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TypeTitleAuthor(s)YearViews
Depletion of annexin A5, annexin A6 and collagen X causes no gross changes in matrix vesicle mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 response.Grskovic, I; Kutsch, A; Frie, C; Groma, G; Stermann, J,; Schlötzer-Schrehardt, U; Niehoff, A,; Moss, SE; Rosenbaum S, S; Pöschl, E; Chmielewski, M; Rappl, G; Abken, H; Bateman, JF; Cheah, KSE; Paulsson, M; Brachvogel, B201290
 
In vivo cellular adaptation to ER stress: Survival strategies with double-edged consequencesTsang, KY; Chan, D; Bateman, JF; Cheah, KSE2010235
 
Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and function.Tsang, KY; Chan, D; Cheslett, D; Chan, WC; So, CL; Melhado, IG; Chan, TW; Kwan, KM; Hunziker, EB; Yamada, Y; Bateman, JF; Cheung, KM; Cheah, KS200795
 
Chondrocytes survive ER stress caused by unfolded proteins via re-programmingCheah, KSE; Tsang, KY; Cheslett, D; Chan, WCW; So, CL; Kwan, KM; Hunziker, EB; Yamada, Y; Bateman, JF; Cheung, KMC; Chan, D200590
 
Misfolding of collagen X chains harboring schmid metaphyseal chondrodysplasia mutations results in aberrant disulfide bond formation, intracellular retention, and activation of the unfolded protein responseWilsoni, R; Freddi, S; Chan, D; Cheah, KSE; Bateman, JF2005106
 
Abnormal chondrocyte differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia col10a1 mutationTsang, KY; Chan, D; Cheslett, D; Kwan, KM; Cheung, KMC; Hunziker, E; Sillence, D; Boot-Handford, R; Bateman, JF; Cheah, KSE2002108
 
Abnormal cell cycle regulation and chondrocyte differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia mutation in COL10A1.Cheah, KSE; Tsang, KY; Chan, D; Cheslett, D; Kwan, KM; Cheung, KMC; Hunziker, E; Sillence, D; Bateman, JF2002121
 
MT1-MMP-dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: Regulation by fibrillar collagenRuangpanit, N; Price, JT; Holmbeck, K; BirkedalHansen, H; Guenzler, V; Huang, X; Chan, D; Bateman, JF; Thompson, EW2002105
 
Abnormal chondroctye differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia Col10al mutationTsang, KY; Chan, D; Kwan, KM; Cheung, KMC; Hunziker, E; Sillence, D; Bateman, JF; Cheah, KSE2002129
 
A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic miceJacenko, O; Chan, D; Franklin, A; Ito, S; Underhill, CB; Bateman, JF; Campbell, MR2001243
 
Gelatinase A (MMP-2) activation by skin fibroblasts: dependence on MT1-MMP expression and fibrillar collagen formRuangpanit, N; Chan, D; Holmbeck, K; BirkedalHansen, H; Polarek, J; Yang, C; Bateman, JF; Thompson, EW2001148
 
Interaction of collagen a1(X) containing engineered NC1 mutations with normal alpha1(X) in vitro. Implications for the molecular basis of schmid metaphyseal chondrodysplasiaChan, D; Freddi, S; Weng, YM; Bateman, JF199990
 
Interaction of collagen α1(X) containing engineered NC1 mutations with normal α1(X) in vitro. Implications for the molecular basis of Schmid metaphyseal chondrodysplasiaChan, D; Freddi, S; Weng, YM; Bateman, JF199969
 
A type III collagen Gly559 to arg helix mutation in Ehler's danlos syndrome type IVBateman, JF; Chiodo, AA; Weng, YM; Chan, D; Haan, E199856
 
Collagen II is essential for the removal of the notochord and the formation of intervertebral discsAszódi, A; Chan, D; Hunziker, E; Bateman, JF; Fässler, R199893
 
In vitro expression analysis of collagen biosynthesis and assemblyChan, D; Lamandé, SR; Mcquillan, DJ; Bateman, JF1997106
 
An α1(II) Gly913 to Cys substitution prevents the matrix incorporation of type II collagen which is replaced with type I and III collagens in cartilage from a patient with hypochondrogenesisMundlos, S; Chan, D; Mcgill, J; Bateman, JF199697
 
Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened α2(I) chains show differential incorporation into the bone and skin extracellular matrixMundlos, S; Chan, D; Weng, YM; Sillence, DO; Cole, WG; Bateman, JF199683
 
Type X collagen NC1 mutations produced by site-directed mutagenesis prevent in vitro assemblyChan, D; Weng, YM; Golub, S; Bateman, JF199658
 
Disrupted growth plates and progressive deformities in osteogenesis imperfecta as a result of the substitution of glycine 585 by valine in the α2(I) chain of type I collagenCole, WG; Chan, D; Chow, CW; Rogers, JG; Bateman, JF199697
 
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