186 related articles for article (PubMed ID: 19302917)
1. Silencing of genes required for glycosylphosphatidylinositol anchor biosynthesis in Burkitt lymphoma.
Hu R; Mukhina GL; Lee SH; Jones RJ; Englund PT; Brown P; Sharkis SJ; Buckley JT; Brodsky RA
Exp Hematol; 2009 Apr; 37(4):423-434.e2. PubMed ID: 19302917
[TBL] [Abstract][Full Text] [Related]
2. Mutations in PIGU Impair the Function of the GPI Transamidase Complex, Causing Severe Intellectual Disability, Epilepsy, and Brain Anomalies.
Knaus A; Kortüm F; Kleefstra T; Stray-Pedersen A; Đukić D; Murakami Y; Gerstner T; van Bokhoven H; Iqbal Z; Horn D; Kinoshita T; Hempel M; Krawitz PM
Am J Hum Genet; 2019 Aug; 105(2):395-402. PubMed ID: 31353022
[TBL] [Abstract][Full Text] [Related]
3. Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies.
Ilkovski B; Pagnamenta AT; O'Grady GL; Kinoshita T; Howard MF; Lek M; Thomas B; Turner A; Christodoulou J; Sillence D; Knight SJ; Popitsch N; Keays DA; Anzilotti C; Goriely A; Waddell LB; Brilot F; North KN; Kanzawa N; Macarthur DG; Taylor JC; Kini U; Murakami Y; Clarke NF
Hum Mol Genet; 2015 Nov; 24(21):6146-59. PubMed ID: 26293662
[TBL] [Abstract][Full Text] [Related]
4. Both PIGA and PIGL mutations cause GPI-a deficient isolates in the Tk6 cell line.
Nicklas JA; Carter EW; Albertini RJ
Environ Mol Mutagen; 2015 Oct; 56(8):663-73. PubMed ID: 25970100
[TBL] [Abstract][Full Text] [Related]
5. Glycosylphosphatidylinositol (GPI) anchored protein deficiency serves as a reliable reporter of Pig-a gene Mutation: Support from an in vitro assay based on L5178Y/Tk
Bemis JC; Avlasevich SL; Labash C; McKinzie P; Revollo J; Dobrovolsky VN; Dertinger SD
Environ Mol Mutagen; 2018 Jan; 59(1):18-29. PubMed ID: 29115020
[TBL] [Abstract][Full Text] [Related]
6. Loss of the GPI-anchor in B-lymphoblastic leukemia by epigenetic downregulation of PIGH expression.
Loeff FC; Rijs K; van Egmond EHM; Zoutman WH; Qiao X; Kroes WGM; Veld SAJ; Griffioen M; Vermeer MH; Neefjes J; Frederik Falkenburg JH; Halkes CJM; Jedema I
Am J Hematol; 2019 Jan; 94(1):93-102. PubMed ID: 30370942
[TBL] [Abstract][Full Text] [Related]
7. Molecular analysis of GPI-anchor biosynthesis pathway genes in rat strains used for the Pig-a gene mutation assay.
Dad A; Dobrovolsky VN; Heflich RH; Revollo JR
Mutat Res Genet Toxicol Environ Mutagen; 2020; 858-860():503256. PubMed ID: 33198937
[TBL] [Abstract][Full Text] [Related]
8. Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia.
Mukhina GL; Buckley JT; Barber JP; Jones RJ; Brodsky RA
Br J Haematol; 2001 Nov; 115(2):476-82. PubMed ID: 11703352
[TBL] [Abstract][Full Text] [Related]
9. Functional analysis of T-cell mutants defective in the biosynthesis of glycosylphosphatidylinositol anchor. Relative importance of glycosylphosphatidylinositol anchor versus N-linked glycosylation in T-cell activation.
Thomas LJ; DeGasperi R; Sugiyama E; Chang HM; Beck PJ; Orlean P; Urakaze M; Kamitani T; Sambrook JF; Warren CD
J Biol Chem; 1991 Dec; 266(34):23175-84. PubMed ID: 1835975
[TBL] [Abstract][Full Text] [Related]
10. The in vitro PIG-A gene mutation assay: mutagenicity testing via flow cytometry based on the glycosylphosphatidylinositol (GPI) status of TK6 cells.
