Zeitschriftenartikel zum Thema „Genetic polymorphisms“
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Siddique, Imad, K. Scott Brimble, Louise Walkin, Angela Summers, Paul Brenchley, Sarah Herrick und Peter J. Margetts. „Genetic Polymorphisms and Peritoneal Membrane Function“. Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis 35, Nr. 5 (September 2015): 517–29. http://dx.doi.org/10.3747/pdi.2014.00049.
Delluc, Aurélien, Lénaïck Gourhant, Karine Lacut, Bernard Mercier, Marie-Pierre Audrezet, Emmanuel Nowak, Emmanuel Oger et al. „Association of common genetic variations and idiopathic venous thromboembolism“. Thrombosis and Haemostasis 103, Nr. 06 (2010): 1161–69. http://dx.doi.org/10.1160/th09-07-0430.
Somberg, John C. „Genetic Polymorphisms“. American Journal of Therapeutics 9, Nr. 4 (Juli 2002): 271. http://dx.doi.org/10.1097/00045391-200207000-00001.
Verloop, Herman, Olaf M. Dekkers, Robin P. Peeters, Jan W. Schoones und Johannes W. A. Smit. „GENETICS IN ENDOCRINOLOGY: Genetic variation in deiodinases: a systematic review of potential clinical effects in humans“. European Journal of Endocrinology 171, Nr. 3 (September 2014): R123—R135. http://dx.doi.org/10.1530/eje-14-0302.
Ventriglio, A., A. Petito, A. Gentile, G. Vitrani, I. Bonfitto, A. C. Cecere, A. Rinaldi et al. „Pharmacodynamic targets of psychotic patients treated with a long-acting therapy“. European Psychiatry 41, S1 (April 2017): S366—S367. http://dx.doi.org/10.1016/j.eurpsy.2017.02.370.
Simmonds, Rachel, José Hermida, Suely Rezende und David Lane. „Haemostatic Genetic Risk Factors in Arterial Thrombosis“. Thrombosis and Haemostasis 86, Nr. 07 (2001): 374–85. http://dx.doi.org/10.1055/s-0037-1616235.
Muiño, Elena, Jurek Krupinski, Caty Carrera, Cristina Gallego-Fabrega, Joan Montaner und Israel Fernández-Cadenas. „An Inflammatory Polymorphisms Risk Scoring System for the Differentiation of Ischemic Stroke Subtypes“. Mediators of Inflammation 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/569714.
Makowska-Kaczmarska, Marzena, Anna Okoń und Elżbieta Olszewska. „Role of polymorphism of the interleukin-1B gene and other genetic polymorphisms in the aetiology of root resorption in patients receiving orthodontic treatment“. Forum Ortodontyczne 13, Nr. 1 (01.03.2017): 36–42. http://dx.doi.org/10.5604/01.3001.0010.2604.
Bouchet, Valérie, Heather Huot und Richard Goldstein. „Molecular Genetic Basis of Ribotyping“. Clinical Microbiology Reviews 21, Nr. 2 (April 2008): 262–73. http://dx.doi.org/10.1128/cmr.00026-07.
Kasyanov, E. D., T. V. Zhilyaeva und G. E. Maso. „Association of affective disorders and MTHFR, MTR, and MTRR gene polymorphisms: preliminary results of a family study“. Neurology, Neuropsychiatry, Psychosomatics 14, Nr. 5 (21.10.2022): 13–21. http://dx.doi.org/10.14412/2074-2711-2022-5-13-21.
Matsuo, Hitoshi, Tomonori Segawa, Sachiro Watanabe, Kimihiko Kato, Takeshi Hibino, Kiyoshi Yokoi, Sahoko Ichihara et al. „Assessment of genetic risk for myocardial infarction“. Thrombosis and Haemostasis 96, Nr. 08 (2006): 220–27. http://dx.doi.org/10.1160/th06-02-0117.
Angelova, Lyudmila, Maria Tsvetkova und Mariya Levkova. „CHROMOSOMAL POLYMORPHISM IN BULGARIAN PATIENTS WITH REPRODUCTIVE PROBLEMS – ONE GENETIC CENTRE EXPERIENCE“. Journal of IMAB - Annual Proceeding (Scientific Papers) 27, Nr. 4 (02.12.2021): 4133–38. http://dx.doi.org/10.5272/jimab.2021274.4133.
