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Results of search for 'au:"Müller-Hocker, J"', page 2 of 7
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Authors
Belohradsky, B H
Bise, K
Brenner, P
Deufel, T
Dichgans, M
Gerbitz, K D
Hammer, C
Horvath, R
Horváth, R
Hübner, G
Jaksch, M
Kadenbach, B
Lochmüller, H
Müller-Höcker, J
Münscher, C
Obermaier-Kusser, B
Pongratz, D
Schäfer, S
Seibel, P
Weiss, M
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DNA, Mitochondrial
Electron Transport Complex IV
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Humans
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Microscopy, Electron
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analysis
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21.
Immunocytochemical localization of mitochondrial single-stranded DNA-binding protein in mitochondria-rich cells of normal and neoplastic human tissue.
[electronic resource]
by
Müller-Höcker, J
Schäfer, S
Li, K
Producer:
20020213
In:
Applied immunohistochemistry & molecular morphology : AIMM
vol. 9
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22.
Human aging is associated with various point mutations in tRNA genes of mitochondrial DNA.
[electronic resource]
by
Münscher, C
Müller-Höcker, J
Kadenbach, B
Producer:
19940415
In:
Biological chemistry Hoppe-Seyler
vol. 374
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23.
[Surgical therapy of polytopic vertebral metastasis in malignant pheochromocytoma].
[electronic resource]
by
Krödel, A
Lohscheidt, K
Müller-Höcker, J
Producer:
19950622
In:
Zeitschrift fur Orthopadie und ihre Grenzgebiete
vol. 133
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24.
Relapsing poly(peri)chondritis diagnosed by biopsy during inflammatory free interval: destructive polychondritis versus fibrosing perichondritis.
[electronic resource]
by
Jung, C
Müller-Höcker, J
Rauh, G
Producer:
19980217
In:
European journal of medical research
vol. 1
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25.
[Schistosomiasis in a leiomyoma of the uterus].
[electronic resource]
by
Mayr, D
Straub, J
Müller-Höcker, J
Producer:
20051004
In:
Der Pathologe
vol. 26
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26.
Spindle-cell lipoma of the skin.
[electronic resource]
by
Duve, S
Müller-Höcker, J
Worret, W I
Producer:
19960424
In:
The American Journal of dermatopathology
vol. 17
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27.
[Leiomyosarcoma of the tongue].
[electronic resource]
by
Wollenberg, B
Müller-Höcker, J
Wustrow, T P
Producer:
19931014
In:
Laryngo- rhino- otologie
vol. 72
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28.
Deregulated expression of cell cycle-associated proteins in solid pseudopapillary tumor of the pancreas.
[electronic resource]
by
Müller-Höcker, J
Zietz, C H
Sendelhofert, A
Producer:
20010517
In:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
vol. 14
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29.
[Congenital fibrosis syndrome. Considerations on etiology, genetics and surgical therapy].
[electronic resource]
by
Boergen, K P
Lorenz, B
Müller-Höcker, J
Producer:
19901231
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 197
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30.
[Arteriopathia calcificans infantum in an infant with mucoviscidosis].
[electronic resource]
by
Rübe, C
Nerlich, A
Späth, A
Müller-Höcker, J
Producer:
19890418
In:
Der Pathologe
vol. 10
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31.
Cytochrome c oxidase defects of the human substantia nigra in normal aging.
[electronic resource]
by
Itoh, K
Weis, S
Mehraein, P
Müller-Höcker, J
Producer:
19971204
In:
Neurobiology of aging
vol. 17
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32.
P53 gene product and EGF-receptor are highly expressed in placental site trophoblastic tumor.
[electronic resource]
by
Müller-Höcker, J
Obernitz, N
Johannes, A
Löhrs, U
Producer:
19971211
In:
Human pathology
vol. 28
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33.
Different in situ hybridization patterns of mitochondrial DNA in cytochrome c oxidase-deficient extraocular muscle fibres in the elderly.
[electronic resource]
by
Müller-Höcker, J
Seibel, P
Schneiderbanger, K
Kadenbach, B
Producer:
19930322
In:
Virchows Archiv. A, Pathological anatomy and histopathology
vol. 422
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34.
The application of a biotin-anti-biotin gold technique providing a significant signal intensification in electron microscopic immunocytochemistry: a comparison with the ultrasmall immunogold silver staining procedure.
[electronic resource]
by
Müller-Höcker, J
Schäfer, S
Sendelhofert, A
Weis, S
Producer:
19980421
In:
Histochemistry and cell biology
vol. 109
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35.
Rapidly progredient scoliosis associated with multicore disease.
[electronic resource]
by
Pellengahr, C
Krödel, A
Müller-Höcker, J
Pongratz, D
Producer:
19981117
In:
Archives of orthopaedic and trauma surgery
vol. 117
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36.
Fibrillary glomerulonephritis mimicking membranous nephropathy--a diagnostic pitfall.
[electronic resource]
by
Müller-Höcker, J
Weiss, M
Sitter, Th
Samtleben, W
Producer:
20090818
In:
Pathology, research and practice
vol. 205
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37.
Focal deficiency of cytochrome c oxidase and of mitochondrial ATPase with histochemical evidence of loosely coupled oxidative phosphorylation in a mitochondrial myopathy of a patient with bilateral ptosis. An enzyme histochemical, immunocytochemical and fine structural study.
[electronic resource]
by
Müller-Höcker, J
Stünkel, S
Pongratz, D
Hübner, G
Producer:
19850822
In:
Journal of the neurological sciences
vol. 69
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38.
The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages.
[electronic resource]
by
Münscher, C
Rieger, T
Müller-Höcker, J
Kadenbach, B
Producer:
19930305
In:
FEBS letters
vol. 317
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39.
Overexpression of cyclin D1, D3, and p21 in an infantile renal carcinoma with Xp11.2 TFE3-gene fusion.
[electronic resource]
by
Müller-Höcker, J
Babaryka, G
Schmid, I
Jung, A
Producer:
20080925
In:
Pathology, research and practice
vol. 204
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40.
[Morphology and diagnosis of Zellweger syndrome. A contribution to combined cytochemical-finestructural identification of peroxisomes in autopsy material and frozen liver tissue with case report].
[electronic resource]
by
Müller-Höcker, J
Bise, K
Endres, W
Hübner, G
Producer:
19821202
In:
Virchows Archiv. A, Pathological anatomy and histology
vol. 393
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