Browsing "Department of Biochemistry" by Author bateman, jf

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TitleAuthor(s)Issue DateViews
 
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
Journal:American Journal of Medical Genetics - Seminars in Medical Genetics
Mundlos, SChan, DMcgill, JBateman, JF
1996
139
 
Type X collagen NC1 mutations produced by site-directed mutagenesis prevent in vitro assembly
Proceeding/Conference:Annals of the New York Academy of Sciences
Chan, DWeng, YMGolub, SBateman, JF
1996
93
 
Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the α1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia
Journal:Journal of Biological Chemistry
Chan, DCole, WGRogers, JGBateman, JF
1995
159
 
A type III collagen Gly559 to arg helix mutation in Ehler's danlos syndrome type IV
Journal:Human Mutation
Bateman, JFChiodo, AAWeng, YMChan, DHaan, E
1998
108
 
Two-dimensional assays of peptide fragments
Journal:Methods in Enzymology
Cole, WGChan, DBateman, JF
1987
98
 
Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and function.
Journal:PLoS biology
Tsang, KYChan, DCheslett, DChan, WCSo, CLMelhado, IGChan, TWKwan, KMHunziker, EBYamada, YBateman, JFCheung, KMCheah, KS
2007
203
 
Substitution of arginine for glycine 664 in the collagen α1(I) chain in lethal perinatal osteogenesis imperfecta. Demonstration of the peptide defect by in vitro expression of the mutant cDNA
Journal:Journal of Biological Chemistry
Bateman, JFLamande, SRDahl, HHMChan, DCole, WG
1988
153
 
A structural mutation of the collagen α1(I)CB7 peptide in lethal perinatal osteogenesis imperfecta
Journal:Journal of Biological Chemistry
Bateman, JFMascara, TChan, DCole, WG
1987
144
 
Site-directed mutagenesis of human type X collagen. Expression of α1(X) NC1, NC2, and helical mutations in vitro and in transfected cells
Journal:Journal of Biological Chemistry
Chan, DYi Ma WengHocking, AMGolub, SMcquillan, DJBateman, JF
1996
101
 
Regulation of procollagen synthesis and processing during ascorbate-induced extracellular matrix accumulation in vitro
Journal:Biochemical Journal
Chan, DLamande, SRCole, WGBateman, JF
1990
108
 
Recurrent substitutions of arginine 789 by cysteine in pro-α1 (II) collagen chains produce spondyloepiphyseal dysplasia congenita
Proceeding/Conference:Journal of Rheumatology
Chan, DRogers, JFBateman, JFCole, WG
1995
102
 
Rapid fractionation of collagen chains and peptides by high-performance liquid chromatography
Journal:Analytical Biochemistry
Bateman, JFMascara, TChan, DCole, WG
1986
145
 
Peptide analysis of collagen produced from cDNA by transcription and translation in vitro.
Journal:Biochemical Journal
Bateman, JFLamande, SChan, DCole, WG
1987
134
 
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
Journal:Journal of Biological Chemistry
Mundlos, SChan, DWeng, YMSillence, DOCole, WGBateman, JF
1996
97
 
MT1-MMP-dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: Regulation by fibrillar collagen
Journal:Experimental Cell Research
Ruangpanit, NPrice, JTHolmbeck, KBirkedalHansen, HGuenzler, VHuang, XChan, DBateman, JFThompson, EW
2002
104
 
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
Journal:Journal of Biological Chemistry
Wilsoni, RFreddi, SChan, DCheah, KSEBateman, JF
2005
124
 
Lethal perinatal osteogenesis imperfecta due to the substitution of arginine for glycine at residue 391 of the α1(I) chain of type I collagen
Journal:Journal of Biological Chemistry
Bateman, JFChan, DWalker, ID
1987
127
 
Lethal perinatal osteogenesis imperfecta due to a type I collagen α2(I) gly to arg substitution detected by chemical cleavage of an mRNA:cDNA sequence mismatch
Journal:Human Mutation
Bateman, JFMoeller, IHannagan, MChan, DCole, WG
1992
144
 
Interaction of Collagen α1(X) Containing Engineered NC1 Mutations with Normal α1(X) in Vitro: Implications for the molecular basis of schmid metaphyseal chondrodysplasia
Journal:Journal of Biological Chemistry
Chan, DFreddi, SWeng, YMBateman, JF
1999
107
 
Interaction of collagen α1(X) containing engineered NC1 mutations with normal α1(X) in vitro. Implications for the molecular basis of Schmid metaphyseal chondrodysplasia
Journal:Journal of Biological Chemistry
Chan, DFreddi, SWeng, YMBateman, JF
1999
142
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