Citation Impact
Citing Papers
Host Defenses against Copper Toxicity
1990
Animal mitochondrial genomes
1999 Standout
Mitochondria and Ageing
1992
Inclusion body myositis and myopathies
1995 Standout
Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase
1995 Standout
The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages
1993
Cytochrome c Oxidase and the Regulation of Oxidative Phosphorylation
2001
The biochemical basis of mitochondrial diseases
1988
Genetic associations with human longevity at the APOE and ACE loci
1994 Standout
Copper-associated liver disease in childhood
1995
Progressive loss of cytochrome c oxidase in the human extraocular muscles in ageing — a cytochemical-immunohistochemical study
1992
ATP synthase from bovine mitochondria: complementary DNA sequence of the import precursor of a heart isoform of the .alpha. subunit
1989 StandoutNobel
Reactive oxygen and DNA damage in mitochondria
1992
Premature ageing in mice expressing defective mitochondrial DNA polymerase
2004 StandoutNature
Copper toxicity, oxidative stress, and antioxidant nutrients
2003 Standout
Idiopathic copper toxicosis
1998
Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR
1992
Mitochondrial DNA mutations in human diseases: a review
1992
Oxidative damage to mitochondrial DNA and its relationship to ageing
1995
Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies
1991
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Two bovine genes for mitochondrial ADP/ATP translocase expressed differently in various tissues
1989 StandoutNobel
DNA sequences of two expressed nuclear genes for human mitochondrial ADP/ATP translocase
1989 StandoutNobel
Determination of the structures of respiratory enzyme complexes from mammalian mitochondria
1995 StandoutNobel
Lipid metabolism in Zellweger's syndrome
1989
Mitochondria, Oxidants, and Aging
2005 Standout
The molecular basis of copper-transport diseases
2001
Wilson disease and idiopathic copper toxicosis
1996
Cytochrome c oxidase deficient fibres in the limb muscle and diaphragm of man without muscular disease: An age-related alteration
1990
The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains
1992 StandoutNobel
Understanding the Odd Science of Aging
2005 Standout
Clinical features of melas and mitochondrial DNA mutations
1995
Metabolism of highly unsaturated n-3 and n-6 fatty acids
2000 Standout
Pyrrolizidine alkaloids in food: a spectrum of potential health consequences
2011
Recent developments in the molecular genetics of mitochondrial disorders
1998
PPARγ Is Required for Placental, Cardiac, and Adipose Tissue Development
1999 Standout
A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
1990 StandoutNature
Superoxide dismutases of muscle in mitochondrial encephalomyopathies
1995
Is non-Indian childhood cirrhosis caused by excess dietary copper?
1994
The growing use of herbal medicines: issues relating to adverse reactions and challenges in monitoring safety
2014 Standout
Mitochondrial myopathies
1984
Oxidative damage and mitochondrial decay in aging.
1994 Standout
Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
1989
The Free Radical Theory of Aging Matures
1998 Standout
Toxic effects of metals
1991 Standout
Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study.
1989
Muscle Diseases: The Muscular Dystrophies
2007
Present interpretation of the role of copper in Indian childhood cirrhosis
1996
The cerebro‐hepato‐renal (Zellweger) syndrome: Prenatal detection based on impaired biosynthesis of plasmalogens
1985
Mitochondrial Diseases in Man and Mouse
1999 StandoutScience
Mitochondrial myopathies
1985
Fluorescent Sensors for Measuring Metal Ions in Living Systems
2014 Standout
Role of copper in Indian childhood cirrhosis
1998
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
1988
Isolation and properties of cytochrome c oxidase from rat liver and quantification of immunological differences between isozymes from various rat tissues with subunit-specific antisera
1985
Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System
2001 Standout
Mitochondrial Dysfunction and Type 2 Diabetes
2005 StandoutScience
Genetic Dissection of Complex Traits
1994 StandoutScience
The development of mitochondrial medicine.
1994
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Long term survival in Indian childhood cirrhosis treated with D-penicillamine.
1996
Prospects for the genetics of human longevity
1993
Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer
1996 Standout
A new locus for hemiplegic migraine maps to chromosome 1q31
1997
Works of J. M�ller-H�cker being referenced
A specific point mutation in the mitochondrial genome of Caucasians with MELAS
1991
Variable reduction of caveolin-3 in patients with LGMD2B/MM
2003
Mutations of mitochondrial DNA and human death
1990
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes
1990
Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome
1984
Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia
1983
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine
1982
Fatal copper storage disease of the liver in a German infant resembling Indian childhood cirrhosis
1987