List of works - Julia Calzada-Wack

A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model

article

Abnormal brain iron metabolism in Irp2 deficient mice is associated with mild neurological and behavioral impairments

scientific article

Allelic loss of chromosomes 8 and 19 in MENX-associated rat pheochromocytoma.

scientific article

An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease

scientific article

Analysis of signal transducer and activator of transcription 3 (Stat 3) pathway in multiple myeloma: Stat 3 activation and cyclin D1 dysregulation are mutually exclusive events

scientific article published on May 2003

Analysis of the PTCH coding region in human rhabdomyosarcoma

scientific article

CIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes Infection

scientific article (publication date: 2016)

Calcitonin controls bone formation by inhibiting the release of sphingosine 1-phosphate from osteoclasts

scientific article

DKK2 mediates osteolysis, invasiveness, and metastatic spread in Ewing sarcoma

scientific article published on 30 November 2012

Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

scientific article published on 7 August 2014

Extensive phenotypic characterization of a new transgenic mouse reveals pleiotropic perturbations in physiology due to mesenchymal hGH minigene expression

scientific article

Formalin-fixed paraffin-embedded (FFPE) proteome analysis using gel-free and gel-based proteomics

scientific article published on September 2010

Heterotopic Cervical Heart Transplantation in Mice

scientific article published on 25 August 2015

Innovations in phenotyping of mouse models in the German Mouse Clinic

scientific article

Introducing the German Mouse Clinic: open access platform for standardized phenotyping.

scientific article

Label-free protein profiling of formalin-fixed paraffin-embedded (FFPE) heart tissue reveals immediate mitochondrial impairment after ionising radiation

scientific article

Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system

scientific article

MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy

scientific article

MiR-34a deficiency accelerates medulloblastoma formation in vivo

scientific article

Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice

scientific article published on 22 December 2009

Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia

scientific journal article

Mouse Genetics and Metabolic Mouse Phenotyping

article

Mouse phenotyping

scientific article

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis

scientific article

Peptidase inhibitor 16 is a membrane-tethered regulator of chemerin processing in the myocardium

scientific article published on 15 August 2016

Profiling the molecular difference between Patched- and p53-dependent rhabdomyosarcoma

scientific article published in November 2004

Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse.

scientific article

Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice

scientific article

Srgap3⁻/⁻ mice present a neurodevelopmental disorder with schizophrenia-related intermediate phenotypes

scientific article published on 20 July 2012

Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice

scientific article published on 17 August 2017

Systemic first-line phenotyping

scientific article published on January 2009

The German Mouse Clinic – Running an Open Access Platform

article

The endochondral bone protein CHM1 sustains an undifferentiated, invasive phenotype, promoting lung metastasis in Ewing sarcoma

scientific article

The posterior HOXD locus: Its contribution to phenotype and malignancy of Ewing sarcoma

scientific article published on 30 May 2016

Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells

scientific article

Unbalanced overexpression of the mutant allele in murine Patched mutants

scientific article

Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic

scientific article

List of works by Julia Calzada-Wack

A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model

Abnormal brain iron metabolism in Irp2 deficient mice is associated with mild neurological and behavioral impairments

Allelic loss of chromosomes 8 and 19 in MENX-associated rat pheochromocytoma.

An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease

Analysis of signal transducer and activator of transcription 3 (Stat 3) pathway in multiple myeloma: Stat 3 activation and cyclin D1 dysregulation are mutually exclusive events

Analysis of the PTCH coding region in human rhabdomyosarcoma

CIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes Infection

Calcitonin controls bone formation by inhibiting the release of sphingosine 1-phosphate from osteoclasts

DKK2 mediates osteolysis, invasiveness, and metastatic spread in Ewing sarcoma

Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

Extensive phenotypic characterization of a new transgenic mouse reveals pleiotropic perturbations in physiology due to mesenchymal hGH minigene expression

Formalin-fixed paraffin-embedded (FFPE) proteome analysis using gel-free and gel-based proteomics

Heterotopic Cervical Heart Transplantation in Mice

Innovations in phenotyping of mouse models in the German Mouse Clinic

Introducing the German Mouse Clinic: open access platform for standardized phenotyping.

Label-free protein profiling of formalin-fixed paraffin-embedded (FFPE) heart tissue reveals immediate mitochondrial impairment after ionising radiation

Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system

MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy

MiR-34a deficiency accelerates medulloblastoma formation in vivo

Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice

Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia

Mouse Genetics and Metabolic Mouse Phenotyping

Mouse phenotyping

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis

Peptidase inhibitor 16 is a membrane-tethered regulator of chemerin processing in the myocardium

Profiling the molecular difference between Patched- and p53-dependent rhabdomyosarcoma

Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse.

Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice

Srgap3⁻/⁻ mice present a neurodevelopmental disorder with schizophrenia-related intermediate phenotypes

Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice

Systemic first-line phenotyping

The German Mouse Clinic – Running an Open Access Platform

The endochondral bone protein CHM1 sustains an undifferentiated, invasive phenotype, promoting lung metastasis in Ewing sarcoma

The posterior HOXD locus: Its contribution to phenotype and malignancy of Ewing sarcoma

Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells

Unbalanced overexpression of the mutant allele in murine Patched mutants

Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic