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The Journal of Biological Chemistry
|
October 27, 1997
Pathophysiology of the MELAS 3243 transition mutation
A Flierl, H Reichmann, P Seibel
European Neurology
|
January 1, 1996
Ragged red or ragged blue fibers
H Reichmann, L Vogler, P Seibel
Journal of Gerontology
|
January 1, 1990
Empirical clusters of disordered behavior among older psychiatric inpatients
R L Ownby, H P Seibel
Ultrastructural Pathology
|
March 10, 1998
Hashimoto thyroiditis is associated with defects of cytochrome-c oxidase in oxyphil Askanazy cells and with the common deletion (4,977) of mitochondrial DNA
J Müller-Höcker, U Jacob, P Seibel
Gene
|
March 25, 1994
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
O C Mell, P Seibel, B Kadenbach
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 1, 1998
The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome
J Müller-Höcker, U Jacob, P Seibel
Biochemical and Biophysical Research Communications
|
April 29, 1994
A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies
P Seibel, A Flierl, M Kottlors, et al.
Nucleic Acids Research
|
April 11, 1991
Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases
J Lauber, C Marsac, B Kadenbach, et al.
Leukemia
|
February 13, 2009
Antiepileptic drugs reduce efficacy of methotrexate chemotherapy by downregulation of Reduced folate carrier transport activity
S Halwachs, I Schäfer, P Seibel, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1993
Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly
J Müller-Höcker, P Seibel, K Schneiderbanger, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
The Journal of Biological Chemistry
|
October 27, 1997
Pathophysiology of the MELAS 3243 transition mutation
A Flierl, H Reichmann, P Seibel
European Neurology
|
January 1, 1996
Ragged red or ragged blue fibers
H Reichmann, L Vogler, P Seibel
Journal of Gerontology
|
January 1, 1990
Empirical clusters of disordered behavior among older psychiatric inpatients
R L Ownby, H P Seibel
Ultrastructural Pathology
|
March 10, 1998
Hashimoto thyroiditis is associated with defects of cytochrome-c oxidase in oxyphil Askanazy cells and with the common deletion (4,977) of mitochondrial DNA
J Müller-Höcker, U Jacob, P Seibel
Gene
|
March 25, 1994
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
O C Mell, P Seibel, B Kadenbach
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 1, 1998
The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome
J Müller-Höcker, U Jacob, P Seibel
Biochemical and Biophysical Research Communications
|
April 29, 1994
A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies
P Seibel, A Flierl, M Kottlors, et al.
Nucleic Acids Research
|
April 11, 1991
Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases
J Lauber, C Marsac, B Kadenbach, et al.
Leukemia
|
February 13, 2009
Antiepileptic drugs reduce efficacy of methotrexate chemotherapy by downregulation of Reduced folate carrier transport activity
S Halwachs, I Schäfer, P Seibel, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1993
Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly
J Müller-Höcker, P Seibel, K Schneiderbanger, et al.
Page
of 5