Pages that link to "Q35755147"

The following pages link to High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes (Q35755147):

Displaying 38 items.

• Rapid phenotyping of knockout mice to identify genetic determinants of bone strength (Q28066355) (← links)
• Using GWAS to identify novel therapeutic targets for osteoporosis (Q30275429) (← links)
• Defective enamel and bone development in sodium-dependent citrate transporter (NaCT) Slc13a5 deficient mice (Q33562785) (← links)
• Role of WNT16 in the regulation of periosteal bone formation in female mice (Q35088791) (← links)
• Diacylglycerol Lipase α Knockout Mice Demonstrate Metabolic and Behavioral Phenotypes Similar to Those of Cannabinoid Receptor 1 Knockout Mice (Q35672654) (← links)
• MicroRNA 224 Regulates Ion Transporter Expression in Ameloblasts To Coordinate Enamel Mineralization (Q35868382) (← links)
• Adult Tph2 knockout mice without brain serotonin have moderately elevated spine trabecular bone but moderately low cortical bone thickness (Q35892276) (← links)
• Constitutively Elevated Blood Serotonin Is Associated with Bone Loss and Type 2 Diabetes in Rats. (Q35933172) (← links)
• Dynamic interplay between bone and multiple myeloma: emerging roles of the osteoblast (Q36086488) (← links)
• Fatty acid desaturase 1 knockout mice are lean with improved glycemic control and decreased development of atheromatous plaque (Q37042588) (← links)
• ROCK1 via LIM kinase regulates growth, maturation and actin based functions in mast cells (Q37086168) (← links)
• Inhibition of AAK1 Kinase as a Novel Therapeutic Approach to Treat Neuropathic Pain (Q37206282) (← links)
• Real-Time Analysis of Endogenous Wnt Signalling in 3D Mesenchymal Stromal Cells. (Q37271085) (← links)
• The function of orthologues of the human Parkinson's disease gene LRRK2 across species: implications for disease modelling in preclinical research (Q37513500) (← links)
• Evolution of gremlin 2 in cetartiodactyl mammals: gene loss coincides with lack of upper jaw incisors in ruminants (Q37611145) (← links)
• Role and mechanism of action of leucine-rich repeat kinase 1 in bone (Q37697750) (← links)
• Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse (Q38371715) (← links)
• Genetic Approaches To Identifying Novel Osteoporosis Drug Targets (Q38400680) (← links)
• Genetic Screening of WNT4 and WNT5B in Two Populations with Deviating Bone Mineral Densities (Q38771580) (← links)
• Quantitative metabolic flux analysis reveals an unconventional pathway of fatty acid synthesis in cancer cells deficient for the mitochondrial citrate transport protein. (Q39179854) (← links)
• Identification of genetic elements in metabolism by high-throughput mouse phenotyping (Q47643645) (← links)
• Screening Gene Knockout Mice for Variation in Bone Mass: Analysis by μCT and Histomorphometry. (Q52366178) (← links)
• SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects (Q58063397) (← links)
• NOTUM inhibition increases endocortical bone formation and bone strength (Q60915886) (← links)
• Identification of gene biomarkers in patients with postmenopausal osteoporosis (Q60958909) (← links)
• Investigation of transcriptome mechanism associated with osteoporosis explored by microarray analysis (Q64056342) (← links)
• Mouse Models and Online Resources for Functional Analysis of Osteoporosis Genome-Wide Association Studies (Q64255307) (← links)
• A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. (Q64941014) (← links)
• Predicting human disease mutations and identifying drug targets from mouse gene knockout phenotyping campaigns. (Q64994782) (← links)
• Zinc Homeostasis in Bone: Zinc Transporters and Bone Diseases (Q89720184) (← links)
• High Fidelity of Mouse Models Mimicking Human Genetic Skeletal Disorders (Q89965056) (← links)
• Pilot GWAS of caries in African-Americans shows genetic heterogeneity (Q90166007) (← links)
• KISS1 in metastatic cancer research and treatment: potential and paradoxes (Q90173564) (← links)
• The role of GPCRs in bone diseases and dysfunctions (Q90913018) (← links)
• A road map for understanding molecular and genetic determinants of osteoporosis (Q91621630) (← links)
• Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7 (Q92357954) (← links)
• Sfrp4 repression of the Ror2/Jnk cascade in osteoclasts protects cortical bone from excessive endosteal resorption (Q93023515) (← links)
• Pleiotropic role of Drosophila phosphoribosyl pyrophosphate synthetase in autophagy and lysosome homeostasis (Q93122281) (← links)