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Denny Schanze (1979-)

Molekularmediziner

Name	Denny Schanze
Zeit	1979- (Lebensdaten)
Ort	Chemnitz (Geburtsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr. rer. nat. (an der Naturwissenschaftlichen Fakultät der Universität Erlangen-Nürnberg) (2015)
Beruf	Molekularmediziner (charakteristischer Beruf)
Datensatztyp	Person
GND-Nummer	1080204431
Datensatz-ID	1080204431
Beteiligt an alle anzeigen Somatic RIT1 delins in arteriovenous malformations hyperactivate RAS-MAPK signaling amenable to MEK inhibition Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma Extracranial vascular anomalies driven by RAS/MAPK variants: spectrum and genotype–phenotype correlations Somatic RIT1 delins in arteriovenous malformations hyperactivate RAS-MAPK signaling amenable to MEK inhibition Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood Microbial composition of tumorous and adjacent gastric tissue is associated with prognosis of gastric cancer Molecular and cellular evidence for the impact of a hypertrophic cardiomyopathy-associated RAF1 variant on the structure and function of contractile machinery in bioartificial cardiac tissues Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome Characteristic dental pattern with hypodontia and short roots in Fraser syndrome The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered Characteristic dental pattern with hypodontia and short roots in Fraser syndrome Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders Requirements analysis and specification for a molecular tumor board platform based on cBioPortal Requirements Analysis and Specification for a Molecular Tumor Board Platform Based on cBioPortal Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants A postzygotic SMO mutation caused the original case of Happle–Tinschert syndrome Genetic Polymorphisms as Predictive Markers of Response to Growth Hormone Therapy in Children with Growth Hormone Deficiency Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy Systematische Analysen zur Identifikation der genetischen Ursache der periodischen Katatonie

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Katalog der Deutschen Nationalbibliothek

Denny Schanze (1979-)

Somatic RIT1 delins in arteriovenous malformations hyperactivate RAS-MAPK signaling amenable to MEK inhibition

Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study

Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma

Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice

Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma

Extracranial vascular anomalies driven by RAS/MAPK variants: spectrum and genotype–phenotype correlations

Somatic RIT1 delins in arteriovenous malformations hyperactivate RAS-MAPK signaling amenable to MEK inhibition

Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood

Microbial composition of tumorous and adjacent gastric tissue is associated with prognosis of gastric cancer

Molecular and cellular evidence for the impact of a hypertrophic cardiomyopathy-associated RAF1 variant on the structure and function of contractile machinery in bioartificial cardiac tissues

Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome

Characteristic dental pattern with hypodontia and short roots in Fraser syndrome

The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered

The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered

Characteristic dental pattern with hypodontia and short roots in Fraser syndrome

Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders

Requirements analysis and specification for a molecular tumor board platform based on cBioPortal

Requirements Analysis and Specification for a Molecular Tumor Board Platform Based on cBioPortal

Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants

A postzygotic SMO mutation caused the original case of Happle–Tinschert syndrome

Genetic Polymorphisms as Predictive Markers of Response to Growth Hormone Therapy in Children with Growth Hormone Deficiency

Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy

Systematische Analysen zur Identifikation der genetischen Ursache der periodischen Katatonie