Protein kinase B/Akt is present in activated form throughout the entire replicative cycle of deltaU(S)3 mutant virus but only at early times after infection with wild-type herpes simplex virus 1 (Q34545781)

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Language	Label	Description	Also known as
English	Protein kinase B/Akt is present in activated form throughout the entire replicative cycle of deltaU(S)3 mutant virus but only at early times after infection with wild-type herpes simplex virus 1	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Protein kinase B/Akt is present in activated form throughout the entire replicative cycle of deltaU(S)3 mutant virus but only at early times after infection with wild-type herpes simplex virus 1 (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Bernard Roizman

2

object named as

Bernard Roizman

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Luca Benetti

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

language of work or name

0 references

publication date

1 April 2006

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Journal of Virology

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

80

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

3341-3348

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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1 reference

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1 reference

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1 reference

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The activation of Akt/PKB signaling pathway and cell survival.

1 reference

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PDK1, the master regulator of AGC kinase signal transduction

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Herpes simplex virus protein kinase US3 activates and functionally overlaps protein kinase A to block apoptosis

1 reference

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Kaposi's sarcoma-associated herpesvirus induces the phosphatidylinositol 3-kinase-PKC-zeta-MEK-ERK signaling pathway in target cells early during infection: implications for infectivity

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Ultrastructural localization of the herpes simplex virus type 1 UL31, UL34, and US3 proteins suggests specific roles in primary envelopment and egress of nucleocapsids

1 reference

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Human cytomegalovirus major immediate-early proteins and simian virus 40 large T antigen can inhibit apoptosis through activation of the phosphatidylinositide 3'-OH kinase pathway and the cellular kinase Akt.

1 reference

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The herpes simplex virus type 2 R1 protein kinase (ICP10 PK) blocks apoptosis in hippocampal neurons, involving activation of the MEK/MAPK survival pathway

1 reference

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Physiological substrates of cAMP-dependent protein kinase

1 reference

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Dynamics of cAMP-dependent protein kinase

1 reference

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AKT plays a central role in tumorigenesis

1 reference

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The US3 protein kinase of herpes simplex virus 1 mediates the posttranslational modification of BAD and prevents BAD-induced programmed cell death in the absence of other viral proteins

1 reference

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Human cytomegalovirus up-regulates the phosphatidylinositol 3-kinase (PI3-K) pathway: inhibition of PI3-K activity inhibits viral replication and virus-induced signaling

1 reference

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The U(S)3 protein kinase blocks apoptosis induced by the d120 mutant of herpes simplex virus 1 at a premitochondrial stage

1 reference

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Protein phosphatase 2A: a highly regulated family of serine/threonine phosphatases implicated in cell growth and signalling

1 reference

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1 reference

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Antiapoptotic activity of herpes simplex virus type 2: the role of US3 protein kinase gene

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Cellular survival: a play in three Akts

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1 reference

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Transduction of interleukin-2 antiapoptotic and proliferative signals via Akt protein kinase

1 reference

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1 reference

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Suppression of apoptotic DNA fragmentation in herpes simplex virus type 1-infected cells.

1 reference

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HSV and glycoprotein J inhibit caspase activation and apoptosis induced by granzyme B or Fas.

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12 December 2020

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Identifiers

10.1128/JVI.80.7.3341-3348.2006

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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