Zobrazeno 1 - 10
of 820
pro vyhledávání: '"J. Castaner"'
Autor:
Grace Robinson Kick, Rebecca E.H. Whiting, Juri Ota-Kuroki, Leilani J. Castaner, Brandie Morgan-Jack, Julianna C. Sabol, Elizabeth J. Meiman, Francheska Ortiz, Martin L. Katz
Publikováno v:
Experimental Eye Research. 226:109344
CLN2 neuronal ceroid lipofuscinosis is a rare hereditary neurodegenerative disorder characterized by deleterious sequence variants in TPP1 that result in reduced or abolished function of the lysosomal enzyme tripeptidyl peptidase 1 (TPP1). Children w
Autor:
Sundeep Chandra, Katherine Bibi, Charles A. O'Neill, John Sinclair, Daniella P. Vansteenkiste, Martin L. Katz, Jacqueline W. Pearce, Annalisa Nguyen, Grace Robinson Kick, Stefanie Lim, Leilani J. Castaner, Rebecca E.H. Whiting
Publikováno v:
Exp Eye Res
CLN2 neuronal ceroid lipofuscinosis is a hereditary neurodegenerative disorder characterized by progressive vision loss, neurological decline, and seizures. CLN2 disease results from mutations in TPP1 that encodes the lysosomal enzyme tripeptidyl pep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f993cf47b7dc132a777799fb9a5ae6ab
https://europepmc.org/articles/PMC7484259/
https://europepmc.org/articles/PMC7484259/
Autor:
Rebecca E.H. Whiting, Annalisa Nguyen, Charles A. O'Neill, Martin L. Katz, Joseph B. Kowal, Cheryl A. Jensen, Stefanie Lim, Carley R. Corado, Grace Robinson Kick, Leilani J. Castaner, Juri Ota-Kuroki
Publikováno v:
Exp Eye Res
CLN2 neuronal ceroid lipofuscinosis is a rare recessive hereditary retinal and neurodegenerative disease resulting from deleterious sequence variants in TPP1 that encodes the soluble lysosomal enzyme tripeptidyl peptidase-1 (TPP1). Children with this
Autor:
Elizabeth J. Meiman, Martin L. Katz, Juri Ota-Kuroki, Grace Robinson Kick, Leilani J. Castaner, Julianna C. Sabol, Cheryl A. Jensen, Rebecca E.H. Whiting
Publikováno v:
Exp Eye Res
CLN5 neuronal ceroid lipofuscinosis is a hereditary neurodegenerative disease characterized by progressive neurological decline, vision loss and seizures. Visual impairment in children with CLN5 disease is attributed to a progressive decline in retin
Autor:
Daniella P. Vansteenkiste, Christopher J. Tracy, Rebecca E.H. Whiting, Baye G. Williamson, Martin L. Katz, Jacqueline W. Pearce, Cheryl A. Jensen, Leilani J. Castaner, Jeffrey N. Bryan, Joan R. Coates, Lauren Elizabeth Gillespie
Publikováno v:
Experimental Eye Research. 152:77-87
The CLN2 form of neuronal ceroid lipofuscinosis is a neurodegenerative disease that results from mutations in the TPP1 gene. Affected children exhibit progressive declines in most neurological functions including vision. Functional declines are accom
Autor:
Ann P. Bosiack, Erica K. Creighton, William K. Suedmeyer, Annie Oh, Michael Selig, Barbara Gandolfi, Leslie A. Lyons, Rebecca E.H. Whiting, Jacqueline W. Pearce, Leilani J. Castaner, Ellen B. Belknap
Publikováno v:
Scientific Reports. 8
Scientific Reports 7: Article number: 43918; published online: 21 March 2017; updated: 18 May 2018 The Acknowledgements section in this Article is incomplete. “Funding was provided by The University of Missouri, College of Veterinary Medicine Clini
Autor:
Rebecca E.H. Whiting, Rebecca J. Katz, Cheryl A. Jensen, Martin L. Katz, D. Gilliam, Jacqueline W. Pearce, Leilani J. Castaner
Publikováno v:
Experimental Eye Research. 134:123-132
The CLN2 form of neuronal ceroid lipofuscinosis is an autosomal recessively inherited lysosomal storage disease that is characterized by progressive vision loss culminating in blindness, cognitive and motor decline, neurodegeneration, and premature d
Autor:
