about
Cellular electron microscopy imaging reveals the localization of the Hfq protein close to the bacterial membraneViral Replication Protein Inhibits Cellular Cofilin Actin Depolymerization Factor to Regulate the Actin Network and Promote Viral Replicase AssemblyVirus factories: associations of cell organelles for viral replication and morphogenesisMultilamellar structures and filament bundles are found on the cell surface during bunyavirus egress.Membrane remodelling during vaccinia virus morphogenesis.Visualization of proteins in intact cells with a clonable tag for electron microscopy.Three-dimensional structure of Rubella virus factories.Cryo-electron tomography of vaccinia virus.Endoplasmic reticulum-Golgi intermediate compartment membranes and vimentin filaments participate in vaccinia virus assemblyNoncanonical role for the host Vps4 AAA+ ATPase ESCRT protein in the formation of Tomato bushy stunt virus replicaseCo-opted oxysterol-binding ORP and VAP proteins channel sterols to RNA virus replication sites via membrane contact sites.Coexistence of multivalent and monovalent TCRs explains high sensitivity and wide range of response.Role of Viral RNA and Co-opted Cellular ESCRT-I and ESCRT-III Factors in Formation of Tombusvirus Spherules Harboring the Tombusvirus Replicase.Reovirus forms neo-organelles for progeny particle assembly within reorganized cell membranes.Virus factories: biogenesis and structural design.Three-Dimensional Imaging of Viral Infections.Virus assembly factories in a lipid world.Metallothioneins for correlative light and electron microscopy.The major core protein P4a (A10L gene) of vaccinia virus is essential for correct assembly of viral DNA into the nucleoprotein complex to form immature viral particles.Self-protection and survival of arbovirus-infected mosquito cells.Polymorphism and structural maturation of bunyamwera virus in Golgi and post-Golgi compartmentsThree-dimensional imaging of the intracellular assembly of a functional viral RNA replicase complex.The unique architecture of Bunyamwera virus factories around the Golgi complex.The ESCRT machinery is not required for human cytomegalovirus envelopment.Novel replication complex architecture in rubella replicon-transfected cells.Intracellular Salmonella induces aggrephagy of host endomembranes in persistent infections.The A17L gene product of vaccinia virus is exposed on the surface of IMV.The coat protein of Rabbit hemorrhagic disease virus contains a molecular switch at the N-terminal region facing the inner surface of the capsid.Influenza virus genome reaches the plasma membrane via a modified endoplasmic reticulum and Rab11-dependent vesicles.Elemental maps from EFTEM images using two different background subtraction models.The TRiC chaperonin controls reovirus replication through outer-capsid folding.Biochemical and electron microscopy analysis of the endotoxin binding to microtubules in vitro.Studying cellular architecture in three dimensions with improved resolution: Ta replicas revisitedThe Coat and Cylindrical Inclusion Proteins of a Potyvirus Are Associated with Connections between Plant CellsTargeting host lipid flows: Exploring new antiviral and antibiotic strategies
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Cristina Risco
@ast
Cristina Risco
@en
Cristina Risco
@es
Cristina Risco
@nl
type
label
Cristina Risco
@ast
Cristina Risco
@en
Cristina Risco
@es
Cristina Risco
@nl
prefLabel
Cristina Risco
@ast
Cristina Risco
@en
Cristina Risco
@es
Cristina Risco
@nl
P106
P1153
56251715300
P21
P31
P496
0000-0001-7501-5934