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John Bateman

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Daniele Belluoccio; Christopher B Little; Lynn Rowley; John F Bateman
Maintaining mRNA integrity during decalcification of mineralized tissues.
Trevor L Cameron; Eleanor J Mackie; Ben T McDermott; M Helen Rajpar; Liliana Tatarczuch; Katrina M Bell; Raymond P Boot-Handford; John F Bateman
Transcriptional profiling of chondrodysplasia growth plate cartilage reveals adaptive ER-stress networks that allow survival but disrupt hypertrophy.
Kwok Yeung Tsang; Danny Chan; John F Bateman; Kathryn S E Cheah
In vivo cellular adaptation to ER stress: survival strategies with double-edged consequences.

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All Publications

2013: Daniele Belluoccio; Christopher B Little; Lynn Rowley; John F Bateman
Maintaining mRNA integrity during decalcification of mineralized tissues.
PloS one 2013;8(3):e58154.
2011: Trevor L Cameron; Eleanor J Mackie; Ben T McDermott; M Helen Rajpar; Liliana Tatarczuch; Katrina M Bell; Raymond P Boot-Handford; John F Bateman
Transcriptional profiling of chondrodysplasia growth plate cartilage reveals adaptive ER-stress networks that allow survival but disrupt hypertrophy.
PloS one 2011;6(9):e24600.
2010: Kwok Yeung Tsang; Danny Chan; John F Bateman; Kathryn S E Cheah
In vivo cellular adaptation to ER stress: survival strategies with double-edged consequences.
Journal of cell science 2010;123(Pt 13):2145-54.
2010: Richard Wilson; Anders F Diseberg; Lavinia Gordon; Snezana Zivkovic; Liliana Tatarczuch; Eleanor J Mackie; Jeffrey J Gorman; John F Bateman
Comprehensive profiling of cartilage extracellular matrix formation and maturation using sequential extraction and label-free quantitative proteomics.
Molecular & cellular proteomics : MCP 2010;9(6):1296-313.
2010: Peter Kannu; John F Bateman; Susan Randle; Shannon Cowie; Desiree du Sart; Shaun McGrath; Matthew Edwards; Ravi Savarirayan
Premature arthritis is a distinct type II collagen phenotype.
Arthritis and rheumatism 2010;62(5):1421-30.
2010: Daniele Belluoccio; Ivan Grskovic; Anja Niehoff; Ursula Schlötzer-Schrehardt; Sabrina Rosenbaum; Julia Etich; Christian Frie; Friedericke Pausch; Stephen E Moss; Ernst Pöschl; John F Bateman; Bent Brachvogel
Deficiency of annexins A5 and A6 induces complex changes in the transcriptome of growth plate cartilage but does not inhibit the induction of mineralization.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2010;25(1):141-53.
2009: Justin M Allen; Laura Zamurs; Bent Brachvogel; Ursula Schlötzer-Schrehardt; Uwe Hansen; Shireen R Lamandé; Lynn Rowley; David J (Jamie) Fitzgerald; John F Bateman
Mice lacking the extracellular matrix protein WARP develop normally but have compromised peripheral nerve structure and function.
The Journal of biological chemistry 2009;284(18):12020-30.
2009: John F Bateman; Raymond P Boot-Handford; Shireen R Lamandé
Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations.
Nature reviews. Genetics 2009;10(3):173-83.
2009: Trevor L Cameron; Daniele Belluoccio; Peter G Farlie; Bent Brachvogel; John F Bateman
Global comparative transcriptome analysis of cartilage formation in vivo.
BMC developmental biology 2009;9():20.
2008: Rishika A Pace; Rachel Peat; Naomi L Baker; Laura Zamurs; Matthias Mörgelin; Melita Irving; Naomi E Adams; John F Bateman; David Mowat; Nicholas J C Smith; Phillipa J Lamont; Steven A Moore; Katherine D Mathews; Kathryn N North; Shireen R Lamandé
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
Annals of neurology 2008;64(3):294-303.
2008: Richard Wilson; Daniele Belluoccio; John F Bateman
Proteomic analysis of cartilage proteins.
Methods (San Diego, Calif.) 2008;45(1):22-31.
