Lista de obras - John F. Bateman - Dominio Público Uruguay

1H NMR spectroscopy of serum reveals unique metabolic fingerprints associated with subtypes of surgically induced osteoarthritis in sheep

artículo científico publicado en 2012

A [4,5-3H]lysine:[14C]lysine dual-label method to measure lysine hydroxylation in collagen

artículo científico publicado en 1986

A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats.

artículo científico publicado en 2016

A microarray approach for comparative expression profiling of the discrete maturation zones of mouse growth plate cartilage.

artículo científico publicado en 2008

A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

artículo científico publicado en 2014

A robust method for proteomic characterization of mouse cartilage using solubility-based sequential fractionation and two-dimensional gel electrophoresis

artículo científico publicado en 2008

ADAMTS-1-knockout mice do not exhibit abnormalities in aggrecan turnover in vitro or in vivo

artículo científico publicado en 2005

Ablation of the miRNA Cluster 24 Has Profound Effects on Extracellular Matrix Protein Abundance in Cartilage

scientific article published on 09 June 2020

Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion

artículo científico publicado en 1999

Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research

artículo científico publicado en 2015

Bulldog dwarfism in Dexter cattle is caused by mutations in ACAN.

artículo científico publicado en 2007

Cartilage intermediate layer protein 2 (CILP-2) is expressed in articular and meniscal cartilage and down-regulated in experimental osteoarthritis.

artículo científico publicado en 2011

Cartilage microRNA dysregulation during the onset and progression of mouse osteoarthritis is independent of aggrecanolysis and overlaps with candidates from end-stage human disease.

artículo científico publicado en 2017

Cartilage proteomics: Challenges, solutions and recent advances ⬇️

artículo científico publicado el 1 de febrero de 2008

Cartilage-specific ablation of XBP1 signaling in mouse results in a chondrodysplasia characterized by reduced chondrocyte proliferation and delayed cartilage maturation and mineralization

artículo científico publicado en 2015

Catabolic cytokines disrupt the circadian clock and the expression of clock-controlled genes in cartilage via an NFкB-dependent pathway.

artículo científico publicado en 2015

Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome

scientific journal article

Changes in the chondrocyte and extracellular matrix proteome during post-natal mouse cartilage development

artículo científico publicado en 2011

Chemical cleavage method for the detection of RNA base changes: experience in the application to collagen mutations in osteogenesis imperfecta

artículo científico publicado en 1993

Clinical phenotypes associated with type II collagen mutations

artículo científico publicado en 2011

Collagen II is essential for the removal of the notochord and the formation of intervertebral discs

scientific journal article

Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells

artículo científico publicado en 2002

Collagen protein abnormalities produced by site-directed mutagenesis of the pro alpha 1(I) gene

scientific article published on 01 January 1989

Comparative proteomic analysis of normal and collagen IX null mouse cartilage reveals altered extracellular matrix composition and novel components of the collagen IX interactome.

artículo científico publicado en 2013

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

artículo científico publicado en 2008

Comprehensive analysis of collagen metabolism in vitro using [4(3H)]/[14C]proline dual-labeling and polyacrylamide gel electrophoresis

scientific article published on 01 January 1988

Comprehensive profiling of cartilage extracellular matrix formation and maturation using sequential extraction and label-free quantitative proteomics

artículo científico publicado en 2010

Correlation of clinical and molecular biological abnormalities in osteogenesis imperfecta

artículo científico publicado en 1989

Deficiency of annexins A5 and A6 induces complex changes in the transcriptome of growth plate cartilage but does not inhibit the induction of mineralization

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Deposition and selective degradation of structurally-abnormal type I collagen in a collagen matrix produced by osteogenesis imperfecta fibroblasts in vitro

artículo científico publicado en 1994

Detection and localization of base changes in RNA using a chemical cleavage method

artículo científico publicado en 1989

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome

artículo científico publicado en 1995

Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy

scientific article published on 24 November 2004

Effect of rapamycin on bone mass and strength in the α2(I)-G610C mouse model of osteogenesis imperfecta.

artículo científico publicado en 2018

Effects of relaxin, pregnancy and parturition on collagen metabolism in the rat pubic symphysis

scientific article published on 01 October 1998

Employing molecular genetics of chondrodysplasias to inform the study of osteoarthritis

scientific article published on February 2009

Epitope specificity of antibodies to type II collagen in rheumatoid arthritis and systemic lupus erythematosus

artículo científico publicado en 1992

Familial digital arthropathy-brachydactyly

artículo científico publicado en 2002

Formation of proline metabolites in chick embryo bone: interference with the measurement of free hydroxyproline by ion-exchange chromatography

artículo científico publicado en 1982

Gelatinase A (MMP-2) activation by skin fibroblasts: dependence on MT1-MMP expression and fibrillar collagen form

