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LEE, BRENDAN

One or more keywords matched the following items that are connected to LEE, BRENDAN

Item Type	Name
Academic Article	Early childhood presentation of Czech dysplasia.
Academic Article	Proteoglycan 4 expression protects against the development of osteoarthritis.
Concept	Collagen Type V
Concept	Collagen Type II
Concept	Collagen Type I
Concept	Collagen Type IV
Concept	Collagen
Academic Article	Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues.
Academic Article	Excessive transforming growth factor-? signaling is a common mechanism in osteogenesis imperfecta.
Academic Article	Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations.
Academic Article	Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice.
Academic Article	Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.
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	Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone.
Academic Article	Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia.
Academic Article	MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-? signalling in osteoblasts.
Academic Article	mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development.
Grant	Dysregulation of 3-prolyl-hydroxylation in Human Skeletal Dysplasias
Grant	BRITTLE BONE DISORDERS CONSORTIUM OF THE RARE DISEASE CLINICAL RESEARCH NETWORK
Grant	Pathogenesis of Novel Forms of Osteogenesis Imperfecta
Academic Article	Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study.
Academic Article	Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta.
Academic Article	Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome.
Academic Article	4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta.

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Collagen