2007: Naomi L Baker; Matthias Mörgelin; Rishika A Pace; Rachel Peat; Naomi E Adams; R J McKinlay Gardner; Lewis P Rowland; Geoffrey Miller; Peter De Jonghe; Berten Ceulemans; Mark C Hannibal; Matthew Edwards; Elizabeth M Thompson; Richard Jacobson; Ros C M Quinlivan; Salim Aftimos; Andrew J Kornberg; Kathryn N North; John F Bateman; Shireen R Lamandé
Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
Annals of neurology 2007;62(4):390-405.
2007: Kwok Yeung Tsang; Danny Chan; Deborah Cheslett; Wilson C W Chan; Chi Leong So; Ian G Melhado; Tori W Y Chan; Kin Ming Kwan; Ernst B Hunziker; Yoshihiko Yamada; John F Bateman; Kenneth M C Cheung; Kathryn S E Cheah
Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and function.
PLoS biology 2007;5(3):e44.
2006: Justin M Allen; John F Bateman; Uwe Hansen; Richard Wilson; Peter Bruckner; Rick T Owens; Takako Sasaki; Rupert Timpl; David J (Jamie) Fitzgerald
WARP is a novel multimeric component of the chondrocyte pericellular matrix that interacts with perlecan.
The Journal of biological chemistry 2006;281(11):7341-9.
2005: George McGillivray; Ravi Savarirayan; Timothy C Cox; C Stojkoski; Robyn McNeil; Agnes Bankier; John F Bateman; Tony Roscioli; R J McKinlay Gardner; Shireen R Lamandé
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.
Journal of medical genetics 2005;42(8):656-62.
2005: John F Bateman
Genetic aspects of osteoarthritis.
Seminars in arthritis and rheumatism 2005;34(6 Suppl 2):15-8.
2005: John F Bateman; Richard Wilson; Susanna Freddi; Shireen R Lamandé; Ravi Savarirayan
Mutations of COL10A1 in Schmid metaphyseal chondrodysplasia.
Human mutation 2005;25(6):525-34.
2005: Richard Wilson; Susanna Freddi; Danny Chan; Kathryn S E Cheah; John F Bateman
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.
The Journal of biological chemistry 2005;280(16):15544-52.
2005: Naomi L Baker; Matthias Mörgelin; Rachel Peat; Nathalie Goemans; Kathryn N North; John F Bateman; Shireen R Lamandé
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy.
Human molecular genetics 2005;14(2):279-93.
2004: David J (Jamie) Fitzgerald; John F Bateman
Why mice have lost genes for COL21A1, STK17A, GPR145 and AHRI: evidence for gene deletion at evolutionary breakpoints in the rodent lineage.
Trends in genetics : TIG 2004;20(9):408-12.
2004: John F Bateman; Susanna Freddi; Robyn McNeil; Elizabeth Thompson; Pia Hermanns; Ravi Savarirayan; Shireen R Lamandé
Identification of four novel COL10A1 missense mutations in schmid metaphyseal chondrodysplasia: further evidence that collagen X NC1 mutations impair trimer assembly.
Human mutation 2004;23(4):396.
2003: Charlotte Wiberg; Andreas R Klatt; Raimund Wagener; Mats Paulsson; John F Bateman; Dick Heinegård; Matthias Mörgelin
Complexes of matrilin-1 and biglycan or decorin connect collagen VI microfibrils to both collagen II and aggrecan.
The Journal of biological chemistry 2003;278(39):37698-704.
2003: John F Bateman; Susanna Freddi; Gary Nattrass; Ravi Savarirayan
Tissue-specific RNA surveillance? Nonsense-mediated mRNA decay causes collagen X haploinsufficiency in Schmid metaphyseal chondrodysplasia cartilage.
Human molecular genetics 2003;12(3):217-25.
2002: David J (Jamie) Fitzgerald; Su Tay Ting; John F Bateman
WARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteins.
FEBS letters 2002;517(1-3):61-6.
2002: Richard Wilson; Susanna Freddi; John F Bateman
Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells.
The Journal of biological chemistry 2002;277(15):12516-24.
2002: David J Amor; Coral Tudball; R J McKinlay Gardner; Shireen R Lamandé; John F Bateman; Ravi Savarirayan
Familial digital arthropathy-brachydactyly.
American journal of medical genetics 2002;108(3):235-40.
2002: Shireen R Lamandé; Matthias Mörgelin; Carly Selan; G Joost Jöbsis; Frank Baas; John F Bateman
Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations.
The Journal of biological chemistry 2002;277(3):1949-56.
2001: David J (Jamie) Fitzgerald; John F Bateman
A new FACIT of the collagen family: COL21A1.
FEBS letters 2001;505(2):275-80.
2001: David J (Jamie) Fitzgerald; Matthias Mörgelin; Carly Selan; Charlotte Wiberg; D R Keene; Shireen R Lamandé; John F Bateman
The N-terminal N5 subdomain of the alpha 3(VI) chain is important for collagen VI microfibril formation.
The Journal of biological chemistry 2001;276(1):187-93.
2001: John F Bateman
The molecular genetics of inherited cartilage disease.
Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2001;9 Suppl A():S141-9.
2000: Susanna Freddi; Ravi Savarirayan; John F Bateman
Molecular diagnosis of Stickler syndrome: a COL2A1 stop codon mutation screening strategy that is not compromised by mutant mRNA instability.
American journal of medical genetics 2000;90(5):398-406.
1999: Shireen R Lamandé; John F Bateman
Procollagen folding and assembly: the role of endoplasmic reticulum enzymes and molecular chaperones.
Seminars in cell & developmental biology 1999;10(5):455-64.
1999: Lesley C Adès; R Davies; Eric A Haan; Katherine J Holman; K C Watson; D Sreetharan; Shi-Nian Cao; Dianna M Milewicz; John F Bateman; A A Chiodo; M Eccles; LA McNoe; M Harbord
Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent.
Clinical dysmorphology 1999;8(4):269-76.
1999: David J (Jamie) Fitzgerald; Shireen R Lamandé; John F Bateman
Proteasomal degradation of unassembled mutant type I collagen pro-alpha1(I) chains.
The Journal of biological chemistry 1999;274(39):27392-8.
1999: Shireen R Lamandé; K A Shields; Andrew J Kornberg; Lloyd K Shield; John F Bateman
Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion.
The Journal of biological chemistry 1999;274(31):21817-22.
1999: Danny Chan; Susanna Freddi; YM Weng; John F Bateman
Interaction of collagen alpha1(X) containing engineered NC1 mutations with normal alpha1(X) in vitro. Implications for the molecular basis of schmid metaphyseal chondrodysplasia.
The Journal of biological chemistry 1999;274(19):13091-7.
1999: John F Bateman; Susanna Freddi; Shireen R Lamandé; P Byers; Steven Nasioulas; J Douglas; Robyn Otway; M R J Kohonen-Corish; E Edkins; S Forrest
Reliable and sensitive detection of premature termination mutations using a protein truncation test designed to overcome problems of nonsense-mediated mRNA instability.
Human mutation 1999;13(4):311-7.
1998: Chrishan S Samuel; JP Coghlan; John F Bateman
Effects of relaxin, pregnancy and parturition on collagen metabolism in the rat pubic symphysis.
The Journal of endocrinology 1998;159(1):117-25.
1998: Shireen R Lamandé; John F Bateman; W Hutchison; RJ McKinlay Gardner; S P Bower; E Byrne; Hans-Henrik M Dahl
Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiency.
Human molecular genetics 1998;7(6):981-9.
1998: Danny Chan; YM Weng; H K Graham; D O Sillence; John F Bateman
A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.
The Journal of clinical investigation 1998;101(7):1490-9.
1998: Shireen R Lamandé; E Sigalas; Te-Cheng Pan; Mon-Li Chu; Marie A Dziadek; Rupert Timpl; John F Bateman
The role of the alpha3(VI) chain in collagen VI assembly. Expression of an alpha3(VI) chain lacking N-terminal modules N10-N7 restores collagen VI assembly, secretion, and matrix deposition in an alpha3(VI)-deficient cell line.
The Journal of biological chemistry 1998;273(13):7423-30.
1998: John F Bateman; A A Chiodo; YM Weng; D Chan; Eric A Haan
A type III collagen Gly559 to Arg helix mutation in Ehler's-Danlos syndrome type IV.
Human mutation 1998;Suppl 1():S257-9.
1997: D Chan; Shireen R Lamandé; David J McQuillan; John F Bateman
In vitro expression analysis of collagen biosynthesis and assembly.
Journal of biochemical and biophysical methods 1997;36(1):11-29.
1996: Lesley C Adès; W B Knight; R W Byard; John F Bateman; J A Esquivel; R B Mee; Eric A Haan; Dianna M Milewicz
Clinicopathologic findings in congenital aneurysms of the great vessels.
American journal of medical genetics 1996;66(3):289-99.
1996: Stefan Mundlos; D Chan; Y M Weng; D O Sillence; W G Cole; John F Bateman
Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened alpha2(I) chains show differential incorporation into the bone and skin extracellular matrix.
The Journal of biological chemistry 1996;271(35):21068-74.
1996: D Chan; Y M Weng; S Golub; John F Bateman
Type X collagen NC1 mutations produced by site-directed mutagenesis prevent in vitro assembly.
Annals of the New York Academy of Sciences 1996;785():231-3.
1996: D Chan; Y M Weng; Anne M Hocking; S Golub; David J McQuillan; John F Bateman
Site-directed mutagenesis of human type X collagen. Expression of alpha1(X) NC1, NC2, and helical mutations in vitro and in transfected cells.
The Journal of biological chemistry 1996;271(23):13566-72.
1996: Stefan Mundlos; D Chan; J McGill; John F Bateman
An alpha 1(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.
American journal of medical genetics 1996;63(1):129-36.
1995: A A Chiodo; D O Sillence; W G Cole; John F Bateman
Abnormal type III collagen produced by an exon-17-skipping mutation of the COL3A1 gene in Ehlers-Danlos syndrome type IV is not incorporated into the extracellular matrix.
The Biochemical journal 1995;311 ( Pt 3)():939-43.
1995: Lesley C Adès; R D Waltham; A A Chiodo; John F Bateman
Myocardial infarction resulting from coronary artery dissection in an adolescent with Ehlers-Danlos syndrome type IV due to a type III collagen mutation.
British heart journal 1995;74(2):112-6.
1995: Shireen R Lamandé; John F Bateman
The type I collagen pro alpha 1(I) COOH-terminal propeptide N-linked oligosaccharide. Functional analysis by site-directed mutagenesis.
The Journal of biological chemistry 1995;270(30):17858-65.
1995: Lesley C Adès; L L Morris; R G Power; M Wilson; Eric A Haan; John F Bateman; Dianna M Milewicz; D O Sillence
Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome.
American journal of medical genetics 1995;57(4):565-72.
1995: Shireen R Lamandé; S D Chessler; S B Golub; P H Byers; D Chan; W G Cole; D O Sillence; John F Bateman
Endoplasmic reticulum-mediated quality control of type I collagen production by cells from osteogenesis imperfecta patients with mutations in the pro alpha 1 (I) chain carboxyl-terminal propeptide which impair subunit assembly.
The Journal of biological chemistry 1995;270(15):8642-9.
1995: David J McQuillan; M D Richardson; John F Bateman
Matrix deposition by a calcifying human osteogenic sarcoma cell line (SAOS-2).
Bone 1995;16(4):415-26.
1995: D Chan; W G Cole; J G Rogers; John F Bateman
Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the alpha 1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia.
The Journal of biological chemistry 1995;270(9):4558-62.
1995: D Chan; J F Rogers; John F Bateman; W G Cole
Recurrent substitutions of arginine 789 by cysteine in pro-alpha 1 (II) collagen chains produce spondyloepiphyseal dysplasia congenita.
The Journal of rheumatology. Supplement 1995;43():37-8.
1995: D Chan; W G Cole; C W Chow; Stefan Mundlos; John F Bateman
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilage.
The Journal of biological chemistry 1995;270(4):1747-53.
1994: John F Bateman; D Chan; I Moeller; M Hannagan; W G Cole
A 5' splice site mutation affecting the pre-mRNA splicing of two upstream exons in the collagen COL1A1 gene. Exon 8 skipping and altered definition of exon 7 generates truncated pro alpha 1(I) chains with a non-collagenous insertion destabilizing the triple helix.
The Biochemical journal 1994;302 ( Pt 3)():729-35.
1994: John F Bateman; S B Golub
Deposition and selective degradation of structurally-abnormal type I collagen in a collagen matrix produced by osteogenesis imperfecta fibroblasts in vitro.
