Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: Syndrome and MAX[original query] |
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Cytokine-related genotypic differences in peak interleukin-6 blood levels of patients with SIRS and septic complications. The Journal of trauma 2005 12 59 (5): 1181-9; discussion 1189-90. Watanabe Eizo, Hirasawa Hiroyuki, Oda Shigeto, Shiga Hidetoshi, Matsuda Kenichi, Nakamura Masataka, Abe Ryuzo, Nakada Takaa |
Dietary saturated fat modulates the association between STAT3 polymorphisms and abdominal obesity in adults. The Journal of nutrition 2009 Nov 139 (11): 2011-7. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Field Martyn R, Peloso Gina M, Shen Jian, McManus Ross, Hercberg Serge, Lairon Denis, Planells Richard, Roche Helen |
Leptin receptor polymorphisms interact with polyunsaturated fatty acids to augment risk of insulin resistance and metabolic syndrome in adults. The Journal of nutrition 2010 Feb 140 (2): 238-44. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Field Martyn R, Ordovas Jose M, Cupples L Adrienne, Defoort Catherine, Lovegrove Julie A, Drevon Christian A, Blaak Ellen E, Gibney Michael J, Kiec-Wilk Beata, Karlstrom Britta, Lopez-Miranda Jose, McManus Ross, Hercberg Serge, Lairon Denis, Planells Richard, Roche Helen |
Gene-nutrient interactions in the metabolic syndrome: single nucleotide polymorphisms in ADIPOQ and ADIPOR1 interact with plasma saturated fatty acids to modulate insulin resistance. The American journal of clinical nutrition 2009 Dec . Ferguson JF, Phillips CM, Tierney AC, Pérez-Martínez P, Defoort C, Helal O, Lairon D, Planells R, Shaw DI, Lovegrove JA, Gjelstad IM, Drevon CA, Blaak EE, Saris WH, Leszczynska-Golabek I, Kiec-Wilk B, Risérus U, Karlström B, Miranda JL, Roche HM |
Complement component 3 polymorphisms interact with polyunsaturated fatty acids to modulate risk of metabolic syndrome. The American journal of clinical nutrition 2009 Dec 90 (6): 1665-73. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Ferguson Jane F, Field Martyn R, Kelly Enda D, Peloso Gina M, Cupples L Adrienne, Shen Jian, Ordovas Jose M, McManus Ross, Hercberg Serge, Portugal Henri, Lairon Denis, Planells Richard, Roche Helen |
ACC2 gene polymorphisms, metabolic syndrome, and gene-nutrient interactions with dietary fat. Journal of lipid research 2010 Dec 51 (12): 3500-7. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Field Martyn R, Cupples L Adrienne, Ordovas Jose M, McMonagle Jolene, Defoort Catherine, Lovegrove Julie A, Drevon Christian A, Blaak Ellen E, Kiec-Wilk Beata, Riserus Ulf, Lopez-Miranda Jose, McManus Ross, Hercberg Serge, Lairon Denis, Planells Richard, Roche Helen |
Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome. Journal of lipid research 2010 Jul 51 (7): 1793-800. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Field Martyn R, Cupples L Adrienne, Ordovas Jose M, Defoort Catherine, Lovegrove Julie A, Drevon Christian A, Gibney Michael J, Blaak Ellen E, Kiec-Wilk Beata, Karlstrom Britta, Lopez-Miranda Jose, McManus Ross, Hercberg Serge, Lairon Denis, Planells Richard, Roche Helen |
Gene-nutrient interactions and gender may modulate the association between ApoA1 and ApoB gene polymorphisms and metabolic syndrome risk. Atherosclerosis 2011 Feb 214 (2): 408-14. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Field Martyn R, McManus Ross, Hercberg Serge, Lairon Denis, Planells Richard, Roche Helen |
Additive effect of polymorphisms in the IL-6, LTA, and TNF-{alpha} genes and plasma fatty acid level modulate risk for the metabolic syndrome and its components. The Journal of clinical endocrinology and metabolism 2010 Mar 95 (3): 1386-94. Phillips Catherine M, Goumidi Louisa, Bertrais Sandrine, Ferguson Jane F, Field Martyn R, Kelly Enda D, Mehegan John, Peloso Gina M, Cupples L Adrienne, Shen Jian, Ordovas Jose M, McManus Ross, Hercberg Serge, Portugal Henri, Lairon Denis, Planells Richard, Roche Helen |
G-protein ß3 subunit 825CC genotype is associated with postprandial distress syndrome with impaired gastric emptying and with the feeling of hunger in Japanese. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2011 Dec 23 (12): 1073-80. Shimpuku M, Futagami S, Kawagoe T, Nagoya H, Shindo T, Horie A, Kodaka Y, Itoh T, Sakamoto |
Genetic variations at the lipoprotein lipase gene influence plasma lipid concentrations and interact with plasma n-6 polyunsaturated fatty acids to modulate lipid metabolism. Atherosclerosis 2011 Oct 218 (2): 416-22. Garcia-Rios Antonio, Delgado-Lista Javier, Perez-Martinez Pablo, Phillips Catherine M, Ferguson Jane F, Gjelstad Ingrid M F, Williams Christine M, Karlström Brita, Kie?-Wilk Beata, Blaak Ellen E, Lairon Denis, Planells Richard, Malczewska-Malec Ma?gorzata, Defoort Catherine, Riserus Ulf, Saris Wim H M, Lovegrove Julie A, Drevon Christian A, Roche Helen M, Lopez-Miranda Jo |
