153 related articles for article (PubMed ID: 19556740)
1. Genetic polymorphisms of the serotonin transporter, but not the 2a receptor or nitric oxide synthetase, are associated with pulmonary hypertension in chronic obstructive pulmonary disease.
Ulrich S; Hersberger M; Fischler M; Nussbaumer-Ochsner Y; Treder U; Russi EW; Speich R
Respiration; 2010; 79(4):288-95. PubMed ID: 19556740
[TBL] [Abstract][Full Text] [Related]
2. [Gene polymorphism of the endothelial nitric oxide synthase enzyme and pulmonary hypertension in patient with chronic obstructive pulmonary disease].
Sun LR; Wang C; Wu AQ; Yan BM; Li DM; Zhang JL; Wang GJ; Zhang Y; Li XQ; Zhang QZ
Zhonghua Jie He He Hu Xi Za Zhi; 2008 May; 31(5):335-40. PubMed ID: 18953956
[TBL] [Abstract][Full Text] [Related]
3. Sequence variants in BMPR2 and genes involved in the serotonin and nitric oxide pathways in idiopathic pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension: relation to clinical parameters and comparison with left heart disease.
Ulrich S; Szamalek-Hoegel J; Hersberger M; Fischler M; Garcia JS; Huber LC; Grünig E; Janssen B; Speich R
Respiration; 2010; 79(4):279-87. PubMed ID: 19844076
[TBL] [Abstract][Full Text] [Related]
4. Associations between endothelial nitric oxide synthase A/B, angiotensin converting enzyme I/D and serotonin transporter L/S gene polymorphisms with pulmonary hypertension in COPD patients.
Ulasli SS; Eyuboglu FO; Verdi H; Atac FB
Mol Biol Rep; 2013 Oct; 40(10):5625-33. PubMed ID: 24057178
[TBL] [Abstract][Full Text] [Related]
5. Polymorphisms in the serotonin transporter protein (SERT) gene in patients with pulmonary arterial hypertension.
Baloira A; Núñez M; Cifrian J; Vilariño C; Ojeda M; Valverde D
Arch Bronconeumol; 2012 Mar; 48(3):77-80. PubMed ID: 22177971
[TBL] [Abstract][Full Text] [Related]
6. Cardiopulmonary exercise test characteristics in patients with chronic obstructive pulmonary disease and associated pulmonary hypertension.
Holverda S; Bogaard HJ; Groepenhoff H; Postmus PE; Boonstra A; Vonk-Noordegraaf A
Respiration; 2008; 76(2):160-7. PubMed ID: 17960052
[TBL] [Abstract][Full Text] [Related]
7. Endothelial nitric oxide synthase polymorphisms associated with abnormal nitric oxide production are not over-represented in children with Down syndrome.
Cua CL; Cooke G; Taylor M; Hayes J; Waldon L; Lipowski P; Kossman B; Nash PL
Congenit Heart Dis; 2006 Jul; 1(4):169-74. PubMed ID: 18377542
[TBL] [Abstract][Full Text] [Related]
8. Prevalence, predictors, and survival in pulmonary hypertension related to end-stage chronic obstructive pulmonary disease.
Andersen KH; Iversen M; Kjaergaard J; Mortensen J; Nielsen-Kudsk JE; Bendstrup E; Videbaek R; Carlsen J
J Heart Lung Transplant; 2012 Apr; 31(4):373-80. PubMed ID: 22226804
[TBL] [Abstract][Full Text] [Related]
9. Pulmonary hypertension in chronic obstructive pulmonary disease and interstitial lung diseases.
Weitzenblum E; Chaouat A; Canuet M; Kessler R
Semin Respir Crit Care Med; 2009 Aug; 30(4):458-70. PubMed ID: 19634085
[TBL] [Abstract][Full Text] [Related]
10. Polymorphism of the serotonin transporter gene and pulmonary hypertension in chronic obstructive pulmonary disease.
Eddahibi S; Chaouat A; Morrell N; Fadel E; Fuhrman C; Bugnet AS; Dartevelle P; Housset B; Hamon M; Weitzenblum E; Adnot S
Circulation; 2003 Oct; 108(15):1839-44. PubMed ID: 14530202
[TBL] [Abstract][Full Text] [Related]
11. Serotonin-induced smooth muscle hyperplasia in various forms of human pulmonary hypertension.
Marcos E; Fadel E; Sanchez O; Humbert M; Dartevelle P; Simonneau G; Hamon M; Adnot S; Eddahibi S
Circ Res; 2004 May; 94(9):1263-70. PubMed ID: 15059929
[TBL] [Abstract][Full Text] [Related]
12. Association study of serotonin 2A receptor (5-HT2A) and serotonin transporter (5-HTT) gene polymorphisms with schizophrenia.
Sáiz PA; García-Portilla MP; Arango C; Morales B; Alvarez V; Coto E; Fernández JM; Bascarán MT; Bousoño M; Bobes J
Prog Neuropsychopharmacol Biol Psychiatry; 2007 Apr; 31(3):741-5. PubMed ID: 17291660
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 19758204
[TBL] [Abstract][Full Text] [Related]
14. Pulmonary hypertension associated with chronic obstructive pulmonary disease.
Chhabra SK
Indian J Chest Dis Allied Sci; 2010; 52(1):29-40. PubMed ID: 20364612
[TBL] [Abstract][Full Text] [Related]
15. Allelic variation in the serotonin transporter (5HTT) gene contributes to idiopathic pulmonary hypertension in children.
Vachharajani A; Saunders S
Biochem Biophys Res Commun; 2005 Aug; 334(2):376-9. PubMed ID: 16009349
[TBL] [Abstract][Full Text] [Related]
16. Pulmonary hypertension in COPD: a review and consideration of the role of arterial vasodilators.
Burger CD
COPD; 2009 Apr; 6(2):137-44. PubMed ID: 19378227
[TBL] [Abstract][Full Text] [Related]
17. Pulmonary arterial lesions in explanted lungs after transplantation correlate with severity of pulmonary hypertension in chronic obstructive pulmonary disease.
Carlsen J; Hasseriis Andersen K; Boesgaard S; Iversen M; Steinbrüchel D; Bøgelund Andersen C
J Heart Lung Transplant; 2013 Mar; 32(3):347-54. PubMed ID: 23265910
[TBL] [Abstract][Full Text] [Related]
18. [Pulmonary hypertension in COPD and interstitial lung diseases].
Markart P; Ghofrani HA; Grimminger F; Günther A
Dtsch Med Wochenschr; 2009 Aug; 134 Suppl 5():S164-6. PubMed ID: 19718606
[TBL] [Abstract][Full Text] [Related]
19. The association between serotonin-related gene polymorphisms and panic disorder.
Yoon HK; Yang JC; Lee HJ; Kim YK
J Anxiety Disord; 2008 Dec; 22(8):1529-34. PubMed ID: 18436425
[TBL] [Abstract][Full Text] [Related]
20. Association of serotonin transporter gene variation with smoking, chronic obstructive pulmonary disease, and its depressive symptoms.
Ishii T; Wakabayashi R; Kurosaki H; Gemma A; Kida K
J Hum Genet; 2011 Jan; 56(1):41-6. PubMed ID: 20981038
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]