[HTML][HTML] Mitotic disassembly and reassembly of nuclear pore complexes

U Kutay, R Jühlen, W Antonin - Trends in Cell Biology, 2021 - cell.com
Nuclear pore complexes (NPCs) are huge protein assemblies within the nuclear envelope (NE)
that serve as selective gates for macromolecular transport between nucleus and …

Moonlighting nuclear pore proteins: tissue-specific nucleoporin function in health and disease

R Jühlen, B Fahrenkrog - Histochemistry and cell biology, 2018 - Springer
The nuclear pore complex is the main transportation hub for exchange between the cytoplasm
and the nucleus. It is built from nucleoporins that form distinct subcomplexes to establish …

The European Spondylarthropathy Study Group preliminary criteria for the classification of spondylarthropathy

M Dougados, SVD Linden, R Juhlin… - … : Official Journal of …, 1991 - Wiley Online Library
Juhlin, and B. Huitfeldt). This first reduction resulted in 25 candidate variables: 1) spinal
pain, 2) … Rasch, and R. Scaillet for their participation as monitors of the study, to C. Bini, I. …

Sulfasalazine in the treatment of spondylarthropathy

…, M Leirisalo‐Repo, B Huitfeldt, R Juhlin… - … : Official Journal of …, 1995 - Wiley Online Library
Objective. To assess the efficacy and tolerability of sulfasalazine (SSZ) in the treatment of
spondyl‐arthropathy. Methods. We conducted a 6‐month randomized, placebo‐controlled, …

From the sideline: Tissue‐specific nucleoporin function in health and disease, an update

R Jühlen, B Fahrenkrog - FEBS letters, 2023 - Wiley Online Library
The subcellular compartmentalisation of eukaryotic cells requires selective exchange between
the cytoplasm and the nucleus. Intact nucleocytoplasmic transport is vital for normal cell …

Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations

…, A Satoh, T Ogata, M Fukami, R Jühlen… - Journal of medical …, 2018 - jmg.bmj.com
Background Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital
phenotypes and enteropathy (MIRAGE) syndrome is a recently described congenital disorder …

A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima

…, F Reschke, S Kutzner, R Jühlen… - Journal of Medical …, 2017 - jmg.bmj.com
Background Triple A syndrome (MIM #231550) is associated with mutations in the AAAS
gene. However, about 30% of patients with triple A syndrome symptoms but an unresolved …

[HTML][HTML] Role of ALADIN in human adrenocortical cells for oxidative stress response and steroidogenesis

R Jühlen, J Idkowiak, AE Taylor, B Kind, W Arlt… - PLoS …, 2015 - journals.plos.org
Triple A syndrome is caused by mutations in AAAS encoding the protein ALADIN. We
investigated the role of ALADIN in the human adrenocortical cell line NCI-H295R1 by either over-…

[HTML][HTML] Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence

E Bonnin, P Cabochette, A Filosa, R Jühlen… - PLoS …, 2018 - journals.plos.org
Nucleoporins build the nuclear pore complex (NPC), which, as sole gate for nuclear-cytoplasmic
exchange, is of outmost importance for normal cell function. Defects in the process of …

[HTML][HTML] Alteration of actin cytoskeletal organisation in fetal akinesia deformation sequence

R Jühlen, L Grauer, V Martinelli, C Rencurel… - Scientific Reports, 2024 - nature.com
… Regression models for cell migration rate and wound closure were fitted in R using
package mgcv (version 1.9-0) based on generalized additive models (GAM) 60 . Differences in …