BACKGROUND: Mutations in the presenilin (PSEN) genes are associated with early-onset familial Alzheimer's disease (FAD). Biochemical characterizations and comparisons have revealed that many PSEN mutations alter gamma-secretase activity to promote accumulation of toxic Abeta42 peptides. In this study, we compared the histopathologic and biochemical profiles of ten FAD cases expressing independent PSEN mutations and determined the degradation patterns of amyloid-beta precursor protein (AbetaPP), Notch, N-cadherin and Erb-B4 by gamma-secretase. In addition, the levels of Abeta40/42 peptides were quantified by ELISA. RESULTS: We observed a wide variation in type, number and distribution of amyloid deposits and neurofibrillary tangles. Fou...
International audienceBackgroundAmyloid protein precursor (APP), presenilin-1 (PSEN1), and presenili...
International audienceBackgroundAmyloid protein precursor (APP), presenilin-1 (PSEN1), and presenili...
Background: There are more than 300 presenilin-1 (PSEN1) mutations identified but a thorough postmor...
Abstract Background Mutations in the presenilin (PSEN) genes are associated with early-onset familia...
BACKGROUND: Mutations in the presenilin (PSEN) genes are associated with early-onset familial Alzh...
Mutations in human presenilin (PS) genes cause aggressive forms of familial Alzheimer's disease. Pre...
Recently it was proposed that the familial Alzheimer's disease (FAD) causing presenilin (PSEN) mutat...
Recently it was proposed that the familial Alzheimer's disease (FAD) causing presenilin (PSEN) mutat...
Mutations in the Presenilin 1 (PSEN1) gene are the most common cause of autosomal dominant familial ...
BACKGROUND: Mutations linked to early onset, familial forms of Alzheimer's disease (FAD) are found m...
Mutations in presenilin 1 (PSEN1), presenilin 2 (PSEN2), and amyloid precursor protein (APP) are maj...
Presenilin (PS) mutations enhance the production of the Abeta42 peptide that is derived from the amy...
Background: Alzheimer's disease (AD) is associated with deposition of amyloid beta (A beta) in the b...
Presenilin (PSEN) pathogenic mutations cause familial Alzheimer's disease (AD [FAD]) in an autosomal...
Background: Alzheimer's disease (AD) is associated with deposition of amyloid beta (A beta) in the b...
International audienceBackgroundAmyloid protein precursor (APP), presenilin-1 (PSEN1), and presenili...
International audienceBackgroundAmyloid protein precursor (APP), presenilin-1 (PSEN1), and presenili...
Background: There are more than 300 presenilin-1 (PSEN1) mutations identified but a thorough postmor...
Abstract Background Mutations in the presenilin (PSEN) genes are associated with early-onset familia...
BACKGROUND: Mutations in the presenilin (PSEN) genes are associated with early-onset familial Alzh...
Mutations in human presenilin (PS) genes cause aggressive forms of familial Alzheimer's disease. Pre...
Recently it was proposed that the familial Alzheimer's disease (FAD) causing presenilin (PSEN) mutat...
Recently it was proposed that the familial Alzheimer's disease (FAD) causing presenilin (PSEN) mutat...
Mutations in the Presenilin 1 (PSEN1) gene are the most common cause of autosomal dominant familial ...
BACKGROUND: Mutations linked to early onset, familial forms of Alzheimer's disease (FAD) are found m...
Mutations in presenilin 1 (PSEN1), presenilin 2 (PSEN2), and amyloid precursor protein (APP) are maj...
Presenilin (PS) mutations enhance the production of the Abeta42 peptide that is derived from the amy...
Background: Alzheimer's disease (AD) is associated with deposition of amyloid beta (A beta) in the b...
Presenilin (PSEN) pathogenic mutations cause familial Alzheimer's disease (AD [FAD]) in an autosomal...
Background: Alzheimer's disease (AD) is associated with deposition of amyloid beta (A beta) in the b...
International audienceBackgroundAmyloid protein precursor (APP), presenilin-1 (PSEN1), and presenili...
International audienceBackgroundAmyloid protein precursor (APP), presenilin-1 (PSEN1), and presenili...
Background: There are more than 300 presenilin-1 (PSEN1) mutations identified but a thorough postmor...