme DDHD2 is a principal brain triglyceride lipase.
Inloes JM; Hsu KL; Dix MM; Viader A; Masuda K; Takei T; Wood MR; Cravatt BF
Proc Natl Acad Sci U S A; 2014 Oct; 111(41):14924-9. PubMed ID: 25267624
[TBL] [Abstract][Full Text] [Related]
17. Misregulation of a DDHD Domain-containing Lipase Causes Mitochondrial Dysfunction in Yeast.
Yadav PK; Rajasekharan R
J Biol Chem; 2016 Aug; 291(35):18562-81. PubMed ID: 27402848
[TBL] [Abstract][Full Text] [Related]
18. The phospholipase DDHD1 as a new target in colorectal cancer therapy.
Raimondo S; Cristaldi M; Fontana S; Saieva L; Monteleone F; Calabrese G; Giavaresi G; Parenti R; Alessandro R
J Exp Clin Cancer Res; 2018 Apr; 37(1):82. PubMed ID: 29653539
[TBL] [Abstract][Full Text] [Related]
19. ABHD12 controls brain lysophosphatidylserine pathways that are deregulated in a murine model of the neurodegenerative disease PHARC.
Blankman JL; Long JZ; Trauger SA; Siuzdak G; Cravatt BF
Proc Natl Acad Sci U S A; 2013 Jan; 110(4):1500-5. PubMed ID: 23297193
[TBL] [Abstract][Full Text] [Related]
20. Structure and function of extracellular phospholipase A1 belonging to the pancreatic lipase gene family.
Aoki J; Inoue A; Makide K; Saiki N; Arai H
Biochimie; 2007 Feb; 89(2):197-204. PubMed ID: 17101204
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]