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5. Ablation of the pro-inflammatory master regulator miR-155 does not mitigate neuroinflammation or neurodegeneration in a vertebrate model of Gaucher's disease. Watson L; Keatinge M; Gegg M; Bai Q; Sandulescu MC; Vardi A; Futerman AH; Schapira AHV; Burton EA; Bandmann O Neurobiol Dis; 2019 Jul; 127():563-569. PubMed ID: 30981829 [TBL] [Abstract][Full Text] [Related]
6. Impact of Gba2 on neuronopathic Gaucher's disease and α-synuclein accumulation in medaka (Oryzias latipes). Nakanishi E; Uemura N; Akiyama H; Kinoshita M; Masanori S; Taruno Y; Yamakado H; Matsuzawa SI; Takeda S; Hirabayashi Y; Takahashi R Mol Brain; 2021 May; 14(1):80. PubMed ID: 33971917 [TBL] [Abstract][Full Text] [Related]
7. Minos-insertion mutant of the Drosophila GBA gene homologue showed abnormal phenotypes of climbing ability, sleep and life span with accumulation of hydroxy-glucocerebroside. Kawasaki H; Suzuki T; Ito K; Takahara T; Goto-Inoue N; Setou M; Sakata K; Ishida N Gene; 2017 May; 614():49-55. PubMed ID: 28286087 [TBL] [Abstract][Full Text] [Related]
8. Sucrose gradient analysis of phospholipid-activated beta-glucosidase in type 1 and type 2 Gaucher's disease. Garrett KO; Prence EM; Glew RH Arch Biochem Biophys; 1985 Apr; 238(1):344-52. PubMed ID: 3920967 [TBL] [Abstract][Full Text] [Related]
9. Comparison of rates of hydrolysis of N-oleoyl and N-stearoyl glucocerebroside in patients with Gaucher's disease. Peters SP; Aquino L; Naccarato WF; Gilbertson JR; Diven WF; Glew RH Biochim Biophys Acta; 1979 Oct; 575(1):27-36. PubMed ID: 508779 [TBL] [Abstract][Full Text] [Related]
10. Activator protein deficient Gaucher's disease. A second patient with the newly identified lipid storage disorder. Christomanou H; Chabás A; Pámpols T; Guardiola A Klin Wochenschr; 1989 Oct; 67(19):999-1003. PubMed ID: 2615292 [TBL] [Abstract][Full Text] [Related]
11. A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease. Tsuji S; Choudary PV; Martin BM; Stubblefield BK; Mayor JA; Barranger JA; Ginns EI N Engl J Med; 1987 Mar; 316(10):570-5. PubMed ID: 2880291 [TBL] [Abstract][Full Text] [Related]
12. Ultrastructural localization of glucocerebrosidase in cultured Gaucher's disease fibroblasts by immunocytochemistry. Willemsen R; van Dongen JM; Ginns EI; Sips HJ; Schram AW; Tager JM; Barranger JA; Reuser AJ J Neurol; 1987 Jan; 234(1):44-51. PubMed ID: 3819786 [TBL] [Abstract][Full Text] [Related]
13. Lessons from glucosylceramide and Gaucher's disease. Luft FC J Mol Med (Berl); 1998 Oct; 76(11):723-4. PubMed ID: 9826117 [No Abstract] [Full Text] [Related]
14. Enzymic differentiation of neurologic and nonneurologic forms of Gaucher's disease. Glew RH; Daniels LB; Clark LS; Hoyer SW J Neuropathol Exp Neurol; 1982 Nov; 41(6):630-41. PubMed ID: 6813430 [TBL] [Abstract][Full Text] [Related]
15. Comparison of N-acyl phosphatidylethanolamines with different N-acyl groups as activators of glucocerebrosidase in various forms of Gaucher's disease. Basu A; Prence E; Garrett K; Glew RH; Ellingson JS Arch Biochem Biophys; 1985 Nov; 243(1):28-34. PubMed ID: 3933429 [TBL] [Abstract][Full Text] [Related]
16. [Molecular basis of treatment in Gaucher's disease]. Pocoví M Med Clin (Barc); 2011 Sep; 137 Suppl 1():32-8. PubMed ID: 22230123 [TBL] [Abstract][Full Text] [Related]
17. Type I Gaucher's disease with homozygous R463C mutation without neurological involvement. Bolaman Z; Kadikoylu G; Levi E; Barutca S; Temucin K Haematologia (Budap); 2002; 32(4):487-93. PubMed ID: 12803123 [TBL] [Abstract][Full Text] [Related]
18. Gaucher's disease in the presence of normal glucocerebrosidase activity. Schofield DE; Scott CR; Lage JM; Farrell DF Hum Pathol; 1992 May; 23(5):588-92. PubMed ID: 1568755 [TBL] [Abstract][Full Text] [Related]
19. Substrate compositional variation with tissue/region and Gba1 mutations in mouse models--implications for Gaucher disease. Sun Y; Zhang W; Xu YH; Quinn B; Dasgupta N; Liou B; Setchell KD; Grabowski GA PLoS One; 2013; 8(3):e57560. PubMed ID: 23520473 [TBL] [Abstract][Full Text] [Related]
20. Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation). Zimmer KP; le Coutre P; Aerts HM; Harzer K; Fukuda M; O'Brien JS; Naim HY J Pathol; 1999 Aug; 188(4):407-14. PubMed ID: 10440752 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]