P. Seibel

P. Seibel, C. Hübner, B. Finckh, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Generation of ρ0 cells utilizing a mitochondrially targeted restriction endonuclease and comparative analyses

P. Seibel, G. Krohne, C. Kukat, 2008, Nucleic acids research.

Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study

M. Battaglia, A. Moschetta, P. Seibel, 2021, Scientific Reports.

Unaltered respiratory chain enzyme activity and mitochondrial DNA in skeletal muscle from patients with idiopathic Parkinson's syndrome.

H. Reichmann, L. Schöls, H. Przuntek, 1994, European neurology.

Antiepileptic drugs reduce efficacy of methotrexate chemotherapy by downregulation of Reduced folate carrier transport activity

P. Seibel, S. Halwachs, W. Honscha, 2009, Leukemia.

Processing of Artificial Peptide-DNA-Conjugates by the Mitochondrial Intermediate Peptidase (MIP)

H. Reichmann, P. Seibel, G. Isaya, 1999, Biological chemistry.

Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo31P-MRS in a patient with mitochondrial cytopathy

H. Reichmann, P. Zaniol, B. Barbiroli, 1995, Journal of Neurology.

The Antiepileptic Drugs Phenobarbital and Carbamazepine Reduce Transport of Methotrexate in Rat Choroid Plexus by Down-Regulation of the Reduced Folate Carrier

P. Seibel, S. Halwachs, W. Honscha, 2011, Molecular Pharmacology.

Assessment of ABCG2-mediated transport of xenobiotics across the blood–milk barrier of dairy animals using a new MDCKII in vitro model

P. Seibel, S. Halwachs, L. Wassermann, 2013, Archives of Toxicology.

Mitochondrial diseases and aging.

S. Papa, P. Seibel, S. Scacco, 1996, Molecular aspects of medicine.

Defects of the respiratory chain in the normal human liver and in cirrhosis during aging

D. Aust, P. Seibel, B. Kadenbach, 1997, Hepatology.

3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome

G. Deuschl, H. Reichmann, P. Seibel, 2004, Acta Neuropathologica.

Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study

R. Horvath, P. Seibel, W. Copeland, 2009, Journal of cellular and molecular medicine.

Mitochondrial dysfunction with myoclonus epilepsy and ragged‐red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple isymmetric lipomatosis

H. Reichmann, M. Naumann, C. Sommer, 1997, Muscle & nerve.

In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy.

K. Gerbitz, P. Seibel, B. Kadenbach, 1992, Human pathology.

Strategy toward Gene Therapy of Mitochondrial DNA Disorders

A. Flierl, P. Seibel, M. Schliebs, 1999 .

Gene Therapy of Mitochondrial DNA Diseases

A. Flierl, P. Seibel, C. Bachmann, 1998 .

VACTERL with the mitochondrial np 3243 point mutation.

H. Reichmann, P. Seibel, W. Dorndorf, 1996, American journal of medical genetics.

Clinical spectrum of the MELAS mutation in a large pedigree

H. Reichmann, P. Seibel, W. Dorndorf, 1995, Acta neurologica Scandinavica.

A functional test of Neandertal and modern human mitochondrial targeting sequences.

S. Pääbo, P. Seibel, I. Schäfer, 2010, Biochemical and biophysical research communications.

Glucocorticoid and thyroid hormone receptors in mitochondria of animal cells.

P. Seibel, C. Sekeris, K. Scheller, 2003, International review of cytology.

Peroxisome proliferator-activated receptor-γ coactivator 1-α (PGC1α) is a metabolic regulator of intestinal epithelial cell fate

C. Lelliott, A. Vidal-Puig, A. Moschetta, 2011, Proceedings of the National Academy of Sciences.

Efficient Repopulation of Genetically Derived Rho Zero Cells with Exogenous Mitochondria

P. Seibel, Mario Krehan, S. Heller, 2013, PloS one.

Mitochondrial Transfer by Human Mesenchymal Stromal Cells Ameliorates Hepatocyte Lipid Load in a Mouse Model of NASH

S. Kalkhof, B. Christ, P. Seibel, 2020, Biomedicines.

Multiple symmetric lipomatosis

H. Reichmann, M. Naumann, K. Reiners, 1994, Neurology.

Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)

N. Romero, B. Eymard, P. Seibel, 1991, Journal of the Neurological Sciences.

Defects of the respiratory chain in oxyphil and chief cells of the normal parathyroid and in hyperfunction.

P. Seibel, C. Münscher, S. Schneeweiss, 1996, Human pathology.

Immunohistochemical detection of human mtDNA polymerase gamma and of human mitochondrial transcription factor A in cytochrome-c-oxidase-deficient oxyphil cells of hyperfunctional parathyroids

R. Wiesner, P. Seibel, W. Copeland, 1998, Virchows Archiv.

Oxyphil cell metaplasia in the parathyroids is characterized by somatic mitochondrial DNA mutations in NADH dehydrogenase genes and cytochrome c oxidase activity-impairing genes.

H. Blum, H. Prokisch, W. Kunz, 2014, The American journal of pathology.

Generation of Rho Zero Cells: Visualization and Quantification of the mtDNA Depletion Process

P. Seibel, S. Heller, I. Schäfer, 2015, International journal of molecular sciences.

Tight control of mitochondrial membrane potential by cytochrome c oxidase.

