(Q33640527)

English

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

28 July 2017

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17 (English)

1 reference

Europe PubMed Central

28 July 2017

Alzheimer's disease

0 references

1 reference

based on heuristic

inferred from title

early-onset autosomal dominant Alzheimer disease

1 reference

based on heuristic

inferred from title

Jonathan L Haines

7

object named as

J L Haines

1 reference

Europe PubMed Central

28 July 2017

James F. Gusella

9

object named as

J F Gusella

1 reference

Europe PubMed Central

28 July 2017

author name string

S V Cheng

1

1 reference

Europe PubMed Central

28 July 2017

J H Nadeau

2

1 reference

Europe PubMed Central

28 July 2017

R E Tanzi

3

1 reference

Europe PubMed Central

28 July 2017

P C Watkins

4

1 reference

Europe PubMed Central

28 July 2017

J Jagadesh

5

1 reference

Europe PubMed Central

28 July 2017

B A Taylor

6

1 reference

Europe PubMed Central

28 July 2017

N Sacchi

8

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 August 1988

1 reference

Europe PubMed Central

28 July 2017

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

1 reference

Europe PubMed Central

28 July 2017

85

1 reference

Europe PubMed Central

28 July 2017

16

1 reference

Europe PubMed Central

28 July 2017

6032-6036

1 reference

Europe PubMed Central

28 July 2017

Lengths of chromosomal segments conserved since divergence of man and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

The alpha-globin pseudogene on mouse chromosome 17 is closely linked to H-2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Confidence limits for estimates of gene linkage based on analysis of recombinant inbred strains.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Isolation of polymorphic DNA segments from human chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Human Cu/Zn superoxide dismutase cDNA: isolation of clones synthesising high levels of active or inactive enzyme from an expression library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Complete structure of the alpha B-crystallin gene: conservation of the exon-intron distribution in the two nonlinked alpha-crystallin genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

The putative oncogene Pim-1 in the mouse: its linkage and variation among t haplotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

The ets sequence from the transforming gene of avian erythroblastosis virus, E26, has unique domains on human chromosomes 11 and 21: both loci are transcriptionally active

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

The locus encoding alpha A-crystallin is closely linked to H-2K on mouse chromosome 17

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Genetic basis for a mouse model of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Molecular genetics of human chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Glyoxalase I polymorphism in the mouse: a new genetic marker linked to H-2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Precise localization of human beta-globin gene complex on chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281899

21 June 2018

Report of the committee on comparative mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic control of the quantitative variation of erythrocytic glyoxalase-1(GLO-1) in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the mouse alpha A-crystallin structural gene to chromosome 17

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of Prm-1, Igl-1, Smst, Mtv-6, Sod-1, and Ets-2 and localization of the Down syndrome region on mouse chromosome 16

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion and duplication of DNA sequences is associated with the embryonic lethal phenotype of the t9 complementation group of the mouse t complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/2901095

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.85.16.6032

1 reference

Europe PubMed Central

28 July 2017

1988PNAS...85.6032C

0 references

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33640527&oldid=1964349638"