Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Katherine A. Dalton"'
Autor:
Benjamin M. Jacobs, Cyrus Daruwalla, Mollie O. McKeon, Raghda Al-Najjar, Andrea Simcock-Davies, Katherine Tuite-Dalton, J. William L. Brown, Ruth Dobson, Jeff Rodgers, Rod Middleton
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-6 (2023)
Abstract Understanding the associations and potential drivers of long-term disability in Multiple Sclerosis (MS) is of clinical and prognostic value. Previous data have suggested a link between depression and disability accrual in MS. We aimed to det
Externí odkaz:
https://doaj.org/article/d72350bc2bba4056a62e8cab9c02ceb1
Autor:
Gavin Giovannoni, Eli Silber, Ruth Dobson, Riffat Tanveer, Jade Harris, Tarunya Arun, Miriam Mattoscio, Ghaniah Hassan-Smith, Huw Morris, Rod Middleton, Emma Tallantyre, David Rog, Nikos Evangelou, Benjamin M Jacobs, Antonio Scalfari, Waqar Rashid, Helen L Ford, Charles A Mein, Stephen Sawcer, Cord Spilker, Bruno Gran, Martin O'Malley, Ashwini Nandoskar, Emeka Uzochukwu, Katila George, Sadid Hoque, Luisa Schalk, Angie Dunne, Charlotte Sellers, Elisa Visentin, Elizabeth Lindsey Bezzina, Eva Wozniak, Eve Sacre, Joan Bradley, Joshua Breedon, Judith Brooke, Karim L Kreft, Katherine Tuite Dalton, Maria Papachatzaki, Michelle Peter, Neisha Rhule, Nimisha Vinod, Outi Quinn, Ramya Shamji, Rashmi Kaimal, Rebecca Boulton, Roxanne Murray, Ruth Bellfield, Shakeelah Patel, Sonia Raj, Stephanie Gumus, Stephanie Mitchell, Tatiana Pogreban, Terri-Louise Brown, Thamanna Begum, Veronica Antoine
Publikováno v:
BMJ Open, Vol 13, Iss 5 (2023)
Purpose Genetic studies of multiple sclerosis (MS) susceptibility and severity have focused on populations of European ancestry. Studying MS genetics in other ancestral groups is necessary to determine the generalisability of these findings. The gene
Externí odkaz:
https://doaj.org/article/dfaa829aa3244981a9b0642497517dd8
Autor:
Benjamin M Jacobs, Luisa Schalk, Angie Dunne, Antonio Scalfari, Ashwini Nandoskar, Bruno Gran, Charles A Mein, Charlotte Sellers, Cord Spilker, David Rog, Elisa Visentin, Elizabeth Lindsey Bezzina, Emeka Uzochukwu, Emma Tallantyre, Eva Wozniak, Eve Sacre, Ghaniah Hassan-Smith, Helen L Ford, Jade Harris, Joan Bradley, Joshua Breedon, Judith Brooke, Karim L Kreft, Katherine Tuite Dalton, Katila George, Maria Papachatzaki, Martin O'Malley, Michelle Peter, Miriam Mattoscio, Neisha Rhule, Nikos Evangelou, Nimisha Vinod, Outi Quinn, Ramya Shamji, Rashmi Kaimal, Rebecca Boulton, Riffat Tanveer, Rod Middleton, Roxanne Murray, Ruth Bellfield, Sadid Hoque, Shakeelah Patel, Sonia Raj, Stephanie Gumus, Stephanie Mitchell, Stephen Sawcer, Tarunya Arun, Tatiana Pogreban, Terri-Louise Brown, Thamanna Begum, Veronica Antoine, Waqar Rashid, Alastair J Noyce, Eli Silber, Huw Morris, Gavin Giovannoni, Ruth Dobson
Publikováno v:
BMJ Open. 13:e071656
PurposeGenetic studies of multiple sclerosis (MS) susceptibility and severity have focused on populations of European ancestry. Studying MS genetics in other ancestral groups is necessary to determine the generalisability of these findings. The genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83f58e358e30a9b7550a2125fd244877
https://doi.org/10.1136/bmjopen-2023-071656
https://doi.org/10.1136/bmjopen-2023-071656
Autor:
Annalaura Lerede, Rodden Middleton, Jeff Rodgers, Katherine Tuite-Dalton, William Trender, Peter Hellyer, Richard Nicholas, Adam Hampshire
