Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Marianne Hallupp"'
Autor:
Lisa J. Oyston, Stephanie Ubiparipovic, Lauren Fitzpatrick, Marianne Hallupp, Lauren M. Boccanfuso, John B. Kwok, Carol Dobson-Stone
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Identified genetic mutations cause 20% of frontotemporal dementia (FTD) and 5-10% of amyotrophic lateral sclerosis (ALS) cases: however, for the remainder of patients the origin of disease is uncertain. The overlap in genetic, clinical and p
Externí odkaz:
https://doaj.org/article/d6b114cd448a4c3994d1dd8d4af96bb4
Autor:
Theresa N. T. Dang, Carol Dobson-Stone, Elias N. Glaros, Woojin S. Kim, Marianne Hallupp, Lauren Bartley, Olivier Piguet, John R. Hodges, Glenda M. Halliday, Kay L. Double, Peter R. Schofield, Peter J. Crouch, John B. J. Kwok
Publikováno v:
Disease Models & Mechanisms, Vol 6, Iss 5, Pp 1198-1204 (2013)
SUMMARY Frontotemporal dementia (FTD) is associated with motor neurone disease (FTD-MND), corticobasal syndrome (CBS) and progressive supranuclear palsy syndrome (PSPS). Together, this group of disorders constitutes a major cause of young-onset demen
Externí odkaz:
https://doaj.org/article/652819affd724e67a4c39f977e1db999
Autor:
Kirsten G Coupland, Woojin S Kim, Glenda M Halliday, Marianne Hallupp, Carol Dobson-Stone, John B J Kwok
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157924 (2016)
Studies investigating the pathogenic role of the microtubule associated protein tau (MAPT) gene in Parkinson's disease (PD) have indicated that DNA methylation of the promoter region is aberrant in disease, leading to dysregulated MAPT expression. We
Externí odkaz:
https://doaj.org/article/b992be44fc05475faa2ae26b0d71a048
Autor:
Carol Dobson-Stone, Marianne Hallupp, Clement T Loy, Elizabeth M Thompson, Eric Haan, Carolyn M Sue, Peter K Panegyres, Cristina Razquin, Manuel Seijo-Martínez, Ramon Rene, Jordi Gascon, Jaume Campdelacreu, Birgit Schmoll, Alexander E Volk, William S Brooks, Peter R Schofield, Pau Pastor, John B J Kwok
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56899 (2013)
A hexanucleotide repeat expansion in C9ORF72 has been established as a common cause of frontotemporal dementia (FTD). However, the minimum repeat number necessary for disease pathogenesis is not known. The aims of our study were to determine the freq
Externí odkaz:
https://doaj.org/article/34d9fa3edd3248f2999405cb91c6ba3c
Autor:
Lisa J. Oyston, Lauren M. Boccanfuso, Lauren Fitzpatrick, Johnny Zhang, Marianne Hallupp, John B. Kwok, Carol Dobson-Stone
BackgroundFrontotemporal dementia (FTD) is one of the most common forms of younger-onset dementia. FTD is genetically, pathologically and clinically related to amyotrophic lateral sclerosis (ALS), a rapidly progressive neurodegenerative disorder. Mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::651498a8f064ad2fbae39415653052ff
https://doi.org/10.1101/2022.06.02.494603
https://doi.org/10.1101/2022.06.02.494603
Autor:
Marianne Hallupp, Colin D. Field, Kelly L. Williams, Emily P. McCann, Garth A. Nicholson, Claire E. Shepherd, John R. Hodges, John Landers, Agnes Luty, William S. Brooks, Thomas Fath, Glenda M. Halliday, Mark F. Bennett, Peter K. Panegyres, Peter R. Schofield, Jennifer A. Fifita, Bradley N. Smith, Ian P. Blair, Janice M. Fullerton, Esmeralda Paric, Neil Rajan, Olivier Piguet, John B.J. Kwok, Jane Hecker, Alex D. Shaw, Cathy L. Short, Melanie Bahlo, Carol Dobson-Stone, Shankaracharya, Audrey Ragagnin, Holly Stefen, Hamideh Shahheydari, Francine Carew-Jones, Elizabeth Thompson, Julie D. Atkin, Zac Chatterton, Peter C. Blumbergs, Simon Topp, Christopher Shaw
Publikováno v:
Brain
Frontotemporal dementia and amyotrophic lateral sclerosis are clinically and pathologically overlapping disorders with shared genetic causes. We previously identified a disease locus on chromosome 16p12.1-q12.2 with genome-wide significant linkage in
Autor:
Lauren Fitzpatrick, Carol Dobson-Stone, Marianne Hallupp, Stephanie Ubiparipovic, Lauren Boccanfuso, Lisa J. Oyston, John B.J. Kwok
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Identified genetic mutations cause 20% of frontotemporal dementia (FTD) and 5-10% of amyotrophic lateral sclerosis (ALS) cases: however, for the remainder of patients the origin of disease is uncertain. The overlap in genetic, clinical and pathologic
Autor:
Ubiparipovic S, Fitzpatrick L, John B.J. Kwok, Lisa J. Oyston, Carol Dobson-Stone, Marianne Hallupp, Lauren Boccanfuso
BackgroundIdentified genetic mutations cause 20% of frontotemporal dementia (FTD) and 5-10% of amyotrophic lateral sclerosis (ALS) cases: however, for the remainder of patients the origin of the disease is uncertain. The overlap in genetic, clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf0deb5603489b71ed3027aa4ba1d7f
https://doi.org/10.1101/2021.03.07.433817
https://doi.org/10.1101/2021.03.07.433817
Autor:
Carol Dobson-Stone, Albert Lee, Lisa J. Oyston, Lauren Boccanfuso, Marianne Hallupp, John B.J. Kwok, Roger S. Chung
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Neil Rajan, Lisa J. Oyston, Marianne Hallupp, Carol Dobson-Stone, Zac Chatterton, John B.J. Kwok
Publikováno v:
Brain : a journal of neurology. 143(8)