(Q46358786)

English

Identification and characterization of a new Down syndrome model, Ts[Rb(12.1716)]2Cje, resulting from a spontaneous Robertsonian fusion between T(171)65Dn and mouse chromosome 12.

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scholarly article

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

Identification and characterization of a new Down syndrome model, Ts[Rb(12.1716)]2Cje, resulting from a spontaneous Robertsonian fusion between T(171)65Dn and mouse chromosome 12. (English)

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

1 reference

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author name string

Angela J Villar

1

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

Pavel V Belichenko

2

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

Anne Marie Gillespie

3

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

Heather M Kozy

4

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

William C Mobley

5

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

Charles J Epstein

6

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

publication date

1 February 2005

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Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

number of pages

12

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Mammalian Genome

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

16

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Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

2

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

79-90

1 reference

Europe PubMed Central

21 December 2017

http://europepmc.org/abstract/MED/15859352

https://scigraph.springernature.com/pub.10.1007/s00335-004-2428-7

0 references

Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

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inferred from PubMed ID database lookup

Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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Synaptic structural abnormalities in the Ts65Dn mouse model of Down Syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

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An improved method for preparing G-banded chromosomes from mouse peripheral blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

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Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome.

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https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

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Novel mutations in an otherwise strictly conserved domain of CuZn superoxide dismutase

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neuropsychology of mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

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Rapid real-time fluorescent PCR gene dosage test for the diagnosis of DNA duplications and deletions

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https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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CYP2D6 genotyping strategy based on gene copy number determination by TaqMan real-time PCR.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

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The DNA sequence of human chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

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A behavioral assessment of Ts65Dn mice: a putative Down syndrome model.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the 3-dimensional architecture of dendritic spines and varicosities in human cortex by confocal laser scanning microscopy and Lucifer yellow microinjections

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15859352

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00335-004-2428-7

1 reference

https://api.fatcat.wiki/v0/release/rqtheq2w4zb7hf5cofkc2uop2q

30 July 2022

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mapped directly with Wikidata item

release_rqtheq2w4zb7hf5cofkc2uop2q

1 reference

https://api.fatcat.wiki/v0/release/rqtheq2w4zb7hf5cofkc2uop2q

30 July 2022

based on heuristic

mapped directly with Wikidata item

1 reference

https://api.fatcat.wiki/v0/release/rqtheq2w4zb7hf5cofkc2uop2q

30 July 2022

based on heuristic

mapped directly with Wikidata item

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