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1

Human Aging is Associated with Various Point Mutations in tRNA Genes of Mitochondrial DNA

MÜNSCHER, Christof, MÜLLER-HÖCKER, Josef, KADENBACH, Bernhard

Journal:

Biological Chemistry Hoppe-Seyler

Year:

1993

Language:

english

File:

PDF, 973 KB

english, 1993

2

Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome

H. S. A. Heymans, H. v. d. Bosch, R. B. H. Schutgens, W. H. H. Tegelaers, J. -U. Walther, J. Müller-Höcker, P. Borst

Journal:

European Journal of Pediatrics

Year:

1984

Language:

english

File:

PDF, 876 KB

english, 1984

3

A Key Role for E-cadherin in Intestinal Homeostasis and Paneth Cell Maturation

Schneider, Marlon R., Dahlhoff, Maik, Horst, David, Hirschi, Benjamin, Trülzsch, Konrad, Müller-Höcker, Josef, Vogelmann, Roger, Allgäuer, Michael, Gerhard, Markus, Steininger, Sylvia, Wolf, Eckhard,

Journal:

Year:

2010

Language:

english

File:

PDF, 20.14 MB

english, 2010

4

A specific point mutation in the mitochondrial genome of Caucasians with MELAS

C. Enter, J. Müller-Höcker, S. Zierz, G. Kurlemann, D. Pongratz, C. Förster, B. Obermaier-Kusser, K. -D. Gerbitz

Journal:

Year:

1991

Language:

english

File:

PDF, 427 KB

english, 1991

5

Chief cell proliferation of the gastric mucosa mimicking early gastric cancer: an unusual variant of fundic gland polyp

J. Müller-Höcker,P. Rellecke

Journal:

Virchows Archiv

Year:

2003

Language:

english

File:

PDF, 618 KB

english, 2003

6

MesP1 drives vertebrate cardiovascular differentiation through Dkk-1-mediated blockade of Wnt-signalling

David, R., Brenner, C., Stieber, J., Schwarz, F., Brunner, S., Vollmer, M., Mentele, E., Müller-Höcker, J., Kitajima, S., Lickert, H.

Journal:

Nature Cell Biology

Year:

2008

Language:

english

File:

PDF, 1.82 MB

english, 2008

7

Defects of cytochrome c oxidase in the substantia nigra of Parkinson's disease: An immunohistochemical and morphometric study

Kyoko Itoh, Dr. Serge Weis, Parviz Mehraein, Josef Müller-Höcker

Journal:

Movement Disorders

Year:

1997

Language:

english

File:

PDF, 1.85 MB

english, 1997

8

Dysregulation of the cell cycle and chromosomal imbalances in juxtaglomerular cell tumors – A comparative study with endocrine tumors of the pancreas

Gerald Assmann, Irmgard Verdorfer, Andreas Jung, Markus Bader, Josef Müller-Höcker

Journal:

Pathology - Research and Practice

Year:

2011

Language:

english

File:

PDF, 2.55 MB

english, 2011

9

Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy

Peter Reilich, Nicolai Schramm, Benedikt Schoser, Peter Schneiderat, Nicola Strigl-Pill, Josef Müller-Höcker, Wolfram Kress, Andreas Ferbert, Sabine Rudnik-Schöneborn, Johannes Noth, Hanns Lochmüller,

Journal:

Journal of Neurology

Year:

2010

Language:

english

File:

PDF, 578 KB

english, 2010

10

Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNALeu(UUR)]

B. Obermaier-Kusser, I. Paetzke-Brunner, C. Enter, J. Müller-Höcker, S. Zierz, W. Ruitenbeek, K.-D. Gerbitz

Journal:

Year:

1991

Language:

english

File:

PDF, 522 KB

english, 1991

11

Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy

R. Horváth, B.G.H. Schoser, J. Müller-Höcker, M. Völpel, M. Jaksch, H. Lochmüller

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 316 KB

english, 2005

12

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

J. Müller-Höcker, S. Stünkel, D. Pongratz, G. Hübner

Journal:

Journal of the Neurological Sciences

Year:

1985

Language:

english

File:

PDF, 1.60 MB

english, 1985

13

IGFBP3 impedes aggressive growth of pediatric liver cancer and is epigenetically silenced in vascular invasive and metastatic tumors

