Results 11 to 20 of about 3,013,569 (257)

Stria Gravidarum Is Genetic But Not Related With Collagen Gene Polymorphism [PDF]

, 2013
BACKGROUND: Striae Gravidarum (SG) is a common problem that complicates the pregnancies. We aimed to evaluate the possible etiologic factors of SG and the possible importance of collagen polymorphism on SG.
Gungor, Cakir A. N., Gencer, M., Silan, F., Uysal, A., Isik, S., Oguz, S., Uludag, A.   +6 more
core   +4 more sources

Angiotensin-converting enzyme insertion/deletion polymorphism does not influence the restenosis rate after coronary stent implantation [PDF]

, 2002
Background. Experimental studies have shown an activation of the angiotensin-converting enzyme (ACE) system as a response to endothelial injury. Recent publications have elucidated the hypothesis that the ACE gene polymorphism may influence the level of ...
Hausmann, Dirk, Koschyk, Dietmar H., Grip, Lars, Ferrari, Markus, de Jaegere, Peter, Rieber, Johannes, Figulla, Hans R., Mudra, Harald, Schächinger, Volker, Rothman, Martin, Voudris, Vassilis   +10 more
core   +1 more source

Association of the CCR5 gene with juvenile idiopathic arthritis [PDF]

, 2010
The CC chemokine receptor 5 (CCR5) has been shown to be important in the recruitment of T-helper cells to the synovium, where they accumulate, drive the inflammatory process and the consequent synovitis and joint destruction.
Martin, P., BSPAR Study Group, Barton, A., UKRAG Consortium, Worthington, J., Gardner-Medwin, J. [CAPS and BSPAR Study Groups], Thomson, W., W Thomson, Flynn, E., A Hinks, E Flynn, J Packham, Packham, J., Hinks, A., S Eyre, J Worthington, Eyre, S.; id_orcid, Eyre, S., Barton, A.; id_orcid, P Martin, Childhood Arthritis Prospective Study (CAPS), Martin, P.; id_orcid, A Barton   +22 more
core   +1 more source

Polymorphism of the tryptophan hydroxylase 2 (TPH2) gene is associated with chimpanzee neuroticism [PDF]

, 2011
In the brain, serotonin production is controlled by tryptophan hydroxylase 2 (TPH2), a genotype. Previous studies found that mutations on the TPH2 locus in humans were associated with depression and studies of mice and studies of rhesus macaques have ...
Alexander Weiss, Murayama, Yuichi, Tatyana Humle, Humle, Tatyana, Toshifumi Udono, Morimura, Naruki, Ikuo Hayasaka, Inoue-Murayama, Miho, Yuichi Murayama, Miho Inoue-Murayama, Shin'ichi Ito, Weiss, Alexander, Kyung-Won Hong, Hayasaka, Ikuo, Ito, Shin'ichi, Hong, Kyung-Won, Udono, Toshifumi, Naruki Morimura   +17 more
core   +2 more sources

Glu298Asp endothelial nitric oxide synthase gene polymorphism interacts with environmental and dietary factors to influence endothelial function [PDF]

, 2002
An endothelial nitric oxide synthase (eNOS) gene polymorphism (Glu298Asp) has been associated with cardiovascular disease. We investigated whether carriage of the polymorphism was associated with functional changes in the endothelium, and how genotype ...
Jeerooburkhan, N., Muller, D.P.R., Mullen, M.J., Deanfield, J.E., Muller, DP, Deanfield, JE, Humphries, SE, Kattenhorn, M., Cole, T.J., Lucas, A, Humphries, S.E., Leeson, Christopher, Kattenhorn, M, Hingorani, AD, Jeerooburkhan, N, Hingorani, S.D., Leeson, CP, Mullen, MJ, Leeson, C.P.M., Cole, TJ, Lucas, A.   +20 more
core   +1 more source

Allelic drop-out may occur with a primer binding site polymorphism for the commonly used RFLP assay for the -1131T>C polymorphism of the Apolipoprotein AV gene. [PDF]

