Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Randy S Daughters"'
Autor:
Tijana Martinov, Rose Glenn-Finer, Sarah Burley, Elena Tonc, Evelyn Balsells, Alyssa Ashbaugh, Linnea Swanson, Randy S Daughters, Devavani Chatterjea
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e78673 (2013)
The interplay among pain, allergy and dysregulated inflammation promises to yield significant conceptual advances in immunology and chronic pain. Hapten-mediated contact hypersensitivity reactions are used to model skin allergies in rodents but have
Externí odkaz:
https://doaj.org/article/90ae823e5e4347999de57c326e27cd15
Publikováno v:
PLoS ONE, Vol 4, Iss 9, p e7003 (2009)
Facioscapulohumeral muscular dystrophy (FSHD) is caused by contractions of D4Z4 repeats at 4q35.2 thought to induce misregulation of nearby genes, one of which, DUX4, is actually localized within each repeat. A conserved ORF (mDUX), embedded within D
Externí odkaz:
https://doaj.org/article/d28e3d3db3a7470d91533709e57fb4a5
Autor:
Randy S Daughters, Daniel L Tuttle, Wangcai Gao, Yoshio Ikeda, Melinda L Moseley, Timothy J Ebner, Maurice S Swanson, Laura P W Ranum
Publikováno v:
PLoS Genetics, Vol 5, Iss 8, p e1000600 (2009)
Microsatellite expansions cause a number of dominantly-inherited neurological diseases. Expansions in coding-regions cause protein gain-of-function effects, while non-coding expansions produce toxic RNAs that alter RNA splicing activities of MBNL and
Externí odkaz:
https://doaj.org/article/63cb96186ac94be394aa5608c69b80a5
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 17 (2024)
Externí odkaz:
https://doaj.org/article/375dab9c70fb402cbb4548fc99a0f891
Autor:
Brian T. Fife, Beebie Boo, Elena Tonc, Jasmine Landry, Jaclyn Kline, Hanna Mengistu, Devavani Chatterjea, Linnea Swanson, Jyothi Dhanwada, Tijana Martinov, Randy S. Daughters, Charles J. Benck
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 2, p e0169672 (2017)
PLoS ONE, Vol 12, Iss 2, p e0169672 (2017)
Background Vulvodynia is a remarkably prevalent chronic pain condition of unknown etiology. Epidemiologic studies associate the risk of vulvodynia with a history of atopic disease. We used an established model of hapten-driven contact hypersensitivit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14a7032dcae1a5ba73189d68b4ebc1f
https://pubmed.ncbi.nlm.nih.gov/28158195
https://pubmed.ncbi.nlm.nih.gov/28158195
Publikováno v:
The Cerebellum. 7:150-158
Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21. The expansion mutation was isolated directly from the DNA of a single pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b9226c9e881916398aba30c52ffd5c3
https://doi.org/10.1007/s12311-008-0010-7
https://doi.org/10.1007/s12311-008-0010-7
Autor:
John W. Day, Gang Chen, Laura P.W. Ranum, Marcy R Weatherspoon, Wangcai Gao, Yoshio Ikeda, Anne K Mosemiller, Randy S. Daughters, Timothy J. Ebner, H. Brent Clark, Tao Zu, Melinda L. Moseley
Publikováno v:
Nature Genetics. 38:758-769
We previously reported that a (CTG)n expansion causes spinocerebellar ataxia type 8 (SCA8), a slowly progressive ataxia with reduced penetrance. We now report a transgenic mouse model in which the full-length human SCA8 mutation is transcribed using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::037731aa8ddd887387ddf7f0a163e554
https://doi.org/10.1038/ng1827
https://doi.org/10.1038/ng1827
Autor:
Patricia L. Faris, Randy S. Daughters, Suck Won Kim, Emil H. Ivanov, José V. Pardo, Robert L. Goodale, Boyd K. Hartman, Patricia A. Costello, Elke Stephan
Publikováno v:
Journal of Gastrointestinal Surgery. 7:740-749
This study aimed to measure brain activation during gastric distention as a way to investigate short-term satiety. We estimated regional cerebral blood flow with positron emission tomography (15O-water) during gastric balloon inflation and deflation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8f84dae6396cefa61b0156d0619aa9
https://doi.org/10.1016/s1091-255x(03)00071-4
https://doi.org/10.1016/s1091-255x(03)00071-4
Autor:
Rimon Bengiamin, Jun Li, Donald A. Simone, John Brennan, Randy S. Daughters, Christopher Bullis, Mark W. Stucky
Publikováno v:
Pain. 81:25-33
Although it is well known that cannabinoids produce antinociception in acute pain models, there is less information on the ability of cannabinoids to alleviate hyperalgesia. In the present study, we determined whether cannabinoids attenuated the deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26a403598cc7675b95ecce06212031ee
https://doi.org/10.1016/s0304-3959(98)00263-2
https://doi.org/10.1016/s0304-3959(98)00263-2
Publikováno v:
Bosnakovski, D, Daughters, R S, Xu, Z, Slack, J & Kyba, M 2009, ' Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats ', PLoS ONE, vol. 4, no. 9 . https://doi.org/10.1371/journal.pone.0007003
PLoS ONE
PLoS ONE, Vol 4, Iss 9, p e7003 (2009)
PLoS ONE
PLoS ONE, Vol 4, Iss 9, p e7003 (2009)
Facioscapulohumeral muscular dystrophy (FSHD) is caused by contractions of D4Z4 repeats at 4q35.2 thought to induce misregulation of nearby genes, one of which, DUX4, is actually localized within each repeat. A conserved ORF (mDUX), embedded within D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6029ad2d327afb2b6695df1765029574
https://purehost.bath.ac.uk/ws/files/69541066/Published_version.pdf
https://purehost.bath.ac.uk/ws/files/69541066/Published_version.pdf