Ivonne Regel, Melanie Eichenmüller, Saskia Joppien, Johanna Liebl, Beate Häberle, Josef Müller-Höcker, Angelika Vollmar, Dietrich von Schweinitz, Roland Kappler

Journal:

Molecular Cancer

Year:

2012

Language:

english

File:

PDF, 633 KB

english, 2012

14

Novel mutation in Hermansky–Pudlak syndrome type 2 with mild immunological phenotype

Kurnik, Karin, Bartsch, Ingrid, Maul-Pavicic, Andrea, Ehl, Stephan, Sandrock-Lang, Kirstin, Bidlingmaier, Christoph, Rombach, Nina, Busse, Anja, Belohradsky, Bernd H., Müller-Höcker, Josef, Aslanidis,

Journal:

Year:

2013

Language:

english

File:

PDF, 636 KB

english, 2013

15

FAMILIAL' INFANTILE LIVER CIRRHOSIS AND HEMOLYTIC ANEMIA DUE TO CHRONIC COPPER INTOXICATION VIA TAP WATER FROM COPPER PIPES

Eife, R, Müller-Höcker, J, Wei, M, Schramel, P, Dieter, H, Feist, D, Reiter, K

Journal:

Pediatric Research

Year:

1989

Language:

english

File:

PDF, 135 KB

english, 1989

16

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

J Muller-Hocker, D Aust, H Rohrbach, J Napiwotzky, A Reith, T A Link, P Seibel, D Holzel, B Kadenbach

Journal:

Year:

1997

Language:

english

File:

PDF, 1.88 MB

english, 1997

17

Die onkozytäre Metaplasie/Neoplasie – Morphologie, Biochemie, Molekulargenetik

J. Müller-Höcker

Journal:

Year:

1998

Language:

german

File:

PDF, 3.35 MB

german, 1998

18

Rapidly progredient scoliosis associated with multicore disease

C. Pellengahr, A. Krödel, J. Müller-Höcker, D. Pongratz

Journal:

Archives of Orthopaedic and Trauma Surgery

Year:

1998

Language:

english

File:

PDF, 918 KB

english, 1998

19

Rupture of splenic artery aneurysm in a pregnant patient with portal hypertension

Peter Hillemanns, Reinhold Knitza, Josef Müller-Höcker

Journal:

American Journal of Obstetrics and Gynecology

Year:

1996

Language:

english

File:

PDF, 159 KB

english, 1996

20

De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

H.J Durling, P Reilich, J Müller-Höcker, B Mendel, D Pongratz, C Wallgren-Pettersson, P Gunning, H Lochmüller, N.G Laing

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 327 KB

english, 2002

21

Metallothionein, copper and zinc in fetal and neonatal human liver: changes during development

Klein, D., Scholz, P., Drasch, G.A., Müller-Höcker, J., Summer, Karl H.

Journal:

Toxicology Letters

Year:

1991

Language:

english

File:

PDF, 480 KB

english, 1991

22

Clinicopathological analysis of the homozygous p.W1327X AGL mutation in glycogen storage disease type 3

Benedikt Schoser, Dieter Gläser, Josef Müller-Höcker

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 217 KB

english, 2008

23

Adenoma of the middle ear mucosa

B. Arnold, C. Zietz, J. Müller-Höcker, T. P. U. Wustrow

Journal:

European Archives of Oto-Rhino-Laryngology

Year:

1996

Language:

english

File:

PDF, 410 KB

english, 1996

24

Mutations of mitochondrial DNA and human death

Bernhard Kadenbach, Josef Müller-Höcker

Journal:

Naturwissenschaften (The Science of Nature)

Year:

1990

Language:

english

File:

PDF, 511 KB

english, 1990

25

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

J. Müller-Höcker, S. Schäfer, A. Sendelhofert, S. Weis

Journal:

Histochemistry and Cell Biology

Year:

1998

Language:

english

File:

PDF, 1.94 MB

english, 1998

26

Expression of bcl-2, Bax and Fas in oxyphil cells of Hashimoto thyroiditis

J. Müller-Höcker

Journal:

Virchows Archiv

Year:

2000

Language:

english

File:

