M. Chiotis

发表

Functional respiratory chain analyses in murid xenomitochondrial cybrids expose coevolutionary constraints of cytochrome b and nuclear subunits of complex III.

C. Pinkert, I. Trounce, M. McKenzie, 2003, Molecular biology and evolution.

Limb–girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis

D. MacArthur, K. North, J. Seto, 2008, Neuromuscular Disorders.

Chemical cleavage of mismatch (CCM) to locate base mismatches in heteroduplex DNA

T. Tabone, R. Cotton, M. Chiotis, 2006, Nature Protocols.

Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection

S. Collins, J. Chin, P. Mckelvie, 2009, Journal of Clinical Neuroscience.

Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysis

D. Kirby, S. Collins, J. Chin, 2011, Journal of Clinical Neuroscience.

Chapter 3 – Enzymatic and Chemical Cleavage Methods to Identify Genetic Variation

A. Godwin, R. Cotton, E. Nicolas, 2010 .

Detection rates and phenotypic spectrum of m.3243A>G in the MT-TL1 gene: a molecular diagnostic laboratory perspective.

S. Collins, J. Chin, R. Marotta, 2014, Mitochondrion.

Capture of Somatic mtDNA Point Mutations with Severe Effects on Oxidative Phosphorylation in Synaptosome Cybrid Clones from Human Brain

R. Cotton, I. Trounce, M. McKenzie, 2014, Human Mutation.

Molecular Evidence for a Jurassic Origin of Ants

R. Crozier, L. Jermiin, M. Chiotis, 1997, Naturwissenschaften.

Long-term screening for primary mitochondrial DNA variants associated with Leber Hereditary Optic Neuropathy: incidence, penetrance and clinical features.

S. Collins, J. Chin, N. Shuey, 2020, Mitochondrion.

A molecular framework for the phylogeny of the ant subfamily dolichoderinae.

R. Crozier, L. Jermiin, M. Chiotis, 2000, Molecular phylogenetics and evolution.