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Search results 101 to 107 out of 107 for Pkn3

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0.017s
Type Details Score
Publication
First Author: zur Nedden S
Year: 2018
Journal: J Clin Invest
Title: Protein kinase N1 critically regulates cerebellar development and long-term function.
Volume: 128
Issue: 5
Pages: 2076-2088
Publication
First Author: Francois AA
Year: 2018
Journal: Cardiovasc Res
Title: Loss of Protein Kinase Novel 1 (PKN1) is associated with mild systolic and diastolic contractile dysfunction, increased phospholamban Thr17 phosphorylation, and exacerbated ischaemia-reperfusion injury.
Volume: 114
Issue: 1
Pages: 138-157
Genotype
Symbol: Pkn1/Pkn1
Background: B6.129P2-Pkn1
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Pkn1/Pkn1 Pkn3/Pkn3
Background: involves: 129P2/OlaHsd * C57BL/6NTac
Zygosity: cx
Has Mutant Allele: true
Publication
First Author: Danno S
Year: 2017
Journal: Genes Cells
Title: PKN2 is essential for mouse embryonic development and proliferation of mouse fibroblasts.
Volume: 22
Issue: 2
Pages: 220-236
Genotype
Symbol: Pkn1/Pkn1 Pkn2/Pkn2<+> Pkn3/Pkn3
Background: involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac
Zygosity: cx
Has Mutant Allele: true
Publication
First Author: Marshall JJT
Year: 2022
Journal: Biochem J
Title: PKN2 deficiency leads both to prenatal 'congenital' cardiomyopathy and defective angiotensin II stress responses.
Volume: 479
Issue: 13
Pages: 1467-1486