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Search Results to Roy Morello

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Morello, Roy

One or more keywords matched the following items that are connected to Morello, Roy

Item Type	Name
Academic Article	CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Concept	Mice, Inbred C57BL
Concept	Mice, Inbred BALB C
Concept	Mice, Transgenic
Concept	Mice, Knockout
Concept	Mice, Mutant Strains
Concept	Mice
Academic Article	The nuclear genes Mtfr1 and Dufd1 regulate mitochondrial dynamic and cellular respiration.
Academic Article	Brachy-syndactyly caused by loss of Sfrp2 function.
Academic Article	Generalized connective tissue disease in Crtap-/- mouse.
Academic Article	Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.
Academic Article	Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis.
Academic Article	Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues.
Academic Article	Ascorbate synthesis pathway: dual role of ascorbate in bone homeostasis.
Academic Article	New roles for INSL3 in adults.
Academic Article	Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation.
Academic Article	Impact of sarA and Phenol-Soluble Modulins on the Pathogenesis of Osteomyelitis in Diverse Clinical Isolates of Staphylococcus aureus.
Academic Article	P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA.
Academic Article	Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome.
Academic Article	Modeling Rare Bone Diseases in Animals.
Academic Article	Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim).
Academic Article	Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm.
Grant	Targeted Enzyme Replacement Therapy for Rare Forms of Osteogenesis Imperfecta
Grant	Role of the Leprecan Genes in Skeletal Formation
Grant	Crtap function during skeletal homeostasis
Grant	Primary lung defects in mouse models of osteogenesis imperfecta
Academic Article	Determinants of vascular permeability in the kidney glomerulus.
Academic Article	The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis Imperfecta.
Academic Article	Dental and craniofacial defects in the Crtap-/- mouse model of osteogenesis imperfecta type VII.
Academic Article	Respiratory defects in the CrtapKO mouse model of osteogenesis imperfecta.
Academic Article	cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein
Academic Article	Loss of alpha3/alpha4(IV) Collagen from the Glomerular Basement Membrane Induces a Strain-Dependent Isoform Switch to alpha5alpha6(IV) Collagen Associated with Longer Renal Survival in Col4a3-/- Alport Mice
Academic Article	Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers-Danlos syndrome.
Academic Article	The NAD salvage pathway in mesenchymal cells is indispensable for skeletal development in mice.
Academic Article	A Rab33b missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylation.
Academic Article	Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta.
Academic Article	Discovery of small molecule agonists of the Relaxin Family Peptide Receptor 2.
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta.
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta
Grant	Lung developmental defects caused by type I collagen mutations in mouse models of osteogenesis imperfecta

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