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Transmitochondrial mice carrying resistance to chloramphenicol on mitochondrial DNA: Developing the first mouse model of mitochondrial DNA disease

Nature medicine, 1999-08, Vol.5 (8), p.957-960

1999

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Mutations at the mitochondrial DNA polymerase ( POLG ) locus associated with male infertility

Nature genetics, 2001-11, Vol.29 (3), p.261-262

2001

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Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications

Reproduction (Cambridge, England), 2002-06, Vol.123 (6), p.751-755

2002

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Mosaicism for mitochondrial DNA polymorphic variants in placenta has implications for the feasibility of prenatal diagnosis in mtDNA diseases

European journal of human genetics : EJHG, 2006-07, Vol.14 (7), p.816-823

2006

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Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases

Neuromuscular disorders : NMD, 2000-10, Vol.10 (7), p.484-487

2000

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Do Sequence Variants in the Major Non-Coding Region of the Mitochondrial Genome Influence Mitochondrial Mutations Associated with Disease?

Human molecular genetics, 1996-04, Vol.5 (4), p.473-479

1996

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Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene

Archives of neurology (Chicago), 2005-12, Vol.62 (12), p.1920

2005

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Long term culture of rat soleus muscle in vitro: Its effects on glucose utilization and insulin sensitivity

FEBS letters, 1990-10, Vol.273 (1-2), p.91-94

1990

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Regulation of hepatic tyrosine aminotransferase in genetically obese rats

Biochimica et biophysica acta, 1983-04, Vol.756 (3), p.297-307

1983

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Stereocontrolled synthesis of novel enantiomerically pure sulfides and selenides from (+)-camphor and (+)-camphor-10-sulfonyl chloride

Tetrahedron, 1999-07, Vol.55 (31), p.9611-9622

1999

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Duplications of mitochondrial DNA in Kearns-Sayre syndrome

Muscle & nerve, 1995, Vol.18 (S14), p.S154-S158

1995

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Transmitochondrial mice carrying resistance to chloramphenicol on mitochondrial DNA: Developing the first mouse model of mitochondrial DNA disease

Mutations at the mitochondrial DNA polymerase ( POLG ) locus associated with male infertility

Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications

Mosaicism for mitochondrial DNA polymorphic variants in placenta has implications for the feasibility of prenatal diagnosis in mtDNA diseases

Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases

A prevalent POLG CAG microsatellite length allele in humans and African great apes

Do Sequence Variants in the Major Non-Coding Region of the Mitochondrial Genome Influence Mitochondrial Mutations Associated with Disease?

Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene

Long term culture of rat soleus muscle in vitro: Its effects on glucose utilization and insulin sensitivity

Regulation of hepatic tyrosine aminotransferase in genetically obese rats

Stereocontrolled synthesis of novel enantiomerically pure sulfides and selenides from (+)-camphor and (+)-camphor-10-sulfonyl chloride

Duplications of mitochondrial DNA in Kearns-Sayre syndrome

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