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

Human pathology, 2012-11, Vol.43 (11), p.1815-1827

2012

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Electrophoretic Analysis of the Mitochondrial Outer Membrane Rupture Induced by Permeability Transition

Analytical chemistry (Washington), 2008-07, Vol.80 (13), p.5051-5058

2008

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A key role for E-cadherin in intestinal homeostasis and Paneth cell maturation

PloS one, 2010-12, Vol.5 (12), p.e14325-e14325

2010

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The cytokine midkine supports neutrophil trafficking during acute inflammation by promoting adhesion via β2 integrins (CD11/CD18)

Blood, 2014-03, Vol.123 (12), p.1887-1896

2014

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Midkine acts as proangiogenic cytokine in hypoxia-induced angiogenesis

American journal of physiology. Heart and circulatory physiology, 2012-08, Vol.303 (4), p.H429-H438

2012

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Blocking the hedgehog pathway inhibits hepatoblastoma growth

Hepatology (Baltimore, Md.), 2009-02, Vol.49 (2), p.482-490

2009

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

American journal of medical genetics. Part A, 2008-11, Vol.146A (22), p.2911-2915

2008

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Immunohistochemical analysis of Mallory bodies in Wilsonian and non‐Wilsonian hepatic copper toxicosis

Hepatology (Baltimore, Md.), 2004-04, Vol.39 (4), p.963-969

2004

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Selective methylation of CpGs at regulatory binding sites controls NNAT expression in Wilms tumors

PloS one, 2013-06, Vol.8 (6), p.e67605-e67605

2013

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

European journal of cancer (1990), 2012-10, Vol.48 (15), p.2442-2450

2012

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The p.G154S mutation of the alpha-B crystallin gene ( CRYAB ) causes late-onset distal myopathy

Neuromuscular disorders : NMD, 2010-04, Vol.20 (4), p.255-259

2010

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

Molecular cancer, 2012-03, Vol.11 (1), p.9-9, Article 9

2012

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Generalized crystal-storing histiocytosis associated with monoclonal gammopathy: molecular analysis of a disorder with rapid clinical course and review of the literature

Blood, 2002-09, Vol.100 (5), p.1817-1827

2002

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Immunoreactivity of p53, Ki-67, and Bcl-2 in oncocytic adenomas and carcinomas of the thyroid gland

Human pathology, 1999-08, Vol.30 (8), p.926-933

Müller-Höcker, Josef

1999

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Mitochondria and Ageing

Brain pathology (Zurich, Switzerland), 1992-04, Vol.2 (2), p.149-158

Müller-Höcker, Josef

1992

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

Movement disorders, 1997-01, Vol.12 (1), p.9-16

1997

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Vessel adherent growth represents a major challenge in the surgical resection of neuroblastoma and Is associated with adverse outcome

Journal of pediatric surgery, 2019-11, Vol.54 (11), p.2336-2342

2019

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Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

European journal of human genetics : EJHG, 2000-04, Vol.8 (4), p.280-285

2000

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P53 gene product and egf-receptor are highly expressed in placental site trophoblastic tumor

Human pathology, 1997-11, Vol.28 (11), p.1302-1306

1997

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Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies

Biochemical and biophysical research communications, 2007-08, Vol.359 (4), p.947-951

2007

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Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Human molecular genetics, 2001-12, Vol.10 (26), p.3025-3035

2001

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Oxyphil Cell Metaplasia in the Parathyroids Is Characterized by Somatic Mitochondrial DNA Mutations in NADH Dehydrogenase Genes and Cytochrome c Oxidase Activity–Impairing Genes

The American journal of pathology, 2014-11, Vol.184 (11), p.2922-2935

2014

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Epigallocatechin-3-Gallate Inhibits Hepatoblastoma Growth by Reactivating the Wnt Inhibitor SFRP1

Nutrition and cancer, 2013, Vol.65 (8), p.1200-1207

2013

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

Clinical research in cardiology, 2011-12, Vol.100 (12), p.1087-1093

2011

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNAser(UCN) gene

Annals of neurology, 1998-10, Vol.44 (4), p.635-640

1998

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

Electrophoretic Analysis of the Mitochondrial Outer Membrane Rupture Induced by Permeability Transition

A key role for E-cadherin in intestinal homeostasis and Paneth cell maturation

The cytokine midkine supports neutrophil trafficking during acute inflammation by promoting adhesion via β2 integrins (CD11/CD18)

Midkine acts as proangiogenic cytokine in hypoxia-induced angiogenesis

Blocking the hedgehog pathway inhibits hepatoblastoma growth

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

Immunohistochemical analysis of Mallory bodies in Wilsonian and non‐Wilsonian hepatic copper toxicosis

Selective methylation of CpGs at regulatory binding sites controls NNAT expression in Wilms tumors

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

The p.G154S mutation of the alpha-B crystallin gene ( CRYAB ) causes late-onset distal myopathy

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

Generalized crystal-storing histiocytosis associated with monoclonal gammopathy: molecular analysis of a disorder with rapid clinical course and review of the literature

Immunoreactivity of p53, Ki-67, and Bcl-2 in oncocytic adenomas and carcinomas of the thyroid gland

Mitochondria and Ageing

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

Vessel adherent growth represents a major challenge in the surgical resection of neuroblastoma and Is associated with adverse outcome

Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

P53 gene product and egf-receptor are highly expressed in placental site trophoblastic tumor

Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies

Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Oxyphil Cell Metaplasia in the Parathyroids Is Characterized by Somatic Mitochondrial DNA Mutations in NADH Dehydrogenase Genes and Cytochrome c Oxidase Activity–Impairing Genes

Epigallocatechin-3-Gallate Inhibits Hepatoblastoma Growth by Reactivating the Wnt Inhibitor SFRP1

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

Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNAser(UCN) gene

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