Structural and functional characterization of H2 haplotype MAPT promoter: unique neurospecific domains and a hypoxia-inducible element would enhance rationally targeted tauopathy research for Alzheimer's disease. (Q36081610)

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English	Structural and functional characterization of H2 haplotype MAPT promoter: unique neurospecific domains and a hypoxia-inducible element would enhance rationally targeted tauopathy research for Alzheimer's disease.	scientific article

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22 January 2020

Structural and functional characterization of H2 haplotype MAPT promoter: unique neurospecific domains and a hypoxia-inducible element would enhance rationally targeted tauopathy research for Alzheimer's disease (English)

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22 January 2020

Alzheimer's disease

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22 January 2020

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Debomoy K Lahiri

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30 January 2012

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22 January 2020

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22 January 2020

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22 January 2020

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22 January 2020

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22 January 2020

Functional activity of the novel Alzheimer's amyloid β-peptide interacting domain (AβID) in the APP and BACE1 promoter sequences and implications in activating apoptotic genes and in amyloidogenesis

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The world of dementia beyond 2020.

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Imaging as a strategy for premortem diagnosis and staging of tauopathies

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Association of the MAPT locus with Parkinson's disease

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Pathological substrates of cognitive decline in Alzheimer's disease

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Evolutionary toggling of the MAPT 17q21.31 inversion region

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Promoter polymorphisms which modulate insulin degrading enzyme expression may increase susceptibility to Alzheimer's disease.

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Tau pathology and neurodegeneration: an obvious but misunderstood link.

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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

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Functional domains of the BACE1 and BACE2 promoters and mechanisms of transcriptional suppression of the BACE2 promoter in normal neuronal cells

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BACE1 gene promoter is differentially regulated: detection of a novel promoter region for its cell type-specific regulation

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A partial failure of membrane protein turnover may cause Alzheimer's disease: a new hypothesis.

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Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease

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Reelin promoter hypermethylation in schizophrenia

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NF-(kappa)B mediates amyloid beta peptide-stimulated activity of the human apolipoprotein E gene promoter in human astroglial cells

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Characterization of the APP proximal promoter and 5'-untranslated regions: identification of cell type-specific domains and implications in APP gene expression and Alzheimer's disease.

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Tau haplotypes regulate transcription and are associated with Parkinson's disease.

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27 July 2018

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23 September 2018

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23 September 2018

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23 September 2018

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23 September 2018

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23 September 2018

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23 September 2018

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23 September 2018

Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia.

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23 September 2018

Promoter polymorphisms which modulate APP expression may increase susceptibility to Alzheimer's disease.

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23 September 2018

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.

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23 September 2018

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23 September 2018

Tau protein expression in frontotemporal dementias

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23 September 2018

High expression of apolipoprotein E mRNA in the brains with sporadic Alzheimer's disease

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23 September 2018

Neuroinflammation and Alzheimer's disease: critical roles for cytokine/Abeta-induced glial activation, NF-kappaB, and apolipoprotein E.

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23 September 2018

Alzheimer's disease hyperphosphorylated tau sequesters normal tau into tangles of filaments and disassembles microtubules.

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23 September 2018

A tau promoter region without neuronal specificity

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23 September 2018

Identification of a tau promoter region mediating tissue-specific-regulated expression in PC12 cells

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23 September 2018

Exploring gene-environment interactions in Parkinson’s disease

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21 October 2018

The Effect of MAPT H1 and APOE ε4 on Transition from Mild Cognitive Impairment to Dementia

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3391566

5 December 2018

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

1 reference

https://pubmed.ncbi.nlm.nih.gov/22310385

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of insertions, deletions, and alignment errors on the branch-site test of positive selection

1 reference

https://pubmed.ncbi.nlm.nih.gov/22310385

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Using RepeatMasker to identify repetitive elements in genomic sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/22310385

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.GENE.2012.01.049

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22310385%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

release_icg36bqhgfdp7flpsovgw4z2ki

1 reference

https://api.fatcat.wiki/v0/release/icg36bqhgfdp7flpsovgw4z2ki

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22310385%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22310385%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

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