P. Seibel, C. Kukat, T. Cocco, 2011, Mitochondrion.

Expression of human cytochrome c oxidase subunits during fetal development.

P. Seibel, G. Bonne, B. Kadenbach, 1993, European journal of biochemistry.

Identification of point mutations by mispairing PCR as exemplified in MERRF disease.

N. Romero, P. Seibel, B. Kadenbach, 1990, Biochemical and biophysical research communications.

Mitochondrial haplogroups and expression studies of commonly used human cell lines.

Christine S. Siegismund, P. Seibel, H. Schultheiss, 2016, Mitochondrion.

Pathophysiology of the MELAS 3243 Transition Mutation*

H. Reichmann, A. Flierl, P. Seibel, 1997, The Journal of Biological Chemistry.

Mitochondrial DNA in migraine with aura

H. Diener, H. Reichmann, P. Seibel, 1996, Neurology.

Hashimoto thyroiditis is associated with defects of cytochrome-c oxidase in oxyphil Askanazy cells and with the common deletion (4,977) of mitochondrial DNA.

P. Seibel, J. Müller‐Höcker, U. Jacob, 1998, Ultrastructural pathology.

Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseases

Gaetano Villani, Peter Seibel, Jörg Trappe, 1995, Nucleic Acids Res..

Mitochondrial disorders in degenerative ataxias

H. Reichmann, H. Przuntek, P. Seibel, 1996 .

Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) gene.

H. Reichmann, P. Seibel, T. Klopstock, 1994, Biochemical and biophysical research communications.

Nitric Oxide-associated Protein 1 (NOA1) Is Necessary for Oxygen-dependent Regulation of Mitochondrial Respiratory Complexes*

I. Wittig, P. Seibel, M. Krüger, 2011, The Journal of Biological Chemistry.

Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain

A. Munnich, G. Brown, M. Zeviani, 2001, Journal of Inherited Metabolic Disease.

Neuropsychological status of mitochondrial encephalomyopathies

H. Reichmann, P. Seibel, A. Engelhardt, 1995, European journal of neurology.

Mitochondrial DNA Mutations Associated with Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction

D. Wallace, M. Lott, J. Shoffner, 1990, Pediatric Research.

Assessment of ABCG2-mediated transport of pesticides across the rabbit placenta barrier using a novel MDCKII in vitro model.

C. Kneuer, P. Seibel, S. Halwachs, 2016, Toxicology and applied pharmacology.

Expression Pattern of Mitochondrial Respiratory Chain Enzymes in Skeletal Muscle of Patients Harboring the A3243G Point Mutation or Large‐Scale Deletions of Mitochondrial DNA

C. Elger, W. Kunz, P. Seibel, 2002, Journal of neuropathology and experimental neurology.

Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletions

H. Reichmann, T. Klockgether, P. Seibel, 2001, Neurology.

New Insights into the Metabolic Consequences of Large‐Scale mtDNA Deletions: A Quantitative Analysis of Biochemical, Morphological, and Genetic Findings in Human Skeletal Muscle

C. Elger, H. Reichmann, T. Klockgether, 2000, Journal of neuropathology and experimental neurology.

Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly

P. Seibel, B. Kadenbach, J. Müller‐Höcker, 2005, Virchows Archiv A.

Mutations of mitochondrial DNA: the molecular basis of mitochondrial encephalo-myopathies and ageing

Margaret A. Johnson, D. Turnbull, P. Seibel, 1991 .

Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases.

P. Seibel, B. Kadenbach, C. Marsac, 1991, Nucleic acids research.

Investigation on the mitochondrial transfer RNALeu(UUR) in blood cells from patients with cluster headache

H. Diener, H. Reichmann, T. Grünewald, 1996, Journal of Neurology.

P. Seibel, S. Halwachs, L. Wassermann, 2013, Archives of Toxicology.

N-Terminal Ile-Orn- and Trp-Orn-Motif Repeats Enhance Membrane Interaction and Increase the Antimicrobial Activity of Apidaecins against Pseudomonas aeruginosa

R. Hoffmann, P. Seibel, E. Veldhuizen, 2016, Front. Cell Dev. Biol..

Antiepileptic Drugs Reduce the Efficacy of Methotrexate Chemotherapy through Accelerated Degradation of the Reduced Folate Carrier by the Ubiquitin-Proteasome Pathway

Peter Seibel, Walther Honscha, P. Seibel, 2011, Chemotherapy.

Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybrids

G. Comi, P. Seibel, C. Kukat, 2008, Nucleic Acids Research.

Chronic progressive external ophthalmoplegia with a novel mitochondrial DNA deletion and a mutation in the tRNALEU(UUR) gene

H. Reichmann, H. Goebel, T. Grünewald, 1999 .

Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study

H. Reichmann, R. Gold, M. Naumann, 2004, Acta Neuropathologica.

Differential expression of myosin heavy-chain mRNA in muscles of mastication during functional advancement of the mandible in pigs.

P. Seibel, W. Harzer, T. Gedrange, 2001, Archives of oral biology.

Defects of the respiratory chain in the normal human liver and in cirrhosis during aging

D. Aust, P. Seibel, B. Kadenbach, 1997, Hepatology.

Intracellular Toxicity of Proline-Rich Antimicrobial Peptides Shuttled into Mammalian Cells by the Cell-Penetrating Peptide Penetratin

R. Hoffmann, P. Seibel, Anne Hansen, 2012, Antimicrobial Agents and Chemotherapy.