Dietary saturated fat, gender and genetic variation at the TCF7L2 locus predict the development of metabolic syndrome. The Journal of nutritional biochemistry 2011 May . Phillips CM, Goumidi L, Bertrais S, Field MR, McManus R, Hercberg S, Lairon D, Planells R, Roche HM |
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors. Familial cancer 2012 Mar 11 (1): 19-26. Rahner Nils, Brockschmidt Felix F, Steinke Verena, Kahl Philip, Becker Tim, Vasen Hans F A, Wijnen Juul T, Tops Carli J M, Holinski-Feder Elke, Ligtenberg Marjolijn J L, Spruijt Liesbeth, Görgens Heike, Stemmler Susanne, Kloor Matthias, Dietmaier Wolfgang, , Schumacher Johannes, Nöthen Markus M, Propping Pet |
High dietary saturated fat intake accentuates obesity risk associated with the fat mass and obesity-associated gene in adults. The Journal of nutrition 2012 Mar . Phillips CM, Kesse-Guyot E, McManus R, Hercberg S, Lairon D, Planells R, Roche HM |
Evaluation of 5-fluorouracil pharmacokinetics in cancer patients with a c.1905+1G>A mutation in DPYD by means of a Bayesian limited sampling strategy. Clinical pharmacokinetics 2012 Mar 51 (3): 163-74. van Kuilenburg André B P, Häusler Peter, Schalhorn Andreas, Tanck Michael W T, Proost Johannes H, Terborg Christoph, Behnke Detlev, Schwabe Wolfgang, Jabschinsky Kati, Maring Jan Gera |
Could familial Mediterranean fever gene mutations be related to PFAPA syndrome? Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2015 Sep . Celiksoy Mehmet Halil, Ogur Gonul, Yaman Elif, Abur Ummet, Fazla Semanur, Sancak Recep, Yildiran Alis |
A study on association of leptin receptor gene polymorphism with obstructive sleep apnea syndrome in overweight and obese north Indian subjects. Indian journal of physiology and pharmacology 0 58 (3): 222-8. Dubey Abhishek, Kant Surya, Agarwal Sarita, Dixit Swati, Mahadi Abbas Ali, Tiwari Suni |
[Population pharmacokinetics and pharmacodynamics of clopidogrel in patients with acute coronary syndrome]. Yao xue xue bao = Acta pharmaceutica Sinica 2014 Oct 49 (10): 1426-32. Xie Cheng, Ding Xiao-Liang, Xue Ling, Jiang Bin, Hang Yong-Fu, Gao Jie, Miao Li-Y |
Assessing the midface in Muenke syndrome: A cephalometric analysis and review of the literature. Journal of plastic, reconstructive & aesthetic surgery : JPRAS 2016 Jul . Samra Fares, Bauder Andrew R, Swanson Jordan W, Whitaker Linton A, Bartlett Scott P, Taylor Jesse |
Abdominal paraganglioma in a young woman with 1p36 deletion syndrome. American journal of medical genetics. Part A 2016 Oct . Murakoshi Miki, Takasawa Kei, Nishioka Masato, Asakawa Masahiro, Kashimada Kenichi, Yoshimoto Takanobu, Yamamoto Toshiyuki, Takekoshi Kazuhiro, Ogawa Yoshihiro, Shimohira Masayu |
Increased psoriasis frequency in patients with familial Mediterranean fever. Upsala journal of medical sciences 2018 1 123 (1): 57-61. Erden Abdulsamet, Batu Ezgi Deniz, Seyho?lu Emrah, Sari Alper, Sönmez Hafize Emine, Armagan Berkan, Demir Selcan, Bilgin Emre, Kilic Levent, Karadag Omer, Akdogan Ali, Bilginer Yelda, Ertenli Ihsan, Kiraz Sedat, Apras Bilgen Sule, Kalyoncu Um |
Urine concentrating defect as presenting sign of progressive renal failure in Bardet-Biedl syndrome patients. Clinical kidney journal 2021 6 14 (6): 1545-1551. Zacchia Miriam, Blanco Francesca Del Vecchio, Torella Annalaura, Raucci Raffaele, Blasio Giancarlo, Onore Maria Elena, Marchese Emanuela, Trepiccione Francesco, Vitagliano Caterina, Iorio Valentina Di, Alessandra Perna, Simonelli Francesca, Nigro Vincenzo, Capasso Giovambattista, Viggiano Davi |
Epilepsy in a cohort of children with Noonan syndrome and related disorders. European journal of pediatrics 2022 5 181 (8): 2919-2926. Davico Chiara, D'Alessandro Rossella, Borgogno Marta, Campagna Filippa, Torta Francesca, Ricci Federica, Amianto Federico, Vittorini Roberta, Carli Diana, Mussa Alessandro, Vitiello Benedetto, Ferrero Giovanni Battis |
Caveolin-1 rs1997623 variant and adult metabolic syndrome-Assessing the association in three ethnic cohorts of Arabs, South Asians and South East Asians. Frontiers in genetics 2022 11 13 1034892. Al Madhoun Ashraf, Hebbar Prashantha, Nizam Rasheeba, Haddad Dania, Melhem Motasem, Abu-Farha Mohamed, Thanaraj Thangavel Alphonse, Al-Mulla Fa |
Genetic Predisposition to Pheochromocytoma and Paraganglioma: 21 Years' Experience in the Field. Annales d'endocrinologie 2024 5 . Catherine Cardot-Bauters, Marie-Christine Vantyghem, Christine Do Cao, Rachel Desailloud, Michael Joubert, Lucie Coppin, Marie-Francoise Odou, Pascal Pig |
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