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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	Role of cartilage-associated protein in skeletal development.
Academic Article	Mutations in SERPINF1 cause osteogenesis imperfecta type VI.
Academic Article	CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Concept	Bone Diseases
Concept	Bone Development
Concept	Bone Diseases, Metabolic
Concept	Bone Density
Concept	Fractures, Bone
Concept	Bone and Bones
Academic Article	Brachy-syndactyly caused by loss of Sfrp2 function.
Academic Article	Generalized connective tissue disease in Crtap-/- mouse.
Academic Article	Mutations in the insulin-like factor 3 receptor are associated with osteoporosis.
Academic Article	Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis.
Academic Article	Osteogenesis Imperfecta: a Translational Approach to Brittle Bone Disease
Academic Article	CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with Osteogenesis Imperfecta type VII
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	Extensive Remineralization of Large Pelvic Lytic Lesions Following Total Therapy Treatment in Patients With Multiple Myeloma.
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	Modeling Rare Bone Diseases in Animals.
Academic Article	Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim).
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	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	Matrix-mediated effects on Bone Marrow Stromal Cells (BMSCs)
Academic Article	Evaluation of a Polyurethane Platform for Delivery of Nanohydroxyapatite and Decellularized Bone Particles in a Porous Three-Dimensional Scaffold
Academic Article	The Osteocyte Transcriptome: Discovering Messages Buried Within Bone.
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.
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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