Krüger CT; Hofmann M; Hartwig A
Arch Toxicol; 2015 Dec; 89(12):2429-43. PubMed ID: 25417052
[TBL] [Abstract][Full Text] [Related]
11. CHO glycosylation mutants: GPI anchor.
Maeda Y; Ashida H; Kinoshita T
Methods Enzymol; 2006; 416():182-205. PubMed ID: 17113867
[TBL] [Abstract][Full Text] [Related]
12. Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.
Hansen L; Tawamie H; Murakami Y; Mang Y; ur Rehman S; Buchert R; Schaffer S; Muhammad S; Bak M; Nöthen MM; Bennett EP; Maeda Y; Aigner M; Reis A; Kinoshita T; Tommerup N; Baig SM; Abou Jamra R
Am J Hum Genet; 2013 Apr; 92(4):575-83. PubMed ID: 23561846
[TBL] [Abstract][Full Text] [Related]
13. Biosynthesis and deficiencies of glycosylphosphatidylinositol.
Kinoshita T
Proc Jpn Acad Ser B Phys Biol Sci; 2014; 90(4):130-43. PubMed ID: 24727937
[TBL] [Abstract][Full Text] [Related]
14. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin.
Brodsky RA; Mukhina GL; Li S; Nelson KL; Chiurazzi PL; Buckley JT; Borowitz MJ
Am J Clin Pathol; 2000 Sep; 114(3):459-66. PubMed ID: 10989647
[TBL] [Abstract][Full Text] [Related]
15. Detection of PIGO-deficient cells using proaerolysin: a valuable tool to investigate mechanisms of mutagenesis in the DT40 cell system.
Nakamura J; Gul H; Tian X; Bultman SJ; Swenberg JA
PLoS One; 2012; 7(3):e33563. PubMed ID: 22428069
[TBL] [Abstract][Full Text] [Related]
16. PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome.
Krawitz PM; Murakami Y; Rieß A; Hietala M; Krüger U; Zhu N; Kinoshita T; Mundlos S; Hecht J; Robinson PN; Horn D
Am J Hum Genet; 2013 Apr; 92(4):584-9. PubMed ID: 23561847
[TBL] [Abstract][Full Text] [Related]
17. Glycosylphosphatidylinositol anchors regulate glycosphingolipid levels.
Loizides-Mangold U; David FP; Nesatyy VJ; Kinoshita T; Riezman H
J Lipid Res; 2012 Aug; 53(8):1522-34. PubMed ID: 22628614
[TBL] [Abstract][Full Text] [Related]
18. Generating anchors only to lose them: The unusual story of glycosylphosphatidylinositol anchor biosynthesis and remodeling in yeast and fungi.
Komath SS; Singh SL; Pratyusha VA; Sah SK
IUBMB Life; 2018 May; 70(5):355-383. PubMed ID: 29679465
[TBL] [Abstract][Full Text] [Related]
19. The in vitro PIG-A gene mutation assay: glycosylphosphatidylinositol (GPI)-related genotype-to-phenotype relationship in TK6 cells.
Krüger CT; Fischer BM; Armant O; Morath V; Strähle U; Hartwig A
Arch Toxicol; 2016 Jul; 90(7):1729-36. PubMed ID: 27100116
[TBL] [Abstract][Full Text] [Related]
20. Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis--The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes.
Jezela-Stanek A; Ciara E; Piekutowska-Abramczuk D; Trubicka J; Jurkiewicz E; Rokicki D; Mierzewska H; Spychalska J; Uhrynowska M; Szwarc-Bronikowska M; Buda P; Said AR; Jamroz E; Rydzanicz M; Płoski R; Krajewska-Walasek M; Pronicka E
Eur J Paediatr Neurol; 2016 May; 20(3):462-73. PubMed ID: 26879448
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
