Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Janis Bennion"'
Autor:
Miller, Louise, Rollinson, Sara, Callister, Janis Bennion, Young, Kate, Harris, Jenny, Gerhard, Alex, Neary, David, Richardson, Anna, Snowden, Julie, Mann, David M.A., Pickering-Brown, Stuart M.
Publikováno v:
In Neurobiology of Aging March 2015 36(3):1603-1603
Autor:
Stuart Pickering-Brown, Marilou Bouffard, Janis Bennion Callister, Pierre Drapeau, Amrutha Swaminathan, Gary A. B. Armstrong, Sarah Ryan, Meijiang Liao
Publikováno v:
Human Molecular Genetics. 27:1754-1762
Large expansions of hexanucleotide GGGGCC (G4C2) repeats (hundreds to thousands) in the first intron of the chromosome 9 open reading frame 72 (C9orf72) locus are the strongest known genetic factor associated with amyotrophic lateral sclerosis and fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7614ea457a7bd67393b2fb70df2e8cf
https://doi.org/10.1093/hmg/ddy083
https://doi.org/10.1093/hmg/ddy083
Publikováno v:
Rollinson, S, Young, K, Bennion-Callister, J & Pickering-Brown, S 2016, ' Identification of biological pathways regulated by PGRN and GRN peptide treatments using transcriptome analysis ', European Journal of Neuroscience, vol. 44, no. 5, pp. 2214-2225 . https://doi.org/10.1111/ejn.13297
Mutations in progranulin (PGRN) have been linked to two neurodegenerative disorders, heterozygote mutations with frontotemporal lobar degeneration (FTLD) and homozygote mutations with neuronal ceroid lipofuscinosis (NCL). Human PGRN is 593aa secreted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469949580f81637de07445e90e68a6c9
https://doi.org/10.1111/ejn.13297
https://doi.org/10.1111/ejn.13297
Autor:
Rollinson, Sara, Halliwell, Nicola, Young, Kate, Callister, Janis Bennion, Toulson, Greg, Gibbons, Linda, Davidson, Yvonne S., Robinson, Andrew C., Gerhard, Alex, Richardson, Anna, Neary, David, Snowden, Julie, Mann, David M.A., Pickering-Brown, Stuart M.
Publikováno v:
In Neurobiology of Aging August 2012 33(8):1846-1846
Publikováno v:
Alzheimer's & Dementia. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::476f00ea7936f0da17f1cd2fe2d17056
https://doi.org/10.1016/j.jalz.2017.06.091
https://doi.org/10.1016/j.jalz.2017.06.091
Publikováno v:
Alzheimer's & Dementia. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddbd9d4f9c65ae850f725c3221b15dc9
https://doi.org/10.1016/j.jalz.2017.06.023
https://doi.org/10.1016/j.jalz.2017.06.023
Akademický článek
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Publikováno v:
Human Molecular Genetics
C9orf72 expansions are the most common genetic cause of FTLD and MND identified to date. Although being intronic, the expansion is translated into five different dipeptide repeat proteins (DPRs) that accumulate within patients’ neurons. Attempts ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e22c28d89e0f1d34a9b54a3ba8162b5b
https://pubmed.ncbi.nlm.nih.gov/27798094
https://pubmed.ncbi.nlm.nih.gov/27798094
Autor:
Stuart Pickering-Brown, Johanna Donovan, Janis Bennion, Aurelie Doyotte, Sandra Taylor, Kim Brownhill, Flavia Stefani, Ling Zhang, Philip G. Woodman, Sara Rollinson
Publikováno v:
Current Biology. 21:1245-1250
SummaryEndosomal sorting complexes required for transport (ESCRTs) regulate several events involving membrane invagination, including multivesicular body (MVB) biogenesis, viral budding, and cytokinesis [1]. In each case, upstream ESCRTs combine with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::892a6976939cefcf1b5aa07c330f2cab
https://doi.org/10.1016/j.cub.2011.06.028
https://doi.org/10.1016/j.cub.2011.06.028
Autor:
Sara Rollinson, Louise Miller, Stuart Pickering-Brown, David M. A. Mann, Julie S. Snowden, Alexander Gerhard, David Neary, Janis Bennion Callister, Anna Richardson, Kate Young, Jenny Harris
Publikováno v:
Neurobiology of aging. 36(3)
Mutations in the gene p62/SQSTM1 have been reported as a relatively rare cause of frontotemporal lobar degeneration (FTLD). To establish whether this was the case for cases of FTLD from the United Kingdom, we sequenced the sequenced the entire open r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e3e8c365e384dfdf59f8b37b5c6b16
https://pubmed.ncbi.nlm.nih.gov/25433461
https://pubmed.ncbi.nlm.nih.gov/25433461