Jacqueline W. Pearce, Christopher B. Kaelin, Tosso Leeb, Holly C. Beale, Hannes Lohi, Leilani J. Castaner, Rebecca E.H. Whiting, William K. Suedmeyer, Wesley C. Warren, Adam R. Boyko, Niels C Pedersen, Marta Castelhano, Dorian J. Garrick, N. Matthew Ellinwood, Annie Oh, William F. Swanson, Michael J. Montague, Michael Selig, Max F. Rothschild, Erica K. Creighton, Patricia P. Chan, Karen A. Terio, Paulo C. Alves, Leslie A. Lyons, John S. Munday, Rory J. Todhunter, Richard Malik, Gregory S. Barsh, Maria Longeri, William J. Murphy, Christopher R Helps, Danielle Aderdein, Ann P. Bosiack, Barbara Gandolfi, Ellen B. Belknap
Publikováno v:
Scientific Reports
Oh, A, Pearce, J W, Gandolfi, B, Creighton, E K, Suedmeyer, W K, Selig, M, Bosiack, A P, Castaner, L J, Whiting, R E H, Belknap, E B, Lyons, L A, Aderdein, D, Alves, P C, Barsh, G S, Beale, H C, Boyko, A R, Castelhano, M G, Chan, P, Ellinwood, N M, Garrick, D J, Helps, C R, Kaelin, C B, Leeb, T, Lohi, H, Longeri, M, Malik, R, Montague, M J, Munday, J S, Murphy, W J, Pedersen, N C, Rothschild, M F, Swanson, W F, Terio, K A, Todhunter, R J & Warren, W C 2017, ' Early-onset progressive retinal atrophy associated with an IQCB1 variant in African black-footed cats (Felis nigripes) ', Scientific Reports, vol. 7, 43918 . https://doi.org/10.1038/srep43918
Scientific reports, vol 7, iss 1
Oh, Annie; Pearce, Jacqueline W; Gandolfi, Barbara; Creighton, Erica K; Suedmeyer, William K; Selig, Michael; Bosiack, Ann P; Castaner, Leilani J; Whiting, Rebecca E H; Belknap, Ellen B; Lyons, Leslie A; 99 Lives, Consortium (2017). Early-Onset Progressive Retinal Atrophy Associated with an IQCB1 Variant in African Black-Footed Cats (Felis nigripes). Scientific Reports, 7(43918), p. 43918. Nature Publishing Group 10.1038/srep43918
Oh, A, Pearce, J W, Gandolfi, B, Creighton, E K, Suedmeyer, W K, Selig, M, Bosiack, A P, Castaner, L J, Whiting, R E H, Belknap, E B, Lyons, L A, Aderdein, D, Alves, P C, Barsh, G S, Beale, H C, Boyko, A R, Castelhano, M G, Chan, P, Ellinwood, N M, Garrick, D J, Helps, C R, Kaelin, C B, Leeb, T, Lohi, H, Longeri, M, Malik, R, Montague, M J, Munday, J S, Murphy, W J, Pedersen, N C, Rothschild, M F, Swanson, W F, Terio, K A, Todhunter, R J & Warren, W C 2017, ' Early-onset progressive retinal atrophy associated with an IQCB1 variant in African black-footed cats (Felis nigripes) ', Scientific Reports, vol. 7, 43918 . https://doi.org/10.1038/srep43918
Scientific reports, vol 7, iss 1
Oh, Annie; Pearce, Jacqueline W; Gandolfi, Barbara; Creighton, Erica K; Suedmeyer, William K; Selig, Michael; Bosiack, Ann P; Castaner, Leilani J; Whiting, Rebecca E H; Belknap, Ellen B; Lyons, Leslie A; 99 Lives, Consortium (2017). Early-Onset Progressive Retinal Atrophy Associated with an IQCB1 Variant in African Black-Footed Cats (Felis nigripes). Scientific Reports, 7(43918), p. 43918. Nature Publishing Group 10.1038/srep43918
African black-footed cats (Felis nigripes) are endangered wild felids. One male and full-sibling female African black-footed cat developed vision deficits and mydriasis as early as 3 months of age. The diagnosis of early-onset progressive retinal atr
Autor:
Kristina Narfström, Brittanie N. Dougherty, Gang Yao, Martin L. Katz, Jacqueline W. Pearce, Derek Kennedy, Brian R. Vuillemenot, Leilani J. Castaner, Cheryl A. Jensen, Charles A. O'Neill, Joan R. Coates, Rebecca E.H. Whiting
Publikováno v:
Experimental Eye Research. 125:164-172
Late-infantile neuronal ceroid lipofuscinosis (CLN2 disease) is a hereditary neurological disorder characterized by progressive retinal degeneration and vision loss, cognitive and motor decline, seizures, and pronounced brain atrophy. This fatal pedi
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