(Q52589275)

4 May 2018

title

Evidence that SIZN1 is a candidate X-linked mental retardation gene. (English)

1 reference

4 May 2018

author name string

Ginam Cho

1

1 reference

4 May 2018

Shambhu S Bhat

2

1 reference

4 May 2018

Jinsong Gao

3

1 reference

4 May 2018

Julianne S Collins

4

1 reference

4 May 2018

R Curtis Rogers

5

1 reference

4 May 2018

Richard J Simensen

6

1 reference

4 May 2018

Charles E Schwartz

7

1 reference

4 May 2018

Jeffrey A Golden

8

1 reference

4 May 2018

Anand K Srivastava

9

1 reference

4 May 2018

language of work or name

English

0 references

publication date

1 October 2008

1 reference

4 May 2018

American Journal of Medical Genetics

published in

1 reference

4 May 2018

volume

146A

1 reference

4 May 2018

issue

20

1 reference

4 May 2018

page(s)

2644-2650

1 reference

4 May 2018

Sizn1 is a novel protein that functions as a transcriptional coactivator of bone morphogenic protein signaling

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

X-linked mental retardation: many genes for a complex disorder

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Down regulation of trk but not p75NTR gene expression in single cholinergic basal forebrain neurons mark the progression of Alzheimer's disease

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Reduction of cortical TrkA but not p75(NTR) protein in early-stage Alzheimer's disease.

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Developmental origins of the age-related decline in cortical cholinergic function and associated cognitive abilities

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

The epidemiology of mental retardation: challenges and opportunities in the new millennium

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Molecular-clinical spectrum of the ATR-X syndrome

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Loss of cholinergic phenotype in basal forebrain coincides with cognitive decline in a mouse model of Down's syndrome

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Cognitive functions of the basal forebrain

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

The etiology of developmental delay

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

The prevalence of mental retardation: a critical review of recent literature.

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Ageing: the cholinergic hypothesis of cognitive decline.

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

X-linked mental retardation

22 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2575800

Single nucleotide polymorphism genotyping using allele-specific PCR and fluorescence melting curves

29 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18798319

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A theory of X-linkage of major intellectual traits. Response to Dr. Anastasi and to the Drs. Nance and Engel

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18798319

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.A.32472

1 reference

4 May 2018

PMC publication ID

2575800

1 reference

4 May 2018

PubMed publication ID

18798319

1 reference

4 May 2018