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Building Finite Element Models to Investigate Zebrafish Jaw Biomechanics.Finite element modelling predicts changes in joint shape and cell behaviour due to loss of muscle strain in jaw developmentSpinal deformity in aged zebrafish is accompanied by degenerative changes to their vertebrae that resemble osteoarthritis.Entpd5 is essential for skeletal mineralization and regulates phosphate homeostasis in zebrafish.Cellular dynamics of regeneration reveals role of two distinct Pax7 stem cell populations in larval zebrafish muscle repairUsing transgenic reporters to visualize bone and cartilage signaling during development in vivo.Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish.Expression of glycosaminoglycan epitopes during zebrafish skeletogenesis.Wnt signalling controls the response to mechanical loading during zebrafish joint development.The Golgi matrix protein giantin is required for normal cilia function in zebrafish.Differential effects of altered patterns of movement and strain on joint cell behaviour and skeletal morphogenesis.New tools for studying osteoarthritis genetics in zebrafish.Trpv5/6 is vital for epithelial calcium uptake and bone formation.Fgf8 drives myogenic progression of a novel lateral fast muscle fibre population in zebrafish.Two populations of endochondral osteoblasts with differential sensitivity to Hedgehog signalling.Myotome adaptability confers developmental robustness to somitic myogenesis in response to fibre number alteration.Giantin-knockout models reveal a feedback loop between Golgi function and glycosyltransferase expression.Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth.Regulator of calcineurin-2 is a centriolar protein with a role in cilia length control.The mechanical impact of loss on joints; mutant zebrafish show changes to joint development and function, which leads to early-onset osteoarthritisBone Regenerates via Dedifferentiation of Osteoblasts in the Zebrafish FinZebrafish as an Emerging Model for Osteoporosis: A Primary Testing Platform for Screening New Osteo-Active CompoundsA rare SMAD9 mutation identifies the BMP signalling pathway as a potential osteoanabolic targetIn ovo temperature manipulation influences embryonic motility and growth of limb tissues in the chick (Gallus gallus)A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for OsteoporosisFinite element and deformation analyses predict pattern of bone failure in loaded zebrafish spines
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description
researcher, ORCID id # 0000-0002-4935-6724
@en
wetenschapper
@nl
name
Chrissy L Hammond
@ast
Chrissy L Hammond
@en
Chrissy L Hammond
@es
Chrissy L Hammond
@nl
type
label
Chrissy L Hammond
@ast
Chrissy L Hammond
@en
Chrissy L Hammond
@es
Chrissy L Hammond
@nl
prefLabel
Chrissy L Hammond
@ast
Chrissy L Hammond
@en
Chrissy L Hammond
@es
Chrissy L Hammond
@nl
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P1153
12784989900
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P496
0000-0002-4935-6724