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Déjà vu with a twist: transglutaminases in bioenergetics and transcriptional dysfunction in Huntington's disease

EMBO molecular medicine, 2010-09, Vol.2 (9), p.335-337

2010

Volltextzugriff (PDF)

Multiple-stress analysis for isolation of Drosophila longevity genes

Proceedings of the National Academy of Sciences - PNAS, 2004-08, Vol.101 (34), p.12610-12615

2004

Volltextzugriff (PDF)

Proteomics of Dense Core Secretory Vesicles Reveal Distinct Protein Categories for Secretion of Neuroeffectors for Cell−Cell Communication

Journal of proteome research, 2010-10, Vol.9 (10), p.5002-5024

2010

Volltextzugriff (PDF)

Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies

Human molecular genetics, 1995-04, Vol.4 (4), p.523-527

1995

Volltextzugriff (PDF)

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

Nature genetics, 1998-02, Vol.18 (2), p.150-154

1998

Volltextzugriff (PDF)

A Drosophila ortholog of the human MRJ modulates polyglutamine toxicity and aggregation

Neurobiology of disease, 2006-11, Vol.24 (2), p.226-244

2006

Volltextzugriff (PDF)

Genetic Suppression of Polyglutamine Toxicity in Drosophila

Science (American Association for the Advancement of Science), 2000-03, Vol.287 (5459), p.1837-1840

2000

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Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

Nature genetics, 1993-10, Vol.5 (2), p.184-188

1993

Volltextzugriff (PDF)

Suppression of polyglutamine toxicity by a Drosophila homolog of myeloid leukemia factor 1

Human molecular genetics, 2002-10, Vol.11 (21), p.2657-2672

2002

Volltextzugriff (PDF)

Aberrant histone acetylation, altered transcription, and retinal degeneration in a Drosophila model of polyglutamine disease are rescued by CREB-binding protein

Genes & development, 2003-06, Vol.17 (12), p.1463-1468

2003

Volltextzugriff (PDF)

HIP1 , a human homologue of S. cerevisiae Sla2p , interacts with membrane-associated huntingtin in the brain

Nature genetics, 1997-05, Vol.16 (1), p.44-53

1997

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X-linked muscular atrophy and the androgen receptor

Trends in Endocrinology & Metabolism, 1994-12, Vol.5 (10), p.416-421

1994

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Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes

Molecular endocrinology (Baltimore, Md.), 1993, Vol.7 (1), p.37-46

1993

Volltextzugriff (PDF)

Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance

The Journal of clinical investigation, 1994-08, Vol.94 (2), p.546-554

1994

Volltextzugriff (PDF)

Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations

Kazemi-Esfarjani, Parsa

1997

Volltextzugriff (PDF)

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Déjà vu with a twist: transglutaminases in bioenergetics and transcriptional dysfunction in Huntington's disease

Multiple-stress analysis for isolation of Drosophila longevity genes

Proteomics of Dense Core Secretory Vesicles Reveal Distinct Protein Categories for Secretion of Neuroeffectors for Cell−Cell Communication

Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

A Drosophila ortholog of the human MRJ modulates polyglutamine toxicity and aggregation

Genetic Suppression of Polyglutamine Toxicity in Drosophila

Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

Suppression of polyglutamine toxicity by a Drosophila homolog of myeloid leukemia factor 1

Aberrant histone acetylation, altered transcription, and retinal degeneration in a Drosophila model of polyglutamine disease are rescued by CREB-binding protein

HIP1 , a human homologue of S. cerevisiae Sla2p , interacts with membrane-associated huntingtin in the brain

X-linked muscular atrophy and the androgen receptor

Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes

Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance

Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations

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