artículo científico publicado en 2001

Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing

artículo científico publicado en 2019

Generation of a heterozygous COL1A1 (c.3969_3970insT) osteogenesis imperfecta mutation human iPSC line, MCRIi001-A-1, using CRISPR/Cas9 editing

scientific article published on 23 April 2019

Genetic Disorders of the Extracellular Matrix

scientific article published on 15 February 2019

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations

artículo científico publicado en 2009

Genomic sequence of mouse COL1A1 encoding the collagen propeptides

artículo científico publicado en 1993

Gingival fibromatosis and Klippel-Trénaunay-Weber syndrome. Case report

scientific article published on 01 May 1995

Global comparative transcriptome analysis of cartilage formation in vivo

artículo científico publicado en 2009

Heterogeneity in dermatosparaxis is shown by contraction of collagen gels

artículo científico publicado en 1991

Human cells unable to express decoron produced disorganized extracellular matrix lacking "shape modules" (interfibrillar proteoglycan bridges).

artículo científico publicado en 1998

Identification of TGFβ-related genes regulated in murine osteoarthritis and chondrocyte hypertrophy by comparison of multiple microarray datasets

artículo científico publicado en 2018

Identification of Two Independent COL5A1 Variants in Dogs with Ehlers-Danlos Syndrome

artículo científico publicado en 2019

Identification of the skeletal progenitor cells forming osteophytes in osteoarthritis

scientific article published on 22 September 2020

In vitro expression analysis of collagen biosynthesis and assembly

artículo científico publicado en 1997

In vivo cellular adaptation to ER stress: survival strategies with double-edged consequences

artículo científico publicado en 2010

Increased chondrocyte sclerostin may protect against cartilage degradation in osteoarthritis

artículo científico publicado en 2011

Interaction of collagen alpha1(X) containing engineered NC1 mutations with normal alpha1(X) in vitro. Implications for the molecular basis of schmid metaphyseal chondrodysplasia

artículo científico publicado en 1999

Introduction of the human pro alpha 1(I) collagen gene into pro alpha 1(I)-deficient Mov-13 mouse cells leads to formation of functional mouse-human hybrid type I collagen

artículo científico publicado en 1987

Is there an evolutionary relationship between WARP (von Willebrand factor A-domain-related protein) and the FACIT and FACIT-like collagens?

artículo científico publicado en 2003

Isolated Anxa5+/Sca-1+ perivascular cells from mouse meningeal vasculature retain their perivascular phenotype in vitro and in vivo

artículo científico publicado en 2007

Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations

artículo científico publicado en 2001

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

artículo científico publicado en 1992

MT1-MMP-dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: regulation by fibrillar collagen

artículo científico publicado en 2002

Maintaining mRNA integrity during decalcification of mineralized tissues

artículo científico publicado en 2013

Mammalian skeletogenesis and extracellular matrix: what can we learn from knockout mice?

artículo científico publicado en 2000

Matrix deposition by a calcifying human osteogenic sarcoma cell line (SAOS-2)

artículo científico publicado en 1995

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

artículo científico publicado en 2005

Molecular consequences of dominant Bethlem myopathy collagen VI mutations

article

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

artículo científico publicado en 1996

Mutations in TRPV4 cause an inherited arthropathy of hands and feet.

artículo científico publicado en 2011

Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia

artículo científico publicado en 2009

Mutations of COL10A1 in Schmid metaphyseal chondrodysplasia

artículo científico publicado en 2005

Novel Elements of the Chondrocyte Stress Response Identified Using an in Vitro Model of Mouse Cartilage Degradation

artículo científico publicado en 2016

Osteogenic capacity of collagen in repair of established periodontal defects

artículo científico publicado en 1992

Ovine skin collagen dysplasia

artículo científico publicado en 1982

Precipitation of collagens by polyethylene glycols

scientific article published on 01 September 1984

Premature arthritis is a distinct type II collagen phenotype.

scientific article published on May 2010

Proteasomal degradation of unassembled mutant type I collagen pro-alpha1(I) chains

artículo científico publicado en 1999

Proteomic analysis of mouse growth plate cartilage

scientific article published on 01 December 2006

Proteomic characterization of mouse cartilage degradation in vitro

artículo científico publicado en 2008

Proteomics makes progress in cartilage and arthritis research

artículo científico publicado en 2009

Rapid fractionation of collagen chains and peptides by high-performance liquid chromatography

scientific article published on 01 April 1986

Recurrent Dominant Mutations Affecting Two Adjacent Residues in the Motor Domain of the Monomeric Kinesin KIF22 Result in Skeletal Dysplasia and Joint Laxity

artículo científico publicado en 2012

Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity

artículo científico publicado en 2011

Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiency

artículo científico publicado en 1998

Regulation of alkaline phosphatase expression in a neonatal rat clonal calvarial cell strain by retinoic acid

artículo científico publicado en 1988

Reliable and sensitive detection of premature termination mutations using a protein truncation test designed to overcome problems of nonsense-mediated mRNA instability

artículo científico publicado en 1999

S100A8 and S100A9 in experimental osteoarthritis.

