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Prof. Dr. Heinrich Sticht
List of publications:
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Professur für Bioinformatik
Award(s)
(1)
Project Leads
(1)
Project Memberships
(3)
Publications
(256)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype (2021)
Averdunk L, Sticht H, Surowy H, Luedecke HJ, Koch-Hogrebe M, Alsaif HS, Kahrizi K, et al.
Journal article
Computational decomposition reveals reshaping of the SARS‐CoV‐2–ACE2 interface among viral variants expressing the N501Y mutation (2021)
Socher E, Conrad M, Heger L, Paulsen F, Sticht H, Zunke F, Arnold P
Journal article, Original article
Specific engineered G protein coupling to histamine receptors revealed from cellular assay experiments and accelerated molecular dynamics simulations (2021)
Höring C, Conrad M, Söldner C, Wang J, Sticht H, Strasser A, Miao Y
Journal article, Original article
A novel strain-specific neutralizing epitope on glycoprotein H of human cytomegalovirus (2021)
Thomas M, Kropff B, Schneider A, Winkler T, Görzer I, Sticht H, Britt WJ, et al.
Journal article, Original article
Molecular Simulations and Alzheimer׳s Disease (2021)
Söldner C, Sticht H, Horn A
Book chapter / Article in edited volumes
A pair of non‐competing neutralizing human monoclonal antibodies protecting from disease in a SARS‐CoV‐2 infection model (2021)
Peter AS, Roth E, Schulz S, Fraedrich K, Steinmetz T, Damm D, Hauke M, et al.
Journal article, Original article
Inhibition of SARS CoV Envelope Protein by Flavonoids and Classical Viroporin Inhibitors (2021)
Breitinger U, Ali NK, Sticht H, Breitinger HG
Journal article
Functional Relevance of the Interaction between Human Cyclins and the Cytomegalovirus-Encoded CDK-Like Protein Kinase pUL97 (2021)
Schütz M, Steingruber M, Socher E, Müller R, Wagner S, Kögel M, Sticht H, Marschall M
Journal article, Original article
Mutations in the B.1.1.7 SARS-CoV-2 Spike Protein Reduce Receptor-Binding Affinity and Induce a Flexible Link to the Fusion Peptide (2021)
Socher E, Conrad M, Heger L, Paulsen F, Sticht H, Zunke F, Arnold P
Journal article
Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1 (2021)
Appelhof B, Wagner M, Hoefele J, Heinze A, Roser T, Koch-Hogrebe M, Roosendaal SD, et al.
Journal article
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