Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nicholas R. Boyle"'
Autor:
Skylar E. Davis, Anna K. Cook, Justin A. Hall, Yuliya Voskobiynyk, Nancy V. Carullo, Nicholas R. Boyle, Ahmad R. Hakim, Kristian M. Anderson, Kierra P. Hobdy, Derian A. Pugh, Charles F. Murchison, Laura J. McMeekin, Micah Simmons, Katherine A. Margolies, Rita M. Cowell, Alissa L. Nana, Salvatore Spina, Lea T. Grinberg, Bruce L. Miller, William W. Seeley, Andrew E. Arrant
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-19 (2023)
Abstract Loss of function progranulin (GRN) mutations are a major autosomal dominant cause of frontotemporal dementia (FTD). Patients with FTD due to GRN mutations (FTD-GRN) develop frontotemporal lobar degeneration with TDP-43 pathology type A (FTLD
Externí odkaz:
https://doaj.org/article/cb7d9e8149f4472c81b6d7612826356c
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
Publikováno v:
Neurotherapeutics. 20:140-153
Heterozygous loss-of-function mutations in progranulin (GRN) cause frontotemporal dementia (FTD), a leading cause of early-onset dementia characterized clinically by behavioral, social, and language deficits. There are currently no FDA-approved thera
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
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
Autor:
Erik D. Roberson, Andrew E. Arrant, Bruce L. Miller, Lea T. Grinberg, William W. Seeley, Nicholas R. Boyle, Jonathan R. Roth, Alissa Nana Li, Salvatore Spina
Publikováno v:
Alzheimer's & Dementia. 15:P308-P308