(Q39226546)

English

Linkage of human cytomegalovirus glycoprotein gO variant groups identified from worldwide clinical isolates with gN genotypes, implications for disease associations and evidence for N-terminal sites of positive selection

scientific article published on January 2004

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scholarly article

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Europe PubMed Central

PubMed publication ID

10 September 2017

Linkage of human cytomegalovirus glycoprotein gO variant groups identified from worldwide clinical isolates with gN genotypes, implications for disease associations and evidence for N-terminal sites of positive selection (English)

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Europe PubMed Central

PubMed publication ID

10 September 2017

Cytomegalovirus

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William D. Rawlinson

6

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Europe PubMed Central

PubMed publication ID

10 September 2017

author name string

Mattick C

1

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Europe PubMed Central

PubMed publication ID

10 September 2017

Dewin D

2

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10 September 2017

Polley S

3

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Europe PubMed Central

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10 September 2017

Sevilla-Reyes E

4

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Europe PubMed Central

PubMed publication ID

10 September 2017

Pignatelli S

5

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Europe PubMed Central

PubMed publication ID

10 September 2017

Wilkinson G

7

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Europe PubMed Central

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10 September 2017

Dal Monte P

8

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Europe PubMed Central

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10 September 2017

Gompels UA

9

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Europe PubMed Central

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10 September 2017

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publication date

1 January 2004

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Europe PubMed Central

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10 September 2017

number of pages

16

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10 September 2017

318

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10 September 2017

2

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582-597

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10 September 2017

Two novel spliced genes in human cytomegalovirus

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Fast screening procedures for random transposon libraries of cloned herpesvirus genomes: mutational analysis of human cytomegalovirus envelope glycoprotein genes

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Survival in children with perinatal HIV infection and very low CD4 lymphocyte counts

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Human cytomegalovirus persistence and latency in endothelial cells and macrophages

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Pseudorabies virus glycoprotein M inhibits membrane fusion

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Cytomegalovirus infection and HIV-1 disease progression in infants born to HIV-1-infected women. Pediatric Pulmonary and Cardiovascular Complications of Vertically Transmitted HIV Infection Study Group

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Glycoproteins M and N of human herpesvirus 8 form a complex and inhibit cell fusion.

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Epstein-Barr virus that lacks glycoprotein gN is impaired in assembly and infection

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Definitions of cytomegalovirus infection and disease in transplant recipients

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Greater CD8+ TCR heterogeneity and functional flexibility in HIV-2 compared to HIV-1 infection

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Complex formation by human cytomegalovirus glycoproteins M (gpUL100) and N (gpUL73).

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Transmission of human cytomegalovirus from infected uterine microvascular endothelial cells to differentiating/invasive placental cytotrophoblasts.

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DIALIGN: finding local similarities by multiple sequence alignment

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The human herpesvirus 6 U100 gene product is the third component of the gH-gL glycoprotein complex on the viral envelope

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Machine learning approaches for the prediction of signal peptides and other protein sorting signals

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A role for human cytomegalovirus glycoprotein O (gO) in cell fusion and a new hypervariable locus

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Cytomegalovirus encodes a potent alpha chemokine

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gpUL73 (gN) genomic variants of human cytomegalovirus isolates are clustered into four distinct genotypes

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Human cytomegalovirus glycoprotein N (gpUL73-gN) genomic variants: identification of a novel subgroup, geographical distribution and evidence of positive selective pressure.

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Intrauterine cytomegalovirus infection and glycoprotein N (gN) genotypes

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A review of genetic differences between limited and extensively passaged human cytomegalovirus strains

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The genes encoding the gCIII complex of human cytomegalovirus exist in highly diverse combinations in clinical isolates

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Inter- and intragenic variations complicate the molecular epidemiology of human cytomegalovirus

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In vitro selection of human cytomegalovirus variants unable to transfer virus and virus products from infected cells to polymorphonuclear leukocytes and to grow in endothelial cells.

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10.1016/J.VIROL.2003.09.036

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Europe PubMed Central

PubMed publication ID

10 September 2017

PubMed publication ID

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Europe PubMed Central

PubMed publication ID

10 September 2017

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