(Q21198881)

English

Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy

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scholarly article

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Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy (English)

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multiple system atrophy

1 reference

based on heuristic

inferred from title

author name string

Hidenao Sasaki

1

author given names

Hidenao

author last names

Sasaki

1 reference

Dimensions Publication ID

17 August 2022

Mitsuru Emi

2

author given names

Mitsuru

author last names

Emi

1 reference

Dimensions Publication ID

17 August 2022

Hiroshi Iijima

3

author given names

Hiroshi

author last names

Iijima

1 reference

Dimensions Publication ID

17 August 2022

Noriko Ito

4

author given names

Noriko

author last names

Ito

1 reference

Dimensions Publication ID

17 August 2022

Hidenori Sato

5

author given names

Hidenori

author last names

Sato

1 reference

Dimensions Publication ID

17 August 2022

Ichiro Yabe

6

author given names

Ichiro

author last names

Yabe

1 reference

Dimensions Publication ID

17 August 2022

Takeo Kato

7

author given names

Takeo

author last names

Kato

1 reference

Dimensions Publication ID

17 August 2022

Jun Utsumi

8

author given names

Jun

author last names

Utsumi

1 reference

Dimensions Publication ID

17 August 2022

Kenichi Matsubara

9

author given names

Kenichi

author last names

Matsubara

1 reference

Dimensions Publication ID

17 August 2022

language of work or name

0 references

publication date

2011

0 references

Molecular Brain

0 references

4

0 references

1

0 references

24

0 references

Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Second consensus statement on the diagnosis of multiple system atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Large recurrent microdeletions associated with schizophrenia

1 reference

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19 March 2017

Two pacemaker channels from human heart with profoundly different activation kinetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Interactive cloning with the SH3 domain of N-src identifies a new brain specific ion channel protein, with homology to eag and cyclic nucleotide-gated channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Segmental duplications and copy-number variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Mechanisms and consequences of somatic mosaicism in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

N-Shc and Sck, two neuronally expressed Shc adapter homologs. Their differential regional expression in the brain and roles in neurotrophin and Src signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Origins and functional impact of copy number variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

19 March 2017

Missing heritability and strategies for finding the underlying causes of complex disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

7 April 2017

''R"--project for statistical computing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

7 April 2017

Augmented currents of an HCN2 variant in patients with febrile seizure syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

CNS elevation of vascular and not mucosal addressin cell adhesion molecules in patients with multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

SNCA variants are associated with increased risk for multiple system atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Population analysis of large copy number variants and hotspots of human genetic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Genomic rearrangements and sporadic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

FGF22 and its close relatives are presynaptic organizing molecules in the mammalian brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Somatic gene mutation and human disease other than cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

12 September 2017

Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

30 May 2018

The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3141657

30 May 2018

HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.

1 reference

https://api.crossref.org/works/10.1186%2F1756-6606-4-24

21 January 2018

Segmental copy number variation shapes tissue transcriptomes.

1 reference

https://api.crossref.org/works/10.1186%2F1756-6606-4-24

21 January 2018

Multiplex families with multiple system atrophy

1 reference

https://api.crossref.org/works/10.1186%2F1756-6606-4-24

21 January 2018

The mammalian ShcB and ShcC phosphotyrosine docking proteins function in the maturation of sensory and sympathetic neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/21658278

12 December 2020

based on heuristic

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Identifiers

10.1186/1756-6606-4-24

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Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1756-6606-4-24

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