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Author Details
Full Name
Wolfgang Wurst
Affiliation
Institute of Developmental Genetics, German Research Center for Environmental Health
ORCID
Career Start Year
1984
Papers
452
H Index
90
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36529279
Identification of ocular regulatory functions of core histone variant H3.2.
Exp Eye Res
2023
37996418
A reversible state of hypometabolism in a human cellular model of sporadic Parkinson's disease.
Nat Commun
2023
37988467
Unrestrained cleavage of Roquin-1 by MALT1 induces spontaneous T cell activation and the development of autoimmunity.
Proc Natl Acad Sci U S A
2023
36993625
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
medRxiv
2023
37230398
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease.
Biochim Biophys Acta Mol Basis Dis
2023
37130781
Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain.
Life Sci Alliance
2023
37428903
Systemic deletion of <i>DMD</i> exon 51 rescues clinically severe Duchenne muscular dystrophy in a pig model lacking <i>DMD</i> exon 52.
Proc Natl Acad Sci U S A
2023
36995669
Gene Editing in Mouse Zygotes Using the CRISPR/Cas9 System.
Methods Mol Biol
2023
36878826
Corrigendum to Semaphorin 4C and 4G are ligands of Plexin-B2 required in cerebellar development [Mol. Cell. Neurosci., 2011 Feb;46(2):419-31].
Mol Cell Neurosci
2023
36538124
A rationale for considering heart/brain axis control in neuropsychiatric disease.
Mamm Genome
2023
34927460
Susceptibility to diet-induced obesity at thermoneutral conditions is independent of UCP1.
Am J Physiol Endocrinol Metab
2022
35373464
Parkinson's disease motor symptoms rescue by CRISPRa-reprogramming astrocytes into GABAergic neurons.
EMBO Mol Med
2022
35370007
Chapter 5 - "Parkinson's disease - A role of non-enzymatic posttranslational modifications in disease onset and progression?"
Mol Aspects Med
2022
35659494
Pig models for Duchenne muscular dystrophy - from disease mechanisms to validation of new diagnostic and therapeutic concepts.
Neuromuscul Disord
2022
35618940
PARK7/DJ-1 promotes pyruvate dehydrogenase activity and maintains T<sub>reg</sub> homeostasis during ageing.
Nat Metab
2022
36535974
Toxicity of extracellular alpha-synuclein is independent of intracellular alpha-synuclein.
Sci Rep
2022
36002575
Phosphorylation of muramyl peptides by NAGK is required for NOD2 activation.
Nature
2022
36369285
Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice.
Nat Commun
2022
36270613
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome.
Mol Metab
2022
35974013
Primary cilia and SHH signaling impairments in human and mouse models of Parkinson's disease.
Nat Commun
2022
35159329
Innate Immune Pathways Promote Oligodendrocyte Progenitor Cell Recruitment to the Injury Site in Adult Zebrafish Brain.
Cells
2022
35308871
Concept of the Munich/Augsburg Consortium Precision in Mental Health for the German Center of Mental Health.
Front Psychiatry
2022
34964047
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk.
Dis Model Mech
2022
33202244
CRISPR-Mediated Induction of Neuron-Enriched Mitochondrial Proteins Boosts Direct Glia-to-Neuron Conversion.
Cell Stem Cell
2021
33597771
Simple and reliable detection of CRISPR-induced on-target effects by qgPCR and SNP genotyping.
Nat Protoc
2021
33512427
Mammalian VPS45 orchestrates trafficking through the endosomal system.
Blood
2021
33729986
Mutant non-coding RNA resource in mouse embryonic stem cells.
Dis Model Mech
2021
33667363
CRISPR-Mediated Induction of Neuron-Enriched Mitochondrial Proteins Boosts Direct Glia-to-Neuron Conversion.
Cell Stem Cell
2021
33531685
Genome editing for Duchenne muscular dystrophy: a glimpse of the future?
Gene Ther
2021
33748099
Comprehensive miRNome-Wide Profiling in a Neuronal Cell Model of Synucleinopathy Implies Involvement of Cell Cycle Genes.
Front Cell Dev Biol
2021
34474098
Determination of morphine and norlaudanosoline in murine brain regions by dispersive liquid-liquid micro-extraction and liquid chromatograpy-electrochemical detection.
Neurochem Int
2021
34811541
Disrupting Roquin-1 interaction with Regnase-1 induces autoimmunity and enhances antitumor responses.
Nat Immunol
2021
34750991
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes.
EMBO Mol Med
2021
34390512
Endoglycan (PODXL2) is proteolytically processed by ADAM10 (a disintegrin and metalloprotease 10) and controls neurite branching in primary neurons.
FASEB J
2021
34767456
TRAF6 prevents fatal inflammation by homeostatic suppression of MALT1 protease.
Sci Immunol
2021
34532319
iPS Cell-Based Model for <i>MAPT</i> Haplotype as a Risk Factor for Human Tauopathies Identifies No Major Differences in TAU Expression.
Front Cell Dev Biol
2021
34043061
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse.
Mamm Genome
2021
34083785
Non-invasive and high-throughput interrogation of exon-specific isoform expression.
Nat Cell Biol
2021
33999436
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism.
Ann Neurol
2021
33449167
DGK and DZHK position paper on genome editing: basic science applications and future perspective.
Basic Res Cardiol
2021
33131190
Diabetes type 2 risk gene Dusp8 is associated with altered sucrose reward behavior in mice and humans.
Brain Behav
2021
33264576
Dose-dependent long-term effects of a single radiation event on behaviour and glial cells.
Int J Radiat Biol
2021
31591642
Soft windowing application to improve analysis of high-throughput phenotyping data.
Bioinformatics
2020
32060626
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes.
Mamm Genome
2020
31908000
Mouse brain proteomics establishes MDGA1 and CACHD1 as in vivo substrates of the Alzheimer protease BACE1.
FASEB J
2020
32029747
Sox2 controls Schwann cell self-organization through fibronectin fibrillogenesis.
Sci Rep
2020
32015554
Global site-specific neddylation profiling reveals that NEDDylated cofilin regulates actin dynamics.
Nat Struct Mol Biol
2020
32015326
Alpha-synuclein fragments trigger distinct aggregation pathways.
Cell Death Dis
2020
32066665
A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neurons.
Transl Psychiatry
2020
32103165
Publisher Correction: Global site-specific neddylation profiling reveals that NEDDylated cofilin regulates actin dynamics.
Nat Struct Mol Biol
2020
1 - 50 of 452
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German Research Centre for Environmental Health
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85
Valerie Gailus-Durner
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers
78
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Institute of Experimental Genetics, German Mouse Clinic
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77
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Co-authored papers
43
Martin Klingenspor
Technical University of Munich
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Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
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14
Glauco P Tocchini-Valentini
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers
11
Kent C Lloyd
University of California davis
Co-authored papers
10
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers
10
Fabian J Theis
Technical University of Munich
Co-authored papers
10
Janet Rossant
The Hospital for Sick Children
Co-authored papers
10
Colin McKerlie
The Hospital for Sick Children
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10
Christian Haass
German Center for Neurodegenerative Diseases (DZNE) Munich
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10
William C Skarnes
Wellcome Trust Sanger Institute
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10
Jacqueline K White
Wellcome Trust Sanger Institute
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9
Ann-Marie Mallon
The Turing Institute
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9
Jeremy Mason
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