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Expression of human cytochrome c oxidase subunits during fetal development.
Bonne G, Seibel P, Possekel S, Marsac C, Kadenbach B. Bonne G, et al. Among authors: seibel p. Eur J Biochem. 1993 Nov 1;217(3):1099-107. doi: 10.1111/j.1432-1033.1993.tb18342.x. Eur J Biochem. 1993. PMID: 8223633
Hashimoto thyroiditis is associated with defects of cytochrome-c oxidase in oxyphil Askanazy cells and with the common deletion (4,977) of mitochondrial DNA.
Müller-Höcker J, Jacob U, Seibel P. Müller-Höcker J, et al. Among authors: seibel p. Ultrastruct Pathol. 1998 Jan-Feb;22(1):91-100. doi: 10.3109/01913129809032263. Ultrastruct Pathol. 1998. PMID: 9491221
Structural organisation of the rat genes encoding liver- and heart-type of cytochrome c oxidase subunit VIa and a pseudogene related to the COXVIa-L cDNA.
Mell OC, Seibel P, Kadenbach B. Mell OC, et al. Among authors: seibel p. Gene. 1994 Mar 25;140(2):179-86. doi: 10.1016/0378-1119(94)90542-8. Gene. 1994. PMID: 8144025
Immunohistochemical detection of human mtDNA polymerase gamma and of human mitochondrial transcription factor A in cytochrome-c-oxidase-deficient oxyphil cells of hyperfunctional parathyroids.
Müller-Höcker J, Schäfer S, Copeland WC, Wiesner R, Seibel P. Müller-Höcker J, et al. Among authors: seibel p. Virchows Arch. 1998 Dec;433(6):529-36. doi: 10.1007/s004280050285. Virchows Arch. 1998. PMID: 9870686
The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome.
Müller-Höcker J, Jacob U, Seibel P. Müller-Höcker J, et al. Among authors: seibel p. Mod Pathol. 1998 Mar;11(3):295-301. Mod Pathol. 1998. PMID: 9521479
Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNA.
Klopstock T, Naumann M, Schalke B, Bischof F, Seibel P, Kottlors M, Eckert P, Reiners K, Toyka KV, Reichmann H. Klopstock T, et al. Among authors: seibel p. Neurology. 1994 May;44(5):862-6. doi: 10.1212/wnl.44.5.862. Neurology. 1994. PMID: 8190288
Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletions.
Kornblum C, Broicher R, Walther E, Seibel P, Reichmann H, Klockgether T, Herberhold C, Schröder R. Kornblum C, et al. Among authors: seibel p. Neurology. 2001 May 22;56(10):1409-12. doi: 10.1212/wnl.56.10.1409. Neurology. 2001. PMID: 11376201
A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
Seibel P, Flierl A, Kottlors M, Reichmann H. Seibel P, et al. Biochem Biophys Res Commun. 1994 Apr 29;200(2):938-42. doi: 10.1006/bbrc.1994.1540. Biochem Biophys Res Commun. 1994. PMID: 8179630
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF).
Seibel P, Degoul F, Bonne G, Romero N, François D, Paturneau-Jouas M, Ziegler F, Eymard B, Fardeau M, Marsac C, et al. Seibel P, et al. J Neurol Sci. 1991 Oct;105(2):217-24. doi: 10.1016/0022-510x(91)90148-z. J Neurol Sci. 1991. PMID: 1661776
Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases.
Lauber J, Marsac C, Kadenbach B, Seibel P. Lauber J, et al. Among authors: seibel p. Nucleic Acids Res. 1991 Apr 11;19(7):1393-7. doi: 10.1093/nar/19.7.1393. Nucleic Acids Res. 1991. PMID: 1709275 Free PMC article.
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