A. Neueder

发表

A common gene expression signature in Huntington’s disease patient brain regions

G. Bates, A. Neueder, Andreas Neueder, 2014, BMC Medical Genomics.

Cre recombinase expression or topical tamoxifen treatment do not affect retinal structure and function, neuronal vulnerability or glial reactivity in the mouse eye

E. Tamm, H. Jägle, C. Sippl, 2016, Neuroscience.

Contesting the dogma of an age-related heat shock response impairment: implications for cardiac-specific age-related disorders

G. Bates, S. Moussaoui, A. Neueder, 2014, Human molecular genetics.

Retinitis Pigmentosa Results in Neurodegeneration Concomitant With Neuroinflammation, Extracellular Matrix Disorganization and the Upregulation of Neuroprotective Pathways in Glial Cells and Neurons

E. Tamm, S. Ergün, Christina B. Bielmeier, 2020 .

Silencing Srsf6 does not modulate incomplete splicing of the huntingtin gene in Huntington’s disease models

Aikaterini S. Papadopoulou, G. Bates, K. Sathasivam, 2020, Scientific Reports.

Novel Isoforms of Heat Shock Transcription Factor 1, HSF1γα and HSF1γβ, Regulate Chaperone Protein Gene Transcription

G. Bates, S. Moussaoui, A. Neueder, 2014, The Journal of Biological Chemistry.

Aberrantly spliced HTT, a new player in Huntington’s disease pathogenesis

D. Housman, N. Wexler, G. Bates, 2013, RNA biology.

Phenotype onset in Huntington’s disease knock‐in mice is correlated with the incomplete splicing of the mutant huntingtin gene

M. Chesselet, G. Bates, M. Hickey, 2019, Journal of neuroscience research.

Targeting Tau Mitigates Mitochondrial Fragmentation and Oxidative Stress in Amyotrophic Lateral Sclerosis

Derek H. Oakley, S. Haggarty, B. Hyman, 2021, Molecular Neurobiology.

Small Ribosomal Protein RPS0 Stimulates Translation Initiation by Mediating 40S-Binding of eIF3 via Its Direct Contact with the eIF3a/TIF32 Subunit

L. Valášek, Vanda Munzarová, Stanislava Gunišová, 2012, PloS one.

Targeting Tau Mitigates Mitochondrial Fragmentation and Oxidative Stress in Amyotrophic Lateral Sclerosis

Derek H. Oakley, S. Haggarty, B. Hyman, 2021, Molecular Neurobiology.

Density, Relative Permittivity, and Viscosity of Propylene Carbonate + Dimethoxyethane Mixtures from 25 °C to 125 °C

J. Barthel, A. Neueder, Hadumar Roch, 2000 .

Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease

D. Housman, P. Detloff, R. Roos, 2013, Proceedings of the National Academy of Sciences.

Characterization of r-protein variants in Saccharomyces cerevisiae

A. Neueder, Andreas Neueder, 2011 .

Analysis of the in vivo assembly pathway of eukaryotic 40S ribosomal proteins.

H. Tschochner, A. Neueder, Sébastien Ferreira-Cerca, 2007, Molecular cell.

PhysiologyDavid and Wolfgang-Michael Franz From Pluripotency to Distinct Cardiomyocyte Subtypes

G. Bates, S. Moussaoui, A. Neueder, 2015 .

Deficiency in Retinal TGFβ Signaling Aggravates Neurodegeneration by Modulating Pro-Apoptotic and MAP Kinase Pathways

E. Tamm, S. Ergün, J. Hillenkamp, 2022, International journal of molecular sciences.

Mitochondrial biology and the identification of biomarkers of Huntington's disease.

M. Orth, A. Neueder, Andreas Neueder, 2020, Neurodegenerative disease management.

G. Bates, A. Neueder, Andreas Neueder, 2018, Advances in experimental medicine and biology.

Three Huntington’s Disease Specific Mutation-Carrying Human Embryonic Stem Cell Lines Have Stable Number of CAG Repeats upon In Vitro Differentiation into Cardiomyocytes

D. Ilic, C. Hobbs, M. Mioulane, 2015, PloS one.

RNA-Mediated Disease Mechanisms in Neurodegenerative Disorders.

A. Neueder, Andreas Neueder, 2019, Journal of molecular biology.

rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins

J. Woolford, Tobias Braun, H. Tschochner, 2009, PloS one.

A Local Role for the Small Ribosomal Subunit Primary Binder rpS5 in Final 18S rRNA Processing in Yeast

H. Tschochner, R. Deutzmann, A. Neueder, 2010, PloS one.

Interrelationships between Yeast Ribosomal Protein Assembly Events and Transient Ribosome Biogenesis Factors Interactions in Early Pre-Ribosomes

J. Griesenbeck, H. Tschochner, R. Deutzmann, 2012, PloS one.

Nucleolar stress controls mutant Huntington toxicity and monitors Huntington’s disease progression

F. Tuorto, B. Liss, M. Orth, 2021, Cell Death & Disease.

Regulatory mechanisms of incomplete huntingtin mRNA splicing

G. Bates, A. Neueder, A. Dumas, 2018, Nature Communications.

Regulatory mechanisms of incomplete huntingtin mRNA splicing

G. Bates, A. Neueder, A. Dumas, 2018, Nature Communications.

The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington’s disease patients

S. Tabrizi, R. Faull, R. Myers, 2017, Scientific Reports.

HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse models

D. Housman, G. Bates, P. Paganetti, 2017, Scientific Reports.

PolyQ length-dependent metabolic alterations and DNA damage drive human astrocyte dysfunction in Huntington’s disease

S. Tabrizi, M. Duchen, P. Ferretti, 2023, Progress in Neurobiology.

HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse models

D. Housman, G. Bates, P. Paganetti, 2017, Scientific Reports.

Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa

E. Tamm, S. Ergün, Christina B. Bielmeier, 2021, International journal of molecular sciences.

HSF1-dependent and -independent regulation of the mammalian in vivo heat shock response and its impairment in Huntington's disease mouse models

D. Housman, G. Bates, P. Paganetti, 2017, Scientific Reports.

Abnormal molecular signatures of inflammation, energy metabolism, and vesicle biology in human Huntington disease peripheral tissues

S. Tabrizi, D. Lavery, S. Haider, 2022, Genome Biology.

Dysfunction of the CNS-Heart Axis in Mouse Models of Huntington's Disease

G. Bates, Georgina F Osborne, A. Protti, 2014, PLoS genetics.

Myostatin inhibition prevents skeletal muscle pathophysiology in Huntington’s disease mice

Tobias C. Wood, S. Tabrizi, L. Greensmith, 2017, Scientific Reports.