(Q53728593)

18 May 2018

title

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype. (English)

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18 May 2018

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linkage disequilibrium

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1

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18 May 2018

Jeffery M. Vance

9

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18 May 2018

Kenichiro Fujiwara

object named as

Kenichiro Fujiwara

5

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author name string

William K Scott

2

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18 May 2018

Fengyu Zhang

3

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18 May 2018

Jeffrey M Stajich

4

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18 May 2018

Michael Hauser

6

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18 May 2018

Burton L Scott

7

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18 May 2018

Margaret A Pericak-Vance

8

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18 May 2018

Eden R Martin

10

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18 May 2018

publication date

8 June 2004

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18 May 2018

published in

Neurogenetics

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18 May 2018

volume

5

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18 May 2018

issue

3

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18 May 2018

page(s)

147-155

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18 May 2018

Colocalization of Tau and Alpha-Synuclein Epitopes in Lewy Bodies

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS10048-004-0180-5

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

21 January 2018

1 reference

12 December 2020

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease

1 reference

12 December 2020

Rotenone inhibition of spindle microtubule assembly in mammalian cells.

1 reference

12 December 2020

A genomic sequence analysis of the mouse and human microtubule-associated protein tau.

1 reference

12 December 2020

The family based association test method: strategies for studying general genotype--phenotype associations.

1 reference

12 December 2020

Microtubule assembly is directly affected by MPP(+)in vitro

1 reference

12 December 2020

Possible association of the tau H1/H1 genotype with primary progressive aphasia

1 reference

12 December 2020

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

1 reference

12 December 2020

Further extension of the H1 haplotype associated with progressive supranuclear palsy

1 reference

12 December 2020

Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Complete genomic screen in Parkinson disease: evidence for multiple genes.

1 reference

12 December 2020

Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus

1 reference

12 December 2020

Genetic evidence for the involvement of tau in progressive supranuclear palsy

1 reference

12 December 2020

Association between the extended tau haplotype and frontotemporal dementia.

1 reference

12 December 2020

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

1 reference

12 December 2020

GOLD--graphical overview of linkage disequilibrium

1 reference

12 December 2020

Genotype‐based association test for general pedigrees: The genotype‐PDT

1 reference

12 December 2020

The structure of haplotype blocks in the human genome

1 reference

12 December 2020

Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

1 reference

12 December 2020

Parkin binds to alpha/beta tubulin and increases their ubiquitination and degradation

1 reference

12 December 2020

A comparison of linkage disequilibrium measures for fine-scale mapping

1 reference

12 December 2020

Corticotropin-releasing factor receptors: physiology, pharmacology, biochemistry and role in central nervous system and immune disorders

1 reference

12 December 2020

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

1 reference

12 December 2020

An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy

1 reference

12 December 2020

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

1 reference

12 December 2020

The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population

1 reference

12 December 2020

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease

1 reference

12 December 2020

Parkin mutations and susceptibility alleles in late-onset Parkinson's disease

1 reference

12 December 2020

A first-generation linkage disequilibrium map of human chromosome 22

1 reference

12 December 2020

The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease.

1 reference

12 December 2020

Extent and distribution of linkage disequilibrium in three genomic regions

1 reference

12 December 2020

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

1 reference

12 December 2020

A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease

1 reference

12 December 2020

Identification of a novel family of presenilin homologues

1 reference

12 December 2020

Pick's disease is associated with mutations in the tau gene.

1 reference

12 December 2020

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

1 reference

12 December 2020

Case-control study of the extended tau gene haplotype in Parkinson's disease

1 reference

12 December 2020

Influence of MPP+ on the state of tubulin polymerisation in NGF-differentiated PC12 cells

1 reference

12 December 2020

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

1 reference

12 December 2020

Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

1 reference

12 December 2020

Haplotype tagging for the identification of common disease genes

1 reference

12 December 2020

10.1007/S10048-004-0180-5

Identifiers

DOI

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18 May 2018

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18 May 2018