No evidence for parental imprinting of mouse 22q11 gene orthologs (Q37145622)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16897343%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

No evidence for parental imprinting of mouse 22q11 gene orthologs (English)

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28 December 2019

1

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28 December 2019

author name string

Daniel W Meechan

2

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28 December 2019

Clifford C Heindel

3

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28 December 2019

Amanda Z Peters

4

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28 December 2019

Robert M Hamer

5

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28 December 2019

Jeffrey A Lieberman

6

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28 December 2019

Anthony-Samuel LaMantia

7

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28 December 2019

publication date

4 August 2006

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28 December 2019

number of pages

11

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inferred from page(s)

published in

Mammalian Genome

1 reference

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28 December 2019

volume

17

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28 December 2019

issue

8

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28 December 2019

page(s)

822-832

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https://scigraph.springernature.com/pub.10.1007/s00335-006-0011-0

28 December 2019

exact match

0 references

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Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

6 September 2017

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6 September 2017

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Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.

6 September 2017

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6 September 2017

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Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization

6 September 2017

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Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

6 September 2017

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Allelic inactivation regulates olfactory receptor gene expression

6 September 2017

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Comparative sequence analysis of imprinted genes between human and mouse to reveal imprinting signatures

6 September 2017

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3 September 2018

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3 September 2018

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3 September 2018

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3 September 2018

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3 September 2018

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Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16897343

12 December 2020

inferred from PubMed ID database lookup

Analysis of candidate imprinted genes linked to Dlk1-Gtl2 using a congenic mouse line

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16897343

12 December 2020

inferred from PubMed ID database lookup

Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16897343

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00335-006-0011-0

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16897343%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16897343%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference