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Search Results to Roy Morello

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

Item TypeName
Academic Article CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Concept Animals
Concept Disease Models, Animal
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.
Grant Crtap function during skeletal homeostasis
Academic Article Determinants of vascular permeability in the kidney glomerulus.
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 Osteogenesis imperfecta: an update on clinical features and therapies.
Grant Respiratory Function in Animal Models of Skeletal Dysplasias
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 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.

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