Current Projects Molecular dissection of mutations in ACTB and ACTG1 causing non-muscle actinopathies Functional characterizations of mutations in non-muscle myosin-2A causing MYH9 -related disorders
children and adolescents in Germany: does social background play a role? Archives of Public Health , 81 (1), 1-12. https://doi.org/10.1186/s13690-023-01173-5 Krüger K , Lapstich AM, Reber KC, Sehlen S, Liersch [...] integrated care AOK Junior: protocol for a mixed-method study. BMC Health Services Research 2020, 20(1), 1-10. DOI: https://doi.org/10.1186/s12913-020-05088-7 . Krauth C, Rossol S, Ortsäter G, Kautz A, Krüger [...] longitudinal retrospective cohort study. BMC pediatrics, 23:164. https://doi.org/10.1186/s12887-023-03988-1 Krüger K , Oedingen C, Kautz A, Langenbacher D, Rossol S, Stahmeyer JT, Krauth C (2023). Lifestyle
III. BMC Mol Biol. 12(1):43. Linkner, J., Witte, G., Stradal, T., Curth, U. and Faix, J. (2011) High-Resolution X-Ray Structure of the Trimeric Scar/WAVE-Complex Precursor Brk1 PLoS One 6, e21327 Winkler [...] switches of the SARS-CoV-2 main protease in vitro provide opportunities for drug design. Nat Commun 15(1): 411. Oleshko, O., N. Vollack-Hesse, A. Tiede, J. Hegermann, U. Curth and S. Werwitzke (2023). Von [...] and mechanistic basis of capsule O-acetylation in Neisseria meningitidis serogroup A. Nat Commun 11(1), 4723. Zhang, L., Lin, D., Sun, X., Curth, U., Drosten, C., Sauerhering, L., Becker, S., Rox, K., and
Interactions Using Uptake and Surface Display by Nontypeable Haemophilus influenzae. mBio. 2021 Jan 19;12(1):e03226-20. doi: 10.1128/mBio.03226-20. PMID: 33468699 Free PMC article. Kawanishi K, Saha S, Diaz S [...] ketodeoxynonulosonic acid production is independent of sialoglycan biosynthesis. J Clin Invest. 2021 Mar 1;131(5):e137681. doi: 10.1172/JCI137681. PMID: 33373330 Free PMC article. 2019 Niculovic KM , Blume L [...] (2018), Sialic acid is a critical fetal defense against maternal complement attack, J Clin Invest . 129(1), 422-436. Sieve I , Münster-Kühnel AK , Hilfiker-Kleiner D (2018), Regulation and function of endothelial
L, Kispert A, Al-Hasani H, Haffner D, Weber RG. Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary [...] Krauss JK, Feuerhake F, Hartmann C, Wiese B, Brand F, Weber RG. Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families. Acta Neuropathol Commun [...] Preller M, Aretz S, Wiese B, Hartmann C, Weber RG. Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin. Acta Neuropathol
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Adresse: Medizinische Hochschule Hannover Klinik für Psychosomatik und Psychotherapie Carl-Neuberg-Str. 1 30625 Hannover Tel: +49 511 532 6436 E-mail : stephan.michael @ mh-hannover.de Raum : K21 - SO - 1040
Adresse: Medizinische Hochschule Hannover Klinik für Psychosomatik und Psychotherapie Carl-Neuberg-Straße 1 30625 Hannover Tel: +49 511 532 6448 E-mail: Westenberger.Adrian @ mh-hannover.de Raum: K21 - O3 - 1012