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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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Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

Molecular psychiatry, 2002-01, Vol.7 (10), p.1064-1074

2002

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A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder

Molecular psychiatry, 2003, Vol.8 (1), p.83-89

2003

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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

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Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families

Nature (London), 1987-09, Vol.329 (6135), p.153-155

1987

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Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease

Human molecular genetics, 2000-11, Vol.9 (18), p.2589

2000

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A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21

American journal of human genetics, 1994-10, Vol.55 (4), p.714-727

1994

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Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3

Human molecular genetics, 1995-12, Vol.4 (12), p.2363-2371

1995

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Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3

Nature genetics, 1992-12, Vol.2 (4), p.335-339

1992

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Immunoreactivity for p53 and mdm2 and the detection of p53 mutations in human malignant mesothelioma

Virchows Archiv : an international journal of pathology, 1995-12, Vol.427 (4), p.431-436

1995

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Expression of Glial Fibrillary Acidic Protein in Rat C6 Glioma Relates to Vimentin and Is Independent of Cell‐Cell Contact

Journal of neurochemistry, 1987-08, Vol.49 (2), p.348-354

1987

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Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type

Annals of neurology, 1997-07, Vol.42 (1), p.108-110

1997

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Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression

Human molecular genetics, 2000-02, Vol.9 (3), p.325-331

2000

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WT1 MUTATION IN MALIGNANT MESOTHELIOMA AND WT1 IMMUNOREACTIVITY IN RELATION TO p53 AND GROWTH FACTOR RECEPTOR EXPRESSION, CELL-TYPE TRANSITION, AND PROGNOSIS

The Journal of pathology, 1997-01, Vol.181 (1), p.67-74

1997

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Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased Aβ42 Secretion

Human molecular genetics, 1999-08, Vol.8 (8), p.1529-1540

1999

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Dinucleotide repeat polymorphism at the D21S145 locus

Nucleic acids research, 1992-03, Vol.20 (5), p.1159-1159

1992

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Molecular Genetic Analysis of Autosomal Dominant Cerebellar Ataxia with Retinal Degeneration (ADCA Type II) Caused by CAG Triplet Repeat Expansion

Human molecular genetics, 1998-02, Vol.7 (2), p.177-186

1998

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Dinucleotide repeat polymorphism at the D1S16 locus

Nucleic acids research, 1992-03, Vol.20 (5), p.1159-1159

1992

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Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21

Genomics (San Diego, Calif.), 1992, Vol.12 (1), p.158-160

1992

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Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A beta 42 secretion

Human molecular genetics, 1999-08, Vol.8 (8), p.1529-1540

1999

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APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's disease

Neuroscience letters, 1994-03, Vol.169 (1), p.179-180

1994

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Mutation screening of the tau gene in patients with early-onset Alzheimer's disease

Neuroscience letters, 1999-12, Vol.277 (2), p.137-139

1999

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Dinucleotide repeat polymorphism at the D21S258 locus

Human molecular genetics, 1992-09, Vol.1 (6), p.449-449

1992

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ApoE genotype is a risk factor in nonpresenilin early-onset alzheimer's disease families

American journal of medical genetics, 1998-02, Vol.81 (1), p.117-121

1998

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Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome

Human genetics, 1991-10, Vol.87 (6), p.649-653

1991

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

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder

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

Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families

Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease

A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21

Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3

Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3

Immunoreactivity for p53 and mdm2 and the detection of p53 mutations in human malignant mesothelioma

Expression of Glial Fibrillary Acidic Protein in Rat C6 Glioma Relates to Vimentin and Is Independent of Cell‐Cell Contact

Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression

WT1 MUTATION IN MALIGNANT MESOTHELIOMA AND WT1 IMMUNOREACTIVITY IN RELATION TO p53 AND GROWTH FACTOR RECEPTOR EXPRESSION, CELL-TYPE TRANSITION, AND PROGNOSIS

Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased Aβ42 Secretion

Dinucleotide repeat polymorphism at the D21S145 locus

Molecular Genetic Analysis of Autosomal Dominant Cerebellar Ataxia with Retinal Degeneration (ADCA Type II) Caused by CAG Triplet Repeat Expansion

Dinucleotide repeat polymorphism at the D1S16 locus

Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21

Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A beta 42 secretion

APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's disease

Mutation screening of the tau gene in patients with early-onset Alzheimer's disease

Dinucleotide repeat polymorphism at the D21S258 locus

ApoE genotype is a risk factor in nonpresenilin early-onset alzheimer's disease families

Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome

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