New approaches to prevent LEOPARD syndrome-associated cardiac hypertrophy by specifically targeting Shp2-dependent signaling (Q39419046)

11 September 2017

New approaches to prevent LEOPARD syndrome-associated cardiac hypertrophy by specifically targeting Shp2-dependent signaling (English)

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11 September 2017

Christine Schramm

1

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11 September 2017

Michelle A Edwards

series ordinal

2

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11 September 2017

Maike Krenz

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3

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11 September 2017

language of work or name

English

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publication date

14 May 2013

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Journal of Biological Chemistry

11 September 2017

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11 September 2017

288

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11 September 2017

25

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11 September 2017

18335-18344

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describes a project that uses

11 September 2017

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3689975/fullTextXML

inferred from PubMed Central ID database lookup

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Cyclosporine attenuates cardiomyocyte hypertrophy induced by RAF1 mutants in Noonan and LEOPARD syndromes

11 September 2017

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Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome-associated PTPN11 mutation.

11 September 2017

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11 September 2017

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Hypertrophic cardiomyopathy: from genetics to treatment

11 September 2017

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Functional effects of PTPN11 (SHP2) mutations causing LEOPARD syndrome on epidermal growth factor-induced phosphoinositide 3-kinase/AKT/glycogen synthase kinase 3beta signaling

11 September 2017

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Transient expression of FRNK reveals stage-specific requirement for focal adhesion kinase activity in cardiac growth

11 September 2017

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Phosphatase-defective LEOPARD syndrome mutations in PTPN11 gene have gain-of-function effects during Drosophila development

11 September 2017

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Specific inhibitors of the protein tyrosine phosphatase Shp2 identified by high-throughput docking.

11 September 2017

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Cardiac developmental defects and eccentric right ventricular hypertrophy in cardiomyocyte focal adhesion kinase (FAK) conditional knockout mice

11 September 2017

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Focal adhesion kinase: an essential kinase in the regulation of cardiovascular functions

11 September 2017

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Mediating ERK 1/2 signaling rescues congenital heart defects in a mouse model of Noonan syndrome

11 September 2017

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Akt2 regulates cardiac metabolism and cardiomyocyte survival

11 September 2017

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Regulation of cardiac hypertrophy by intracellular signalling pathways

11 September 2017

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Life with a single isoform of Akt: mice lacking Akt2 and Akt3 are viable but display impaired glucose homeostasis and growth deficiencies

11 September 2017

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Discovery of a novel shp2 protein tyrosine phosphatase inhibitor

11 September 2017

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Reduced phosphatase activity of SHP-2 in LEOPARD syndrome: consequences for PI3K binding on Gab1

11 September 2017

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PTPN11 (Shp2) mutations in LEOPARD syndrome have dominant negative, not activating, effects

11 September 2017

1 reference

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Dosage-dependent effects of Akt1/protein kinase Balpha (PKBalpha) and Akt3/PKBgamma on thymus, skin, and cardiovascular and nervous system development in mice

11 September 2017

1 reference

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Noonan syndrome mutation Q79R in Shp2 increases proliferation of valve primordia mesenchymal cells via extracellular signal-regulated kinase 1/2 signaling.

11 September 2017

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Focal adhesion kinase is upstream of phosphatidylinositol 3-kinase/Akt in regulating fibroblast survival in response to contraction of type I collagen matrices via a beta 1 integrin viability signaling pathway

11 September 2017

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Molecular Mechanism for a Role of SHP2 in Epidermal Growth Factor Receptor Signaling

11 September 2017

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Force-dependent integrin-cytoskeleton linkage formation requires downregulation of focal complex dynamics by Shp2

11 September 2017

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Dwarfism, impaired skin development, skeletal muscle atrophy, delayed bone development, and impeded adipogenesis in mice lacking Akt1 and Akt2.

11 September 2017

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Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene

11 September 2017

1 reference

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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

11 September 2017

1 reference

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Insulin resistance and a diabetes mellitus-like syndrome in mice lacking the protein kinase Akt2 (PKB beta)

11 September 2017

1 reference

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Concerted activity of tyrosine phosphatase SHP-2 and focal adhesion kinase in regulation of cell motility

11 September 2017

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Multiple Lentigenes Syndrome

11 September 2017

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Dynamin 2 mediates PDGFRα-SHP-2-promoted glioblastoma growth and invasion

11 September 2017

1 reference

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LEOPARD-type SHP2 mutant Gln510Glu attenuates cardiomyocyte differentiation and promotes cardiac hypertrophy via dysregulation of Akt/GSK-3β/β-catenin signaling

11 September 2017

1 reference

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Nuclear protein tyrosine phosphatase Shp-2 is one important negative regulator of nuclear export of telomerase reverse transcriptase.

11 September 2017

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Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation

14 September 2017

1 reference

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Phosphatase-dependent and -independent functions of Shp2 in neural crest cells underlie LEOPARD syndrome pathogenesis

14 September 2017

1 reference

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Mutation of Thr466 in SHP2 abolishes its phosphatase activity, but provides a new substrate-trapping mutant

17 June 2018

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GFP-FRNK disrupts focal adhesions and induces anoikis in neonatal rat ventricular myocytes.

17 June 2018

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PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3689975

Negative inotropic effect of rapamycin on isolated human cardiomyocytes

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3689975

A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3689975

Ras/Erk signaling is essential for activation of protein synthesis by Gq protein-coupled receptor agonists in adult cardiomyocytes

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3689975

PTPN11 mutations in LEOPARD syndrome

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3689975

Akt1/PKBalpha is required for normal growth but dispensable for maintenance of glucose homeostasis in mice

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3689975

Akt1 is required for physiological cardiac growth

21 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23673659

12 December 2020

inferred from PubMed ID database lookup

A standard echocardiographic and tissue Doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of Noonan and LEOPARD syndromes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23673659

12 December 2020

inferred from PubMed ID database lookup

The PTPN11 loss-of-function mutation Q510E-Shp2 causes hypertrophic cardiomyopathy by dysregulating mTOR signaling

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23673659

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1074/JBC.M113.483800

1 reference

11 September 2017

1 reference

11 September 2017

PubMed publication ID

23673659

1 reference