(Q34430539)

2 August 2017

title

Associations between human disease genes and overlapping gene groups and multiple amino acid runs (English)

1 reference

2 August 2017

Samuel Karlin

1

1 reference

2 August 2017

Chingfer Chen

series ordinal

2

1 reference

2 August 2017

Andrew J Gentles

series ordinal

3

1 reference

2 August 2017

Michael Cleary

series ordinal

4

1 reference

2 August 2017

language of work or name

English

0 references

publication date

9 December 2002

1 reference

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

2 August 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

2 August 2017

volume

99

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2 August 2017

issue

26

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2 August 2017

page(s)

17008-17013

1 reference

Genes, pseudogenes, and Alu sequence organization across human chromosomes 21 and 22.

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Transcription factor haploinsufficiency: when half a loaf is not enough

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Molecular fossils in the human genome: identification and analysis of the pseudogenes in chromosomes 21 and 22

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Amino acid runs in eukaryotic proteomes and disease associations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Glutamine repeats and neurodegeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

The DNA sequence of human chromosome 21

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

The DNA sequence of human chromosome 22

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Alu repeats and human disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

A common molecular basis for rearrangement disorders on chromosome 22q11

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Isolation of a novel human gene from the Down syndrome critical region of chromosome 21q22.2.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Mechanisms of neuronal degeneration in Alzheimer's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

The gene encoding the glutamate receptor subunit GluR5 is located on human chromosome 21q21.1-22.1 in the vicinity of the gene for familial amyotrophic lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Down syndrome phenotypes: the consequences of chromosomal imbalance

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=139260

Extent of RNA editing of glutamate receptor subunit GluR5 in different brain regions of the rat.

6 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

Linkage mapping of the cystathionine ?-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3? untranslated region

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

Transposable elements are found in a large number of human protein-coding genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

Deconstructing DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

Genomic organization of the human tissue inhibitor of metalloproteinases-3 (TIMP3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.262658799

21 January 2018

Identifiers

DOI

10.1073/PNAS.262658799

1 reference

2 August 2017

0 references

1 reference

2 August 2017

1 reference