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Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome

Proceedings of the National Academy of Sciences - PNAS, 2011-04, Vol.108 (16), p.6543-6548

2011

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Ebselen treatment reduces noise induced hearing loss via the mimicry and induction of glutathione peroxidase

Hearing research, 2007-04, Vol.226 (1), p.44-51

2007

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Reduction of acute cisplatin ototoxicity and nephrotoxicity in rats by oral administration of allopurinol and ebselen

Hearing research, 2005-03, Vol.201 (1), p.81-89

2005

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CTP synthase polymerization in germline cells of the developing Drosophila egg supports egg production

Biology open, 2020-07, Vol.9 (7)

2020

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The geometry of taking flight: Limb morphometrics in Mesozoic theropods

Journal of morphology (1931), 2015-02, Vol.276 (2), p.152-166

2015

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Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss

American journal of human genetics, 2006-01, Vol.78 (1), p.144-152

2006

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Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous

Science (American Association for the Advancement of Science), 1997-11, Vol.278 (5341), p.1315-1318

1997

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Ebselen-Mediated Protection From Single and Repeated Noise Exposure in Rat

The Laryngoscope, 2004-02, Vol.114 (2), p.333-337

2004

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Combined oral delivery of ebselen and allopurinol reduces multiple cisplatin toxicities in rat breast and ovarian cancer models while enhancing anti-tumor activity

Anti-cancer drugs, 2005-06, Vol.16 (5), p.569-579

2005

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Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

Science (American Association for the Advancement of Science), 1998-03, Vol.279 (5358), p.1950-1954

1998

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Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Nature genetics, 1999-12, Vol.23 (4), p.413-419

1999

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The tetrameric kinesin Kif25 suppresses pre-mitotic centrosome separation to establish proper spindle orientation

Nature cell biology, 2017-04, Vol.19 (4), p.384

2017

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

Human molecular genetics, 2001-10, Vol.10 (22), p.2509-2514

2001

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Cloning of the cellular receptor for feline leukemia virus subgroup C (FeLV-C), a retrovirus that induces red cell aplasia

Blood, 2000-02, Vol.95 (3), p.1093-1099

2000

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An Ancient Conserved Gene Expressed in the Human Inner Ear: Identification, Expression Analysis, and Chromosomal Mapping of Human and Mouse Antiquitin (ATQ1)

Genomics (San Diego, Calif.), 1997-12, Vol.46 (2), p.191-199

1997

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SeqHelp: a program to analyze molecular sequences utilizing common computational resources

Genome research, 1998-03, Vol.8 (3), p.306

1998

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Characterization of EZH1, a human homolog of Drosophila enhancer of zeste near BRCA1

Genomics (San Diego, Calif.), 1996-10, Vol.37 (2), p.161-171

1996

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Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization

Genomics (San Diego, Calif.), 1992-06, Vol.13 (2), p.452-454

1992

Volltextzugriff (PDF)

Fractalkine-induced activation of the phosphatidylinositol-3 kinase pathway attentuates microglial activation in vivo and in vitro

Journal of neurochemistry, 2009-09, Vol.110 (5), p.1547-1556

2009

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Therapeutic Inhibition of miR-208a Improves Cardiac Function and Survival During Heart Failure

Circulation (New York, N.Y.), 2011-10, Vol.124 (14), p.1537-1547

2011

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Inhibition of miR-15 Protects Against Cardiac Ischemic Injury

Circulation research, 2012-01, Vol.110 (1), p.71-81

2012

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Potential functional and pathological side effects related to off-target pharmacological activity

Journal of pharmacological and toxicological methods, 2017-09, Vol.87, p.108-126

2017

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Biomimetic and bio-inspired robotics in electric fish research

Journal of experimental biology, 2013-07, Vol.216 (Pt 13), p.2501-2514

2013

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Therapeutic suppression of translation initiation factor eIF4E expression reduces tumor growth without toxicity

The Journal of clinical investigation, 2007-09, Vol.117 (9), p.2638-2648

2007

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GM-CSF increases mucosal and systemic immunogenicity of an H1N1 influenza DNA vaccine administered into the epidermis of non-human primates

PloS one, 2010-06, Vol.5 (6), p.e11021-e11021

2010

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Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome

Ebselen treatment reduces noise induced hearing loss via the mimicry and induction of glutathione peroxidase

Reduction of acute cisplatin ototoxicity and nephrotoxicity in rats by oral administration of allopurinol and ebselen

CTP synthase polymerization in germline cells of the developing Drosophila egg supports egg production

The geometry of taking flight: Limb morphometrics in Mesozoic theropods

Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss

Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous

Ebselen-Mediated Protection From Single and Repeated Noise Exposure in Rat

Combined oral delivery of ebselen and allopurinol reduces multiple cisplatin toxicities in rat breast and ovarian cancer models while enhancing anti-tumor activity

Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

The tetrameric kinesin Kif25 suppresses pre-mitotic centrosome separation to establish proper spindle orientation

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

Cloning of the cellular receptor for feline leukemia virus subgroup C (FeLV-C), a retrovirus that induces red cell aplasia

An Ancient Conserved Gene Expressed in the Human Inner Ear: Identification, Expression Analysis, and Chromosomal Mapping of Human and Mouse Antiquitin (ATQ1)

SeqHelp: a program to analyze molecular sequences utilizing common computational resources

Characterization of EZH1, a human homolog of Drosophila enhancer of zeste near BRCA1

Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization

Fractalkine-induced activation of the phosphatidylinositol-3 kinase pathway attentuates microglial activation in vivo and in vitro

Therapeutic Inhibition of miR-208a Improves Cardiac Function and Survival During Heart Failure

Inhibition of miR-15 Protects Against Cardiac Ischemic Injury

Potential functional and pathological side effects related to off-target pharmacological activity

Biomimetic and bio-inspired robotics in electric fish research

Therapeutic suppression of translation initiation factor eIF4E expression reduces tumor growth without toxicity

GM-CSF increases mucosal and systemic immunogenicity of an H1N1 influenza DNA vaccine administered into the epidermis of non-human primates

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