UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 385

Sortiert nach

Strategies for fighting mitochondrial diseases

Journal of internal medicine, 2020-06, Vol.287 (6), p.665-684

2020

Volltextzugriff (PDF)

AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome

Gene therapy, 2017-10, Vol.24 (10), p.661-667

2017

Volltextzugriff (PDF)

Mitochondrial disorders

Brain (London, England : 1878), 2004-10, Vol.127 (10), p.2153-2172

2004

Volltextzugriff (PDF)

Loss of apoptosis-inducing factor critically affects MIA40 function

Cell death & disease, 2015-07, Vol.6 (7), p.e1814-e1814

2015

Volltextzugriff (PDF)

Idebenone Treatment In Leber's Hereditary Optic Neuropathy

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.e188-e188

2011

Volltextzugriff (PDF)

Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk

Journal of internal medicine, 2009-02, Vol.265 (2), p.174-192

2009

Volltextzugriff (PDF)

Clinical and molecular features of mitochondrial DNA depletion syndromes

Journal of inherited metabolic disease, 2009-04, Vol.32 (2), p.143-158

2009

Volltextzugriff (PDF)

Reduced mitochondrial Ca2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase

Cell death and differentiation, 2016-02, Vol.23 (2), p.231-241

2016

Volltextzugriff (PDF)

Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells

Mitochondrion, 2012-03, Vol.12 (2), p.328-335

2012

Volltextzugriff (PDF)

Revisiting mitochondrial ocular myopathies: a study from the Italian Network

Journal of neurology, 2017-08, Vol.264 (8), p.1777-1784

2017

Volltextzugriff (PDF)

SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype

Biochimica et biophysica acta. Molecular basis of disease, 2018-06, Vol.1864 (6), p.2131-2142

2018

Volltextzugriff (PDF)

Clinical and molecular findings in children with complex I deficiency

Biochimica et biophysica acta, 2004-12, Vol.1659 (2), p.136-147

2004

Volltextzugriff (PDF)

Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

Science (American Association for the Advancement of Science), 2000-08, Vol.289 (5480), p.782-785

2000

Volltextzugriff (PDF)

Properties of a sandy clay loam Haplic Ferralsol and soybean grain yield in a five-year field trial as affected by biochar amendment

Geoderma, 2017-11, Vol.305, p.100-112

2017

Volltextzugriff (PDF)

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

Neurology, 2005-04, Vol.64 (7), p.1204

2005

Volltextzugriff (PDF)

Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease

Journal of medical genetics, 2011-10, Vol.48 (10), p.660-668

2011

Volltextzugriff (PDF)

Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

Neuromuscular disorders : NMD, 2012-12, Vol.22 (3-3), p.S226-S229

2012

Volltextzugriff (PDF)

Local and systemic control of powdery mildew in eucalyptus using essential oils and decoctions from traditional Brazilian medicinal plants

Forest pathology = Journal de pathologie forestière = Zeitschrift für Forstpathologie, 2014-04, Vol.44 (2), p.145-153

2014

Volltextzugriff (PDF)

GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy

Neurology, 2006-07, Vol.67 (2), p.273

2006

Volltextzugriff (PDF)

M.I.3 Nuclear genes involved in mitochondrial syndromes

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.764-765

Zeviani, M

2007

Volltextzugriff (PDF)

Crushed crambe from biodiesel production as replacement for soybean meal in the supplement of steers grazing

Italian journal of animal science, 2019-01, Vol.18 (1), p.316-327

2019

Volltextzugriff (PDF)

Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

Neurology, 2003-04, Vol.60 (8), p.1354

2003

Volltextzugriff (PDF)

EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias

European journal of neurology, 2009-07, Vol.16 (7), p.777-785

2009

Volltextzugriff (PDF)

EFNS guidelines on the molecular diagnosis of mitochondrial disorders

European journal of neurology, 2009-12, Vol.16 (12), p.1255-1264

2009

Volltextzugriff (PDF)

Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1)

Biochimica et biophysica acta, 2009-12, Vol.1792 (12), p.1109-1112

2009

Volltextzugriff (PDF)

1 – 25 von 385

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(362)
Mit Volltextzugriff
(338)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Strategies for fighting mitochondrial diseases

AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome

Mitochondrial disorders

Loss of apoptosis-inducing factor critically affects MIA40 function

Idebenone Treatment In Leber's Hereditary Optic Neuropathy

Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk

Clinical and molecular features of mitochondrial DNA depletion syndromes

Reduced mitochondrial Ca2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase

Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells

Revisiting mitochondrial ocular myopathies: a study from the Italian Network

SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype

Clinical and molecular findings in children with complex I deficiency

Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

Properties of a sandy clay loam Haplic Ferralsol and soybean grain yield in a five-year field trial as affected by biochar amendment

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease

Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

Local and systemic control of powdery mildew in eucalyptus using essential oils and decoctions from traditional Brazilian medicinal plants

GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy

M.I.3 Nuclear genes involved in mitochondrial syndromes

Crushed crambe from biodiesel production as replacement for soybean meal in the supplement of steers grazing

Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias

EFNS guidelines on the molecular diagnosis of mitochondrial disorders

Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1)

Suchergebnisse filtern