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Author Details
Full Name
Herbert Schulz
Affiliation
Clinic for Plastic, Otto von Guericke University
ORCID
Career Start Year
1995
Papers
114
H Index
45
Expertise
CM4AI Collaborator
Kirsten Obernier (CM4AI)
PMID
Paper Title
Journal Title
Published Year
35069110
A Versatile Clustered Regularly Interspaced Palindromic Repeats Toolbox to Study Neurological Ca<sub>V</sub>3.2 Channelopathies by Promoter-Mediated Transcription Control.
Front Mol Neurosci
2022
33319393
Gene expression analysis in epileptic hippocampi reveals a promoter haplotype conferring reduced aldehyde dehydrogenase 5a1 expression and responsiveness.
Epilepsia
2021
34445479
The CellBox-2 Mission to the International Space Station: Thyroid Cancer Cells in Space.
Int J Mol Sci
2021
32308125
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
Pharmacogenomics
2020
30395686
An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
J Bone Miner Res
2019
31293497
Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel <i>KCNQ1</i> Loss-of-Function Mutation.
Front Neurol
2019
31550089
Beneficial Effects of Low Frequency Vibration on Human Chondrocytes in Vitro.
Cell Physiol Biochem
2019
30830987
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
J Bone Miner Res
2019
30719712
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
Epilepsia
2019
29343717
The role of NFκB in spheroid formation of human breast cancer cells cultured on the Random Positioning Machine.
Sci Rep
2018
29985426
Thyroid cancer cells in space during the TEXUS-53 sounding rocket mission - The THYROID Project.
Sci Rep
2018
29949789
Pathway Analysis Hints Towards Beneficial Effects of Long-Term Vibration on Human Chondrocytes.
Cell Physiol Biochem
2018
30545079
Microgravity Affects Thyroid Cancer Cells during the TEXUS-53 Mission Stronger than Hypergravity.
Int J Mol Sci
2018
29459093
Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
Kidney Int
2018
28904069
Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.
Circulation
2017
28232204
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.
Free Radic Biol Med
2017
28161520
Expression profiling of colorectal cancer cells reveals inhibition of DNA replication licensing by extracellular calcium.
Biochim Biophys Acta Mol Cell Res
2017
28148779
Adverse left ventricular remodeling by glycoprotein nonmetastatic melanoma protein B in myocardial infarction.
FASEB J
2017
29142228
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
Nat Commun
2017
28533195
De novo 8p23.1 deletion in a patient with absence epilepsy.
Epileptic Disord
2017
27106802
Embryonic cardiomyocytes can orchestrate various cell protective mechanisms to survive mitochondrial stress.
J Mol Cell Cardiol
2016
27583204
Transcriptional profiling of regenerating embryonic mouse hearts.
Genom Data
2016
27199465
CD74-Downregulation of Placental Macrophage-Trophoblastic Interactions in Preeclampsia.
Circ Res
2016
27211213
Human Engineered Heart Tissue: Analysis of Contractile Force.
Stem Cell Reports
2016
26888427
Ndufc2 Gene Inhibition Is Associated With Mitochondrial Dysfunction and Increased Stroke Susceptibility in an Animal Model of Complex Human Disease.
J Am Heart Assoc
2016
25950944
Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies.
PLoS Genet
2015
26388944
Gene repositioning within the cell nucleus is not random and is determined by its genomic neighborhood.
Epigenetics Chromatin
2015
26192016
Novel candidate genes for impaired nephron development in a rat model with inherited nephron deficit and albuminuria.
Clin Exp Pharmacol Physiol
2015
25889719
Differential gene expression of human chondrocytes cultured under short-term altered gravity conditions during parabolic flight maneuvers.
Cell Commun Signal
2015
25993318
Alternatively spliced isoforms of WT1 control podocyte-specific gene expression.
Kidney Int
2015
25961942
PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
Nat Genet
2015
24196587
Differential gene expression profile and altered cytokine secretion of thyroid cancer cells in space.
FASEB J
2014
25566086
Proteasome inhibition slightly improves cardiac function in mice with hypertrophic cardiomyopathy.
Front Physiol
2014
24770696
Klf4 and Klf5 differentially inhibit mesoderm and endoderm differentiation in embryonic stem cells.
Nat Commun
2014
24790086
Protease inhibitor 15, a candidate gene for abdominal aortic internal elastic lamina ruptures in the rat.
Physiol Genomics
2014
24852842
Functional improvement and maturation of rat and human engineered heart tissue by chronic electrical stimulation.
J Mol Cell Cardiol
2014
24651840
Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy.
PLoS One
2014
24487590
TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction.
J Clin Invest
2014
24410968
Rosuvastatin can block pro-inflammatory actions of transgenic human C-reactive protein without reducing its circulating levels.
Cardiovasc Ther
2014
23038778
Activation of the PTHRP/adenylate cyclase pathway promotes differentiation of rat XEN cells into parietal endoderm, whereas Wnt/β-catenin signaling promotes differentiation into visceral endoderm.
J Cell Sci
2013
24019929
Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1).
PLoS One
2013
23658691
Comparative transcriptional profiling of the axolotl limb identifies a tripartite regeneration-specific gene program.
PLoS One
2013
23675535
Genomic approach to identify factors that drive the formation of three-dimensional structures by EA.hy926 endothelial cells.
PLoS One
2013
23798433
Interfering with Gal-1-mediated angiogenesis contributes to the pathogenesis of preeclampsia.
Proc Natl Acad Sci U S A
2013
23708188
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats.
Nat Genet
2013
23706953
TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue.
Seizure
2013
23319640
Borna disease virus-induced neuronal degeneration dependent on host genetic background and prevented by soluble factors.
Proc Natl Acad Sci U S A
2013
21519850
Specific gene signatures and pathways in mesodermal cells and their derivatives derived from embryonic stem cells.
Stem Cell Rev Rep
2012
22949513
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Hum Mol Genet
2012
22964303
Gravity-sensitive signaling drives 3-dimensional formation of multicellular thyroid cancer spheroids.
FASEB J
2012
1 - 50 of 114
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Per Hoffmann
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Steve Horvath
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