Accès ouvert
2025
article
OpenAlex
Claudia Bastl, Cindy M. Close, Ingo Holtz, Blaise Gatin‐Fraudet et autres
The malaria parasite Plasmodium falciparum affects the lives of millions of people worldwide every year. The detection of replicating parasites within human red blood cells is of paramount importance, requiring appropriate diagnostic tools. Herein, we design and apply a silicon rhodamine-fused glibenclamide …
de, gb, Nigéria, ch, us
(code pays fourni par la source)
Accès ouvert
2025
preprint
OpenAlex
Claudia Bastl, Cindy M. Close, Ingo Holtz, Blaise Gatin‐Fraudet et autres
Abstract The malaria parasite Plasmodium falciparum affects the lives of millions of people worldwide every year. The detection of replicating parasites within human red blood cells is of paramount importance, requiring appropriate diagnostic tools. Herein, we design and apply a silicon rhodamine-fused …
de, gb, ch, Nigéria, us
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Ramona Birke, Julia Ast, Dorien A. Roosen, Joon Lee et autres
self-labelling protein tags. We anticipate that Sulfo549, Sulfo646 and their congeners will be useful for a number of cell biology applications where labelling of intracellular sites interferes with accurate surface protein analysis.
de, gb, us
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Xylena Reed, Melanie M. Cobb, Gaia Skinbinski, Dorien A. Roosen et autres
Reproducibility of expression patterns in iPSC-derived cells from different labs is an important first step in ensuring replication of biochemical or functional assays that are performed in different labs. Here we show that reproducible gene expression patterns from iPSCs and iPSC-derived neurons …
us
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Melissa Conti Mazza, Alexandra G. Beilina, Dorien A. Roosen, David N. Hauser et autres
Mutations in the oncogene PARK7, which codes for DJ-1, have been associated with early-onset autosomal recessive Parkinson's disease (PD); however, the exact role of DJ-1 in PD remains elusive. Fibroblasts from a PD patient with a uniparental disomy, 1 bp deletion in …
us
(code pays fourni par la source)
Accès ouvert
2021
preprint
OpenAlex
Ramona Birke, Julia Ast, Dorien A. Roosen, Bettina Mathes et autres
ABSTRACT Sulfonated rhodamines that endow xanthene dyes with cellular impermeability are presented. We fuse charged sulfonates to red and far-red dyes to obtain Sulfo549 and Sulfo646, respectively, and further link these to SNAP- and Halo-tag substrates for protein self-labelling. Cellular impermeability is …
de, gb
(code pays fourni par la source)
Accès ouvert
2020
article
OpenAlex
Filiz Sila Rizalar, Dorien A. Roosen, Volker Haucke
de
(code pays fourni par la source)
Accès ouvert
2020
article
OpenAlex
Alice Filippini, Veronica Mutti, Gaia Faustini, Francesca Longhena et autres
The progressive neuropathological damage seen in Parkinson's disease (PD) is thought to be related to the spreading of aggregated forms of α-synuclein. Clearance of extracellular α-synuclein released by degenerating neurons may be therefore a key mechanism to control the concentration of α-synuclein …
it, us
(code pays fourni par la source)
Accès ouvert
2020
article
OpenAlex
Alexandra G. Beilina, Luis Bonet‐Ponce, Ravindran Kumaran, Jennifer J. Kordich et autres
Mutations in Leucine-rich repeat kinase 2 (LRRK2) cause Parkinson's disease (PD). However, the precise function of LRRK2 remains unclear. We report an interaction between LRRK2 and VPS52, a subunit of the Golgi-associated retrograde protein (GARP) complex that identifies a function of LRRK2 …
us, gb
(code pays fourni par la source)
Accès ouvert
2020
article
OpenAlex
Lynne Krohn, Francis P. Grenn, Mary B. Makarious, Jonggeol Jeffrey Kim et autres
ca, us
(code pays fourni par la source)
Accès ouvert
2020
preprint
OpenAlex
Lynne Krohn, Francis P. Grenn, Mary B. Makarious, Jonggeol Jeffrey Kim et autres
Abstract Multiple genes have been associated with monogenic Parkinson’s disease and Parkinsonism syndromes. Mutations in PINK1 (PARK6) have been shown to result in autosomal recessive early onset Parkinson’s disease. In the past decade, several studies have suggested that carrying a single heterozygous …
ca, us
(code pays fourni par la source)
Accès ouvert
2019
preprint
OpenAlex
Dorien A. Roosen, Natalie Landeck, Luis Bonet‐Ponce, Jillian H. Kluss et autres
Abstract Parkinson’s disease (PD) is a common neurodegenerative motor disorder characterized in part by neuropathological lesions in the nigrostriatal pathway. Loss of function mutations in Auxilin, the major neuronal clathrin uncoating protein, cause an aggressive form of juvenile onset PD. How mutations …
us, gb
(code pays fourni par la source)