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Items: 1 to 20 of 66

1.

C21orf91 genotypes correlate with herpes simplex labialis (cold sore) frequency: description of a cold sore susceptibility gene.

Kriesel JD, Jones BB, Matsunami N, Patel MK, St Pierre CA, Kurt-Jones EA, Finberg RW, Leppert M, Hobbs MR.

J Infect Dis. 2011 Dec 1;204(11):1654-62. doi: 10.1093/infdis/jir633.

2.

Identification of a herpes simplex labialis susceptibility region on human chromosome 21.

Hobbs MR, Jones BB, Otterud BE, Leppert M, Kriesel JD.

J Infect Dis. 2008 Feb 1;197(3):340-6. doi: 10.1086/525540.

PMID:
18199027
3.

Cold sore susceptibility gene-1 genotypes affect the expression of herpes labialis in unrelated human subjects.

Kriesel JD, Bhatia A, Thomas A.

Hum Genome Var. 2014 Nov 20;1:14024. doi: 10.1038/hgv.2014.24. eCollection 2014.

4.

The first common cold sore susceptibility gene.

Cunningham AL, Booth D.

J Infect Dis. 2011 Dec 1;204(11):1645-7. doi: 10.1093/infdis/jir635. No abstract available.

PMID:
22039567
5.

Immunoglobulin genes and immunity to herpes simplex virus type 1.

Pandey JP.

J Infect Dis. 2012 Jul 1;206(1):143-4. doi: 10.1093/infdis/jis317. Epub 2012 Apr 25. No abstract available.

6.

[Prevention and treatment of Herpes Labialis].

Duquet N.

J Pharm Belg. 2016 Mar;(1):4-11. Review. French.

PMID:
30281218
7.

Herpes simplex virus type 1 shedding in the oral cavity of seropositive patients.

da Silva LM, Guimarães AL, Victória JM, Gomes CC, Gomez RS.

Oral Dis. 2005 Jan;11(1):13-6.

PMID:
15641961
8.
9.

Association of TLR3-hyporesponsiveness and functional TLR3 L412F polymorphism with recurrent herpes labialis.

Yang CA, Raftery MJ, Hamann L, Guerreiro M, Grütz G, Haase D, Unterwalder N, Schönrich G, Schumann RR, Volk HD, Scheibenbogen C.

Hum Immunol. 2012 Aug;73(8):844-51. doi: 10.1016/j.humimm.2012.04.008. Epub 2012 Apr 23.

PMID:
22537752
10.

A 3'-untranslated region polymorphism in the TBX21 gene encoding T-bet is a risk factor for genital herpes simplex virus type 2 infection in humans.

Svensson A, Bergin AM, Löwhagen GB, Tunbäck P, Bellner L, Padyukov L, Eriksson K.

J Gen Virol. 2008 Sep;89(Pt 9):2262-8. doi: 10.1099/vir.0.2008/001305-0.

PMID:
18753235
11.

Longitudinal evaluation of herpes simplex virus DNA load during episodes of herpes labialis.

Boivin G, Goyette N, Sergerie Y, Keays S, Booth T.

J Clin Virol. 2006 Dec;37(4):248-51.

PMID:
17046320
12.
13.
14.

Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.

Nolan DK, Sutton B, Haynes C, Johnson J, Sebek J, Dowdy E, Crosslin D, Crossman D, Sketch MH Jr, Granger CB, Seo D, Goldschmidt-Clermont P, Kraus WE, Gregory SG, Hauser ER, Shah SH.

BMC Genet. 2012 Feb 27;13:12. doi: 10.1186/1471-2156-13-12.

16.

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

Paschou P, Feng Y, Pakstis AJ, Speed WC, DeMille MM, Kidd JR, Jaghori B, Kurlan R, Pauls DL, Sandor P, Barr CL, Kidd KK.

Am J Hum Genet. 2004 Oct;75(4):545-60. Epub 2004 Aug 9.

17.

Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus.

Veal CD, Capon F, Allen MH, Heath EK, Evans JC, Jones A, Patel S, Burden D, Tillman D, Barker JN, Trembath RC.

Am J Hum Genet. 2002 Sep;71(3):554-64. Epub 2002 Jul 29.

18.

LDGIdb: a database of gene interactions inferred from long-range strong linkage disequilibrium between pairs of SNPs.

Wang MC, Chen FC, Chen YZ, Huang YT, Chuang TJ.

BMC Res Notes. 2012 May 2;5:212. doi: 10.1186/1756-0500-5-212.

19.

Association between single-nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population.

Hamada D, Takata Y, Osabe D, Nomura K, Shinohara S, Egawa H, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Miyamoto T, Moritani M, Kunika K, Inoue H, Yasui N, Itakura M.

Arthritis Rheum. 2005 May;52(5):1371-80.

20.

Power and sample size calculations for genetic case/control studies using gene-centric SNP maps: application to human chromosomes 6, 21, and 22 in three populations.

De La Vega FM, Gordon D, Su X, Scafe C, Isaac H, Gilbert DA, Spier EG.

Hum Hered. 2005;60(1):43-60. Epub 2005 Sep 2.

PMID:
16137993

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