(Q35201305)

7 August 2017

Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21 (English)

1 reference

7 August 2017

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3

Hardy JA

1 reference

7 August 2017

Owen MJ

1

1 reference

7 August 2017

James LA

series ordinal

2

1 reference

7 August 2017

Williamson R

series ordinal

4

1 reference

7 August 2017

Goate AM

series ordinal

5

1 reference

7 August 2017

language of work or name

English

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publication date

1 February 1990

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

46

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7 August 2017

316-322

1 reference

7 August 2017

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

7 August 2017

1 reference

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Receptors for human alpha and beta interferon but not for gamma interferon are specified by human chromosome 21

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

A (6;21) translocation, unbalanced, 46 chromosomes. Repository identification no. GM-144.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Human chromosome 21-encoded cDNA clones

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Absence of Linkage of Chromosome 21q21 Markers to Familial Alzheimer's Disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Genetic linkage studies in Alzheimer's disease families.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Isolation and regional mapping of DNA sequences unique to human chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Predisposing locus for Alzheimer's disease on chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

CpG-rich islands and the function of DNA methylation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Biochemical genetics of Chinese hamster cell mutants with deviant purine metabolism: characterization of Chinese hamster cell mutants defective in phosphoribosylpyrophosphate amidotransferase and phosphoribosylglycinamide synthetase and an examinati

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

Studies in aging of the brain: IV. Familial Alzheimer disease: Relation to transmissible dementia, aneuploidy, and microtubular defects

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

A family with histologically confirmed Alzheimer's disease.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684974

A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion

26 September 2018

1 reference

12 December 2020

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene

1 reference

12 December 2020

Genetic linkage map of human chromosome 21

1 reference

12 December 2020

A genetic linkage map of 17 markers on human chromosome 21

1 reference

12 December 2020

Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes

1 reference

12 December 2020

Dementia of the Alzheimer type. Clinical genetics, natural history, and associated conditions

1 reference

12 December 2020

Identifiers

PMCID

1684974

1 reference

7 August 2017

1 reference