User profiles for Marius Ueffing
Marius UeffingProf. Dr. rer. nat., Director, Institute for Ophthalmic Research, University of Tuebingen Verified email at uni-tuebingen.de Cited by 21095 |
[HTML][HTML] Latent membrane protein 1 of Epstein–Barr virus mimics a constitutively active receptor molecule
Latent membrane protein 1 (LMP1) of Epstein–Barr virus (EBV) is an integral membrane
protein which has transforming potential and is necessary but not sufficient for B‐cell …
protein which has transforming potential and is necessary but not sufficient for B‐cell …
The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity
Mutations in the leucine-rich repeat kinase 2 gene (LRRK2) have been recently identified in
families with autosomal dominant late-onset Parkinson disease (PD). The LRRK2 protein …
families with autosomal dominant late-onset Parkinson disease (PD). The LRRK2 protein …
[HTML][HTML] Prevalence of age-related macular degeneration in Europe: the past and the future
Purpose Age-related macular degeneration (AMD) is a frequent, complex disorder in elderly
of European ancestry. Risk profiles and treatment options have changed considerably over …
of European ancestry. Risk profiles and treatment options have changed considerably over …
[HTML][HTML] Latent membrane protein 1 of Epstein–Barr virus interacts with JAK3 and activates STAT proteins
…, C Kaiser, R Zeidler, B Scheffer, M Ueffing… - The EMBO …, 1999 - embopress.org
Latent membrane protein 1 (LMP1) acts like a permanently activated receptor of the tumor
necrosis factor (TNF)‐receptor superfamily and is absolutely required for B cell …
necrosis factor (TNF)‐receptor superfamily and is absolutely required for B cell …
Hydrogen peroxide-induced apoptosis is CD95-independent, requires the release of mitochondria-derived reactive oxygen species and the activation of NF-κB
A Dumont, SP Hehner, TG Hofmann, M Ueffing… - Oncogene, 1999 - nature.com
Reactive oxygen species (ROS) play an important role in cell death induced by many different
stimuli. This study shows that hydrogen peroxide-induced apoptosis in T-cells did not …
stimuli. This study shows that hydrogen peroxide-induced apoptosis in T-cells did not …
LRRK2 controls synaptic vesicle storage and mobilization within the recycling pool
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the single most common cause of
inherited Parkinson's disease. Little is known about its involvement in the pathogenesis of …
inherited Parkinson's disease. Little is known about its involvement in the pathogenesis of …
[HTML][HTML] Epstein–Barr virus latent membrane protein‐1 triggers AP‐1 activity via the c‐Jun N‐terminal kinase cascade
The Epstein–Barr virus latent membrane protein‐1 (LMP‐1) is an integral membrane protein
which transforms fibroblasts and is essential for EBV‐mediated B‐cell immortalization. LMP‐…
which transforms fibroblasts and is essential for EBV‐mediated B‐cell immortalization. LMP‐…
Merging organoid and organ-on-a-chip technology to generate complex multi-layer tissue models in a human retina-on-a-chip platform
10.7554/eLife.46188.001 The devastating effects and incurable nature of hereditary and
sporadic retinal diseases such as Stargardt disease, age-related macular degeneration or …
sporadic retinal diseases such as Stargardt disease, age-related macular degeneration or …
A novel tandem affinity purification strategy for the efficient isolation and characterisation of native protein complexes
Isolation and dissection of native multiprotein complexes is a central theme in functional
genomics. The development of the tandem affinity purification (TAP) tag has enabled an efficient …
genomics. The development of the tandem affinity purification (TAP) tag has enabled an efficient …
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
Defects in primary cilium biogenesis underlie the ciliopathies, a growing group of genetic
disorders. We describe a whole-genome siRNA-based reverse genetics screen for defects in …
disorders. We describe a whole-genome siRNA-based reverse genetics screen for defects in …