PDF, 628 KB

english, 2000

27

Human aging is associated with stochastic somatic mutations of mitochondrial DNA

Bernhard Kadenbach, Christof Münscher, Viola Frank, Josef Müller-Höcker, Jörg Napiwotzki

Journal:

Mutation Research/DNAging

Year:

1995

Language:

english

File:

PDF, 1.06 MB

english, 1995

28

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

J Muller-Hocker, D Aust, H Rohrbach, J Napiwotzky, A Reith, TA Link, P Seibel, D Holzel, B Kadenbach

Journal:

Year:

1997

Language:

english

File:

PDF, 1.88 MB

english, 1997

29

26-jährige Patientin mit unklarer Transaminasen-Erhöhung

K. Martin, B. Schlotter, J. Müller-höcker, K. Loeschke, D. Pongratz, C. Folwaczny

Year:

2002

File:

PDF, 1.68 MB

2002

30

Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: An autopsy-immunocytochemical study

Josef Müller-Höcker, Martin Droste, Bernhard Kadenbach, Dieter Pongratz, Gerhard Hübner

Journal:

Human Pathology

Year:

1989

Language:

english

File:

PDF, 5.20 MB

english, 1989

31

β-Catenin mutations in 2 nested stromal epithelial tumors of the liver—a neoplasia with defective mesenchymal-epithelial transition

Gerald Assmann, Roland Kappler, Evelyn Zeindl-Eberhart, Irene Schmid, Beate Häberle, Christian Graeb, Andreas Jung, Josef Müller-Höcker

Journal:

Human Pathology

Year:

2012

Language:

english

File:

PDF, 4.38 MB

english, 2012

32

Fatal mitochondrial cardiomyopathy in Kearns-Sayre syndrome with deficiency of cytochrome-c-oxidase in cardiac and skeletal muscle

Josef Müller-Höcker, Axel Johannes, Martin Droste, Bernhard Kadenbach, Dieter Pongratz, Gerhard Hühner

Journal:

Virchows Archiv B Cell Pathology Zell-pathologie

Year:

1986-1987

Language:

english

File:

PDF, 4.08 MB

english, 1986-1987

33

Paraneoplastic chronic intestinal pseudoobstruction as a rare complication of bronchial carcinoid.

Gerl, A, Storck, M, Schalhorn, A, Muller-Hocker, J, Jauch, K W, Schildberg, F W, Wilmanns, W

Journal:

Year:

1992

Language:

english

File:

PDF, 1.31 MB

english, 1992

34

Altered expression of key cell cycle regulators in renal cell carcinoma associated with Xp11.2 translocation

H. Barroca, S. Castedo, J. Vieira, M. Teixeira, J. Müller-Höcker

Journal:

Pathology - Research and Practice

Year:

2009

Language:

english

File:

PDF, 510 KB

english, 2009

35

Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

K.-D. Gerbitz, B. Obermaier-Kusser, S. Zierz, D. Pongratz, J. Müller-Höcker, P. Lestienne

Journal:

Journal of Neurology

Year:

1990

Language:

english

File:

PDF, 776 KB

english, 1990

36

Fatal copper storage disease of the liver in a German infant resembling Indian childhood cirrhosis

Josef Müller-Höcker, Michael Weiß, Ulrike Meyer, Peter Schramel, Baldur Wiebecke, Bernd H. Belohradsky, Gerhard Hübner

Journal:

Virchows Archiv

Year:

1987

Language:

english

File:

PDF, 910 KB

english, 1987

37

Technique of immunoapheresis in heterotopic and orthotopic xenotransplantation of pig hearts into cynomolgus and rhesus monkeys

P Brenner, M Schmoeckel, H Reichenspurner, T Felbinger, M Hinz, V Eder, A Rucker, C Wimmer, S Uchita, S Kriegeskorte, B Meiser, J Müller-Höcker, D Seidel, C Hammer, B Reichart

Journal:

Transplantation Proceedings

Year:

2000

Language:

english

File:

PDF, 51 KB

english, 2000

38

Das kongenitale Fibrosesyndrom - Überlegungen zur Ätiologie, Genetik und chirurgischen Therapie

Boergen, K., Lorenz, B., Müller-Höcker, J.