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:e2.3
Neurological conditions present with cognitive impairment that greatly affects the quality of life of the patients and should be routinely evaluated. However, it can be difficult to detect and impractical to monitor with classic in person cognitive a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ef161a24bd0b31f324b027751ee977c
https://doi.org/10.1136/jnnp-2022-abn2.100
https://doi.org/10.1136/jnnp-2022-abn2.100
Autor:
Afagh Garjani, Rodden M Middleton, Graham R Law, Katherine Tuite-Dalton, Rachael Hunter, Roshan das Nair, Nikos Evangelou, Richard Nicholas
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:A93.2-A93
COVID-19 is a concern in people with multiple sclerosis (MS), mostly because of their long-term physical disabilities and immunomodulatory disease-modifying therapies (DMTs). In this community-based pro- spective longitudinal study, we have been moni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf1c09b6333d4f3fde2fbf6fadb266c9
https://doi.org/10.1136/jnnp-2022-abn.302
https://doi.org/10.1136/jnnp-2022-abn.302
Autor:
Yiyun Pan, Timothy A. Bell, Fernando Pardo-Manuel de Villena, Pablo Hock, Darla R. Miller, Katherine A Dalton, Lucy H. Williams, John R. Shorter, Benjamin D. Philpot, Bin Gu, Ginger D. Shaw
Publikováno v:
Epilepsia
OBJECTIVE: Animal studies remain essential for understanding mechanisms of epilepsy and identifying new therapeutic targets. However, existing animal models of epilepsy do not reflect the high level of genetic diversity found in the human population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81e13c5db0e3201b10f4f38c301f8a5b
https://pubmed.ncbi.nlm.nih.gov/32852103
https://pubmed.ncbi.nlm.nih.gov/32852103
Autor:
Marie Rougie, Kelly E. Carstens, Bin Gu, Ellen P. Clark, Benjamin D. Philpot, Matthew C. Judson, Serena M. Dudek, Katherine A Dalton
Publikováno v:
Journal of Clinical Investigation. 129:163-168
Angelman syndrome (AS) is a neurodevelopmental disorder in which epilepsy is common (~90%) and often refractory to antiepileptics. AS is caused by mutation of the maternal allele encoding the ubiquitin protein ligase E3A (UBE3A), but it is unclear ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7064d3d4ce8f2e74e03d1216178ffff
https://doi.org/10.1172/jci120816
https://doi.org/10.1172/jci120816
Publikováno v:
Zoological Research. 38:171-179
Epilepsy, characterized by spontaneous recurrent seizures (SRS), is a serious and common neurological disorder afflicting an estimated 1% of the population worldwide. Animal experiments, especially those utilizing small laboratory rodents, remain ess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60b39dc8a0e4282977998cef7b75741f
https://doi.org/10.24272/j.issn.2095-8137.2017.042
https://doi.org/10.24272/j.issn.2095-8137.2017.042
Autor:
Bin Gu, Shorter, Cooley Bc, Pablo Hock, Timothy A. Bell, Ginger D. Shaw, Pan Y, Katherine A Dalton, Benjamin D. Philpot, Darla R. Miller, Lucy H. Williams, de Villena Fp
Epilepsy is a neurological disorder with complex etiologies and genetic architecture. Animal models have a critical role in understanding the pathophysiology of epilepsy. Here we studied epilepsy utilizing a genetic reference population of Collaborat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c4f07a8db366c387d63de4e7172a95
