Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis

Genetic determinants of fibro-osseous lesions in aged inbred mice

(2016) Annerose Berndt et al.   EXPERIMENTAL AND MOLECULAR PATHOLOGY

Research Progress in Pseudoxanthoma Elasticum and Related Ectopic Mineralization Disorders

(2016) Qiaoli Li et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Mapping Genetic Contributions to Cardiac Pathology Induced by Beta-Adrenergic Stimulation in MiceCLINICAL PERSPECTIVE

(2014) Christoph D. Rau et al.   Circulation-Cardiovascular Genetics

Genetic modulation of nephrocalcinosis in mouse models of ectopic mineralization: the Abcc6 tm1Jfk and Enpp1 asj mutant mice

(2014) Qiaoli Li et al.   LABORATORY INVESTIGATION

Spontaneous asj-2J Mutant Mouse as a Model for Generalized Arterial Calcification of Infancy: A Large Deletion/Insertion Mutation in the Enpp1 Gene

(2014) Qiaoli Li et al.   PLoS One

Identification of Genes Important for Cutaneous Function Revealed by a Large Scale Reverse Genetic Screen in the Mouse

(2014) Tia DiTommaso et al.   PLoS Genetics

Mineralization/Anti-Mineralization Networks in the Skin and Vascular Connective Tissues

(2013) Qiaoli Li et al.   AMERICAN JOURNAL OF PATHOLOGY

Mutant Enpp1asj mice as a model for generalized arterial calcification of infancy

(2013) Q. Li et al.   Disease Models & Mechanisms

Mouse Alopecia Areata and Heart Disease: Know Your Mouse!

(2013) John P. Sundberg et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

A Novel Animal Model for Pseudoxanthoma Elasticum

(2012) Qiaoli Li et al.   AMERICAN JOURNAL OF PATHOLOGY

Quantification of the Calcification Phenotype of Abcc6-Deficient Mice with Microcomputed Tomography

(2012) Yannick Le Corre et al.   AMERICAN JOURNAL OF PATHOLOGY

Ablation of cyclase-associated protein 2 (CAP2) leads to cardiomyopathy

(2012) Vivek S. Peche et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Human Molecular Genetic and Functional Studies Identify TRIM63 , Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy

(2012) Suet Nee Chen et al.   CIRCULATION RESEARCH

A Single-Nucleotide Polymorphism in the Abcc6 Gene Associates with Connective Tissue Mineralization in Mice Similar to Targeted Models for Pseudoxanthoma Elasticum

(2012) Annerose Berndt et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Amelogenesis Imperfecta and Other Biomineralization Defects in Fam20a and Fam20c Null Mice

(2012) P. Vogel et al.   VETERINARY PATHOLOGY

Abcc6 Deficiency Causes Increased Infarct Size and Apoptosis in a Mouse Cardiac Ischemia-Reperfusion Model

(2011) Imran N. Mungrue et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Identification of Fat4 and Tsc22d1 as Novel Candidate Genes for Spontaneous Pulmonary Adenomas

(2011) A. Berndt et al.   CANCER RESEARCH

Exploring the elephant: histopathology in high-throughput phenotyping of mutant mice

(2011) P. N. Schofield et al.   Disease Models & Mechanisms

Animal models with pathological mineralization phenotypes

(2011) Uwe Kornak   JOINT BONE SPINE

Quantitative lymphatic vessel trait analysis suggests Vcam1 as candidate modifier gene of inflammatory bowel disease

(2010) G Jurisic et al.   GENES AND IMMUNITY

Klotho Deficiency Causes Vascular Calcification in Chronic Kidney Disease

(2010) M. C. Hu et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

A survey of airway responsiveness in 36 inbred mouse strains facilitates gene mapping studies and identification of quantitative trait loci

(2010) Adriana S. Leme et al.   MOLECULAR GENETICS AND GENOMICS

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Comparison of unrestrained plethysmography and forced oscillation for identifying genetic variability of airway responsiveness in inbred mice

(2010) Annerose Berndt et al.   PHYSIOLOGICAL GENOMICS

Pathbase and the MPATH Ontology

(2010) P. N. Schofield et al.   VETERINARY PATHOLOGY

Dysferlin Deficiency and the Development of Cardiomyopathy in a Mouse Model of Limb-Girdle Muscular Dystrophy 2B

(2009) Thomas H. Chase et al.   AMERICAN JOURNAL OF PATHOLOGY

Pseudoxanthoma Elasticum: Molecular Genetics and Putative Pathomechanisms

(2009) Jouni Uitto et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Cardiovascular Response to Beta-Adrenergic Blockade or Activation in 23 Inbred Mouse Strains

(2009) Corinne Berthonneche et al.   PLoS One

An Alternative Splice Variant inAbcc6, the Gene Causing Dystrophic Calcification, Leads to Protein Deficiency in C3H/He Mice

(2008) Zouhair Aherrahrou et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Integrating mouse anatomy and pathology ontologies into a phenotyping database: Tools for data capture and training

(2008) John P. Sundberg et al.   MAMMALIAN GENOME

Arterial calcifications and increased expression of vitamin D receptor targets in mice lacking TIF1 

(2008) M. Ignat et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA