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PROF JOHN BATEMAN



Contact Details

Organization: Biochemistry and Molecular Biology
Position: Honorary (Professorial Fellow)
Email:

Research Expertise and International Linkages

Research Expertise

Research Interest Key Words Country of Expertise
Inherited bone and muscle disease, Bone and cartillage development disease Connective tissue research Australia

Qualifications, Honours, Fellowships and Other Awards

Qualifications

Title Institution Date Awarded Abbreviation
Bachelor of Science Monash University 31-Dec-1974
Doctor of Philosophy Monash University 31-Dec-1978

Government Research Classifications

Research Fields, Courses and Discipline Classifications

Socio-Economic Objective Classifications

Grants and Contracts

Research Grants, Contracts and Consultancies awarded to the University of Melbourne as the administering institution (since 2003) as recorded in Themis Agreements.

Grants

Title Role Funding Source Scheme Award Date
MOLECULAR MECHANISMS OF COLLAGEN MATRIX ASSEMBLY IN HEALTH Chief Investigator NHMRC Project Grants 01/01/2000
Molecular pathology of human collagen mutations Chief Investigator NHMRC Research Fellowship 01/01/2001
Research Fellowship Chief Investigator NHMRC Research Fellowship 01/01/2005
mRNA surveillance in human disease: Molecular determinants of nonsense-mediated mRNA decay Chief Investigator NHMRC Project Grants 01/01/2006
Rapid functional analysis of genes involved in skeletal development Chief Investigator AUST RESEARCH COUNCIL Discovery Projects 01/01/2008
Proteomic and transcriptional profiling of cartilage Chief Investigator AUST RESEARCH COUNCIL Discovery Projects

Publications

Publications produced at the University of Melbourne and reported in the Annual Publications Collection and 'Research Report' since 2001. The Themis Publications module, released in November 2006, allows additional publications from previous institutions and publications from past years to be entered.

Publications in 2009

Journal Articles

Publications in 2008

Journal Articles

Publications in 2007

Journal Articles

  • Isolated Anxa5+/Sca-1+ perivascular cells from mouse meningeal vasculature retain their perivascular phenotype in vitro and in vivo
    Year: 2007
    Journal: Experimental Cell Research
    Volume: 313
    Page numbers: 2730-2743
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  • Molecular Consequences of Dominant Bethlem Myopathy Collagen VI Mutations
    Year: 2007
    Journal: Annals of Neurology
    Volume: 62
    Page numbers: 390-405
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  • Surviving Endoplasmic Reticulum Stress Is Coupled to Altered Chondrocyte Differentiation and Function
    Year: 2007
    Journal: PLoS Biology
    Volume: 5
    Issue: 3
    Page numbers: e44
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Publications in 2006

Journal Articles

  • WARP Is a Novel Multimeric Component of the Chondrocyte Pericelluar Matrix That Interacts with Perlecan 


    Year: 2006
    Journal: Journal of Biological Chemistry
    Volume: 281
    Issue: 11
    Page numbers: 7341-7349
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  • Proteomic analysis of mouse growth plate cartilage
    Year: 2006
    Journal: Proteomics
    Volume: 6
    Page numbers: 6549-6553
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Publications in 2005

Journal Articles

  • ADAMTS-1-knockout mice do not exhibit abnormalities in aggrecan turnover in vitro or in vivo
    Year: 2005
    Journal: Arthritis and Rheumatism
    Volume: 52
    Issue: 5
    Page numbers: 1461-1472
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  • Dominant collagen VI mutations are a common cause of Ullrich congential muscular dystrophy.
    Year: 2005
    Journal: Human Molecular Genetics
    Volume: 14
    Issue: 2
    Page numbers: 279-293
    Publisher: Oxford University Press(Oxford)
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  • Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
    Year: 2005
    Journal: Journal of Medical Genetics
    Volume: 42
    Issue: 8
    Page numbers: 656-662
    Publisher: BMJ Publishing Group(London)
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  • Genetic aspects of osteoarthritis
    Year: 2005
    Journal: Seminars in Arthritis and Rheumatism
    Volume: 34
    Issue: 6
    Page numbers: 15-18
    Publisher: WB Saunders Co(Pennsylvania)
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  • Misfolding of collagen X chains harboring Schmid metaphyseal chondrodysplasia mutations result in aberrant disulfide bond formation, intracelluar retention and activaton of the unfolded protein response.
    Year: 2005
    Journal: Journal of Biological Chemistry
    Volume: 280
    Issue: 16
    Page numbers: 15544-15552
    Publisher: American Society for Biochemistry and Molecular Biology(Maryland)
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  • Mutations of COL10A1 in schmid metaphyseal chondrodysplasia
    Year: 2005
    Journal: Human Mutation
    Volume: 25
    Issue: 6
    Page numbers: 525-534
    Publisher: Wiley-Liss(New York)
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Publications in 2004

Journal Articles

  • Identification of four new COL10A1 missense mutations in Schmid metaphyseal chondrodysplasia: further evidence that collagen X NC1 mutations impair trimer assembly
    Year: 2004
    Journal: Human Mutation
    Volume: 693
    Page numbers: 1-7
    Publisher: Wiley-Liss(New York)
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  • Intracellular trafficking and degredation of unassociated proα2 chains of collagen type I
    Year: 2004
    Journal: Experimental Cell Research
    Volume: 296
    Issue: 2
    Page numbers: 307-316
    Publisher: Academic Press(California)
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  • Why mice have lost genes for COL21A1, STK17A, GPR145 and AHRI: evidence for gene deletion at evolutionalry breakpoints in the rodent lineage.
    Year: 2004
    Journal: Trends in Genetics
    Volume: 20
    Issue: 9
    Page numbers: 408-412
    Publisher: Elsevier Science London(London)
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Publications in 2003

Journal Articles

  • Complexes of matrilin-1 and biglycan or decorin connect collagen VI microfibrils to collagen II and aggrecan.
    Year: 2003
    Journal: Journal of Biological Chemistry
    Volume: 278
    Issue: 39
    Page numbers: 37698-37704
    Publisher: American Society for Biochemistry and Molecular Biology(Maryland)
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  • Is there an evolutionary relationship between WARP (von Willebrand factor A-domain-related protein) and the FACIT and FACIT-like collagens?
    Year: 2003
    Journal: FEBS Letters
    Volume: 552
    Issue: 2-3
    Page numbers: 91-94
    Publisher: Elsevier Science(Amsterdam)
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  • Molecular diagnosis in a pregnancy at risk for both spondyloepiphyseal dysplasia congenita and achondroplasia
    Year: 2003
    Journal: Prenatal Diagnosis
    Volume: 23
    Issue: 10
    Page numbers: 861-863
    Publisher: Wiley Europe
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  • Tissue specific RNA surveillance? Nonsense-mediated mRNA decay causes collagen X haploinsufficiency in Schmid metaphyseal chondrodysplasia cartilage.
    Year: 2003
    Journal: Human Molecular Genetics
    Volume: 12
    Issue: 3
    Page numbers: 217-225
    Publisher: Oxford University Press(Oxford)
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Publications in 2002

Journal Articles

  • Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells
    Year: 2002
    Journal: Journal of Biological Chemistry
    Volume: 277
    Page numbers: 12516-12524
    Publisher: American Society for Biochemistry and Molecular Biology(Maryland)
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  • Familial Digital Arthropathy-Brachydactyly
    Year: 2002
    Journal: American Journal of Medical Genetics
    Volume: 108
    Page numbers: 234-240
    Publisher: Wiley-Liss(New York)
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  • Kinked collagen VI tetramers and reduced microfibril formation as a result of bethlem myopathy and introduced triple helical glycine mutations
    Year: 2002
    Journal: Journal of Biological Chemistry
    Volume: 277
    Page numbers: 1949-1956
    Publisher: American Society for Biochemistry and Molecular Biology(Maryland)
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  • MT1-MMP-Dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: Regulation by fibrillar collagen
    Year: 2002
    Journal: Experimental Cell Research
    Volume: 272
    Page numbers: 109-118
    Publisher: Academic Press(California)
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  • The globular domain of the proα1(I) N-propeptide is not required for secretion, processing by procollagen n-proteinase, or fibrillogenesis of type I collagen in mice
    Year: 2002
    Journal: Journal of Biological Chemistry
    Volume: 277
    Page numbers: 2605-2613
    Publisher: American Society for Biochemistry and Molecular Biology(Maryland)
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  • WARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteins
    Year: 2002
    Journal: FEBS Letters
    Volume: 517
    Page numbers: 61-66
    Publisher: Elsevier Science(Amsterdam)
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Publications in 2001

Journal Articles

  • A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic mice
    Year: 2001
    Journal: American Journal of Pathology
    Volume: 159
    Issue: 6
    Page numbers: 2257-2269
    Publisher: American Society of Investigative Pathology Inc(Maryland)
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  • A new FACIT of the collagen family: COL21A1
    Year: 2001
    Journal: FEBS Letters
    Volume: 505
    Page numbers: 275-280
    Publisher: Elsevier Science(Amsterdam)
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  • Gelatinase A (MMP-2) activation by skin fibroblasts: dependence on MT1-MMP expression and fibrillar collagen form
    Year: 2001
    Journal: Matrix Biology
    Volume: 20
    Issue: 3
    Page numbers: 193-203
    Publisher: Elsevier Science(Amsterdam)
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  • The N-terminal N5 Subdomain of the a3(VI) Chain Is Important for Collagen VI Microfibril Formation
    Year: 2001
    Journal: Journal of Biological Chemistry
    Volume: 276
    Issue: 1
    Page numbers: 187-193
    Publisher: American Society for Biochemistry and Molecular Biology(Maryland)
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  • The molecular genetics of inherited cartilage disease
    Year: 2001
    Journal: Osteoarthritis and Cartilage
    Volume: 9
    Page numbers: 141-149
    Publisher: WB Saunders Co
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