Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Vish Koppaka"'
Autor:
Jaclyn Cadaoas, Huimin Hu, Gabrielle Boyle, Elida Gomero, Rosario Mosca, Kartika Jayashankar, Mike Machado, Sean Cullen, Belle Guzman, Diantha van de Vlekkert, Ida Annunziata, Michel Vellard, Emil Kakkis, Vish Koppaka, Alessandra d’Azzo
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss , Pp 191-203 (2021)
Galactosialidosis is a rare lysosomal storage disease caused by a congenital defect of protective protein/cathepsin A (PPCA) and secondary deficiency of neuraminidase-1 and β-galactosidase. PPCA is a lysosomal serine carboxypeptidase that functions
Externí odkaz:
https://doaj.org/article/d34dc77de868405aae409bdba6cc80c5
Autor:
Melita Dvorak-Ewell, Dan Wendt, Chuck Hague, Terri Christianson, Vish Koppaka, Danielle Crippen, Emil Kakkis, Michel Vellard
Publikováno v:
PLoS ONE, Vol 5, Iss 8, p e12194 (2010)
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is a lysosomal storage disorder caused by deficiency of N-acetylgalactosamine-6-sulfatase (GALNS), an enzyme that degrades keratan sulfate (KS). Currently no therapy for MPS IVA is available. We
Externí odkaz:
https://doaj.org/article/7accaaff249d4d5483ec40f96f5417e8
Autor:
Mike Machado, Rosario Mosca, Belle Guzman, Elida Gomero, Michel C. Vellard, Vish Koppaka, Ida Annunziata, Alessandra d'Azzo, Jaclyn Cadaoas, Gabrielle Boyle, Kartika Jayashankar, Huimin Hu, Sean Cullen, Emil D. Kakkis, Diantha van de Vlekkert
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss, Pp 191-203 (2021)
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss, Pp 191-203 (2021)
Galactosialidosis is a rare lysosomal storage disease caused by a congenital defect of protective protein/cathepsin A (PPCA) and secondary deficiency of neuraminidase-1 and β-galactosidase. PPCA is a lysosomal serine carboxypeptidase that functions
Autor:
Jaclyn Cadaoas, Rosario Mosca, Alessandra d'Azzo, Camilo Toro, Cynthia J. Tifft, Emil D. Kakkis, Vish Koppaka, Diantha van de Vlekkert, Simona Allievi, Leigh E. Fremuth, Ida Annunziata, Yvan Campos, Cinzia Gellera, Laura Canafoglia, Gepke Visser
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 3, p 695 (2020)
Journal of Clinical Medicine; Volume 9; Issue 3; Pages: 695
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 9; Issue 3; Pages: 695
Journal of Clinical Medicine
Congenital deficiency of the lysosomal sialidase neuraminidase 1 (NEU1) causes the lysosomal storage disease, sialidosis, characterized by impaired processing/degradation of sialo-glycoproteins and sialo-oligosaccharides, and accumulation of sialylat
Autor:
Chuck Hague, Vish Koppaka, Dan J Wendt, Michel C. Vellard, Terri Christianson, Melita Dvorak-Ewell, Emil D. Kakkis, Danielle Crippen
Publikováno v:
PLoS ONE, Vol 5, Iss 8, p e12194 (2010)
PLoS ONE
PLoS ONE
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is a lysosomal storage disorder caused by deficiency of N-acetylgalactosamine-6-sulfatase (GALNS), an enzyme that degrades keratan sulfate (KS). Currently no therapy for MPS IVA is available. We
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 421
Immunonaffinity chromatography is a powerful technique for rapid purification of proteins. In a single-step purification, it is possible to purify proteins for testing in model systems and for conducting enzyme kinetic studies. Because the immunoaffi
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 421
Dye affinity chromatography is a purification technique offering unique selectivities and high purification factors. Dye ligands may act as substrate analogs, offering affinity interactions with their corresponding enzymes. This chapter describes a d
Publikováno v:
Affinity Chromatography ISBN: 9781588296597
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d36e3685e2d97ca62111cdce78a75680
https://doi.org/10.1007/978-1-59745-582-4_4
https://doi.org/10.1007/978-1-59745-582-4_4
Publikováno v:
Affinity Chromatography ISBN: 9781588296597
Dye affinity chromatography is a purification technique offering unique selectivities and high purification factors. Dye ligands may act as substrate analogs, offering affinity interactions with their corresponding enzymes. This chapter describes a d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e83d0b937a3057f6aef1f2d616623c67
https://doi.org/10.1007/978-1-59745-582-4_5
https://doi.org/10.1007/978-1-59745-582-4_5
Autor:
Vish Koppaka, Michael Vellard, Dan J Wendt, Shilpa Shroff, Melita Dvorak-Ewell, Terri Christianson
Publikováno v:
Molecular Genetics and Metabolism. 96:S22