Journal:

Klinische Monatsblätter für Augenheilkunde

Year:

1990

Language:

german

File:

PDF, 549 KB

german, 1990

39

Brauner Urin

Pietsch, U., Müller-Höcker, C., Filipovic, M.

Journal:

Der Anaesthesist

Year:

2016

Language:

german

File:

PDF, 396 KB

german, 2016

40

Monoclonal gammopathy after low-grade MALT lymphoma: Evidence for a second neoplasm

S. Pachmann, B. Anderegg, J. Müller-Höcker, W. Nathrath, N. Brack, F.J. Tigges, R. Hartenstein, R. Munker

Journal:

American Journal of Hematology

Year:

2002

Language:

english

File:

PDF, 231 KB

english, 2002

41

Fibrilläre Glomerulonephritis Fallbericht zur Differentialdiagnose des nephrotischen Syndroms*

M. Weiss, K. Tzavella, J. Müller-Höcker, A. Nerlich, E. Held

Journal:

Year:

1998

Language:

german

File:

PDF, 645 KB

german, 1998

42

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

J. Müller-Höcker, P. Seibel, K. Schneiderbanger, Ch. Zietz, B. Obermaier-Kusser, K.D. Gerbitz, B. Kadenbach

Journal:

Human Pathology

Year:

1992

Language:

english

File:

PDF, 6.20 MB

english, 1992

43

Novel desmoplakin mutation: juvenile biventricular cardiomyopathy with left ventricular non-compaction and acantholytic palmoplantar keratoderma

Tatjana Williams, Wolfram Machann, Leif Kühler, Henning Hamm, Josef Müller-Höcker, Michael Zimmer, Georg Ertl, Oliver Ritter, Meinrad Beer, Jost Schönberger

Journal:

Clinical Research in Cardiology

Year:

2011

Language:

english

File:

PDF, 648 KB

english, 2011

44

Defects of the respiratory chain in hepatic oncocytes

J. Müller-Höcker

Journal:

Virchows Archiv

Year:

1998

Language:

english

File:

PDF, 2.55 MB

english, 1998

45

The point mutation of mitochondrial DNA characteristic for MERRF disease is found also in healthy people of different ages

C. Münscher, T. Rieger, J. Müller-Höcker, B. Kadenbach

Journal:

Year:

1993

Language:

english

File:

PDF, 443 KB

english, 1993

46

Rapamycin blocks hepatoblastoma growth in vitro and in vivo implicating new treatment options in high-risk patients

Ferdinand Wagner, Bente Henningsen, Christine Lederer, Melanie Eichenmüller, Jan Gödeke, Josef Müller-Höcker, Dietrich von Schweinitz, Roland Kappler

Journal:

European Journal of Cancer

Year:

2012

Language:

english

File:

PDF, 905 KB

english, 2012

47

Congenital Alveolar Capillary Dysplasia: Rare Cause of Persistent Pulmonary Hypertension

Haraida, Sibylle, Lochbühler, Hannelore, Heger, A., Nerlich, A., Diebold, J., Wiest, Irmgard, Müller-Höcker, J., Löhrs, U.

Journal:

Fetal and Pediatric Pathology

Year:

1997

Language:

english

File:

PDF, 4.50 MB

english, 1997

48

Spindle-Cell Lipoma of the Skin

Duve, Stefan, Müller-Höcker, Josef, Worret, Wolf I.

Journal:

American Journal of Dermatopathology

Year:

1995

File:

PDF, 454 KB

1995

49

10.1097/00022744-200109000-00013

Muller-Hocker, J., Schafer, S., Li, K.

Journal:

Applied Immunohistochemistry

Year:

2001

Language:

english

File:

PDF, 2.09 MB

english, 2001

50

The cytokine midkine supports neutrophil trafficking during acute inflammation by promoting adhesion via 2 integrins (CD11/CD18)

Weckbach, L. T., Gola, A., Winkelmann, M., Jakob, S. M., Groesser, L., Borgolte, J., Pogoda, F., Pick, R., Pruenster, M., Muller-Hocker, J., Deindl, E., Sperandio, M., Walzog, B.

Journal:

Year:

2014

Language:

english

File:

PDF, 1.51 MB

english, 2014

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