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Results: 1-17 |
Results: 17

Authors: Bateman, JF
Citation: Jf. Bateman, The molecular genetics of inherited cartilage disease, OSTEO CART, 9, 2001, pp. S141-S149

Authors: Ruangpanit, N Chan, D Holmbeck, K Birkedal-Hansen, H Polarek, J Yang, CL Bateman, JF Thompson, EW
Citation: N. Ruangpanit et al., Gelatinase A (MMP-2) activation by skin fibroblasts: dependence on MT1-MMPexpression and fibrillar collagen form, MATRIX BIOL, 20(3), 2001, pp. 193-203

Authors: Fitzgerald, J Morgelin, M Selan, C Wiberg, C Keene, DR Lamande, SR Bateman, JF
Citation: J. Fitzgerald et al., The N-terminal N5 subdomain of the alpha 3(VI) chain is important for collagen VI microfibril formation, J BIOL CHEM, 276(1), 2001, pp. 187-193

Authors: Fitzgerald, J Bateman, JF
Citation: J. Fitzgerald et Jf. Bateman, A new FACIT of the collagen family: COL21A1, FEBS LETTER, 505(2), 2001, pp. 275-280

Authors: Jacenko, O Chan, D Franklin, A Ito, S Underhill, CB Bateman, JF Campbell, MR
Citation: O. Jacenko et al., A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distributionin transgenic mice, AM J PATH, 159(6), 2001, pp. 2257-2269

Authors: Aszodi, A Bateman, JF Gustafsson, E Boot-Handford, R Fassler, R
Citation: A. Aszodi et al., Mammalian skeletogenesis and extracellular matrix: What can we learn from knockout mice?, CELL STRUCT, 25(2), 2000, pp. 73-84

Authors: Freddi, S Savarirayan, R Bateman, JF
Citation: S. Freddi et al., Molecular diagnosis of Stickler syndrome: A COL2A1 stop codon mutation screening strategy that is not compromised by mutant mRNA instability, AM J MED G, 90(5), 2000, pp. 398-406

Authors: Fitzgerald, J Kennedy, D Viseshakul, N Cohen, BN Mattick, J Bateman, JF Forsayeth, JR
Citation: J. Fitzgerald et al., UNCL, the mammalian homologue of UNC-50, is an inner nuclear membrane RNA-binding protein, BRAIN RES, 877(1), 2000, pp. 110-123

Authors: Lamande, SR Bateman, JF
Citation: Sr. Lamande et Jf. Bateman, Procollagen folding and assembly: The role of endoplasmic reticulum enzymes and molecular chaperones, SEM CELL D, 10(5), 1999, pp. 455-464

Authors: Bateman, JF Freddi, S Lamande, SR Byers, P Nasioulas, S Douglas, J Otway, R Kohonen-Corish, M Edkins, E Forrest, S
Citation: Jf. Bateman et al., Reliable and sensitive detection of premature termination mutations using a protein truncation test designed to overcome problems of nonsense-mediated mRNA instability (vol 13, pg 311, 1998), HUM MUTAT, 14(1), 1999, pp. 86-86

Authors: Bateman, JF Freddi, S Lamande, SR Byers, P Nasioulas, S Douglas, J Otway, R Kohonen-Corish, M Edkins, E Forrest, S
Citation: Jf. Bateman et al., Reliable and sensitive detection of premature termination mutations using a protein truncation test designed to overcome problems of nonsense-mediated mRNA instability, HUM MUTAT, 13(4), 1999, pp. 311-317

Authors: Ades, LC Davies, R Haan, EA Holman, KJ Watson, KC Sreetharan, D Cao, SN Milewicz, DM Bateman, JF Chiodo, AA Eccles, M McNoe, L Harbord, M
Citation: Lc. Ades et al., Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent, CLIN DYSMOR, 8(4), 1999, pp. 269-276

Authors: Aszodi, A Bateman, JF Hirsch, E Baranyi, M Hunziker, EB Hauser, N Bosze, Z Fassler, R
Citation: A. Aszodi et al., Normal skeletal development of mice lacking matrilin 1: Redundant functionof matrilins in cartilage?, MOL CELL B, 19(11), 1999, pp. 7841-7845

Authors: Fitzgerald, J Lamande, SR Bateman, JF
Citation: J. Fitzgerald et al., Proteasomal degradation of unassembled mutant type I collagen pro-alpha 1(I) chains, J BIOL CHEM, 274(39), 1999, pp. 27392-27398

Authors: Lamande, SR Shields, KA Kornberg, AJ Shield, LK Bateman, JF
Citation: Sr. Lamande et al., Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion, J BIOL CHEM, 274(31), 1999, pp. 21817-21822

Authors: Chan, D Freddi, S Weng, YM Bateman, JF
Citation: D. Chan et al., Interaction of collagen alpha 1(X) containing engineered NC1 mutations with normal alpha 1(X) in vitro - Implications for the molecular basis of schmid metaphyseal chondrodysplasia, J BIOL CHEM, 274(19), 1999, pp. 13091-13097

Authors: Aszodi, A Chan, D Hunziker, E Bateman, JF Fassler, R
Citation: A. Aszodi et al., Collagen II is essential for the removal of the notochord and the formation of intervertebral discs, J CELL BIOL, 143(5), 1998, pp. 1399-1412
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