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Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin

The Journal of pathology, 2005-12, Vol.207 (4), p.436-444

2005

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Time-dependent and tissue-specific accumulation of mtDNA and respiratory chain defects in chronic doxorubicin cardiomyopathy

Circulation (New York, N.Y.), 2003-11, Vol.108 (19), p.2423-2429

2003

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Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4

American journal of human genetics, 2007-07, Vol.81 (1), p.158-164

2007

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The 6‐maleimidocaproyl hydrazone derivative of doxorubicin (DOXO‐EMCH) is superior to free doxorubicin with respect to cardiotoxicity and mitochondrial damage

International journal of cancer, 2007-02, Vol.120 (4), p.927-934

2007

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Evidence of nucleoside analogue reverse transcriptase inhibitor--associated genetic and structural defects of mitochondria in adipose tissue of HIV-infected patients

Journal of acquired immune deficiency syndromes (1999), 2002-02, Vol.29 (2), p.117-121

2002

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p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria

Annals of neurology, 2005-01, Vol.57 (1), p.148-151

2005

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Autosomal recessive rippling muscle disease with homozygous CAV3 mutations

Annals of neurology, 2005-02, Vol.57 (2), p.303-304

2005

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Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation

Human molecular genetics, 2004-09, Vol.13 (18), p.2133-2141

2004

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Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients

Brain (London, England : 1878), 2007-12, Vol.130 (12), p.3250-3264

2007

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Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

Human molecular genetics, 2003-02, Vol.12 (3), p.349-356

2003

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Myogenin (Myf4) upregulation in trans-differentiating fibroblasts from a congenital myopathy with arrest of myogenesis and defects of myotube formation

Anatomy and Embryology, 2006-11, Vol.211 (6), p.639-648

2006

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Axonal Neuropathy and Predominance of Type II Myofibers in Infantile Spinal Muscular Atrophy

Journal of child neurology, 1998-07, Vol.13 (7), p.327-331

1998

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Neonatal type IV glycogen storage disease associated with “null” mutations in glycogen branching enzyme 1

The Journal of pediatrics, 2004-11, Vol.145 (5), p.705-709

2004

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Homozygosity Mapping of a Gene Locus for Primary Ciliary Dyskinesia on Chromosome 5p and Identification of the Heavy Dynein Chain DNAH5 as a Candidate Gene

American journal of respiratory cell and molecular biology, 2000-11, Vol.23 (5), p.696-702

2000

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Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency

Neuromuscular disorders : NMD, 2001-11, Vol.11 (8), p.757-759

2001

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Cytochrome C oxidase deficiency and Long-Chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy

Annals of neurology, 1992-01, Vol.31 (1), p.107-109

1992

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Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

Human molecular genetics, 2004-02, Vol.13 (3), p.363-363

2004

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INTRATHYMIC PATHOGENESIS AND DUAL GENETIC CONTROL OF MYASTHENIA GRAVIS

The Lancet (British edition), 1977-03, Vol.309 (8013), p.678-680

1977

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Abundant minute myotubes in a patient who later developed centronuclear myopathy

Acta neuropathologica, 1998-05, Vol.95 (5), p.547-551

1998

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Thymic nurse cells-Ia-bearing epithelium involved in T-lymphocyte differentiation?

Nature (London), 1980-01, Vol.283 (5745), p.402-404

1980

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Rare combination of Becker muscular dystrophy and Klinefelter's syndrome in one patient

Brain & development (Tokyo. 1979), 1997-07, Vol.19 (5), p.359-361

1997

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IN VITRO SELECTION OF RAT AUTOIMMUNE HELPER T-LYMPHOCYTES SPECIFIC FOR ACETYLCHOLINE RECEPTOR (AChR)

Annals of the New York Academy of Sciences, 1981-12, Vol.377 (1), p.831-832

1981

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EARLY DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY

The Lancet (British edition), 1978-07, Vol.312 (8080), p.105-105

1978

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Prenatal diagnosis of X-linked centronuclear myopathy by linkage analysis

Pediatric research, 1993-02, Vol.33 (2), p.201-204

1993

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X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder

Human genetics, 1993-03, Vol.91 (1), p.51-54

1993

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Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin

Time-dependent and tissue-specific accumulation of mtDNA and respiratory chain defects in chronic doxorubicin cardiomyopathy

Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4

The 6‐maleimidocaproyl hydrazone derivative of doxorubicin (DOXO‐EMCH) is superior to free doxorubicin with respect to cardiotoxicity and mitochondrial damage

Evidence of nucleoside analogue reverse transcriptase inhibitor--associated genetic and structural defects of mitochondria in adipose tissue of HIV-infected patients

p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria

Autosomal recessive rippling muscle disease with homozygous CAV3 mutations

Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

Myogenin (Myf4) upregulation in trans-differentiating fibroblasts from a congenital myopathy with arrest of myogenesis and defects of myotube formation

Axonal Neuropathy and Predominance of Type II Myofibers in Infantile Spinal Muscular Atrophy

Neonatal type IV glycogen storage disease associated with “null” mutations in glycogen branching enzyme 1

Homozygosity Mapping of a Gene Locus for Primary Ciliary Dyskinesia on Chromosome 5p and Identification of the Heavy Dynein Chain DNAH5 as a Candidate Gene

Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency

Cytochrome C oxidase deficiency and Long-Chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

INTRATHYMIC PATHOGENESIS AND DUAL GENETIC CONTROL OF MYASTHENIA GRAVIS

Abundant minute myotubes in a patient who later developed centronuclear myopathy

Thymic nurse cells-Ia-bearing epithelium involved in T-lymphocyte differentiation?

Rare combination of Becker muscular dystrophy and Klinefelter's syndrome in one patient

IN VITRO SELECTION OF RAT AUTOIMMUNE HELPER T-LYMPHOCYTES SPECIFIC FOR ACETYLCHOLINE RECEPTOR (AChR)

EARLY DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY

Prenatal diagnosis of X-linked centronuclear myopathy by linkage analysis

X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder

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