human | Q5 |
P106 | occupation | researcher | Q1650915 |
Q36369804 | Annexin A1 Deficiency does not Affect Myofiber Repair but Delays Regeneration of Injured Muscles |
Q34481444 | Are there too many or too few SNAREs in proteoliposomes? |
Q40374927 | Carbohydrate-binding molecules inhibit viral fusion and entry by crosslinking membrane glycoproteins |
Q36824514 | Cationic Cell-Penetrating Peptide Binds to Planar Lipid Bilayers Containing Negatively Charged Lipids but does not Induce Conductive Pores |
Q34202149 | Cell-Penetrating Peptide Induces Leaky Fusion of Liposomes Containing Late Endosome-Specific Anionic Lipid |
Q40692947 | Cell-penetrating peptides. A reevaluation of the mechanism of cellular uptake |
Q40462664 | Cellular uptake of unconjugated TAT peptide involves clathrin-dependent endocytosis and heparan sulfate receptors. |
Q34521574 | Cytosol-dependent membrane fusion in ER, nuclear envelope and nuclear pore assembly: biological implications |
Q36972120 | Delivery of steric block morpholino oligomers by (R-X-R)4 peptides: structure-activity studies. |
Q28475709 | Dengue Virus Ensures Its Fusion in Late Endosomes Using Compartment-Specific Lipids |
Q36184677 | Efficient entry of cell-penetrating peptide nona-arginine into adherent cells involves a transient increase in intracellular calcium |
Q30532065 | Extracellular annexins and dynamin are important for sequential steps in myoblast fusion. |
Q40124025 | Fusion Stage of HIV-1 Entry Depends on Virus-Induced Cell Surface Exposure of Phosphatidylserine |
Q30532780 | Fusion-pore expansion during syncytium formation is restricted by an actin network |
Q47780558 | Influenza hemagglutinins outside of the contact zone are necessary for fusion pore expansion |
Q37447814 | Transmembrane protein-free membranes fuse into xenopus nuclear envelope and promote assembly of functional pores |
Q41080258 | Transmembrane proteins are not required for early stages of nuclear envelope assembly |