Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Charlotte, Forsell"'
Autor:
Homira Behbahani, Charlotte Forsell, Eva-Britt Samuelsson, Saara Tikka, Kirsten Coupland, Mahmod Panahi, Erik Sundström, Naeimeh Yousefi Mesri, Helena Karlström, Matti Viitanen, Bengt Winblad, Caroline Graff
Publikováno v:
Journal of Cellular and Molecular Medicine
Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a familial fatal progressive degenerative disorder. One of the pathological hallmarks of CADASIL is a dramatic reduction of vascular smooth muscle
Publikováno v:
Alzheimer's & Dementia. 10
to be due to the extra dosage of the amyloid precursor protein(APP) gene: an established risk factor for AD. Studying mouse models of DS have led to a greater understanding of the significance of trisomy 21 and its relationship with AD. The Tc1 DS mo
Publikováno v:
American Journal of Medical Genetics. 67:306-311
An association between the {epsilon}4 allele of the apolipoprotein E gene (APOE) and late-onset Alzheimer`s disease (AD) was recently demonstrated. In order to confirm the association and to gauge the ability of standard genetic linkage methods to id
Autor:
Charlotte Forsell, Bengt Winblad, Jorge Andrade, Toru Kimura, Caroline Graff, Anna Sillén, Jacob Odeberg, Lena Lilius, Jesper Brohede
Publikováno v:
Alzheimer's & Dementia. 6
Publikováno v:
Alzheimer's & Dementia. 6
significant variants (P
Autor:
Jacob Odeberg, Lena Lilius, Caroline Graff, Anna Sillén, Jesper Brohede, Hayao Ebise, Charlotte Forsell, Jorge Andrade, Bengt Winblad
Publikováno v:
Alzheimer's & Dementia. 6
Autor:
Lena Lilius, Terho Lehtimäki, Tuula Pirttilä, H. Frey, Juha O. Rinne, Charlotte Forsell, Matias Röyttä, Lars Lannfelt, Kari M. Mattila, Anne Eerola, Peter St George-Hyslop
Publikováno v:
Annals of Neurology. 44:965-967
In early-onset familial Alzheimer's disease (AD) pathogenic mutations have been found in the amyloid precursor protein (APP) gene and in the presenilin (PS)-1 and PS-2 genes. We screened for mutations in these genes in 20 patients with familial AD fr
Autor:
Karin Axelman, Caroline Graff, Päivi Onkamo, Anna Sillén, Juha Kere, Behnosh F. Björk, Charlotte Forsell, Bengt Winblad, Lena Lilius
Publikováno v:
Alzheimer's & Dementia. 2
Autor:
Susanne Froelich Fabre, Lena Lilius, Bengt Winblad, Charlotte Forsell, Karin Dillner, Behnosh F. Björk, Karin Axelman, Caroline Graff
Publikováno v:
Alzheimer's & Dementia. 2
Autor:
Martin Ingelsson, Lena Lilius, Caroline Graff, Michael C. Irizarry, Bradley T. Hyman, Youngah Shin, Charlotte Forsell
Publikováno v:
Current Protocols in Human Genetics
Disease-associated gene polymorphisms provide both scientific insight into pathophysiological mechanisms and clinical information regarding risk and progression. Of special interest is the ɛ4 allele of the apolipoprotein E gene, which has emerged as