| Title | Author(s) | Year | View Count |  | 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, B | 2012 | 87 |
 | In vivo cellular adaptation to ER stress: Survival strategies with double-edged consequences | Tsang, KY; Chan, D; Bateman, JF; Cheah, KSE | 2010 | 243 |
 | 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, KS | 2007 | 89 |
| Misfolding of collagen X chains harboring schmid metaphyseal chondrodysplasia mutations results in aberrant disulfide bond formation, intracellular retention, and activation of the unfolded protein response | Wilsoni, R; Freddi, S; Chan, D; Cheah, KSE; Bateman, JF | 2005 | 119 |
| Chondrocytes survive ER stress caused by unfolded proteins via re-programming | Cheah, KSE; Tsang, KY; Cheslett, D; Chan, WCW; So, CL; Kwan, KM; Hunziker, EB; Yamada, Y; Bateman, JF; Cheung, KMC; Chan, D | 2005 | 90 |
| MT1-MMP-dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: Regulation by fibrillar collagen | Ruangpanit, N; Price, JT; Holmbeck, K; BirkedalHansen, H; Guenzler, V; Huang, X; Chan, D; Bateman, JF; Thompson, EW | 2002 | 139 |
| Abnormal chondroctye differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia Col10al mutation | Tsang, KY; Chan, D; Kwan, KM; Cheung, KMC; Hunziker, E; Sillence, D; Bateman, JF; Cheah, KSE | 2002 | 168 |
| 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, JF | 2002 | 119 |
| Abnormal chondrocyte differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia col10a1 mutation | Tsang, KY; Chan, D; Cheslett, D; Kwan, KM; Cheung, KMC; Hunziker, E; Sillence, D; Boot-Handford, R; Bateman, JF; Cheah, KSE | 2002 | 116 |
| A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic mice | Jacenko, O; Chan, D; Franklin, A; Ito, S; Underhill, CB; Bateman, JF; Campbell, MR | 2001 | 245 |
| Gelatinase A (MMP-2) activation by skin fibroblasts: dependence on MT1-MMP expression and fibrillar collagen form | Ruangpanit, N; Chan, D; Holmbeck, K; BirkedalHansen, H; Polarek, J; Yang, C; Bateman, JF; Thompson, EW | 2001 | 154 |
| Interaction of collagen a1(X) containing engineered NC1 mutations with normal alpha1(X) in vitro. Implications for the molecular basis of schmid metaphyseal chondrodysplasia | Chan, D; Freddi, S; Weng, YM; Bateman, JF | 1999 | 121 |
| Interaction of collagen α1(X) containing engineered NC1 mutations with normal α1(X) in vitro. Implications for the molecular basis of Schmid metaphyseal chondrodysplasia | Chan, D; Freddi, S; Weng, YM; Bateman, JF | 1999 | 95 |
| Collagen II is essential for the removal of the notochord and the formation of intervertebral discs | Aszódi, A; Chan, D; Hunziker, E; Bateman, JF; Fässler, R | 1998 | 131 |
| A type III collagen Gly559 to arg helix mutation in Ehler's danlos syndrome type IV | Bateman, JF; Chiodo, AA; Weng, YM; Chan, D; Haan, E | 1998 | 53 |
| In vitro expression analysis of collagen biosynthesis and assembly | Chan, D; Lamandé, SR; Mcquillan, DJ; Bateman, JF | 1997 | 82 |
| 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 collagen | Cole, WG; Chan, D; Chow, CW; Rogers, JG; Bateman, JF | 1996 | 82 |
| 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 hypochondrogenesis | Mundlos, S; Chan, D; Mcgill, J; Bateman, JF | 1996 | 107 |
| Site-directed mutagenesis of human type X collagen. Expression of α1(X) NC1, NC2, and helical mutations in vitro and in transfected cells | Chan, D; Yi Ma Weng; Hocking, AM; Golub, S; Mcquillan, DJ; Bateman, JF | 1996 | 96 |
| 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 matrix | Mundlos, S; Chan, D; Weng, YM; Sillence, DO; Cole, WG; Bateman, JF | 1996 | 88 |
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