Zobrazeno 1 - 10
of 10
pro vyhledávání: '"John G. Keimel"'
Autor:
Shalini Kot, Subha Karumuthil-Melethil, Evan Woodley, Violeta Zaric, Patrick Thompson, Zhilin Chen, Erik Lykken, John G. Keimel, William F. Kaemmerer, Steven J. Gray, Jagdeep S. Walia
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13, p 6751 (2021)
GM2 gangliosidosis disorders are a group of neurodegenerative diseases that result from a functional deficiency of the enzyme β-hexosaminidase A (HexA). HexA consists of an α- and β-subunit; a deficiency in either subunit results in Tay–Sachs Di
Externí odkaz:
https://doaj.org/article/466f52285cfe442f99f9974dfd0081d6
Autor:
Cliff Heindel, Karlaina J.L. Osmon, Evan Woodley, John G. Keimel, Patrick Thompson, Subha Karumuthil-Melethil, William F. Kaemmerer, Jagdeep S. Walia, Steven J. Gray
Publikováno v:
Current Gene Therapy. 22:262-276
Background: GM2 gangliosidosis is a neurodegenerative, lysosomal storage disease caused by the deficiency of β-hexosaminidase A enzyme (Hex A), an α/β-subunit heterodimer. A novel variant of the human hexosaminidase α-subunit, coded by HEX M, has
Autor:
Patrick Thompson, Michael David Kaytor, Michael B. Tropak, Jagdeep S. Walia, John G. Keimel, Sahana Nagabhushan Kalburgi, Subha Karumuthil-Melethil, Brian L. Mark, Don J. Mahuran, Steven J. Gray
GM2 gangliosidosis is a family of three genetic neurodegenerative disorders caused by the accumulation of GM2 ganglioside (GM2) in neuronal tissue. Two of these are due to the deficiency of the heterodimeric (α–β), “A” isoenzyme of lysosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36beefde55a72fc28286189393911820
https://europepmc.org/articles/PMC5349231/
https://europepmc.org/articles/PMC5349231/
Autor:
Tina Billstrom, William F. Kaemmerer, John G. Keimel, Merry Passage, Rebecca Rose, Linnea Lentz
Publikováno v:
Molecular Genetics and Metabolism.
Autor:
Kot, Shalini1 (AUTHOR) 11sk82@queensu.ca, Karumuthil-Melethil, Subha2 (AUTHOR) subha.km@gmail.com, Woodley, Evan1 (AUTHOR) evan.woodley@gmail.com, Zaric, Violeta2,3 (AUTHOR) violetav@email.unc.edu, Thompson, Patrick4 (AUTHOR) pt24@queensu.ca, Chen, Zhilin4 (AUTHOR) zc@queensu.ca, Lykken, Erik2 (AUTHOR) erik_lykken@med.unc.edu, Keimel, John G.5 (AUTHOR) jack.keimel@newhoperesearch.org, Kaemmerer, William F.5 (AUTHOR) bill.kaemmerer@newhoperesearch.org, Gray, Steven J.2,3 (AUTHOR) Steven.Gray@UTSouthwestern.edu, Walia, Jagdeep S.1,4 (AUTHOR) jagdeep.walia@kingstonhsc.ca
Publikováno v:
International Journal of Molecular Sciences. Jul2021, Vol. 22 Issue 13, p6751-6751. 1p.
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Autor:
Osmon, Karlaina J. L., Woodley, Evan, Thompson, Patrick, Ong, Katalina, Karumuthil-Melethil, Subha, Keimel, John G., Mark, Brian L., Mahuran, Don, Gray, Steven J., Walia, Jagdeep S.
Publikováno v:
Human Gene Therapy; Jul2016, Vol. 27 Issue 7, p497-508, 12p
Autor:
Karumuthil-Melethil, Subha, Kalburgi, Sahana Nagabhushan, Thompson, Patrick, Tropak, Michael, Kaytor, Michael D., Keimel, John G., Mark, Brian L., Mahuran, Don, Walia, Jagdeep S., Gray, Steven J.
Publikováno v:
Human Gene Therapy; Jul2016, Vol. 27 Issue 7, p509-521, 13p
Autor:
Bobdan Romaniuk
National Directory Of Nonprofit Organizations (NDNO) provides names, addresses, and annual income figures of more than 260,000 organizations, 181,000+ of which have incomes in excess of $100,000. In addition, phone numbers are provided for 99.9% of l
Autor:
Bohdan Romaniuk
National Directory Of Nonprofit Organizations (NDNO) provides names, addresses, and annual income figures of more than 260,000 organizations, 181,000+ of which have incomes in excess of $100,000. In addition, phone numbers are provided for 99.9% of l