List of works - Martin John Barron

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy

scientific article published in May 2003

A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta

scientific article

Aged human skin accumulates mast cells with altered functionality which localise to macrophage and VIP nerve fibres

scientific article published on 06 December 2018

Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress ⬇️

scientific article

Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy.

scientific article

Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts

scientific article

Differences in the accumulation of mitochondrial defects with age in mice and humans

scientific article published on 12 October 2011

Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate ⬇️

scientific article

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions

scientific article published on 3 November 2006

Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptors

scientific article published on 15 October 2014

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

scientific article published in April 2004

Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutation.

scientific article

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

scientific article

Is the 32-kDa fragment the functional enamelin unit in all species?

scientific article

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

scientific article

Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission.

scholarly article

Mitochondrial DNA mutations in human colonic crypt stem cells

scientific article published on November 2003

Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta

scientific article

Novel mutations in GJA1 cause oculodentodigital syndrome

scientific article published on November 2008

Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations

scientific article published on 28 June 2012

The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice

scientific journal article

The diagnosis of mitochondrial muscle disease.

scientific article published on April 2004

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

scientific article

List of works by Martin John Barron

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy

A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta

Aged human skin accumulates mast cells with altered functionality which localise to macrophage and VIP nerve fibres

Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress ⬇️

Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy.

Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts

Differences in the accumulation of mitochondrial defects with age in mice and humans

Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate ⬇️

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions

Entry mechanisms of herpes simplex virus 1 into murine epidermis: involvement of nectin-1 and herpesvirus entry mediator as cellular receptors

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutation.

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

Is the 32-kDa fragment the functional enamelin unit in all species?

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission.

Mitochondrial DNA mutations in human colonic crypt stem cells

Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta

Novel mutations in GJA1 cause oculodentodigital syndrome

Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations

The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice

The diagnosis of mitochondrial muscle disease.

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome