(Q34137795)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

review article

1 reference

title

Too much of a good thing: mechanisms of gene action in Down syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

author name string

R H Reeves

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J T Richtsmeier

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

publication date

1 February 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

83-88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

Down syndrome: genetic recombination and the origin of the extra chromosome 21.

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Genotype-phenotype relationships in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Monogenic traits are not simple: lessons from phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Whither Down syndrome critical regions?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

The DNA sequence of human chromosome 21

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Down syndrome—a disruption of homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Down syndrome and mouse models.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutase

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Gene dosage of CuZnSOD and Down's syndrome: diminished prostaglandin synthesis in human trisomy 21, transfected cells and transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected]

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Genetics of mouse behavior: interactions with laboratory environment.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

A mouse model for Down syndrome exhibits learning and behaviour deficits.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Specific impairment of cardiogenesis in mouse ES cells containing a human chromosome 21.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Chromosome engineering in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Down syndrome phenotypes: the consequences of chromosomal imbalance

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Perfect conserved linkage across the entire mouse chromosome 10 region homologous to human chromosome 21

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

Physical and comparative mapping of distal mouse chromosome 16. 5 p5.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902172-7

7 January 2021

10.1016/S0168-9525(00)02172-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11173117%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference