PAPER Weisová P, Alvarez SP, Kilbride SM, Anilkumar U, Baumann B, Jordán J, Bernas T, Huber HJ, Düssmann H, Prehn JH
SEARCH RESULTS
331254 RESULTS
PAPER Delaby C, Gabelle A, Meynier P, Loubiere V, Vialaret J, Tiers L, Ducos J, Hirtz C, Lehmann S
Development and validation of dried matrix spot sampling for the quantitative determination of amyloid β peptides in cerebrospinal fluid.
Clin Chem Lab Med. 2013 Oct 23;:1-7. PubMed: 24150208PAPER Franchi C, Arosio F, Djade CD, Salvini Porro G, Nobili A
Caregivers' perceptions of the therapeutic benefits of drug treatments for dementia.
Aging Clin Exp Res. 2013 Dec;25(6):677-83. PubMed: 24150573PAPER Veerappan CS, Sleiman S, Coppola G
Epigenetics of Alzheimer's disease and frontotemporal dementia.
Neurotherapeutics. 2013 Oct;10(4):709-21. PubMed: 24150812PAPER Morra LF, Donovick PJ
Clinical presentation and differential diagnosis of dementia with Lewy bodies: a review.
Int J Geriatr Psychiatry. 2013 Oct 21; PubMed: 24150834PAPER Scacchi R, Gambina G, Broggio E, Corbo RM
Sex and ESR1 genotype may influence the response to treatment with donepezil and rivastigmine in patients with Alzheimer's disease.
Int J Geriatr Psychiatry. 2013 Oct 22; PubMed: 24150894PAPER Clare L, Woods RT, Nelis SM, Martyr A, Marková IS, Roth I, Whitaker CJ, Morris RG
Trajectories of quality of life in early-stage dementia: individual variations and predictors of change.
Int J Geriatr Psychiatry. 2013 Oct 22; PubMed: 24150910PAPER Bader C, Cyrille C, Jadwiga Z, Joel D, Fichten A, Catherine GJ, Roger B, Olivier B
Estimation of the Lateral Ventricles Volumes from a 2D Image and Its Relationship with Cerebrospinal Fluid Flow.
Biomed Res Int. 2013;2013:215989. PubMed: 24151585Sid Strickland
The Rockefeller UniversityNew York, United States
PSEN1 L166P
MUTATIONS PSEN1 73653577 GRCh37/hg19 rs63750265 T C g.38794T> C g.55399T> C Exon 6 Point, Missense Coding Decreased Aβ (37 + 38 + 40) / (42 + 43) and Aβ37/Aβ42 and increased Aβ42/Aβ40. Increased Aβ42 and Aβ43; endosomal accumulation of APP β-CTF. Also, interf
APPPS1
RESEARCH MODELS Summary APPPS1 mice contain human transgenes for both APP bearing the Swedish mutation and PSEN1 containing an L166P mutation, both under the control of the Thy1 promoter. In these mice, expression of the human APP transgene is approximately 3-fold higher
APPDutch
RESEARCH MODELS Summary This transgenic mouse line bears a mutation that was determined to cause hereditary cerebral hemorrhage with amyloidosis-Dutch type, a rare autosomal dominant disorder characterized by cerebral amyloid angiopathy (CAA), strokes, and dementia. APPD
ADanPP
RESEARCH MODELS This transgenic line bears a mutation that causes Familial Danish Dementia (FDD), a rare autosomal dominant disorder characterized by cerebral deposition of Danish-amyloid (ADan), neuro-inflammation, and neurofibrillary tangles (Vidal et al., 2000). The F
Tg-ArcSwe
RESEARCH MODELS Summary The inclusion of the Arctic mutation along with the Swedish mutation in the transgene results in more prominent Aβ pathology, including elevated soluble Aβ aggregates such as Aβ protofibrils, greater accumulation of Aβ inside neurons, and more rob
PAPER
Parkinson disease: Patients with Parkinson disease show deposition of α-synuclein in cutaneous autonomic nerves.
Autophagy. 2013 Oct 8;9(12) PubMed: 24145375Current Filters
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