Precise Similarity of Many Human Proteins to Proteins of Prokarya [PDF]
Proteins originated in early forms of life and have long survived, because they have always been required. Some recognizably similar proteins are found in all sequence comparisons between species, no matter how distant, including prokaryotes and ...
Roy Britten
core +2 more sources
Forschung für die Praxis: Bullöse Autoimmundermatosen unter Immuncheckpoint‐Inhibitoren [PDF]
Zusammenfassung Immuncheckpoint‐Rezeptoren und ‐Liganden wie das cytotoxic T‐lymphocyte‐associated Protein 4 (CTLA‐4), programmed death‐1 (PD‐1) und ligand‐1 (PD‐L1) werden sowohl auf Immun‐ als auch auf nicht‐Immunzellen in großem Umfang exprimiert und dienen der Feinabstimmung des Aktivierungsniveaus von Immunzellen, wodurch Immunreaktionen ...
Prüßmann J, Prüßmann W, Sadik C.
europepmc +2 more sources
Clinical and Translational Medicine, Volume 13, Issue 11, November 2023.
Meng Liu +5 more
wiley +1 more source
Three LIF-dependent signatures and gene clusters with atypical expression profiles, identified by transcriptome studies in mouse ES cells and early derivatives [PDF]
BACKGROUND: Mouse embryonic stem (ES) cells remain pluripotent in vitro when grown in the presence of the cytokine Leukemia Inhibitory Factor (LIF).
Agapios Sachinidis +14 more
core +4 more sources
Dysferlin mediates the cytoprotective effects of TRAF2 following myocardial ischemia reperfusion injury [PDF]
BACKGROUND: We have demonstrated that tumor necrosis factor (TNF) receptor‐associated factor 2 (TRAF2), a scaffolding protein common to TNF receptors 1 and 2, confers cytoprotection in the heart.
Barger, Philip M +7 more
core +2 more sources
Seltene Form der Epidermolysis bullosa simplex mit homozygoter Mutation im Gen EXPH5
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 21, Issue S2, Page 3-5, April 2023.
Henning Olbrich +2 more
wiley +1 more source
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility [PDF]
The genetic basis of epidermolysis bullosa, a group of genetic disorders characterized by the mechanically induced formation of skin blisters, is largely known, but a number of cases still remain genetically unsolved.
Boerries, Melanie +15 more
core +1 more source
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells [PDF]
H1069Q substitution represents the most frequent mutation of the copper transporter ATP7B causing Wilson disease in Caucasian population. ATP7B localizes to the Golgi complex in hepatocytes but moves in response to copper overload to the endo-lysosomal ...
Allocca, Simona +10 more
core +2 more sources
Calgranulin B is known to be involved in tumor development, but the underlying molecular mechanism is not clear. To gain insight into possible roles of calgranulin B, we screened for calgranulin B-interacting molecules in the SNU-484 gastric cancer and ...
Kyung-Hee Kim +3 more
doaj +1 more source
Defenders and Challengers of Endothelial Barrier Function
Regulated vascular permeability is an essential feature of normal physiology and its dysfunction is associated with major human diseases ranging from cancer to inflammation and ischemic heart diseases. Integrity of endothelial cells also play a prominent
Nader Rahimi
doaj +1 more source

