DC-SIGN and DC-SIGNR interact with the glycoprotein of Marburg virus and the S protein of severe acute respiratory syndrome coronavirus

…, P Möller, AJ Rennekamp, M Krumbiegel… - Journal of …, 2004 - Am Soc Microbiol
The lectins DC-SIGN and DC-SIGNR can augment viral infection; however, the range of
pathogens interacting with these attachment factors is incompletely defined. Here we show that …

Susceptibility to SARS coronavirus S protein-driven infection correlates with expression of angiotensin converting enzyme 2 and infection can be blocked by soluble …

H Hofmann, M Geier, A Marzi, M Krumbiegel… - Biochemical and …, 2004 - Elsevier
The angiotensin converting enzyme 2 (ACE2) has been identified as a receptor for the
severe acute respiratory syndrome associated coronavirus (SARS-CoV). Here we show that …

S protein of severe acute respiratory syndrome-associated coronavirus mediates entry into hepatoma cell lines and is targeted by neutralizing antibodies in infected …

…, A Marzi, T Gramberg, M Geier, M Krumbiegel… - Journal of …, 2004 - Am Soc Microbiol
The severe acute respiratory syndrome-associated coronavirus (SARS-CoV) causes severe
pneumonia with a fatal outcome in approximately 10% of patients. SARS-CoV is not closely …

[HTML][HTML] LSECtin interacts with filovirus glycoproteins and the spike protein of SARS coronavirus

…, P Möller, PF Lalor, A Marzi, M Geier, M Krumbiegel… - Virology, 2005 - Elsevier
Cellular attachment factors like the C-type lectins DC-SIGN and DC-SIGNR (collectively
referred to as DC-SIGN/R) can augment viral infection and might promote viral dissemination in …

Diagnostic yield and novel candidate genes by exome sequencing in 152 consanguineous families with neurodevelopmental disorders

…, C Thiel, S Uebe, AB Ekici, M Krumbiegel… - JAMA …, 2017 - jamanetwork.com
Importance Autosomal recessive inherited neurodevelopmental disorders are highly
heterogeneous, and many, possibly most, of the disease genes are still unknown. Objectives To …

[HTML][HTML] Aberrant phase separation and nucleolar dysfunction in rare genetic diseases

…, K Kahrizi, VM Kalscheuer, A Kan, M Krumbiegel… - Nature, 2023 - nature.com
Thousands of genetic variants in protein-coding genes have been linked to disease.
However, the functional impact of most variants is unknown as they occur within intrinsically …

α-Synuclein oligomers induce early axonal dysfunction in human iPSC-based models of synucleinopathies

…, F Krach, M Krumbiegel… - Proceedings of the …, 2018 - National Acad Sciences
α-Synuclein (α-Syn) aggregation, proceeding from oligomers to fibrils, is one central
hallmark of neurodegeneration in synucleinopathies. α-Syn oligomers are toxic by triggering …

Modulation of different human immunodeficiency virus type 1 Nef functions during progression to AIDS

S Carl, TC Greenough, M Krumbiegel… - Journal of …, 2001 - Am Soc Microbiol
The human immunodeficiency virus type 1 (HIV-1) Nef protein has several independent
functions that might contribute to efficient viral replication in vivo. Since HIV-1 adapts rapidly to …

Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2

…, MP Lux, PA Fasching, M Krumbiegel… - … journal of cancer, 2017 - Wiley Online Library
Breast and ovarian cancer (BC/OC) predisposition has been attributed to a number of high‐
and moderate to low‐penetrance susceptibility genes. With the advent of next generation …

[HTML][HTML] Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma

F Pasutto, M Krumbiegel, CY Mardin… - … & visual science, 2008 - iovs.arvojournals.org
purpose. Three common sequence variants in the lysyl oxidase-like 1 (LOXL1) gene were
recently associated with both pseudoexfoliation (PEX) and pseudoexfoliation glaucoma (…