Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in mice (Q36108365)

12 August 2017

Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in mice (English)

1 reference

12 August 2017

Rosa Chiara Paolicelli

8

Rosa Chiara Paolicelli

1 reference

12 August 2017

Dominika Farley

6

0 references

Tiago Ferreira

Tiago Ferreira

5

0 references

Olga Ermakova

Olga Ermakova

1

0 references

Richard Moriggl

Richard Moriggl

11

0 references

Lukasz Piszczek

2

Lukasz Piszczek

1 reference

12 August 2017

10

Claus Nerlov

1 reference

12 August 2017

Luisa Luciani

3

1 reference

12 August 2017

Florence M G Cavalli

4

1 reference

12 August 2017

Stefania Rizzo

7

1 reference

12 August 2017

Mumna Al-Banchaabouchi

9

1 reference

12 August 2017

Nicholas M Luscombe

12

1 reference

12 August 2017

Cornelius Gross

13

1 reference

12 August 2017

1 January 2011

1 reference

12 August 2017

EMBO Molecular Medicine

1 reference

12 August 2017

3

1 reference

12 August 2017

1

1 reference

12 August 2017

50-66

1 reference

describes a project that uses

12 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3402001/fullTextXML

inferred from PubMed Central ID database lookup

limma

1 reference

22 June 2022

https://europepmc.org/article/PMC/3402001

inferred from PubMed Central ID database lookup

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A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy

2 October 2017

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Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

2 October 2017

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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

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The transcription factors Stat5a/b are not required for islet development but modulate pancreatic beta-cell physiology upon aging

2 October 2017

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A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse

2 October 2017

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Differential involvement of the central amygdala in appetitive versus aversive learning

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Clarifying the role of Stat5 in lymphoid development and Abelson-induced transformation

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2 October 2017

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2 October 2017

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A comparison of wild-caught wood mice and bank voles in the Intellicage: assessing exploration, daily activity patterns and place learning paradigms

2 October 2017

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Inactivation of Stat5 in mouse mammary epithelium during pregnancy reveals distinct functions in cell proliferation, survival, and differentiation

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Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: a fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15.

2 October 2017

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TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

2 October 2017

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Essential role of STAT3 in the control of the acute-phase response as revealed by inducible gene inactivation [correction of activation] in the liver

2 October 2017

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Reduced number of hypocretin neurons in human narcolepsy

2 October 2017

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Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

2 October 2017

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Stat5 activation is uniquely associated with cytokine signaling in peripheral T cells

2 October 2017

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Embryonic lethality and tumorigenesis caused by segmental aneuploidy on mouse chromosome 11.

2 October 2017

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Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

2 October 2017

1 reference

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Diet-induced atherosclerosis in mice heterozygous and homozygous for apolipoprotein E gene disruption

2 October 2017

1 reference

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Transgenic mice expressing high levels of human apolipoprotein B develop severe atherosclerotic lesions in response to a high-fat diet.

2 October 2017

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Chromosome engineering in mice

2 October 2017

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Segmental aneuploidy and the genetic gross structure of the Drosophila genome

2 October 2017

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Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI.

2 October 2017

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The Min (multiple intestinal neoplasia) mutation: its effect on gut epithelial cell differentiation and interaction with a modifier system

2 October 2017

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Evidence for a cluster of genes on chromosome 17q11-q21 controlling susceptibility to tuberculosis and leprosy in Brazilians

2 October 2017

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. 1979.

2 July 2018

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Segmental copy number variation shapes tissue transcriptomes

2 July 2018

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Toward simpler and faster genome-wide mutagenesis in mice

23 September 2018

1 reference

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Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

23 September 2018

1 reference

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Developmental exposure to methylmercury alters learning and induces depression-like behavior in male mice

23 September 2018

1 reference

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CD8+ T cells are effector cells of contact dermatitis to common skin allergens in mice.

23 September 2018

1 reference

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EMPReSS: standardized phenotype screens for functional annotation of the mouse genome.

23 September 2018

1 reference

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Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3402001

Severe growth hormone insensitivity resulting from total absence of signal transducer and activator of transcription 5b.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3402001

Effect of diets on lipoprotein concentrations in heterozygous apolipoprotein E-deficient mice.

23 September 2018

1 reference

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Antigen-specific T cell sensitization is impaired in IL-17-deficient mice, causing suppression of allergic cellular and humoral responses

23 September 2018

1 reference

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Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome

23 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FEMMM.201000112

Cutting edge: An in vivo requirement for STAT3 signaling in TH17 development and TH17-dependent autoimmunity

21 January 2018

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12 December 2020

Allelic phasing of a mouse chromosome 11 deficiency influences p53 tumorigenicity

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12 December 2020

Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populations

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12 December 2020

Genetic variants in STAT3 are associated with nonalcoholic fatty liver disease

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12 December 2020

A new candidate site for a tumor suppressor gene involved in mouse thymic lymphomagenesis is located on the distal part of chromosome 4

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12 December 2020

Growth hormone insensitivity associated with a STAT5b mutation

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12 December 2020

Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)

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12 December 2020

STAT5 activity in pancreatic beta-cells influences the severity of diabetes in animal models of type 1 and 2 diabetes

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12 December 2020

Identifiers

DOI

10.1002/EMMM.201000112

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

21204268

1 reference