Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Madelyn Q. Hoffmann"'
Autor:
Andrew E. Arrant, Jonathan R. Roth, Nicholas R. Boyle, Shreya N. Kashyap, Madelyn Q. Hoffmann, Charles F. Murchison, Eliana Marisa Ramos, Alissa L. Nana, Salvatore Spina, Lea T. Grinberg, Bruce L. Miller, William W. Seeley, Erik D. Roberson
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-17 (2019)
Abstract Loss-of-function mutations in progranulin (GRN) are a major autosomal dominant cause of frontotemporal dementia. Most pathogenic GRN mutations result in progranulin haploinsufficiency, which is thought to cause frontotemporal dementia in GRN
Externí odkaz:
https://doaj.org/article/c318266701f74db1b7c84975e46849dc
Autor:
Andrew E. Arrant, Anthony J. Filiano, Aashka R. Patel, Madelyn Q. Hoffmann, Nicholas R. Boyle, Shreya N. Kashyap, Vincent C. Onyilo, Allen H. Young, Erik D. Roberson
Publikováno v:
Neurobiology of Disease, Vol 124, Iss , Pp 152-162 (2019)
Loss-of-function mutations in progranulin (GRN), most of which cause progranulin haploinsufficiency, are a major autosomal dominant cause of frontotemporal dementia (FTD). Individuals with loss-of-function mutations on both GRN alleles develop neuron
Externí odkaz:
https://doaj.org/article/97e61d56e52648b9bc2c109597052725
Autor:
Shreya N. Kashyap, Erik D. Roberson, Lea T. Grinberg, Madelyn Q. Hoffmann, William W. Seeley, Andrew E. Arrant, Jonathan R. Roth, Alissa L. Nana, Bruce L. Miller, Eliana Marisa Ramos, Charles F. Murchison, Salvatore Spina, Nicholas R. Boyle
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-17 (2019)
Acta Neuropathologica Communications
Acta neuropathologica communications, vol 7, iss 1
Acta Neuropathologica Communications
Acta neuropathologica communications, vol 7, iss 1
Loss-of-function mutations in progranulin (GRN) are a major autosomal dominant cause of frontotemporal dementia. Most pathogenicGRNmutations result in progranulin haploinsufficiency, which is thought to cause frontotemporal dementia inGRNmutation car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ccda55fe93e4f7a531f674858b170c
https://doaj.org/article/c318266701f74db1b7c84975e46849dc
https://doaj.org/article/c318266701f74db1b7c84975e46849dc
Autor:
Madelyn Q. Hoffmann, Anthony J. Filiano, Andrew E. Arrant, Shreya N. Kashyap, Allen H. Young, Erik D. Roberson, Aashka R. Patel, Nicholas R. Boyle, Vincent C. Onyilo
Publikováno v:
Neurobiology of Disease, Vol 124, Iss, Pp 152-162 (2019)
Loss-of-function mutations in progranulin (GRN), most of which cause progranulin haploinsufficiency, are a major autosomal dominant cause of frontotemporal dementia (FTD). Individuals with loss-of-function mutations on both GRN alleles develop neuron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::995a7c10ab86bae13b3772a768dd835e
https://doi.org/10.1016/j.nbd.2018.11.011
https://doi.org/10.1016/j.nbd.2018.11.011