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1رسالة جامعية
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2دورية أكاديمية
المؤلفون: Rajagopal, Sangeerthana, Donaldson, Jasmine, Flower, Michael, Hensman Moss, Davina J, Tabrizi, Sarah J
المصدر: Emerging Topics in Life Sciences , Article ETLS20230015. (2023) (In press).
مصطلحات موضوعية: DNA synthesis and repair, cag repeat, genetic modifier, repeat expansion, somatic DNA expansion, somatic instability
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/10179590/1/etls-2023-0015c.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10179590Test/
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3دورية أكاديمية
المؤلفون: Papoutsi, Marina, Flower, Michael, Hensman Moss, Davina J, Holmans, Peter, Estevez-Fraga, Carlos, Johnson, Eileanoir B, Scahill, Rachael I, Rees, Geraint, Langbehn, Douglas, Tabrizi, Sarah J
المصدر: Brain Communications , 4 (6) , Article fcac279. (2022)
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/10159644/1/fcac279%20%281%29.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10159644Test/
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4
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5دورية أكاديمية
المؤلفون: Estevez-Fraga, Carlos, Magrinelli, Francesca, Hensman Moss, Davina, Mulroy, Eoin, Di Lazzaro, Giulia, Latorre, Anna, Mackenzie, Melissa, Houlden, Henry, Tabrizi, Sarah J, Bhatia, Kailash P
المساهمون: Estevez-Fraga, Carlo, Magrinelli, Francesca, Hensman Moss, Davina, Mulroy, Eoin, Di Lazzaro, Giulia, Latorre, Anna, Mackenzie, Melissa, Houlden, Henry, Tabrizi, Sarah J, Bhatia, Kailash P
مصطلحات موضوعية: Amyotrophic lateral sclerosis, Frontotemporal dementia, Parkinson's disease, Parkinsonism
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33977144; info:eu-repo/semantics/altIdentifier/wos/WOS:000658830100019; volume:7; issue:e575; firstpage:1; lastpage:8; numberofpages:8; journal:NEUROLOGY. GENETICS; http://hdl.handle.net/11562/1045099Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85106878149; https://doi.org/10.1212/NXG.0000000000000575Test
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6دورية أكاديميةMSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1
المؤلفون: Flower, Michael, Lomeikaite, Vilija, Ciosi, Marc, Cumming, Sarah, Morales, Fernando, Lo, Kitty, Hensman Moss, Davina, Jones, Lesley, Holmans, Peter, Monckton, Darren G., Tabrizi, Sarah J., Taylor, Louise, Treweek, Shaun, Hogarth, Fiona, Littleford, Roberta, Donnan, Peter, Hapca, Adrian, Mckenzie, Emma, Rauchhaus, Petra
المصدر: OPTIMISTIC consortium , Flower , M , Lomeikaite , V , Ciosi , M , Cumming , S , Morales , F , Lo , K , Hensman Moss , D , Jones , L , Holmans , P , Monckton , D G , Tabrizi , S J , Taylor , L , Treweek , S , Hogarth , F , Littleford , R , Donnan , P , Hapca , A & Mckenzie , E & Rauchhaus , P 2019 , ' MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1 ' ....
