Pages that link to "Q27469188"
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The following pages link to Transgenic mouse model of the mild dominant form of osteogenesis imperfecta (Q27469188):
Displaying 50 items.
- Defects in tendon, ligament, and enthesis in response to genetic alterations in key proteoglycans and glycoproteins: a review (Q21285116) (← links)
- Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP (Q28200065) (← links)
- Restricted expression of Mov13 mutant alpha 1(I) collagen gene in osteoblasts and its consequences for bone development (Q28508303) (← links)
- Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assembly (Q28589575) (← links)
- A targeted mutation at the known collagenase cleavage site in mouse type I collagen impairs tissue remodeling (Q28589602) (← links)
- Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition (Q28590272) (← links)
- Increased susceptibility to microdamage in Brtl/ mouse model for osteogenesis imperfecta (Q30463549) (← links)
- Generalized connective tissue disease in Crtap-/- mouse (Q30982897) (← links)
- Femoral neck strength of mouse in two loading configurations: method evaluation and fracture characteristics (Q31985110) (← links)
- Perinatal lethal osteogenesis imperfecta. (Q33676390) (← links)
- Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral (Q33891672) (← links)
- A murine skeletal adaptation that significantly increases cortical bone mechanical properties. Implications for human skeletal fragility (Q33904180) (← links)
- Gene therapy for tissue repair and regeneration (Q33933274) (← links)
- An inbred line of transgenic mice expressing an internally deleted gene for type II procollagen (COL2A1). Young mice have a variable phenotype of a chondrodysplasia and older mice have osteoarthritic changes in joints (Q34169901) (← links)
- Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect. (Q34191451) (← links)
- Extracellular Microfibrils Control Osteoblast-supported Osteoclastogenesis by Restricting TGFβ Stimulation of RANKL Production (Q34232152) (← links)
- Procollagen C proteinase enhancer 1 genes are important determinants of the mechanical properties and geometry of bone and the ultrastructure of connective tissues. (Q34233484) (← links)
- Collagen mutation causes changes of the microdamage morphology in bone of an OI mouse model (Q34268022) (← links)
- Effect of mechanical loading on periodontal cells (Q34632705) (← links)
- Continuing to break the sound barrier: genes in hearing (Q34699453) (← links)
- Variable bone fragility associated with an Amish COL1A2 variant and a knock-in mouse model (Q35156234) (← links)
- Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen (Q35195793) (← links)
- Nell-1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2 /− mice (Q35229979) (← links)
- Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagen (Q35889436) (← links)
- Osteogenesis Imperfecta: A Review with Clinical Examples. (Q35932671) (← links)
- OIM and related animal models of osteogenesis imperfecta. (Q35990573) (← links)
- Genetic randomization reveals functional relationships among morphologic and tissue-quality traits that contribute to bone strength and fragility (Q36021383) (← links)
- Multiparametric Classification of Skin from Osteogenesis Imperfecta Patients and Controls by Quantitative Magnetic Resonance Microimaging (Q36077769) (← links)
- New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis (Q36106531) (← links)
- Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta (Q36125438) (← links)
- Role of genetic background in determining phenotypic severity throughout postnatal development and at peak bone mass in Col1a2 deficient mice (oim). (Q36711366) (← links)
- Osteoporosis induced in mice by overproduction of interleukin 4. (Q36716814) (← links)
- Animal models of osteogenesis imperfecta and related syndromes (Q36861283) (← links)
- Characterization of skin abnormalities in a mouse model of osteogenesis imperfecta using high resolution magnetic resonance imaging and Fourier transform infrared imaging spectroscopy (Q37466102) (← links)
- Animal models of human genetic diseases: do they need to be faithful to be useful? (Q37872654) (← links)
- The Role of Collagen Organization on the Properties of Bone (Q38430261) (← links)
- Fell Muir Lecture: Collagen fibril formation in vitro and in vivo. (Q39309215) (← links)
- Enhanced intracellular availability and survival of hammerhead ribozymes increases target ablation in a cellular model of osteogenesis imperfecta (Q40625024) (← links)
- Insertional mutagenesis in transgenic mice (Q40628397) (← links)
- Collagens and their abnormalities in a wide spectrum of diseases (Q40853815) (← links)
- Osteogenesis imperfecta: from phenotype to genotype and back again. (Q41163824) (← links)
- Increased bone formation in osteocalcin-deficient mice. (Q41182577) (← links)
- Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursors (Q41875199) (← links)
- Enhanced Wnt signaling improves bone mass and strength, but not brittleness, in the Col1a1( /mov13) mouse model of type I Osteogenesis Imperfecta (Q42114635) (← links)
- Of mice and men: heritable skeletal disorders (Q42559546) (← links)
- Oesophageal morphometry and residual strain in a mouse model of osteogenesis imperfecta (Q42663249) (← links)
- Effects of the bisphosphonate risedronate on osteopenia in OASIS-deficient mice (Q43213519) (← links)
- Proteoglycans and glycosaminoglycan fine structure in the mouse tail tendon fascicle (Q43603737) (← links)
- Validation of a technique for studying functional adaptation of the mouse ulna in response to mechanical loading (Q44136620) (← links)
- An evaluation of otopathology in the MOV-13 transgenic mutant mouse (Q44934494) (← links)