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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	Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.
Academic Article	Role of cartilage-associated protein in skeletal development.
Academic Article	Mutations in SERPINF1 cause osteogenesis imperfecta type VI.
Academic Article	CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.
Academic Article	CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
Concept	Osteogenesis
Concept	Osteogenesis Imperfecta
Academic Article	Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues.
Academic Article	Osteogenesis
Academic Article	Osteogenesis Imperfecta: a Translational Approach to Brittle Bone Disease
Academic Article	Transitional Care in Osteogenesis Imperfecta: Advances in Biology, Technology, and Clinical Practice
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	Severe Osteogenesis Imperfecta Caused by a Small In-Frame Deletion in CRTAP
Academic Article	Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation.
Academic Article	Osteogenesis imperfecta and therapeutics.
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	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	Osteogenesis imperfecta: an update on clinical features and therapies.
Grant	Role of collagen prolyl 3-hydroxylation in Osteogenesis imperfecta
Grant	Lung alterations in recessive Osteogenesis Imperfecta due to loss of the prolyl 3-hydroxylation complex
Academic Article	Recessive Osteogenesis Imperfecta: rER Genes Take the Stage
Grant	Elucidating the role of type I collagen mutations on respiratory function in osteogenesis imperfecta
Grant	Elucidating the role of type I collagen mutations on respiratory function in osteogenesis imperfecta
Grant	Elucidating the role of type I collagen mutations on respiratory function in osteogenesis imperfecta
Grant	Elucidating the role of type I collagen mutations on respiratory function in osteogenesis imperfecta
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	Elucidating the role of type I collagen mutations on respiratory function in 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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Osteogenesis