مصطلحات موضوعية: association study, Huntington's disease, movement disorders, myotonic dystrophy, transcriptomics, /dk/atira/pure/subjectarea/asjc/2700/2700, name=General Medicine
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.1093/brain/awz115Test
https://discovery.dundee.ac.uk/en/publications/70d59b07-486a-4f0a-8550-b12dacef59cbTest
https://discovery.dundee.ac.uk/ws/files/103612865/awz115.pdfTest
http://www.scopus.com/inward/record.url?scp=85072279766&partnerID=8YFLogxKTest -
7دورية أكاديمية
المؤلفون: Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah, Hensman Moss, Davina, Alshammari, Asma, Flower, Michael, Durr, Alexandra, Leavitt, Blair, Roos, Raymund, Holmans, Peter, Jones, Lesley, Langbehn, Douglas, Kwak, Seung, Tabrizi, Sarah, Monckton, Darren
وصف الملف: application/pdf
العلاقة: https://orca.cardiff.ac.uk/id/eprint/125434/3/1-s2.0-S2352396419306243-main.pdfTest; Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah, Hensman Moss, Davina, Alshammari, Asma, Flower, Michael, Durr, Alexandra, Leavitt, Blair, Roos, Raymund, Holmans, Peter https://orca.cardiff.ac.uk/view/cardiffauthors/A0466487.htmlTest orcid:0000-0003-0870-9412 orcid:0000-0003-0870-9412, Jones, Lesley orcid:0000-0002-3007-4612 orcid:0000-0002-3007-4612, Langbehn, Douglas, Kwak, Seung, Tabrizi, Sarah and Monckton, Darren 2019. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. EBioMedicine 48 , pp. 568-580. 10.1016/j.ebiom.2019.09.020 https://doi.org/10.1016/j.ebiom.2019.09.020Test file https://orca.cardiff.ac.uk/id/eprint/125434/3/1-s2.0-S2352396419306243-main.pdfTest
الإتاحة: https://doi.org/10.1016/j.ebiom.2019.09.020Test
https://orca.cardiff.ac.uk/id/eprint/125434Test/
https://orca.cardiff.ac.uk/id/eprint/125434/3/1-s2.0-S2352396419306243-main.pdfTest -
8دورية أكاديمية
المؤلفون: Goold, Robert, Flower, Michael, Moss, Davina Hensman, Medway, Christopher, Wood-Kaczmar, Alison, Andre, Ralph, Farshim, Pamela, Bates, Gill P, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah J
وصف الملف: application/pdf
العلاقة: https://orca.cardiff.ac.uk/id/eprint/116223/7/ddy375.pdfTest; Goold, Robert, Flower, Michael, Moss, Davina Hensman, Medway, Christopher orcid:0000-0002-1764-0587 orcid:0000-0002-1764-0587, Wood-Kaczmar, Alison, Andre, Ralph, Farshim, Pamela, Bates, Gill P, Holmans, Peter https://orca.cardiff.ac.uk/view/cardiffauthors/A0466487.htmlTest orcid:0000-0003-0870-9412 orcid:0000-0003-0870-9412, Jones, Lesley orcid:0000-0002-3007-4612 orcid:0000-0002-3007-4612 and Tabrizi, Sarah J 2019. FAN1 modifies Huntington's disease progression by stabilising the expanded HTT CAG repeat. Human Molecular Genetics 28 (4) , pp. 650-661. 10.1093/hmg/ddy375 https://doi.org/10.1093/hmg%2Fddy375Test file https://orca.cardiff.ac.uk/id/eprint/116223/7/ddy375.pdfTest
الإتاحة: https://doi.org/10.1093/hmg/ddy375Test
https://orca.cardiff.ac.uk/id/eprint/116223Test/
https://orca.cardiff.ac.uk/id/eprint/116223/7/ddy375.pdfTest -
9مؤتمر
المؤلفون: Hensman Moss, Davina, Dalmia, Anupriya, Galassi Deforie, Valentina, Ibanez, Kristina, Tabrizi, Sarah J, Lahiri, Nayana, Houlden, Henry, Holmans, Peter, Jones, Lesley, Tucci, Arianna
المصدر: C: Genetic modifiers
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10دورية أكاديمية
المؤلفون: Goold, Robert, Flower, Michael, Moss, Davina Hensman, Medway, Chris, Wood-Kaczmar, Alison, Andre, Ralph, Farshim, Pamela, Bates, Gill P, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah J
المساهمون: UK Dementia Research Institute, Medical Research Council, CHDI
المصدر: Human Molecular Genetics ; volume 28, issue 4, page 650-661 ; ISSN 0964-6906 1460-2083
الإتاحة: https://doi.org/10.1093/hmg/ddy375Test
http://academic.oup.com/hmg/article-pdf/28/4/650/27636613/ddy375.pdfTest