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Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes

Nature communications, 2016-10, Vol.7 (1), p.13049-13049, Article 13049

2016

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The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis

PLoS genetics, 2015-01, Vol.11 (1), p.e1004749

2015

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Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3

PLoS genetics, 2015-01, Vol.11 (1), p.e1004834

2015

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Klotho Depletion Contributes to Increased Inflammation in Kidney of the db/db Mouse Model of Diabetes via RelA (Serine)536 Phosphorylation

Diabetes (New York, N.Y.), 2011-07, Vol.60 (7), p.1907-1916

2011

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Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription

eLife, 2019-04, Vol.8

2019

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Design of a bioactive small molecule that targets r(AUUCU) repeats in spinocerebellar ataxia 10

Nature communications, 2016-06, Vol.7 (1), p.11647-11, Article 11647

2016

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Editorial: Neurodegeneration: From Disease Mechanism to Therapeutic Advancement

Frontiers in genetics, 2022-06, Vol.13, p.941846-941846

2022

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Neil2-null Mice Accumulate Oxidized DNA Bases in the Transcriptionally Active Sequences of the Genome and Are Susceptible to Innate Inflammation

The Journal of biological chemistry, 2015-10, Vol.290 (41), p.24636-24648

2015

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Polyglutamine Expansion in Huntingtin and Mechanism of DNA Damage Repair Defects in Huntington's Disease

Frontiers in cellular neuroscience, 2022-04, Vol.16, p.837576-837576

2022

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Preferential Repair of Oxidized Base Damage in the Transcribed Genes of Mammalian Cells

The Journal of biological chemistry, 2011-02, Vol.286 (8), p.6006-6016

2011

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Correction: The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3'-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis

PLoS genetics, 2024-01, Vol.20 (1), p.e1011124-e1011124

2024

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Neutron Imaging: Basics, Techniques and Applications

1, 2022

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Role of Human DNA Glycosylase Nei-like 2 (NEIL2) and Single Strand Break Repair Protein Polynucleotide Kinase 3′-Phosphatase in Maintenance of Mitochondrial Genome

The Journal of biological chemistry, 2012, Vol.287 (4), p.2819-2829

2012

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Ethanol suppresses PGC-1α expression by interfering with the cAMP-CREB pathway in neuronal cells

PloS one, 2014-08, Vol.9 (8), p.e104247

2014

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Purkinje cell loss is the major brain pathology of spinocerebellar ataxia type 10

Journal of neurology, neurosurgery and psychiatry, 2013-12, Vol.84 (12), p.1409-1411

2013

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The future of cancer treatment: combining radiotherapy with immunotherapy

Frontiers in molecular biosciences, 2024-07, Vol.11, p.1409300

2024

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Klotho Ameliorates Chemically Induced Endoplasmic Reticulum (ER) Stress Signaling

Cellular physiology and biochemistry, 2013-01, Vol.31 (4-5), p.659-672

2013

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Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability

European journal of human genetics : EJHG, 2013-11, Vol.21 (11), p.1272-1276

2013

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Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (7), p.2843-2848

2011

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Klotho depletion contributes to increased inflammation in Kidney of the db/db mouse model of diabetes via RelA [.sup.536] phosphorylation

Diabetes (New York, N.Y.), 2011-07, Vol.60 (7), p.1907

2011

Volltextzugriff (PDF)

Deficiency in classical nonhomologous end-joining–mediated repair of transcribed genes is linked to SCA3 pathogenesis

Proceedings of the National Academy of Sciences - PNAS, 2020-04, Vol.117 (14), p.8154-8165

2020

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Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

Nature genetics, 2000-05, Vol.25 (1), p.110-114

2000

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PIAS1 modulates striatal transcription, DNA damage repair, and SUMOylation with relevance to Huntington's disease

Proceedings of the National Academy of Sciences - PNAS, 2021-01, Vol.118 (4)

2021

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Myotonic dystrophy types 1 and 2

Handbook of Clinical Neurology, 2011, Vol.101, p.193-237

2011

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Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: A toxic RNA gain-of-function model

Journal of neuroscience research, 2012-03, Vol.90 (3), p.706-714

2012

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1 – 25 von 1.008

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Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes

The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis

Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3

Klotho Depletion Contributes to Increased Inflammation in Kidney of the db/db Mouse Model of Diabetes via RelA (Serine)536 Phosphorylation

Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription

Design of a bioactive small molecule that targets r(AUUCU) repeats in spinocerebellar ataxia 10

Editorial: Neurodegeneration: From Disease Mechanism to Therapeutic Advancement

Neil2-null Mice Accumulate Oxidized DNA Bases in the Transcriptionally Active Sequences of the Genome and Are Susceptible to Innate Inflammation

Polyglutamine Expansion in Huntingtin and Mechanism of DNA Damage Repair Defects in Huntington's Disease

Preferential Repair of Oxidized Base Damage in the Transcribed Genes of Mammalian Cells

Correction: The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3'-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis

Neutron Imaging: Basics, Techniques and Applications

Role of Human DNA Glycosylase Nei-like 2 (NEIL2) and Single Strand Break Repair Protein Polynucleotide Kinase 3′-Phosphatase in Maintenance of Mitochondrial Genome

Ethanol suppresses PGC-1α expression by interfering with the cAMP-CREB pathway in neuronal cells

Purkinje cell loss is the major brain pathology of spinocerebellar ataxia type 10

The future of cancer treatment: combining radiotherapy with immunotherapy

Klotho Ameliorates Chemically Induced Endoplasmic Reticulum (ER) Stress Signaling

Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability

Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast

Klotho depletion contributes to increased inflammation in Kidney of the db/db mouse model of diabetes via RelA [.sup.536] phosphorylation

Deficiency in classical nonhomologous end-joining–mediated repair of transcribed genes is linked to SCA3 pathogenesis

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

PIAS1 modulates striatal transcription, DNA damage repair, and SUMOylation with relevance to Huntington's disease

Myotonic dystrophy types 1 and 2

Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: A toxic RNA gain-of-function model

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