Results 261 to 270 of about 300,470 (289)
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A novel nuclear export activity in HIV-1 matrix protein required for viral replication
Nature, 1999An important aspect of the pathophysiology of human immunodeficiency virus type-1 (HIV-1) infection is the ability of the virus to replicate in non-dividing cells. HIV-1 matrix (MA), the amino-terminal domain of the Pr55 gag polyprotein (Pr55), bears a nuclear localization signal that promotes localization of the viral preintegration complex to the ...
Dupont, Stefan A. +7 more
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HIV-1 matrix protein: A mysterious regulator of the viral life cycle
Virus Research, 2007Significant progress has been achieved in the last few years concerning the human immunodeficiency virus (HIV-1) life cycle, mostly in the fields of cellular receptors for the virus, virus assembly and budding of virus particles from the cell surface.
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Stronger Together: The role of cysteine residues in Ebola viral matrix protein VP40
The FASEB Journal, 2017Introduction One hallmark of an intracellular Ebola infection is the formation of virus‐like particles, or VLPs, on the extracellular surface of infected cells. The formation of VLPs is known to be facilitated by oligomerization of the viral matrix protein VP40.
Sarah Catherine Briann Baker +2 more
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Microbiology and Immunology, 1999
AbstractTo investigate the nature and intracellular behavior of the matrix (M) protein of an avirulent strain (HEP‐Flury) of rabies virus, we cloned and sequenced the cDNA of the protein. Using expression vectors pZIP‐NeoSV(X)1 and pCDM8, the cDNA was transfected to animal cells (BHK‐21 and COS‐7) with or without coexpression of viral glycoprotein (G).
K, Nakahara +6 more
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AbstractTo investigate the nature and intracellular behavior of the matrix (M) protein of an avirulent strain (HEP‐Flury) of rabies virus, we cloned and sequenced the cDNA of the protein. Using expression vectors pZIP‐NeoSV(X)1 and pCDM8, the cDNA was transfected to animal cells (BHK‐21 and COS‐7) with or without coexpression of viral glycoprotein (G).
K, Nakahara +6 more
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Molecular Phylogenetics and Evolution, 2001
Phylogenetic relationships among the Paramyxoviridae, a broad family of viruses whose members cause devastating diseases of wildlife, livestock, and humans, were examined with both fusion (F) and matrix (M) protein-coding sequences. Neighbor-joining trees of F and M protein sequences showed that the Paramyxoviridae was divided into the two ...
K M, Westover, A L, Hughes
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Phylogenetic relationships among the Paramyxoviridae, a broad family of viruses whose members cause devastating diseases of wildlife, livestock, and humans, were examined with both fusion (F) and matrix (M) protein-coding sequences. Neighbor-joining trees of F and M protein sequences showed that the Paramyxoviridae was divided into the two ...
K M, Westover, A L, Hughes
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Trends in Cell Biology, 1991
Because influenza virus replicates in the nucleus and buds from the plasma membrane, its ribonucleoproteins (RNPs) must undergo bidirectional transport across the nuclear membrane. Export from the nucleus to the cytoplasm was found to depend on the viral matrix protein (M1).
K, Martin, A, Helenius
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Because influenza virus replicates in the nucleus and buds from the plasma membrane, its ribonucleoproteins (RNPs) must undergo bidirectional transport across the nuclear membrane. Export from the nucleus to the cytoplasm was found to depend on the viral matrix protein (M1).
K, Martin, A, Helenius
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The contemporary management of cancers of the sinonasal tract in adults
Ca-A Cancer Journal for Clinicians, 2023Rajat Thawani
exaly
Laboratory investigation; a journal of technical methods and pathology, 1986
Protein synthesis was determined in cultures of human umbilical cord vein endothelial cells (EC) infected with either herpes simplex type 1 (HSV-1) or type 2 (HSV-2). Monolayers were infected for 1 hour with either 5 or 20 infectious virus particles per EC (multiplicity of infection of 5 or 20).
N A, Kefalides, Z, Ziaie
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Protein synthesis was determined in cultures of human umbilical cord vein endothelial cells (EC) infected with either herpes simplex type 1 (HSV-1) or type 2 (HSV-2). Monolayers were infected for 1 hour with either 5 or 20 infectious virus particles per EC (multiplicity of infection of 5 or 20).
N A, Kefalides, Z, Ziaie
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