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Calcium signalling-dependent mitochondrial dysfunction and bioenergetics regulation in respiratory chain Complex II deficiency

Cell death and differentiation, 2010-12, Vol.17 (12), p.1855-1866

2010

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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

Nature genetics, 2001-09, Vol.29 (1), p.57-60

2001

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Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria

Molecular genetics and metabolism, 2008-09, Vol.95 (1), p.107-109

2008

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Structural changes at microtubule ends accompanying GTP hydrolysis: Information from a slowly hydrolyzable analogue of GTP, guanylyl (α,β)methylenediphosphonate

Proceedings of the National Academy of Sciences - PNAS, 1998-03, Vol.95 (7), p.3661-3666

1998

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Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo‐obstruction

Neurogastroenterology and motility, 2011-01, Vol.23 (1), p.24-e1

2011

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Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis

Molecular genetics and metabolism, 2015-03, Vol.2 (C), p.25-31

2015

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Variable outcome of growth hormone administration in respiratory chain deficiency

Molecular genetics and metabolism, 2008-02, Vol.93 (2), p.195-199

2008

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Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B12

Journal of inherited metabolic disease, 2009, Vol.32 (2), p.159-162

2009

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Structural Changes Accompanying GTP Hydrolysis in Microtubules: Information from a Slowly Hydrolyzable Analogue Guanylyl-(α,β)-Methylene-Diphosphonate

The Journal of cell biology, 1995-01, Vol.128 (1/2), p.117-125

1995

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Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosis

Cell death and differentiation, 2007-03, Vol.14 (3), p.597-606

2007

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Lattice Defects in Microtubules: Protofilament Numbers Vary within Individual Microtubules

The Journal of cell biology, 1992-06, Vol.117 (5), p.1031-1040

1992

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Reconstruction of the Centrosome Cycle from Cryoelectron Micrographs

Journal of structural biology, 1997-11, Vol.120 (2), p.117-133

1997

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Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B 12

Journal of inherited metabolic disease, 2009-04, Vol.32 (2), p.159-162

2009

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Limited flexibility of the inter-protofilament bonds in microtubules assembled from pure tubulin

European biophysics journal, 1998-01, Vol.27 (5), p.490-500

1998

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Microtubules switch occasionally into unfavorable configurations during elongation

Journal of molecular biology, 2000-05, Vol.298 (4), p.663-676

2000

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Self-administered prescriptions of oral steroids and antibiotics in chronic obstructive pulmonary disease: are we doing more harm than good?

Chronic respiratory disease, 2007-08, Vol.4 (3), p.143-147

2007

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Determination of microtubule polarity by cryo-electron microscopy

Structure (London), 1996-09, Vol.4 (9), p.1031-1040

1996

Volltextzugriff (PDF)

Respiratory chain deficiency in Alpers syndrome

Neuropediatrics, 2001-06, Vol.32 (3), p.150

2001

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Structure of Growing Microtubule Ends: Two-Dimensional Sheets Close into Tubes at Variable Rates

The Journal of cell biology, 1995-06, Vol.129 (5), p.1311-1328

1995

Volltextzugriff (PDF)

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

Journal of medical genetics, 2004-01, Vol.41 (1), p.14-17

2004

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Biochemical and molecular investigations in respiratory chain deficiencies

Clinica chimica acta, 1994-07, Vol.228 (1), p.35-51

1994

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Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

Molecular genetics and metabolism, 2002-09, Vol.77 (1-2), p.21-30

2002

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The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

European journal of pediatrics, 1999, Vol.158 (1), p.55-58

1999

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Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency

The Journal of pediatrics, 2000-02, Vol.136 (2), p.209-214

2000

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Human cultured skin fibroblasts survive profound inherited ubiquinone depletion

Free radical research, 2001-01, Vol.35 (1), p.11-21

2001

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Calcium signalling-dependent mitochondrial dysfunction and bioenergetics regulation in respiratory chain Complex II deficiency

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria

Structural changes at microtubule ends accompanying GTP hydrolysis: Information from a slowly hydrolyzable analogue of GTP, guanylyl (α,β)methylenediphosphonate

Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo‐obstruction

Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis

Variable outcome of growth hormone administration in respiratory chain deficiency

Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B12

Structural Changes Accompanying GTP Hydrolysis in Microtubules: Information from a Slowly Hydrolyzable Analogue Guanylyl-(α,β)-Methylene-Diphosphonate

Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosis

Lattice Defects in Microtubules: Protofilament Numbers Vary within Individual Microtubules

Reconstruction of the Centrosome Cycle from Cryoelectron Micrographs

Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B 12

Limited flexibility of the inter-protofilament bonds in microtubules assembled from pure tubulin

Microtubules switch occasionally into unfavorable configurations during elongation

Self-administered prescriptions of oral steroids and antibiotics in chronic obstructive pulmonary disease: are we doing more harm than good?

Determination of microtubule polarity by cryo-electron microscopy

Respiratory chain deficiency in Alpers syndrome

Structure of Growing Microtubule Ends: Two-Dimensional Sheets Close into Tubes at Variable Rates

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

Biochemical and molecular investigations in respiratory chain deficiencies

Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency

Human cultured skin fibroblasts survive profound inherited ubiquinone depletion

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