Matrix biology : journal of the International Society for Matrix Biology 1994;14(3):251-62.
1993: S P Fenton; S R Lamande; M Hannagan; A Stacey; Rudolf Jaenisch; John F Bateman
Genomic sequence of mouse COL1A1 encoding the collagen propeptides.
Biochimica et biophysica acta 1993;1216(3):469-74.
1993: Shireen R Lamandé; John F Bateman
A type I collagen reporter gene construct for protein engineering studies. Functional equivalence of transfected reporter COL1A1 and endogenous gene products during biosynthesis and in vitro extracellular matrix accumulation.
The Biochemical journal 1993;293 ( Pt 2)():387-94.
1993: Shireen R Lamandé; John F Bateman
A mouse 3T6 fibroblast cell culture model for the study of normal and protein-engineered collagen synthesis and deposition into the extracellular matrix.
Matrix (Stuttgart, Germany) 1993;13(4):323-30.
1993: John F Bateman; S R Lamande; M Hannagan; I Moeller; Hans-Henrik M Dahl; W G Cole
Chemical cleavage method for the detection of RNA base changes: experience in the application to collagen mutations in osteogenesis imperfecta.
American journal of medical genetics 1993;45(2):233-40.
1992: John F Bateman; I Moeller; M Hannagan; D Chan; W G Cole
Characterization of three osteogenesis imperfecta collagen alpha 1(I) glycine to serine mutations demonstrating a position-dependent gradient of phenotypic severity.
The Biochemical journal 1992;288 ( Pt 1)():131-5.
1992: John F Bateman; I Moeller; M Hannagan; D Chan; W G Cole
Lethal perinatal osteogenesis imperfecta due to a type I collagen alpha 2(I) Gly to Arg substitution detected by chemical cleavage of an mRNA:cDNA sequence mismatch.
Human mutation 1992;1(1):55-62.
1991: John F Bateman; M Hannagan; D Chan; W G Cole
Characterization of a type I collagen alpha 2(I) glycine-586 to valine substitution in osteogenesis imperfecta type IV. Detection of the mutation and prenatal diagnosis by a chemical cleavage method.
The Biochemical journal 1991;276 ( Pt 3)():765-70.
1990: W G Cole; A A Chiodo; S R Lamande; R Janeczko; F Ramirez; Hans-Henrik M Dahl; D Chan; John F Bateman
A base substitution at a splice site in the COL3A1 gene causes exon skipping and generates abnormal type III procollagen in a patient with Ehlers-Danlos syndrome type IV.
The Journal of biological chemistry 1990;265(28):17070-7.
1990: W G Cole; P E Campbell; J G Rogers; John F Bateman
The clinical features of osteogenesis imperfecta resulting from a non-functional carboxy terminal pro alpha 1(I) propeptide of type I procollagen and a severe deficiency of normal type I collagen in tissues.
Journal of medical genetics 1990;27(9):545-51.
1990: D Chan; S R Lamande; W G Cole; John F Bateman
Regulation of procollagen synthesis and processing during ascorbate-induced extracellular matrix accumulation in vitro.
The Biochemical journal 1990;269(1):175-81.
1990: John F Bateman; S B Golub
Assessment of procollagen processing defects by fibroblasts cultured in the presence of dextran sulphate.
The Biochemical journal 1990;267(3):573-7.
1990: W G Cole; C W Chow; J G Rogers; John F Bateman
The clinical features of three babies with osteogenesis imperfecta resulting from the substitution of glycine by arginine in the pro alpha 1(I) chain of type I procollagen.
Journal of medical genetics 1990;27(4):228-35.
1990: H Wu; John F Bateman; A Schnieke; A Sharpe; D Barker; T Mascara; D Eyre; R Bruns; P Krimpenfort; Anton Berns
Human-mouse interspecies collagen I heterotrimer is functional during embryonic development of Mov13 mutant mouse embryos.
Molecular and cellular biology 1990;10(4):1452-60.
1990: A H Ang; G Tachas; J H Campbell; John F Bateman; G R Campbell
Collagen synthesis by cultured rabbit aortic smooth-muscle cells. Alteration with phenotype.
The Biochemical journal 1990;265(2):461-9.
