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Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies

The FEBS journal, 2013-09, Vol.280 (17), p.4149-4164

2013

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Calpains, cleaved mini-dysferlinC72, and L-type channels underpin calcium-dependent muscle membrane repair

The Journal of neuroscience, 2013-03, Vol.33 (12), p.5085-5094

2013

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Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factor

Cardiovascular research, 2016-05, Vol.110 (2), p.178-187

2016

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Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans

Nature genetics, 2007-10, Vol.39 (10), p.1261-1265

2007

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Minimal expression of dysferlin prevents development of dysferlinopathy in dysferlin exon 40a knockout mice

Acta neuropathologica communications, 2023-01, Vol.11 (1), p.15-15, Article 15

2023

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The Murine Stanniocalcin 2 Gene Is a Negative Regulator of Postnatal Growth

Endocrinology (Philadelphia), 2008-05, Vol.149 (5), p.2403-2410

2008

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Loss of calpains-1 and -2 prevents repair of plasma membrane scrape injuries, but not small pores, and induces a severe muscular dystrophy

American Journal of Physiology: Cell Physiology, 2020-06, Vol.318 (6), p.C1226-C1237

2020

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Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling

Cellular signalling, 2017-05, Vol.33, p.30-40

2017

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Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch

Journal of neuropathology and experimental neurology, 2011-04, Vol.70 (4), p.302-313

2011

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Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy

Brain (London, England : 1878), 2011-12, Vol.134 (12), p.3513-3526

2011

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Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development

Gene Expression Patterns, 2007-02, Vol.7 (4), p.396-404

2007

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Membrane lymphotoxin contributes to anti‐leishmanial immunity by controlling structural integrity of lymphoid organs

European journal of immunology, 2002-07, Vol.32 (7), p.1993-2003

2002

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Characterisation of a P140K mutant O 6 ‐methylguanine‐DNA‐methyltransferase (MGMT)‐expressing transgenic mouse line with drug‐selectable bone marrow

The journal of gene medicine, 2006-09, Vol.8 (9), p.1071-1085

2006

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Characterisation of a P140K mutant O6-methylguanine-DNA-methyltransferase (MGMT)-expressing transgenic mouse line with drug-selectable bone marrow

The journal of gene medicine, 2006-09, Vol.8 (9), p.1071-1085

2006

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Unimpaired Autoreactive T-Cell Traffic Within the Central Nervous System During Tumor Necrosis Factor Receptor-Mediated inhibition of Experimental Autoimmune Encephalomyelitis

Proceedings of the National Academy of Sciences - PNAS, 1995-11, Vol.92 (24), p.11066-11070

1995

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Calpains, Cleaved Mini-Dysferlin C72 , and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair

The Journal of neuroscience, 2013-03, Vol.33 (12), p.5085-5094

2013

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Microglia induce CD4 T lymphocyte final effector function and death

The Journal of experimental medicine, 1996-11, Vol.184 (5), p.1737-1745

1996

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Distinct roles for lymphotoxin‐α and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue

European journal of immunology, 1997-10, Vol.27 (10), p.2600-2609

1997

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Critical points of tumor necrosis factor action in central nervous system autoimmune inflammation defined by gene targeting

The Journal of experimental medicine, 1997-11, Vol.186 (9), p.1585-1590

1997

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Challenging cytokine redundancy: inflammatory cell movement and clinical course of experimental autoimmune encephalomyelitis are normal in lymphotoxin-deficient, but not tumor necrosis factor-deficient, mice

The Journal of experimental medicine, 1998-05, Vol.187 (9), p.1517-1528

1998

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Tumor necrosis factor blockade in actively induced experimental autoimmune encephalomyelitis prevents clinical disease despite activated T cell infiltration to the central nervous system

European journal of immunology, 1997-08, Vol.27 (8), p.1973-1981

1997

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Characterisation of a P140K mutant O6-methylguanine-DNA

The journal of gene medicine, 2006-09, Vol.8 (9), p.1071-1085

2006

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Gene targeting in C57BL/6 ES cells. Successful germ line transmission using recipient BALB/c blastocysts developmentally matured in vitro

Nucleic acids research, 1997-02, Vol.25 (4), p.917

1997

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Generation of splenic follicular structure and B cell movement in tumor necrosis factor-deficient mice

The Journal of experimental medicine, 1998-10, Vol.188 (8), p.1503-1510

1998

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Negative Autoregulation of GTF2IRD1 in Williams-Beuren Syndrome via a Novel DNA Binding Mechanism

The Journal of biological chemistry, 2010-02, Vol.285 (7), p.4715-4724

2010

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Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies

Calpains, cleaved mini-dysferlinC72, and L-type channels underpin calcium-dependent muscle membrane repair

Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factor

Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans

Minimal expression of dysferlin prevents development of dysferlinopathy in dysferlin exon 40a knockout mice

The Murine Stanniocalcin 2 Gene Is a Negative Regulator of Postnatal Growth

Loss of calpains-1 and -2 prevents repair of plasma membrane scrape injuries, but not small pores, and induces a severe muscular dystrophy

Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling

Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch

Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy

Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development

Membrane lymphotoxin contributes to anti‐leishmanial immunity by controlling structural integrity of lymphoid organs

Characterisation of a P140K mutant O 6 ‐methylguanine‐DNA‐methyltransferase (MGMT)‐expressing transgenic mouse line with drug‐selectable bone marrow

Characterisation of a P140K mutant O6-methylguanine-DNA-methyltransferase (MGMT)-expressing transgenic mouse line with drug-selectable bone marrow

Unimpaired Autoreactive T-Cell Traffic Within the Central Nervous System During Tumor Necrosis Factor Receptor-Mediated inhibition of Experimental Autoimmune Encephalomyelitis

Calpains, Cleaved Mini-Dysferlin C72 , and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair

Microglia induce CD4 T lymphocyte final effector function and death

Distinct roles for lymphotoxin‐α and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue

Critical points of tumor necrosis factor action in central nervous system autoimmune inflammation defined by gene targeting

Challenging cytokine redundancy: inflammatory cell movement and clinical course of experimental autoimmune encephalomyelitis are normal in lymphotoxin-deficient, but not tumor necrosis factor-deficient, mice

Tumor necrosis factor blockade in actively induced experimental autoimmune encephalomyelitis prevents clinical disease despite activated T cell infiltration to the central nervous system

Characterisation of a P140K mutant O6-methylguanine-DNA

Gene targeting in C57BL/6 ES cells. Successful germ line transmission using recipient BALB/c blastocysts developmentally matured in vitro

Generation of splenic follicular structure and B cell movement in tumor necrosis factor-deficient mice

Negative Autoregulation of GTF2IRD1 in Williams-Beuren Syndrome via a Novel DNA Binding Mechanism

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