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Search results 401 to 409 out of 409 for Actn2

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Type Details Score
Genotype
Genotype
Symbol: Rr593/Rr593
Background: involves: C57BL/6 * SJL
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Rr593/Rr593<+>
Background: involves: C57BL/6 * SJL
Zygosity: ht
Has Mutant Allele: true
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GXD Expression
GXD Expression
Probe: MGI:6714279
Assay Type: Immunohistochemistry
Annotation Date: 2021-06-09
Strength: Weak
Sex: Not Specified
Emaps: EMAPS:3268819
Pattern: Not Specified
Stage: TS19
Assay Id: MGI:6714277
Age: embryonic day 11.5
Image: S9B Ronin KO
Note: Knockout embryos showed little phosphorylated Rps6 in cardiomyocytes. Actn2 expression level remained similar to control.
Specimen Label: S9B Ronin KO
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
Probe: MGI:4438055
Assay Type: Immunohistochemistry
Annotation Date: 2024-02-09
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3268815
Pattern: Not Specified
Stage: TS15
Assay Id: MGI:7580870
Age: embryonic day 9.5
Image: 6 E9.5
Note: Immunopositive striations became more defined in the center of sarcomeres of many myofibrils, alternating with Actn2 striations.
Specimen Label: 6 E9.5
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
Probe: MGI:4438055
Assay Type: Immunohistochemistry
Annotation Date: 2024-02-09
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3268815
Pattern: Not Specified
Stage: TS15
Assay Id: MGI:7580870
Age: embryonic day 9.5
Image: 6 E9.5
Note: Immunopositive striations became more defined in the center of sarcomeres of many myofibrils, alternating with Actn2 striations.
Specimen Label: 6 E9.5
Detected: true
Specimen Num: 4
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DO Term
DOID:0081342 | congenital myopathy 8
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Publication
31629737 | J:294355
 
First Author: Yang KC
Year: 2019
Journal: J Mol Cell Cardiol
Title: Deficiency of nuclear receptor interaction protein leads to cardiomyopathy by disrupting sarcomere structure and mitochondrial respiration.
Volume: 137
Pages: 9-24
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Publication
20089533 | J:158367
First Author: Becanovic K
Year: 2010
Journal: Hum Mol Genet
Title: Transcriptional changes in Huntington disease identified using genome-wide expression profiling and cross-platform analysis.
Volume: 19
Issue: 8
Pages: 1438-52
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Publication
- | J:23000
       
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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