1990: John F Bateman; T Mascara; W G Cole; A Stacey; Rudolf Jaenisch
The study of collagen structure and function by site-directed mutagenesis of collagen genes.
Annals of the New York Academy of Sciences 1990;580():324-9.
1989: Hans-Henrik M Dahl; S R Lamande; R G Cotton; John F Bateman
Detection and localization of base changes in RNA using a chemical cleavage method.
Analytical biochemistry 1989;183(2):263-8.
1989: S R Lamande; Hans-Henrik M Dahl; W G Cole; John F Bateman
Characterization of point mutations in the collagen COL1A1 and COL1A2 genes causing lethal perinatal osteogenesis imperfecta.
The Journal of biological chemistry 1989;264(27):15809-12.
1989: John F Bateman; S R Lamande; Hans-Henrik M Dahl; D Chan; T Mascara; W G Cole
A frameshift mutation results in a truncated nonfunctional carboxyl-terminal pro alpha 1(I) propeptide of type I collagen in osteogenesis imperfecta.
The Journal of biological chemistry 1989;264(19):10960-4.
1989: W G Cole; Rudolf Jaenisch; John F Bateman
New insights into the molecular pathology of osteogenesis imperfecta.
The Quarterly journal of medicine 1989;70(261):1-4.
1989: John F Bateman; T Mascara; W G Cole; A Stacey; Rudolf Jaenisch
Collagen protein abnormalities produced by site-directed mutagenesis of the pro alpha 1(I) gene.
Connective tissue research 1989;20(1-4):205-12; discussion 261-3.
1988: John F Bateman; S R Lamande; Hans-Henrik M Dahl; D Chan; W G Cole
Substitution of arginine for glycine 664 in the collagen alpha 1(I) chain in lethal perinatal osteogenesis imperfecta. Demonstration of the peptide defect by in vitro expression of the mutant cDNA.
The Journal of biological chemistry 1988;263(24):11627-30.
1988: W G Cole; John F Bateman
Regulation and organization of connective tissues.
The Australian and New Zealand journal of surgery 1988;58(4):263-70.
1988: Kong Wah Ng; P R Gummer; V P Michelangeli; John F Bateman; T Mascara; W G Cole; T John Martin
Regulation of alkaline phosphatase expression in a neonatal rat clonal calvarial cell strain by retinoic acid.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 1988;3(1):53-61.
1988: John F Bateman; V Harley; D Chan; W G Cole
Comprehensive analysis of collagen metabolism in vitro using [4(3H)]/[14C]proline dual-labeling and polyacrylamide gel electrophoresis.
Analytical biochemistry 1988;168(1):171-5.
1988: John F Bateman; D Chan; S Lamande; T Mascara; W G Cole
Biochemical heterogeneity of type I collagen mutations in osteogenesis imperfecta.
Annals of the New York Academy of Sciences 1988;543():95-105.
1987: John F Bateman; J. Jane Pillow; T Mascara; S Medvedec; J A Ramshaw; W G Cole
Cell-layer-associated proteolytic cleavage of the telopeptides of type I collagen in fibroblast culture.
The Biochemical journal 1987;245(3):677-82.
1987: John F Bateman; S Lamande; D Chan; W G Cole
Peptide analysis of collagen produced from cDNA by transcription and translation in vitro.
The Biochemical journal 1987;245(2):393-8.
1987: John F Bateman; T Mascara; D Chan; W G Cole
A structural mutation of the collagen alpha 1(I)CB7 peptide in lethal perinatal osteogenesis imperfecta.
The Journal of biological chemistry 1987;262(10):4445-51.
1986: John F Bateman; D Chan; T Mascara; J G Rogers; W G Cole
Collagen defects in lethal perinatal osteogenesis imperfecta.
The Biochemical journal 1986;240(3):699-708.
1986: John F Bateman; T Mascara; D Chan; W G Cole
Rapid fractionation of collagen chains and peptides by high-performance liquid chromatography.
Analytical biochemistry 1986;154(1):338-44.
1986: John F Bateman; W G Cole; J. Jane Pillow; J A Ramshaw
Induction of procollagen processing in fibroblast cultures by neutral polymers.
The Journal of biological chemistry 1986;261(9):4198-203.
1984: John F Bateman; T Mascara; D Chan; W G Cole
Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta.
The Biochemical journal 1984;217(1):103-15.