Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 72

1.

Polymorphisms of adrenergic cardiovascular control genes are associated with adolescent chronic fatigue syndrome.

Sommerfeldt L, Portilla H, Jacobsen L, Gjerstad J, Wyller VB.

Acta Paediatr. 2011 Feb;100(2):293-8. doi: 10.1111/j.1651-2227.2010.02072.x.

PMID:
21059181
2.

Moderate exercise increases expression for sensory, adrenergic, and immune genes in chronic fatigue syndrome patients but not in normal subjects.

Light AR, White AT, Hughen RW, Light KC.

J Pain. 2009 Oct;10(10):1099-112. doi: 10.1016/j.jpain.2009.06.003.

3.

Autoantibodies, polymorphisms in the serotonin pathway, and human leukocyte antigen class II alleles in chronic fatigue syndrome: are they associated with age at onset and specific symptoms?

Ortega-Hernandez OD, Cuccia M, Bozzini S, Bassi N, Moscavitch S, Diaz-Gallo LM, Blank M, Agmon-Levin N, Shoenfeld Y.

Ann N Y Acad Sci. 2009 Sep;1173:589-99. doi: 10.1111/j.1749-6632.2009.04802.x.

PMID:
19758204
4.
5.

Genetic polymorphisms of adrenergic receptors.

Garland EM, Biaggioni I.

Clin Auton Res. 2001 Apr;11(2):67-78. Review.

PMID:
11570606
6.

Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome.

Goertzel BN, Pennachin C, de Souza Coelho L, Gurbaxani B, Maloney EM, Jones JF.

Pharmacogenomics. 2006 Apr;7(3):475-83.

PMID:
16610957
7.

Glucocorticoid receptor polymorphisms and haplotypes associated with chronic fatigue syndrome.

Rajeevan MS, Smith AK, Dimulescu I, Unger ER, Vernon SD, Heim C, Reeves WC.

Genes Brain Behav. 2007 Mar;6(2):167-76.

8.

Polymorphism in COMT is associated with IgG3 subclass level and susceptibility to infection in patients with chronic fatigue syndrome.

Löbel M, Mooslechner AA, Bauer S, Günther S, Letsch A, Hanitsch LG, Grabowski P, Meisel C, Volk HD, Scheibenbogen C.

J Transl Med. 2015 Aug 14;13:264. doi: 10.1186/s12967-015-0628-4.

9.

An integrated approach to infer causal associations among gene expression, genotype variation, and disease.

Lee E, Cho S, Kim K, Park T.

Genomics. 2009 Oct;94(4):269-77. doi: 10.1016/j.ygeno.2009.06.002.

10.

Association between chronic fatigue syndrome and the corticosteroid-binding globulin gene ALA SER224 polymorphism.

Torpy DJ, Bachmann AW, Gartside M, Grice JE, Harris JM, Clifton P, Easteal S, Jackson RV, Whitworth JA.

Endocr Res. 2004 Aug;30(3):417-29.

PMID:
15554358
11.

Genetic evaluation of the serotonergic system in chronic fatigue syndrome.

Smith AK, Dimulescu I, Falkenberg VR, Narasimhan S, Heim C, Vernon SD, Rajeevan MS.

Psychoneuroendocrinology. 2008 Feb;33(2):188-97.

PMID:
18079067
12.

[Catechol-O-methyltransferase gene rs6267 polymorphism in children with attention deficit hyperactivity disorder].

Zhang YB, Luo XR, Liu X, Zhong Y, Zhu F, Chen LY.

Zhongguo Dang Dai Er Ke Za Zhi. 2011 Feb;13(2):127-30. Chinese.

13.

An angiotensin-1 converting enzyme polymorphism is associated with allostatic load mediated by C-reactive protein, interleukin-6 and cortisol.

Smith AK, Maloney EM, Falkenberg VR, Dimulescu I, Rajeevan MS.

Psychoneuroendocrinology. 2009 May;34(4):597-606. doi: 10.1016/j.psyneuen.2008.10.022.

PMID:
19081678
14.

Human liver catechol-O-methyltransferase pharmacogenetics.

Boudíková B, Szumlanski C, Maidak B, Weinshilboum R.

Clin Pharmacol Ther. 1990 Oct;48(4):381-9.

PMID:
2225698
15.

Dopaminergic candidate genes in Tourette syndrome: association between tic severity and 3' UTR polymorphism of the dopamine transporter gene.

Tarnok Z, Ronai Z, Gervai J, Kereszturi E, Gadoros J, Sasvari-Szekely M, Nemoda Z.

Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):900-5.

PMID:
17508355
16.

Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome.

Gürsoy S, Erdal E, Herken H, Madenci E, Alaşehirli B, Erdal N.

Rheumatol Int. 2003 May;23(3):104-7.

PMID:
12739038
17.

Genetic polymorphisms of estrogen receptor alpha, CYP19, catechol-O-methyltransferase are associated with familial prostate carcinoma risk in a Japanese population.

Suzuki K, Nakazato H, Matsui H, Koike H, Okugi H, Kashiwagi B, Nishii M, Ohtake N, Nakata S, Ito K, Yamanaka H.

Cancer. 2003 Oct 1;98(7):1411-6.

18.

[Sudden cardiac death and polymorphism of genes-candidates of cardiovascular diseases].

Voevoda MI, Kulikov IV, Maksimov VN, Maliutina SK, Shakhtshneĭder EV, Kulishova LM, Novoselov VP, Romashenko AG.

Kardiologiia. 2009;49(4):52-7. Russian.

PMID:
19463119
19.

Association between serotonin transporter gene polymorphism and chronic fatigue syndrome.

Narita M, Nishigami N, Narita N, Yamaguti K, Okado N, Watanabe Y, Kuratsune H.

Biochem Biophys Res Commun. 2003 Nov 14;311(2):264-6.

PMID:
14592408
20.

Association analysis of the DRD4 and COMT genes in methamphetamine abuse.

Li T, Chen CK, Hu X, Ball D, Lin SK, Chen W, Sham PC, Loh el-W, Murray RM, Collier DA.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):120-4.

PMID:
15274053
Items per page

Supplemental Content

Support Center