167 related articles for article (PubMed ID: 19607915)
1. Impact of beta-galactosidase mutations on the expression of the canine lysosomal multienzyme complex.
Kreutzer R; Kreutzer M; Sewell AC; Techangamsuwan S; Leeb T; Baumgärtner W
Biochim Biophys Acta; 2009 Oct; 1792(10):982-7. PubMed ID: 19607915
[TBL] [Abstract][Full Text] [Related]
2. New mutations in the PPBG gene lead to loss of PPCA protein which affects the level of the beta-galactosidase/neuraminidase complex and the EBP-receptor.
Malvagia S; Morrone A; Caciotti A; Bardelli T; d'Azzo A; Ancora G; Zammarchi E; Donati MA
Mol Genet Metab; 2004 May; 82(1):48-55. PubMed ID: 15110321
[TBL] [Abstract][Full Text] [Related]
3. Role of beta-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis.
Caciotti A; Donati MA; Boneh A; d'Azzo A; Federico A; Parini R; Antuzzi D; Bardelli T; Nosi D; Kimonis V; Zammarchi E; Morrone A
Hum Mutat; 2005 Mar; 25(3):285-92. PubMed ID: 15714521
[TBL] [Abstract][Full Text] [Related]
4. Intermittent enzyme replacement therapy with recombinant human β-galactosidase prevents neuraminidase 1 deficiency.
Luu AR; Wong C; Agrawal V; Wise N; Handyside B; Lo MJ; Pacheco G; Felix JB; Giaramita A; d'Azzo A; Vincelette J; Bullens S; Bunting S; Christianson TM; Hague CM; LeBowitz JH; Yogalingam G
J Biol Chem; 2020 Sep; 295(39):13556-13569. PubMed ID: 32727849
[TBL] [Abstract][Full Text] [Related]
5. Elastogenesis in cultured dermal fibroblasts from patients with lysosomal beta-galactosidase, protective protein/cathepsin A and neuraminidase-1 deficiencies.
Tatano Y; Takeuchi N; Kuwahara J; Sakuraba H; Takahashi T; Takada G; Itoh K
J Med Invest; 2006 Feb; 53(1-2):103-12. PubMed ID: 16538002
[TBL] [Abstract][Full Text] [Related]
6. Lysosomal high molecular weight multienzyme complex.
Ostrowska H; Krukowska K; Kalinowska J; Orłowska M; Lengiewicz I
Cell Mol Biol Lett; 2003; 8(1):19-24. PubMed ID: 12655352
[TBL] [Abstract][Full Text] [Related]
7. Lysosomal multienzyme complex: pros and cons of working together.
Bonten EJ; Annunziata I; d'Azzo A
Cell Mol Life Sci; 2014 Jun; 71(11):2017-32. PubMed ID: 24337808
[TBL] [Abstract][Full Text] [Related]
8. Lysosomal multienzymatic complex-related diseases: a genetic study among Portuguese patients.
Coutinho MF; Lacerda L; Macedo-Ribeiro S; Baptista E; Ribeiro H; Prata MJ; Alves S
Clin Genet; 2012 Apr; 81(4):379-93. PubMed ID: 21214877
[TBL] [Abstract][Full Text] [Related]
9. Biochemical and molecular characterization of novel mutations in GLB1 and NEU1 in patient cells with lysosomal storage disorders.
Kwak JE; Son MY; Son YS; Son MJ; Cho YS
Biochem Biophys Res Commun; 2015 Feb; 457(4):554-60. PubMed ID: 25600812
[TBL] [Abstract][Full Text] [Related]
10. [Orientation of three lysosomal enzymes in the mouse inner ear and hearing loss in enzyme gene deficiency].
Guo YK; Xie DH; Yang XM
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Feb; 31(1):79-84. PubMed ID: 16562682
[TBL] [Abstract][Full Text] [Related]
11. Cathepsin A/protective protein: an unusual lysosomal multifunctional protein.
Hiraiwa M
Cell Mol Life Sci; 1999 Dec; 56(11-12):894-907. PubMed ID: 11212324
[TBL] [Abstract][Full Text] [Related]
12. Enzymatic activity of lysosomal carboxypeptidase (cathepsin) A is required for proper elastic fiber formation and inactivation of endothelin-1.
Seyrantepe V; Hinek A; Peng J; Fedjaev M; Ernest S; Kadota Y; Canuel M; Itoh K; Morales CR; Lavoie J; Tremblay J; Pshezhetsky AV
Circulation; 2008 Apr; 117(15):1973-81. PubMed ID: 18391110
[TBL] [Abstract][Full Text] [Related]
13. Molecular mechanisms of pathogenesis in a glycosphingolipid and a glycoprotein storage disease.
d'Azzo A; Bonten E
Biochem Soc Trans; 2010 Dec; 38(6):1453-7. PubMed ID: 21118106
[TBL] [Abstract][Full Text] [Related]
14. A duplication in the canine beta-galactosidase gene GLB1 causes exon skipping and GM1-gangliosidosis in Alaskan huskies.
Kreutzer R; Leeb T; Müller G; Moritz A; Baumgärtner W
Genetics; 2005 Aug; 170(4):1857-61. PubMed ID: 15944348
[TBL] [Abstract][Full Text] [Related]
15. Expression and characterization of 14 GLB1 mutant alleles found in GM1-gangliosidosis and Morquio B patients.
Santamaria R; Chabás A; Callahan JW; Grinberg D; Vilageliu L
J Lipid Res; 2007 Oct; 48(10):2275-82. PubMed ID: 17664528
[TBL] [Abstract][Full Text] [Related]
16. Association of N-acetylgalactosamine-6-sulfate sulfatase with the multienzyme lysosomal complex of beta-galactosidase, cathepsin A, and neuraminidase. Possible implication for intralysosomal catabolism of keratan sulfate.
Pshezhetsky AV; Potier M
J Biol Chem; 1996 Nov; 271(45):28359-65. PubMed ID: 8910459
[TBL] [Abstract][Full Text] [Related]
17. Enzyme replacement for GM1-gangliosidosis: Uptake, lysosomal activation, and cellular disease correction using a novel β-galactosidase:RTB lectin fusion.
Condori J; Acosta W; Ayala J; Katta V; Flory A; Martin R; Radin J; Cramer CL; Radin DN
Mol Genet Metab; 2016 Feb; 117(2):199-209. PubMed ID: 26766614
[TBL] [Abstract][Full Text] [Related]
18. Senescence-associated beta-galactosidase is lysosomal beta-galactosidase.
Lee BY; Han JA; Im JS; Morrone A; Johung K; Goodwin EC; Kleijer WJ; DiMaio D; Hwang ES
Aging Cell; 2006 Apr; 5(2):187-95. PubMed ID: 16626397
[TBL] [Abstract][Full Text] [Related]
19. Heterodimerization of the sialidase NEU1 with the chaperone protective protein/cathepsin A prevents its premature oligomerization.
Bonten EJ; Campos Y; Zaitsev V; Nourse A; Waddell B; Lewis W; Taylor G; d'Azzo A
J Biol Chem; 2009 Oct; 284(41):28430-28441. PubMed ID: 19666471
[TBL] [Abstract][Full Text] [Related]
20. Lysosomal multienzyme complex: biochemistry, genetics, and molecular pathophysiology.
Pshezhetsky AV; Ashmarina M
Prog Nucleic Acid Res Mol Biol; 2001; 69():81-114. PubMed ID: 11550799
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
