(Q36637691)

English

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

scientific article published on October 1998

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scholarly article

1 reference

Europe PubMed Central

15 August 2017

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

1 reference

Europe PubMed Central

15 August 2017

neurodegeneration

1 reference

based on heuristic

inferred from title

Zbigniew K Wszolek

3

object named as

Z Wszolek

1 reference

Europe PubMed Central

15 August 2017

Kirk Wilhelmsen

19

object named as

K C Wilhelmsen

1 reference

Europe PubMed Central

15 August 2017

author name string

L N Clark

1

1 reference

Europe PubMed Central

15 August 2017

P Poorkaj

2

1 reference

Europe PubMed Central

15 August 2017

D H Geschwind

4

1 reference

Europe PubMed Central

15 August 2017

Z S Nasreddine

5

1 reference

Europe PubMed Central

15 August 2017

B Miller

6

1 reference

Europe PubMed Central

15 August 2017

D Li

7

1 reference

Europe PubMed Central

15 August 2017

H Payami

8

1 reference

Europe PubMed Central

15 August 2017

F Awert

9

1 reference

Europe PubMed Central

15 August 2017

K Markopoulou

10

1 reference

Europe PubMed Central

15 August 2017

A Andreadis

11

1 reference

Europe PubMed Central

15 August 2017

I D'Souza

12

1 reference

Europe PubMed Central

15 August 2017

V M Lee

13

1 reference

Europe PubMed Central

15 August 2017

L Reed

14

1 reference

Europe PubMed Central

15 August 2017

J Q Trojanowski

15

1 reference

Europe PubMed Central

15 August 2017

V Zhukareva

16

1 reference

Europe PubMed Central

15 August 2017

T Bird

17

1 reference

Europe PubMed Central

15 August 2017

G Schellenberg

18

1 reference

Europe PubMed Central

15 August 2017

language of work or name

0 references

publication date

1 October 1998

1 reference

Europe PubMed Central

15 August 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

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15 August 2017

95

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15 August 2017

22

1 reference

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15 August 2017

13103-13107

1 reference

Europe PubMed Central

15 August 2017

Rapidly progressive autosomal dominant Parkinsonism and dementia with Pallido-Ponto-Nigral Gegeneration (PPND) and Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Familial parkinsonism: Our experience and review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

The cardiac troponin T alternative exon contains a novel purine-rich positive splicing element

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

30 September 2017

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

28 June 2018

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

28 June 2018

Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

28 June 2018

The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

20 September 2018

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

20 September 2018

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

20 September 2018

Genetic evidence for the involvement of tau in progressive supranuclear palsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

20 September 2018

The role of exon sequences in splice site selection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

20 September 2018

Abnormal tau phosphorylation at Ser396 in Alzheimer's disease recapitulates development and contributes to reduced microtubule binding.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23724

20 September 2018

Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789048

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789048

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A splicing enhancer in the human fibronectin alternate ED1 exon interacts with SR proteins and stimulates U2 snRNP binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789048

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.95.22.13103

1 reference

Europe PubMed Central

15 August 2017

1998PNAS...9513103C

0 references

1 reference

Europe PubMed Central

15 August 2017

1 reference

Europe PubMed Central

15 August 2017

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