High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes.
about
Rapid phenotyping of knockout mice to identify genetic determinants of bone strengthUsing GWAS to identify novel therapeutic targets for osteoporosis.Defective enamel and bone development in sodium-dependent citrate transporter (NaCT) Slc13a5 deficient mice.Role of WNT16 in the regulation of periosteal bone formation in female mice.Diacylglycerol Lipase α Knockout Mice Demonstrate Metabolic and Behavioral Phenotypes Similar to Those of Cannabinoid Receptor 1 Knockout Mice.MicroRNA 224 Regulates Ion Transporter Expression in Ameloblasts To Coordinate Enamel Mineralization.Adult Tph2 knockout mice without brain serotonin have moderately elevated spine trabecular bone but moderately low cortical bone thicknessConstitutively Elevated Blood Serotonin Is Associated with Bone Loss and Type 2 Diabetes in Rats.Dynamic interplay between bone and multiple myeloma: emerging roles of the osteoblastFatty acid desaturase 1 knockout mice are lean with improved glycemic control and decreased development of atheromatous plaque.ROCK1 via LIM kinase regulates growth, maturation and actin based functions in mast cells.Inhibition of AAK1 Kinase as a Novel Therapeutic Approach to Treat Neuropathic Pain.Real-Time Analysis of Endogenous Wnt Signalling in 3D Mesenchymal Stromal Cells.The function of orthologues of the human Parkinson's disease gene LRRK2 across species: implications for disease modelling in preclinical research.Evolution of gremlin 2 in cetartiodactyl mammals: gene loss coincides with lack of upper jaw incisors in ruminantsRole and mechanism of action of leucine-rich repeat kinase 1 in bone.Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse.Genetic Approaches To Identifying Novel Osteoporosis Drug Targets.Genetic Screening of WNT4 and WNT5B in Two Populations with Deviating Bone Mineral Densities.Quantitative metabolic flux analysis reveals an unconventional pathway of fatty acid synthesis in cancer cells deficient for the mitochondrial citrate transport protein.Identification of genetic elements in metabolism by high-throughput mouse phenotyping.SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects
P2860
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P2860
High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
High-throughput screening of m ...... and novel skeletal phenotypes.
@ast
High-throughput screening of m ...... and novel skeletal phenotypes.
@en
type
label
High-throughput screening of m ...... and novel skeletal phenotypes.
@ast
High-throughput screening of m ...... and novel skeletal phenotypes.
@en
prefLabel
High-throughput screening of m ...... and novel skeletal phenotypes.
@ast
High-throughput screening of m ...... and novel skeletal phenotypes.
@en
P2093
P2860
P356
P1433
P1476
High-throughput screening of m ...... and novel skeletal phenotypes.
@en
P2093
Arthur T Sands
Brian Zambrowicz
David G Potter
David R Powell
Gwenn M Hansen
Laura L Kirkpatrick
Peter Vogel
Robert Brommage
P2860
P2888
P356
10.1038/BONERES.2014.34
P577
2014-10-28T00:00:00Z