Skip to Main Content

Author Details

Stefan T Arold
1997
165
45
PMIDPaper TitleJournal TitlePublished Year
36979085Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation.2023
36810590SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literature.2023
37452126The combined action of the intracellular regions regulates FGFR2 kinase activity.Commun Biol2023
36805523Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders.2023
37119330AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model.Acta Neuropathol2023
37243525Essential role of the CD docking motif of MPK4 in plant immunity, growth, and development.2023
37540795Leveraging AI Advances and Online Tools for Structure-Based Variant Analysis.2023
34820905A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex Dystonia.Movement Disorders2022
35772173Convection Driven Ultrarapid Protein Detection via Nanobody-Functionalized Organic Electrochemical Transistors.Advanced Materials2022
36231115A Novel Homozygous Founder Variant of <i>RTN4IP1</i> in Two Consanguineous Saudi Families.Cells2022
35945264PYK2 senses calcium through a disordered dimerization and calmodulin-binding element.Communications Biology2022
36071959The exceptionally efficient quorum quenching enzyme LrsL suppresses biofilm production.Frontiers in Microbiology2022
35782862Thicker Ice Improves the Integrity and Angular Distribution of CDC48A Hexamers on Cryo-EM Grids.Frontiers in Molecular Biosciences2022
35782384<i>SPTBN5</i>, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures.Front Mol Neurosci2022
35718708Targeting plant UBX proteins: AI-enhanced lessons from distant cousins.Trends in Plant Science2022
36553519Clinical, Radiological, and Genetic Characterization of a Patient with a Novel Homoallelic Loss-of-Function Variant in .2022
34991250Unraveling the differential impact of PAHs and dioxin-like compounds on AKR1C3 reveals the EGFR extracellular domain as a critical determinant of the AHR response.Environment international2022
35312702Efficient multi-gene expression in cell-free droplet microreactors.PLoS ONE2022
35238175Structural basis for specific inhibition of the highly sensitive ShHTL7 receptor.EMBO Reports2022
34850204Rational design of Striga hermonthica-specific seed germination inhibitors.Plant Physiology2022
35200314How to Find the Right RNA-Sensing CRISPR-Cas System for an Application.Biosensors2022
35052432A Novel Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and Cataracts.Genes2021
33592301Co-occurrence of mcr-1 and mcr-8 genes in multi-drug-resistant Klebsiella pneumoniae from a 2015 clinical isolate.Int J Antimicrob Agents2021
33489165Succinic semialdehyde dehydrogenase deficiency presenting with central hypothyroidism.Clinical Case Reports (discontinued)2021
33748703Comprehensive multi-omics analysis of G6PC3 deficiency-related congenital neutropenia with inflammatory bowel disease.iScience2021
33631427QAUST: Protein Function Prediction Using Structure Similarity, Protein Interaction, and Functional Motifs.Genomics Proteomics Bioinformatics2021
33794377Identifying Novel Drug Targets by iDTPnd: A Case Study of Kinase Inhibitors.Genomics Proteomics Bioinformatics2021
33787846Synergy and allostery in ligand binding by HIV-1 Nef.Biochemical Journal2021
33937142Clinical and Genetic Characterization of Craniosynostosis in Saudi Arabia.Frontiers in Pediatrics2021
34141135Versatile control of the CDC48 segregase by the plant UBX-containing (PUX) proteins.Computational and Structural Biotechnology Journal2021
34031558Rapid single-molecule detection of COVID-19 and MERS antigens via nanobody-functionalized organic electrochemical transistors.Nat Biomed Eng2021
33764426Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking.Brain2021
34345025Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.Genet Med2021
33755318MYH1 is a candidate gene for recurrent rhabdomyolysis in humans.Am J Med Genet A2021
33422522Discriminative SKP2 Interactions with CDK-Cyclin Complexes Support a Cyclin A-Specific Role in p27KIP1 Degradation.J Mol Biol2021
33419940Chromatin phosphoproteomics unravels a function for AT-hook motif nuclear localized protein AHL13 in PAMP-triggered immunity.Proceedings of the National Academy of Sciences of the United States of America2021
33410747Molecular basis for the adaptive evolution of environment-sensing by H-NS proteins.eLife2021
32888189Phenotypic and molecular spectrum of pyridoxamine-5'-phosphate oxidase deficiency: A scoping review of 87 cases of pyridoxamine-5'-phosphate oxidase deficiency.Clinical Genetics2021
34507989Cancer-associated mutations in the p85α N-terminal SH2 domain activate a spectrum of receptor tyrosine kinases.Proc Natl Acad Sci U S A2021
34784417Correction: Synergy and allostery in ligand binding by HIV-1 Nef.Biochemical Journal2021
34382809Molecular Basis for Environment Sensing by a Nucleoid-Structuring Bacterial Protein Filament.Journal of Physical Chemistry Letters2021
34777282Novel Enzymes From the Red Sea Brine Pools: Current State and Potential.Frontiers in Microbiology2021
34380564Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining.Human Genomics2021
34373908Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder.Brain2021
34592986The genome of the zoonotic malaria parasite Plasmodium simium reveals adaptations to host switching.BMC Biol2021
33057074Interleukin-26 activates macrophages and facilitates killing of Mycobacterium tuberculosis.Scientific Reports2020
32373358Synthetic bulky NS4A peptide variants bind to and inhibit HCV NS3 protease.Journal of Advanced Research2020
322452181-Imidazole-2,5-Dicarboxamides as NS4A Peptidomimetics: Identification of a New Approach to Inhibit HCV-NS3 Protease.Biomolecules2020
32006098Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy.Acta Neuropathologica2020
32110744A Novel TBX1 Variant Causing Hypoparathyroidism and Deafness.Journal of the Endocrine Society2020
  • 1 - 50 of 164

Recommended Authors

Collaborators

University of Leeds
Co-authored papers 17
King Faisal Specialist Hospital and Research Center
Co-authored papers 16
King Abdullah University of Science and Technology (KAUST)
Co-authored papers 8
Co-authored papers 6
King Abdullah University of Science and Technology
Co-authored papers 6
Institute of Neurology, University College London (UCL)
Co-authored papers 6
King Abdullah University of Science and Technology (KAUST)
Co-authored papers 4
The University of Texas MD Anderson Cancer Center
Co-authored papers 4
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 3
Hamad Medical Corporation.
Co-authored papers 3
Center for the Development of Therapeutics, Broad Institute of MIT & Harvard
Co-authored papers 3
King Abdullah University of Science and Technology
Co-authored papers 3
King Abdullah University of Science and Technology (KAUST)
Co-authored papers 2
University of Texas MD Anderson Cancer Center
Co-authored papers 2
Co-authored papers 2
Ann & Robert H. Lurie Children's Hospital of Chicago
Co-authored papers 2
Co-authored papers 2
University of British Columbia
Co-authored papers 2
National Cancer Institute
Co-authored papers 2
Children's Cancer Institute, Lowy Cancer Research Centre
Co-authored papers 2
National Cancer Institute
Co-authored papers 2
Co-authored papers 2
University of Manchester
Co-authored papers 2
National Cancer Institute
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
College of Life Sciences
Co-authored papers 2
Broad Institute of Harvard and MIT
Co-authored papers 2
St Jude Children's Research Hospital
Co-authored papers 2
University of California
Co-authored papers 2
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 2