Kinesin light chain 1 gene haplotypes in three conformational diseases. (Q51860683)

14 April 2018

title

Kinesin light chain 1 gene haplotypes in three conformational diseases. (English)

1 reference

14 April 2018

16

Henrik Zetterberg

1 reference

14 April 2018

15

Kaj Blennow

1 reference

14 April 2018

5

Lennart Minthon

1 reference

14 April 2018

3

Staffan Nilsson

1 reference

14 April 2018

Madeleine Zetterberg

13

Madeleine Zetterberg

1 reference

14 April 2018

Ingmar Skoog

9

Ingmar Skoog

1 reference

14 April 2018

Malin von Otter

1

Malin von Otter

1 reference

14 April 2018

Sara Landgren

2

Sara Landgren

1 reference

14 April 2018

Deborah Gustafson

8

Deborah R Gustafson

1 reference

14 April 2018

Gunnar Tasa

14

Gunnar Tasa

1 reference

14 April 2018

Nenad Bogdanovic

6

Nenad Bogdanovic

1 reference

14 April 2018

Caroline Lundvall

4

Caroline Lundvall

1 reference

14 April 2018

author name string

Niels Andreasen

7

1 reference

14 April 2018

Anders Wallin

10

1 reference

14 April 2018

Anna Håkansson

11

1 reference

14 April 2018

Hans Nissbrandt

12

1 reference

14 April 2018

publication date

13 November 2009

1 reference

14 April 2018

published in

NeuroMolecular Medicine

1 reference

14 April 2018

volume

12

1 reference

14 April 2018

page(s)

229-236

1 reference

14 April 2018

issue

3

1 reference

14 April 2018

https://scigraph.springernature.com/pub.10.1007/s12017-009-8103-0

exact match

0 references

cites work

Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12017-009-8103-0

Alternatively spliced products of the human kinesin light chain 1 (KNS2) gene

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12017-009-8103-0

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12017-009-8103-0

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

21 January 2018

1 reference

12 December 2020

Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP

1 reference

12 December 2020

Microtubule-dependent transport in neurons: steps towards an understanding of regulation, function and dysfunction

1 reference

12 December 2020

Gene-environmental effects behind leukoaraiosis: a silent genetic variant of the kinesin protein can be activated in a subject with poorly controlled long-lasting hypertension.

1 reference

12 December 2020

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

1 reference

12 December 2020

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

1 reference

12 December 2020

Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material.

1 reference

12 December 2020

Kinesin gene variability may affect tau phosphorylation in early Alzheimer's disease

1 reference

12 December 2020

Axonal transport of amyloid precursor protein is mediated by direct binding to the kinesin light chain subunit of kinesin-I

1 reference

12 December 2020

Role of short-range protein interactions in lens opacifications

1 reference

12 December 2020

A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.

1 reference

12 December 2020

Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.

1 reference

12 December 2020

Microtubule configuration and membranous vesicle transport in elongating fiber cells of the rat lens

1 reference

12 December 2020

A genetic variant in cytoskeleton motors amplifies susceptibility to leukoaraiosis in hypertensive smokers: gene-environmental interactions behind vascular white matter demyelinization

1 reference

12 December 2020

Inhibition of kinesin synthesis in vivo inhibits the rapid transport of representative proteins for three transport vesicle classes into the axon.

1 reference

12 December 2020

Molecular motors implicated in the axonal transport of tau and alpha-synuclein

1 reference

12 December 2020

Synapsin and synaptic vesicle protein expression during embryonic and post-natal lens fiber cell differentiation.

1 reference

12 December 2020

Tau protein in cerebrospinal fluid: a biochemical marker for axonal degeneration in Alzheimer disease?

1 reference

12 December 2020

Parkinson's Disease Society Brain Bank, London: overview and research

1 reference

12 December 2020

Variability in the kinesin light chain 1 gene may influence risk of age-related cataract.

1 reference

12 December 2020

Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

1 reference

12 December 2020

Axonopathy and transport deficits early in the pathogenesis of Alzheimer's disease

1 reference

12 December 2020

The structure of haplotype blocks in the human genome

1 reference

12 December 2020

Association study of three polymorphisms of kinesin light-chain 1 gene with Alzheimer's disease

1 reference

12 December 2020

Histopathological criteria for progressive dementia disorders: clinical-pathological correlation and classification by multivariate data analysis

1 reference

12 December 2020

Standardization of measurement of beta-amyloid(1-42) in cerebrospinal fluid and plasma.

1 reference

12 December 2020

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease

1 reference

12 December 2020

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

1 reference

12 December 2020

High-resolution whole-genome association study of Parkinson disease.

1 reference

12 December 2020

1 reference

12 December 2020

Axonal transport defects: a common theme in neurodegenerative diseases

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

1 reference

12 December 2020

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

1 reference

12 December 2020

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

1 reference

12 December 2020

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

12 December 2020

1 reference

12 December 2020

Intracellular transport and kinesin superfamily proteins, KIFs: structure, function, and dynamics

1 reference

12 December 2020

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database

1 reference

12 December 2020

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

1 reference

12 December 2020

Degenerative axonal changes in the hippocampus and amygdala in Parkinson's disease.

1 reference

12 December 2020

A cytoskeleton motor protein genetic variant may exert a protective effect on the occurrence of multiple sclerosis: the janus face of the kinesin light-chain 1 56836CC genetic variant

1 reference

12 December 2020

Axonal stress kinase activation and tau misbehavior induced by kinesin-1 transport defects.

1 reference

12 December 2020

Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.

1 reference

12 December 2020

1 reference

12 December 2020

Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease

1 reference

12 December 2020

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

1 reference

12 December 2020

Cell toxicity and conformational disease.

1 reference

12 December 2020

Quantification of tau phosphorylated at threonine 181 in human cerebrospinal fluid: a sandwich ELISA with a synthetic phosphopeptide for standardization.

1 reference

12 December 2020

The International HapMap Project

1 reference

12 December 2020

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

1 reference

12 December 2020

Do disorders of movement cause movement disorders and dementia?

1 reference

12 December 2020

1-Methyl-4-phenylpyridinium affects fast axonal transport by activation of caspase and protein kinase C

1 reference

12 December 2020

Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation

1 reference

12 December 2020

Genome screen of late-onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis

1 reference

12 December 2020

10.1007/S12017-009-8103-0

Identifiers

DOI

1 reference

14 April 2018

PubMed ID

19911314

1 reference

14 April 2018