PubRank

John F Bateman

Author PubWeight™ 54.79‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and function. PLoS Biol 2007 1.82
2 The circadian clock in murine chondrocytes regulates genes controlling key aspects of cartilage homeostasis. Arthritis Rheum 2013 1.82
3 Complexes of matrilin-1 and biglycan or decorin connect collagen VI microfibrils to both collagen II and aggrecan. J Biol Chem 2003 1.72
4 Premature arthritis is a distinct type II collagen phenotype. Arthritis Rheum 2010 1.66
5 Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protection. Mol Biol Cell 2009 1.55
6 Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet 2004 1.51
7 Targeted induction of endoplasmic reticulum stress induces cartilage pathology. PLoS Genet 2009 1.21
8 Global comparative transcriptome analysis of cartilage formation in vivo. BMC Dev Biol 2009 1.18
9 Comprehensive profiling of cartilage extracellular matrix formation and maturation using sequential extraction and label-free quantitative proteomics. Mol Cell Proteomics 2010 1.18
10 Molecular consequences of dominant Bethlem myopathy collagen VI mutations. Ann Neurol 2007 1.15
11 Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity. Ann Neurol 2008 1.14
12 In vivo cellular adaptation to ER stress: survival strategies with double-edged consequences. J Cell Sci 2010 1.13
13 Bulldog dwarfism in Dexter cattle is caused by mutations in ACAN. Mamm Genome 2007 1.11
14 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. J Biol Chem 2005 1.10
15 ADAMTS-1-knockout mice do not exhibit abnormalities in aggrecan turnover in vitro or in vivo. Arthritis Rheum 2005 1.09
16 S100A8 and S100A9 in experimental osteoarthritis. Arthritis Res Ther 2010 1.08
17 Mutations in TRPV4 cause an inherited arthropathy of hands and feet. Nat Genet 2011 1.07
18 Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations. J Biol Chem 2001 1.06
19 Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity. Am J Hum Genet 2011 1.02
20 Proteomic analysis of mouse growth plate cartilage. Proteomics 2006 1.01
21 A microarray approach for comparative expression profiling of the discrete maturation zones of mouse growth plate cartilage. Biochim Biophys Acta 2008 1.01
22 Changes in the chondrocyte and extracellular matrix proteome during post-natal mouse cartilage development. Mol Cell Proteomics 2011 1.01
23 Transcriptional profiling of chondrodysplasia growth plate cartilage reveals adaptive ER-stress networks that allow survival but disrupt hypertrophy. PLoS One 2011 1.00
24 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. J Bone Miner Res 2012 0.99
25 Why mice have lost genes for COL21A1, STK17A, GPR145 and AHRI: evidence for gene deletion at evolutionary breakpoints in the rodent lineage. Trends Genet 2004 0.99
26 Competency for nonsense-mediated reduction in collagen X mRNA is specified by the 3' UTR and corresponds to the position of mutations in Schmid metaphyseal chondrodysplasia. Am J Hum Genet 2008 0.97
27 Isolated Anxa5+/Sca-1+ perivascular cells from mouse meningeal vasculature retain their perivascular phenotype in vitro and in vivo. Exp Cell Res 2007 0.96
28 Proteomic characterization of mouse cartilage degradation in vitro. Arthritis Rheum 2008 0.96
29 Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells. J Biol Chem 2002 0.95
30 Employing molecular genetics of chondrodysplasias to inform the study of osteoarthritis. Arthritis Rheum 2009 0.94
31 Cartilage intermediate layer protein 2 (CILP-2) is expressed in articular and meniscal cartilage and down-regulated in experimental osteoarthritis. J Biol Chem 2011 0.93
32 WARP is a novel multimeric component of the chondrocyte pericellular matrix that interacts with perlecan. J Biol Chem 2006 0.92
33 Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophy. J Biol Chem 2010 0.91
34 Proteomic analysis of cartilage proteins. Methods 2008 0.91
35 A robust method for proteomic characterization of mouse cartilage using solubility-based sequential fractionation and two-dimensional gel electrophoresis. Matrix Biol 2008 0.90
36 Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome. PLoS Genet 2013 0.86
37 The globular domain of the proalpha 1(I) N-propeptide is not required for secretion, processing by procollagen N-proteinase, or fibrillogenesis of type I collagen in mice. J Biol Chem 2001 0.85
38 WARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteins. FEBS Lett 2002 0.84
39 The extracellular matrix protein WARP is a novel component of a distinct subset of basement membranes. Matrix Biol 2008 0.84
40 Mice lacking the extracellular matrix protein WARP develop normally but have compromised peripheral nerve structure and function. J Biol Chem 2009 0.84
41 Deficiency of annexins A5 and A6 induces complex changes in the transcriptome of growth plate cartilage but does not inhibit the induction of mineralization. J Bone Miner Res 2010 0.83
42 Nonsense-mediated mRNA decay of collagen -emerging complexity in RNA surveillance mechanisms. J Cell Sci 2013 0.83
43 MT1-MMP-dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: regulation by fibrillar collagen. Exp Cell Res 2002 0.82
44 Proteomics makes progress in cartilage and arthritis research. Matrix Biol 2009 0.82
45 Comparative proteomic analysis of normal and collagen IX null mouse cartilage reveals altered extracellular matrix composition and novel components of the collagen IX interactome. J Biol Chem 2013 0.81
46 Sorting of growth plate chondrocytes allows the isolation and characterization of cells of a defined differentiation status. J Bone Miner Res 2010 0.81
47 bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1. PLoS One 2013 0.80
48 Intracellular trafficking and degradation of unassociated proalpha2 chains of collagen type I. Exp Cell Res 2004 0.80
49 WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes. PLoS One 2012 0.80
50 Maintaining mRNA integrity during decalcification of mineralized tissues. PLoS One 2013 0.78
51 Is there an evolutionary relationship between WARP (von Willebrand factor A-domain-related protein) and the FACIT and FACIT-like collagens? FEBS Lett 2003 0.78
52 Familial digital arthropathy-brachydactyly. Am J Med Genet 2002 0.78
53 Cartilage proteomics: Challenges, solutions and recent advances. Proteomics Clin Appl 2008 0.77
54 1H NMR spectroscopy of serum reveals unique metabolic fingerprints associated with subtypes of surgically induced osteoarthritis in sheep. J Proteome Res 2012 0.77
55 Molecular diagnosis in a pregnancy at risk for both spondyloepiphyseal dysplasia congenita and achondroplasia. Prenat Diagn 2003 0.75