Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Douglas N. Sanders"'
Autor:
Fabiana H.G. Farias, Rong Zeng, Gary S. Johnson, Fred A. Wininger, Jeremy F. Taylor, Robert D. Schnabel, Stephanie D. McKay, Douglas N. Sanders, Hannes Lohi, Eija H. Seppälä, Claire M. Wade, Kerstin Lindblad-Toh, Dennis P. O'Brien, Martin L. Katz
Publikováno v:
Neurobiology of Disease, Vol 42, Iss 3, Pp 468-474 (2011)
A recessive, adult-onset neuronal ceroid-lipofuscinosis (NCL) occurs in Tibetan terriers. A genome-wide association study restricted this NCL locus to a 1.3 Mb region of canine chromosome 2 which contains canine ATP13A2. NCL-affected dogs were homozy
Externí odkaz:
https://doaj.org/article/f40ebbfe3986422681439c3d7e637cd3
Autor:
Lisa M. Stanek, Bryan Matstis, Leslie C. Wu, Douglas N. Sanders, Laura K. Richman, Ulrich Matzner
Publikováno v:
Molecular Genetics and Metabolism. 135:S115
Autor:
Douglas N. Sanders, Gayle C. Johnson, Martin L. Katz, Gary S. Johnson, Dennis P. O'Brien, Simon R. Platt, Jared E. Decker, Rong Zeng, David A. Wenger
Publikováno v:
Molecular Genetics and Metabolism. 108:70-75
GM2 gangliosidosis is a fatal lysosomal storage disease caused by a deficiency of β-hexosaminidase (EC 3.2.1.52). There are two major isoforms of the enzyme: hexosaminidase A composed of an α and a β subunit (encoded by HEXA and HEXB genes, respec
Autor:
Hannes Lohi, Jeremy F. Taylor, Fabiana H. G. Farias, Martin L. Katz, Rong Zeng, Eija H. Seppälä, Robert D. Schnabel, Fred A. Wininger, Dennis P. O'Brien, Douglas N. Sanders, Stephanie D. McKay, Gary S. Johnson, Claire M. Wade, Kerstin Lindblad-Toh
Publikováno v:
Neurobiology of Disease, Vol 42, Iss 3, Pp 468-474 (2011)
A recessive, adult-onset neuronal ceroid-lipofuscinosis (NCL) occurs in Tibetan terriers. A genome-wide association study restricted this NCL locus to a 1.3 Mb region of canine chromosome 2 which contains canine ATP13A2. NCL-affected dogs were homozy
Autor:
Douglas N. Sanders, Martin L. Katz, Gary S. Johnson, Shahnawaz Khan, Dennis P. O'Brien, Fabiana H. G. Farias, Rong Zeng
Publikováno v:
Journal of Biomedicine and Biotechnology, Vol 2011 (2011)
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology
The childhood neuronal ceroid lipofuscinoses (NCLs) are inherited neurodegenerative diseases that are progressive and ultimately fatal. An Australian Shepherd that exhibited a progressive neurological disorder with signs similar to human NCL was eval
Publikováno v:
Journal of Inherited Metabolic Disease. 30:952-963
The neuronal ceroid lipofuscinoses (NCLs) are inherited neurodegenerative diseases characterized by massive accumulation of autofluorescent storage bodies in neurons and other cells. A late-onset form of NCL occurs in Tibetan terrier dogs. Gel electr
Autor:
Mark D. Kirk, Cheryl A. Jensen, Leilani J. Castaner, Jeffrey N. Bryan, Christopher J. Tracy, Douglas N. Sanders, Martin L. Katz
Publikováno v:
Retinal Degenerative Diseases ISBN: 9783319171203
A number of retinal degenerative diseases may be amenable to treatment with continuous intraocular delivery of therapeutic agents that cannot be delivered effectively to the retina via systemic or topical administration. Among these disorders are lys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a2052894302821bfab0f4f35017b8e9
https://doi.org/10.1007/978-3-319-17121-0_76
https://doi.org/10.1007/978-3-319-17121-0_76
Publikováno v:
American Journal of Veterinary Research. 63:890-895
Objective—To determine whether the late onset form of inherited ceroid lipofuscinosis (CL) in Tibetan Terriers is accompanied by low plasma carnitine concentrations prior to the appearance of clinical signs. Animals—129 healthy Tibetan Terriers,
Autor:
Douglas N. Sanders, Camille A. Flournoy, Dennis P. O'Brien, Lani J. Castaner, Joan R. Coates, Rebecca E.H. Whiting, Fred A. Wininger, Shinichi Kanazono, Martin L. Katz
The neuronal ceroid lipofuscinoses (NCLs) are autosomal recessive lysosomal storage diseases characterized by progressive neurodegeneration and by accumulation of autofluorescent storage material in the central nervous system and other tissues. One o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db66f9d468637243603db80e7ae7c34d
https://europepmc.org/articles/PMC3190059/
https://europepmc.org/articles/PMC3190059/