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H2O2 Determination by the I3- Method and by KMnO4 Titration

Analytical chemistry (Washington), 1994-09, Vol.66 (18), p.2921-2925

1994

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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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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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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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Development of a graphite probe calorimeter for absolute clinical dosimetry

Medical physics (Lancaster), 2013-02, Vol.40 (2), p.020701-n/a

2013

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Sci-Sat AM: Radiation Dosimetry and Practical Therapy Solutions - 09: Stability of a water calorimetry system as a primary standard for absorbed dose to water

Medical physics (Lancaster), 2016-08, Vol.43 (8), p.4960-4961

2016

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Development of a graphite probe calorimeter for absolute clinical dosimetry: Development of a graphite probe calorimeter

Medical physics (Lancaster), 2013-01, Vol.40 (2), p.20701

2013

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

Mammalian genome, 2004-06, Vol.15 (6), p.492-502

2004

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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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Reply to Chinnery et al

American journal of human genetics, 1998-12, Vol.63 (6), p.1910-1911

1998

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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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Clinical and Molecular Features of Encephalomyopathy Due to the A3302G Mutation in the Mitochondrial tRNALeu(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

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

1990

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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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H(2)O(2) determination by the I(3)(negative) method and by KMnO(4) titration

Analytical chemistry (Washington), 1994-09, Vol.66 (18), p.2921

1994

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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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Porcine Aorto-Renal Artery (PARA) model for laparoscopic transcystic common bile duct exploration: the evolution of a training model to meet new clinical needs

Langenbeck's archives of surgery, 2021-06, Vol.406 (4), p.1149-1154

2021

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Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta

Journal of medical genetics, 2010-04, Vol.47 (4), p.257-261

2010

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Editorial

Human resource management journal, 2013-01, Vol.23 (1), p.1-2

2013

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Editorial

Human resource management journal, 2013-01, Vol.23 (1), p.1-2

2013

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Editorial

Human resource management journal, 2013-01, Vol.23 (1), p.1-2

2013

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H2O2 Determination by the I3- Method and by KMnO4 Titration

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

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

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

Development of a graphite probe calorimeter for absolute clinical dosimetry

Sci-Sat AM: Radiation Dosimetry and Practical Therapy Solutions - 09: Stability of a water calorimetry system as a primary standard for absorbed dose to water

Development of a graphite probe calorimeter for absolute clinical dosimetry: Development of a graphite probe calorimeter

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?

Reply to Chinnery et al

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

Clinical and Molecular Features of Encephalomyopathy Due to the A3302G Mutation in the Mitochondrial tRNALeu(UUR) Gene

Long term culture of rat soleus muscle in vitro

Duplications of mitochondrial DNA in Kearns-Sayre syndrome

H(2)O(2) determination by the I(3)(negative) method and by KMnO(4) titration

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

An Analytical Framework for Delirium Research in Palliative Care Settings: Integrated Epidemiologic, Clinician-Researcher, and Knowledge User Perspectives

Porcine Aorto-Renal Artery (PARA) model for laparoscopic transcystic common bile duct exploration: the evolution of a training model to meet new clinical needs

Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta

Editorial

Editorial

Editorial

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