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Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Human molecular genetics, 1998-01, Vol.7 (1), p.43-51

1998

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Current and future implications of basic and translational research on amyloid-β peptide production and removal pathways

Molecular and cellular neuroscience, 2015-05, Vol.66 (Pt A), p.3-11

2015

Volltextzugriff (PDF)

Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model

Molecular psychiatry, 2013-08, Vol.18 (8), p.889-897

2013

Volltextzugriff (PDF)

A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts

Neurology, 2004-05, Vol.62 (10), p.1875

2004

Volltextzugriff (PDF)

Genetic Factors in the Genesis of Alzheimer's Disease

Annals of the New York Academy of Sciences, 2000-01, Vol.924 (1), p.1-7

ST GEORGE-HYSLOP, P. H.

2000

Volltextzugriff (PDF)

Molecular genetics of Alzheimer’s disease

Biological Psychiatry, 2000-02, Vol.47 (3), p.183-199

St George-Hyslop, Peter H

2000

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Nicastrin binds to membrane-tethered Notch

Nature cell biology, 2001-08, Vol.3 (8), p.751-754

2001

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Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian population

Molecular psychiatry, 2002-08, Vol.7 (7), p.776-781

2002

Volltextzugriff (PDF)

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Nature (London), 1995-06, Vol.375 (6534), p.754-760

1995

Volltextzugriff (PDF)

The presenilin 1 protein is a component of a high molecular weight intracellular complex that contains beta-catenin

The Journal of biological chemistry, 1998-06, Vol.273 (26), p.16470-16475

1998

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The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients

Annals of neurology, 1996-12, Vol.40 (6), p.912-917

1996

Volltextzugriff (PDF)

Clinical and genetic study of a large Italian family linked to SPG12 locus

Neurology, 2002-11, Vol.59 (9), p.1395

2002

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Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder

Nature (London), 1990-09, Vol.347 (6289), p.194-197

1990

Volltextzugriff (PDF)

Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: Confirmation of 14q CAG expansion

Annals of neurology, 1995-10, Vol.38 (4), p.684-687

1995

Volltextzugriff (PDF)

PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier

Neurology, 2003-10, Vol.61 (7), p.1005

2003

Volltextzugriff (PDF)

Molecular Genetics of Alzheimer Disease

Seminars in neurology, 1999, Vol.19 (4), p.371-383

St. George-Hyslop, P. H.

1999

Volltextzugriff (PDF)

Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia

Neurology, 1998-04, Vol.50 (4), p.1015

1998

Volltextzugriff (PDF)

Prediction of probable Alzheimer's disease in memory-impaired patients: A prospective longitudinal study

Neurology, 1996-03, Vol.46 (3), p.661

1996

Volltextzugriff (PDF)

Endogenous Presenilin 1 Redistributes to the Surface of Lamellipodia upon Adhesion of Jurkat Cells to a Collagen Matrix

Proceedings of the National Academy of Sciences - PNAS, 1999-07, Vol.96 (14), p.7932-7937

1999

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TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant

EMBO molecular medicine, 2017-10, Vol.9 (10), p.1366-1378

2017

Volltextzugriff (PDF)

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

Nature (London), 1995-08, Vol.376 (6543), p.775-778

1995

Volltextzugriff (PDF)

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

Brain (London, England : 1878), 2010-02, Vol.133 (2), p.591-598

2010

Volltextzugriff (PDF)

The effects of APOE and tau gene variability on risk of frontotemporal dementia

Neurobiology of aging, 2006-05, Vol.27 (5), p.702-709

2006

Volltextzugriff (PDF)

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Nature (London), 1995-06, Vol.375 (6534), p.754-760

1995

Volltextzugriff (PDF)

Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant

Human molecular genetics, 1996-07, Vol.5 (7), p.985-988

1996

Volltextzugriff (PDF)

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Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Current and future implications of basic and translational research on amyloid-β peptide production and removal pathways

Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model

A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts

Genetic Factors in the Genesis of Alzheimer's Disease

Molecular genetics of Alzheimer’s disease

Nicastrin binds to membrane-tethered Notch

Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian population

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

The presenilin 1 protein is a component of a high molecular weight intracellular complex that contains beta-catenin

The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients

Clinical and genetic study of a large Italian family linked to SPG12 locus

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder

Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: Confirmation of 14q CAG expansion

PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier

Molecular Genetics of Alzheimer Disease

Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia

Prediction of probable Alzheimer's disease in memory-impaired patients: A prospective longitudinal study

Endogenous Presenilin 1 Redistributes to the Surface of Lamellipodia upon Adhesion of Jurkat Cells to a Collagen Matrix

TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

The effects of APOE and tau gene variability on risk of frontotemporal dementia

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant

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