, 2006
Apolipoprotein AV (ApoAV) gene variant, -1131T>C, is associated with increased triglyceride concentrations in all ethnic groups studied. An MseI based RFLP analysis is the most commonly used method for genotyping this SNP.
Andrew T Hattersley, Venigalla, Prathyusha NS, Kirsten J Ward, Ward Kirsten J, Hattersley, Andrew T, Ward, Kirsten J, Giriraj R Chandak, Ellard Sian, Timothy M Frayling, Prathyusha NS Venigalla, Frayling, Timothy M, Sian Ellard, Chittaranjan S Yajnik, Hattersley Andrew T, Chandak Giriraj R, Frayling Timothy M, Yajnik Chittaranjan S, Chandak, Giriraj R, Venigalla Prathyusha NS, Ellard, Sian, Yajnik, Chittaranjan S   +20 more
core   +1 more source

Association of the 894G>T polymorphism in the endothelial nitric oxide synthase gene with risk of acute myocardial infarction [PDF]

, 2008
Background: This study was designed to investigate the association of the 894G>T polymorphism in the eNOS gene with risk of acute myocardial infarction (AMI), extent of coronary artery disease (CAD) on coronary angiography, and in-hospital mortality ...
Sakellariou Dimitris C, Tzeis Stylianos E, Richter, Dimitris J., Gialafos Elias J, Gialafos, Elias J., Elias J Gialafos, Andrikopoulos George K, Toutouzas Pavlos K, Richter Dimitris J, George K Andrikopoulos, Edward W Hillhouse, Grammatopoulos, Dimitris, Stefanos G Foussas, Stylianos E Tzeis, Grammatopoulos Dimitris K, Sakellariou, Dimitris C., Michalis N Zairis, Zervou Sevasti I, Manolis Antonis S, Manolis, Antonis S., Toutouzas, Pavlos K., Dimitris K Grammatopoulos, Foussas Stefanos G, Tzeis, Stylianos E., Zairis Michalis N, Christodoulos I Stefanadis, Stefanadis, Christodoulos I., Foussas, Stefanos G., Dimitris C Sakellariou, Sevasti I Zervou, Antonis S Manolis, Zervou, Sevasti I., null null, Andrikopoulos, George K., Zairis, Michalis N., Hillhouse Edward W, Dimitris J Richter, Stefanadis Christodoulos I, Hillhouse, Edward W., Pavlos K Toutouzas   +39 more
core   +2 more sources

The promoter polymorphism -232C/G of the PCK1 gene is associated with type 2 diabetes in a UK-resident South Asian population [PDF]

, 2009
Background: The PCK1 gene, encoding cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C), has previously been implicated as a candidate gene for type 2 diabetes (T2D) susceptibility.
Britten, Abigail C, Barnett Anthony H, Barnett, Anthony, Britten, Abigail C., Bellary, S, Barnett, Anthony H., Anthony H Barnett, Kumar Sudhesh, Rees, Simon D, Britten, Abigail, Sudhesh Kumar, O'Hare, J Paul, Kelly, M Ann, Rees, Simon D., Rees, Simon, Kelly, M. Ann, Kelly, Marilyn, Britten Abigail C, Kelly M Ann, Bellary, Srikanth, Rees Simon D, Srikanth Bellary, Abigail C Britten, J Paul O'Hare, Bellary Srikanth, O'Hare, JP, Kumar, Sudhesh, Barnett, Anthony H, Simon D Rees, Barnett, A. H., O'Hare J Paul, Kumar, S, O'Hare, J. Paul, M Ann Kelly   +33 more
core   +3 more sources

Response to combination therapy with interferon alfa-2a and ribavirin in chronic hepatitis C according to a TNF-alpha promoter polymorphism [PDF]

, 2003
Background. Tumor necrosis factor-alpha (TNF-alpha) is involved in the pathogenesis of chronic active hepatitis C. Polymorphisms in the promoter region of the TNF-alpha gene can alter the TNF-alpha expression and modify the host immune response.
Konig, A., Folwaczny, Christian, Schmidt, F., Simperl, C., Schaefer, M., Torok, P., Glas, J., Schiemann, Uwe, Martin, K.   +8 more
core   +1 more source

The association between vesicle-associated membrane protein - 8 A/G gene polymorphism and the risk of acute myocardial infarction

Revista Colombiana de Cardiología, 2021
Introduction: Until now, only few studies have reported the correlation between vesicle-associated membrane protein-8 (VAMP-8) A/G gene polymorphism and acute myocardial infarction.
Mohammad S. Rohman, Jonny K. Fajar, Rina Y. Novira, Erdo P. Sidarta, Putu N. B. Saka, Teuku Heriansyah   +5 more
doaj   +1 more source