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ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions

American journal of human genetics, 2011-09, Vol.89 (3), p.407-414

2011

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TRIM32 regulates skeletal muscle stem cell differentiation and is necessary for normal adult muscle regeneration

PloS one, 2012-01, Vol.7 (1), p.e30445-e30445

2012

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Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome

American journal of human genetics, 2009-06, Vol.84 (6), p.728-739

2009

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Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

The HUGO journal, 2009-12, Vol.3 (1-4), p.41-49

2009

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The Interaction of Piasy with Trim32, an E3-Ubiquitin Ligase Mutated in Limb-girdle Muscular Dystrophy Type 2H, Promotes Piasy Degradation and Regulates UVB-induced Keratinocyte Apoptosis through NFκB

The Journal of biological chemistry, 2006-09, Vol.281 (35), p.25850-25866

2006

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Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene

American journal of human genetics, 2002-03, Vol.70 (3), p.663-672

2002

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Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

Neuromuscular disorders : NMD, 2000-12, Vol.10 (8), p.553-559

2000

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Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I

European journal of human genetics : EJHG, 2005-08, Vol.13 (8), p.978-982

2005

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A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

American journal of human genetics, 1998-07, Vol.63 (1), p.140-147

1998

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The Interaction of Piasy with Trim32, an E3-Ubiquitin Ligase Mutated in Limb-girdle Muscular Dystrophy Type 2H, Promotes Piasy Degradation and Regulates UVB-induced Keratinocyte Apoptosis through NFÎºB

The Journal of biological chemistry, 2006-09, Vol.281 (35), p.25850

2006

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The interaction of Piasy with Trim32, an E3-ubiquitin ligase mutated in limb-girdle muscular dystrophy type 2H, promotes Piasy degradation and regulates UVB-induced keratinocyte apoptosis through NFkappaB

The Journal of biological chemistry, 2006-09, Vol.281 (35), p.25850

2006

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Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype

American journal of human genetics, 1996-10, Vol.59 (4), p.872-878

1996

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Hutterite brothers both affected with two forms of limb girdle muscular dystrophy : LGMD2H and LGMD21

European journal of human genetics : EJHG, 2005, Vol.13 (8), p.978-982

2005

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Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

The HUGO journal, 2009-12, Vol.3 (1-4), p.83-83

2009

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Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval

American journal of human genetics, 1994-06, Vol.54 (6), p.1050-1059

1994

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The 56 kDa androgen binding protein is an aldehyde dehydrogenase

Biochemical and biophysical research communications, 1991-03, Vol.175 (3), p.831-838

1991

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Untersuchungen uber den Austritt von Zell-Enzymen aus der akut oder chronisch vorgeschadigten, isolierten, perfundierten Ratten-Leber

Wrogemann, Klaus

1966

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Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy

Journal of the neurological sciences, 1992-10, Vol.112 (1), p.133-138

1992

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The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene

Molecular and cellular endocrinology, 1991, Vol.75 (1), p.37-47

1991

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Partial androgen insensitivity—are all tissues equal?

Fertility and sterility, 1993-08, Vol.60 (2), p.366-368

1993

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ENERGY METABOLISM IN PROGRESSIVE MUSCULAR DYSTROPHY; STUDIES ON OXIDATIVE PHOSPHORYLATION OF GENETICALLY DETERMINED MUSCULAR DYSTROPHY IN MICE AND HAMSTERS

WROGEMANN, KLAUS

1969

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Mitochondrial calcium overloading in cardiomyopathic hamsters

Journal of molecular and cellular cardiology, 1978-01, Vol.10 (2), p.185-195

1978

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The 56 kDa androgen-binding protein in human genital skin fibroblasts: its relation to the human androgen receptor

Molecular and cellular endocrinology, 1990-01, Vol.68 (2), p.195-204

1990

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Functional studies on in situ-like mitochondria isolated in the presence of polyvinyl pyrrolidone

Biochimica et biophysica acta. Bioenergetics, 1985, Vol.806 (1), p.1-8

1985

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An abundant 56 kD protein with low affinity androgen binding: Another member of the steroid/thyroid receptor family?

Biochemical and biophysical research communications, 1988-09, Vol.155 (2), p.907-913

1988

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ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions

TRIM32 regulates skeletal muscle stem cell differentiation and is necessary for normal adult muscle regeneration

Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome

Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

The Interaction of Piasy with Trim32, an E3-Ubiquitin Ligase Mutated in Limb-girdle Muscular Dystrophy Type 2H, Promotes Piasy Degradation and Regulates UVB-induced Keratinocyte Apoptosis through NFκB

Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I

A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

The Interaction of Piasy with Trim32, an E3-Ubiquitin Ligase Mutated in Limb-girdle Muscular Dystrophy Type 2H, Promotes Piasy Degradation and Regulates UVB-induced Keratinocyte Apoptosis through NFÎºB

The interaction of Piasy with Trim32, an E3-ubiquitin ligase mutated in limb-girdle muscular dystrophy type 2H, promotes Piasy degradation and regulates UVB-induced keratinocyte apoptosis through NFkappaB

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype

Hutterite brothers both affected with two forms of limb girdle muscular dystrophy : LGMD2H and LGMD21

Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval

The 56 kDa androgen binding protein is an aldehyde dehydrogenase

Untersuchungen uber den Austritt von Zell-Enzymen aus der akut oder chronisch vorgeschadigten, isolierten, perfundierten Ratten-Leber

Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy

The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene

Partial androgen insensitivity—are all tissues equal?

ENERGY METABOLISM IN PROGRESSIVE MUSCULAR DYSTROPHY; STUDIES ON OXIDATIVE PHOSPHORYLATION OF GENETICALLY DETERMINED MUSCULAR DYSTROPHY IN MICE AND HAMSTERS

Mitochondrial calcium overloading in cardiomyopathic hamsters

The 56 kDa androgen-binding protein in human genital skin fibroblasts: its relation to the human androgen receptor

Functional studies on in situ-like mitochondria isolated in the presence of polyvinyl pyrrolidone

An abundant 56 kD protein with low affinity androgen binding: Another member of the steroid/thyroid receptor family?

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