artículo científico publicado en 2010

Sorting of growth plate chondrocytes allows the isolation and characterization of cells of a defined differentiation status

artículo científico publicado en 2010

Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and function

artículo científico publicado en 2007

Targeted induction of endoplasmic reticulum stress induces cartilage pathology

artículo científico publicado en 2009

The N-terminal N5 subdomain of the alpha 3(VI) chain is important for collagen VI microfibril formation

scientific article published on 01 January 2001

The circadian clock in murine chondrocytes regulates genes controlling key aspects of cartilage homeostasis

artículo científico publicado en 2013

The effect of relaxin on collagen metabolism in the nonpregnant rat pubic symphysis: the influence of estrogen and progesterone in regulating relaxin activity

scientific article published on 01 September 1996

The extracellular matrix protein WARP is a novel component of a distinct subset of basement membranes

scientific journal article

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

artículo científico publicado en 2001

The intervertebral disc contains intrinsic circadian clocks that are regulated by age and cytokines and linked to degeneration

artículo científico publicado en 2016

The study of collagen structure and function by site-directed mutagenesis of collagen genes

artículo científico publicado en 1990

The use of simultaneous reprogramming and gene correction to generate an osteogenesis imperfecta patient COL1A1 c. 3936 G>T iPSC line and an isogenic control iPSC line

scientific article published on 04 May 2019

Tissue-specific RNA surveillance? Nonsense-mediated mRNA decay causes collagen X haploinsufficiency in Schmid metaphyseal chondrodysplasia cartilage

artículo científico publicado en 2003

Transcriptional profiling of chondrodysplasia growth plate cartilage reveals adaptive ER-stress networks that allow survival but disrupt hypertrophy

artículo científico publicado en 2011

Transcriptomics of wild-type mice and mice lacking ADAMTS-5 activity identifies genes involved in osteoarthritis initiation and cartilage destruction.

artículo científico publicado en 2013

UNCL, the mammalian homologue of UNC-50, is an inner nuclear membrane RNA-binding protein

scientific journal article

Utility of circulating serum miRNAs as biomarkers of early cartilage degeneration in animal models of post-traumatic osteoarthritis and inflammatory arthritis

artículo científico publicado en 2016

WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes

artículo científico publicado en 2012

WARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteins

scientific journal article

Why mice have lost genes for COL21A1, STK17A, GPR145 and AHRI: evidence for gene deletion at evolutionary breakpoints in the rodent lineage

scientific article published on 01 September 2004

XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease

scientific article published on 01 July 2019

XBP1-Independent UPR Pathways Suppress C/EBP-β Mediated Chondrocyte Differentiation in ER-Stress Related Skeletal Disease

artículo científico publicado en 2015

bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1

artículo científico publicado en 2013

Lista de obras de John F. Bateman

1H NMR spectroscopy of serum reveals unique metabolic fingerprints associated with subtypes of surgically induced osteoarthritis in sheep

A [4,5-3H]lysine:[14C]lysine dual-label method to measure lysine hydroxylation in collagen

A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats.

A microarray approach for comparative expression profiling of the discrete maturation zones of mouse growth plate cartilage.

A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.

A robust method for proteomic characterization of mouse cartilage using solubility-based sequential fractionation and two-dimensional gel electrophoresis

ADAMTS-1-knockout mice do not exhibit abnormalities in aggrecan turnover in vitro or in vivo

Ablation of the miRNA Cluster 24 Has Profound Effects on Extracellular Matrix Protein Abundance in Cartilage

Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion

Breeding Strategy Determines Rupture Incidence in Post-Infarct Healing WARPing Cardiovascular Research

Bulldog dwarfism in Dexter cattle is caused by mutations in ACAN.

Cartilage intermediate layer protein 2 (CILP-2) is expressed in articular and meniscal cartilage and down-regulated in experimental osteoarthritis.

Cartilage microRNA dysregulation during the onset and progression of mouse osteoarthritis is independent of aggrecanolysis and overlaps with candidates from end-stage human disease.

Cartilage proteomics: Challenges, solutions and recent advances ⬇️

Cartilage-specific ablation of XBP1 signaling in mouse results in a chondrodysplasia characterized by reduced chondrocyte proliferation and delayed cartilage maturation and mineralization

Catabolic cytokines disrupt the circadian clock and the expression of clock-controlled genes in cartilage via an NFкB-dependent pathway.

Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome

Changes in the chondrocyte and extracellular matrix proteome during post-natal mouse cartilage development

Chemical cleavage method for the detection of RNA base changes: experience in the application to collagen mutations in osteogenesis imperfecta

Clinical phenotypes associated with type II collagen mutations

Collagen II is essential for the removal of the notochord and the formation of intervertebral discs

Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity

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

Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells

Collagen protein abnormalities produced by site-directed mutagenesis of the pro alpha 1(I) gene

Comparative proteomic analysis of normal and collagen IX null mouse cartilage reveals altered extracellular matrix composition and novel components of the collagen IX interactome.

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

Comprehensive analysis of collagen metabolism in vitro using [4(3H)]/[14C]proline dual-labeling and polyacrylamide gel electrophoresis

Comprehensive profiling of cartilage extracellular matrix formation and maturation using sequential extraction and label-free quantitative proteomics

Correlation of clinical and molecular biological abnormalities in osteogenesis imperfecta

Deficiency of annexins A5 and A6 induces complex changes in the transcriptome of growth plate cartilage but does not inhibit the induction of mineralization

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

Deposition and selective degradation of structurally-abnormal type I collagen in a collagen matrix produced by osteogenesis imperfecta fibroblasts in vitro

Detection and localization of base changes in RNA using a chemical cleavage method

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome

Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy

Effect of rapamycin on bone mass and strength in the α2(I)-G610C mouse model of osteogenesis imperfecta.

Effects of relaxin, pregnancy and parturition on collagen metabolism in the rat pubic symphysis

Employing molecular genetics of chondrodysplasias to inform the study of osteoarthritis

Epitope specificity of antibodies to type II collagen in rheumatoid arthritis and systemic lupus erythematosus

Familial digital arthropathy-brachydactyly

Formation of proline metabolites in chick embryo bone: interference with the measurement of free hydroxyproline by ion-exchange chromatography

Gelatinase A (MMP-2) activation by skin fibroblasts: dependence on MT1-MMP expression and fibrillar collagen form

Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing

Generation of a heterozygous COL1A1 (c.3969_3970insT) osteogenesis imperfecta mutation human iPSC line, MCRIi001-A-1, using CRISPR/Cas9 editing

Genetic Disorders of the Extracellular Matrix

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations

Genomic sequence of mouse COL1A1 encoding the collagen propeptides

Gingival fibromatosis and Klippel-Trénaunay-Weber syndrome. Case report

Global comparative transcriptome analysis of cartilage formation in vivo

Heterogeneity in dermatosparaxis is shown by contraction of collagen gels

Human cells unable to express decoron produced disorganized extracellular matrix lacking "shape modules" (interfibrillar proteoglycan bridges).

Identification of TGFβ-related genes regulated in murine osteoarthritis and chondrocyte hypertrophy by comparison of multiple microarray datasets

Identification of Two Independent COL5A1 Variants in Dogs with Ehlers-Danlos Syndrome

Identification of the skeletal progenitor cells forming osteophytes in osteoarthritis

In vitro expression analysis of collagen biosynthesis and assembly

In vivo cellular adaptation to ER stress: survival strategies with double-edged consequences

Increased chondrocyte sclerostin may protect against cartilage degradation in osteoarthritis

Interaction of collagen alpha1(X) containing engineered NC1 mutations with normal alpha1(X) in vitro. Implications for the molecular basis of schmid metaphyseal chondrodysplasia

Introduction of the human pro alpha 1(I) collagen gene into pro alpha 1(I)-deficient Mov-13 mouse cells leads to formation of functional mouse-human hybrid type I collagen

Is there an evolutionary relationship between WARP (von Willebrand factor A-domain-related protein) and the FACIT and FACIT-like collagens?

Isolated Anxa5+/Sca-1+ perivascular cells from mouse meningeal vasculature retain their perivascular phenotype in vitro and in vivo

Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations

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

MT1-MMP-dependent and -independent regulation of gelatinase A activation in long-term, ascorbate-treated fibroblast cultures: regulation by fibrillar collagen

Maintaining mRNA integrity during decalcification of mineralized tissues

Mammalian skeletogenesis and extracellular matrix: what can we learn from knockout mice?

Matrix deposition by a calcifying human osteogenic sarcoma cell line (SAOS-2)

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

Molecular consequences of dominant Bethlem myopathy collagen VI mutations

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

Mutations in TRPV4 cause an inherited arthropathy of hands and feet.

Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia

Mutations of COL10A1 in Schmid metaphyseal chondrodysplasia

Novel Elements of the Chondrocyte Stress Response Identified Using an in Vitro Model of Mouse Cartilage Degradation

Osteogenic capacity of collagen in repair of established periodontal defects

Ovine skin collagen dysplasia

Precipitation of collagens by polyethylene glycols

Premature arthritis is a distinct type II collagen phenotype.