Calderón, Rosario, Ana M. Pérez-Miranda, Maria Fuciarelli, Giusepina Scano, Mónica Carrión, Miguel A. Alfonso-Sánchez, José A. Peña, Beatriz Ambrosio und GianFranco De Stefano. „Genetic polymorphisms in autochthonous Basques from Northern Navarre“. Anthropologischer Anzeiger 64, Nr. 2 (21.06.2006): 173–87. http://dx.doi.org/10.1127/anthranz/64/2006/173.
Kobayashi, T., T. Nagata, S. Murakami, S. Takashiba, H. Kurihara, Y. Izumi, Y. Numabe et al. „Genetic Risk Factors for Periodontitis in a Japanese Population“. Journal of Dental Research 88, Nr. 12 (05.11.2009): 1137–41. http://dx.doi.org/10.1177/0022034509350037.
Taizhanova, Dana, Roza Bodaubay, Aliya Toleuova, Akerke Kalimbetova, Dmitriy Babenko, Anar Turmukhambetova, Ludmila Akhmaltdinova und Olga Visternichan. „Genetic Polymorphisms Association in Restenosis of Coronary Arteries“. Open Access Macedonian Journal of Medical Sciences 8, B (25.08.2020): 666–72. http://dx.doi.org/10.3889/oamjms.2020.4505.
Kocabaş, Neslihan Aygün, und Bensu Karahalil. „XRCC1 Arg399Gln Genetic Polymorphism in a Turkish Population“. International Journal of Toxicology 25, Nr. 5 (September 2006): 419–22. http://dx.doi.org/10.1080/10915810600870567.
Weeden, Norman F., Bruce I. Reisch und Mary-Howell E. Martens. „Genetic Analysis of Isozyme Polymorphism in Grape“. Journal of the American Society for Horticultural Science 113, Nr. 5 (September 1988): 765–69. http://dx.doi.org/10.21273/jashs.113.5.765.
Cambien, Francois, und Laurence Tiret. „Atherosclerosis: From Genetic Polymorphisms to System Genetics“. Cardiovascular Toxicology 5, Nr. 2 (2005): 143–52. http://dx.doi.org/10.1385/ct:5:2:143.
Miguita, K., Q. Cordeiro, R. G. Shavitt, E. C. Miguel und H. Vallada. „Association study between genetic monoaminergic polymorphisms and OCD response to clomipramine treatment“. Arquivos de Neuro-Psiquiatria 69, Nr. 2b (2011): 283–87. http://dx.doi.org/10.1590/s0004-282x2011000300003.
Singh, Sanjay, Manish Gupta, Rajeev Kumar Seam und Harish Changotra. „E2F1 genetic variants and risk of cervical cancer in Indian women“. International Journal of Biological Markers 33, Nr. 4 (24.04.2018): 389–94. http://dx.doi.org/10.1177/1724600818768459.
Canavy, I., M. Henry, P. E. Morange, L. Tiret, O. Poirier, A. Ebagosti, M. Bory und I. Juhan-Vague. „Genetic Polymorphisms and Coronary Artery Disease in the South of France“. Thrombosis and Haemostasis 83, Nr. 02 (2000): 212–16. http://dx.doi.org/10.1055/s-0037-1613788.
Zihlif, Malek, Amer Imraish, Baeth Al-Rawashdeh, Aya Qteish, Raihan Husami, Rawand Husami, Farah Tahboub, Yazun Jarrar und Su-Jun Lee. „The Association of IgE Levels with ADAM33 Genetic Polymorphisms among Asthmatic Patients“. Journal of Personalized Medicine 11, Nr. 5 (22.04.2021): 329. http://dx.doi.org/10.3390/jpm11050329.
Sorokina, E. Yu, A. V. Pogozheva und D. B. Nikityuk. „Study of the association of gene polymorphism with the risk of non-communicable diseases in martial artists“. Sports medicine: research and practice 11, Nr. 2 (22.09.2021): 25–33. http://dx.doi.org/10.47529/2223-2524.2021.2.5.
Atmoko, Widi, Putu Angga Risky Raharja, Ponco Birowo, Agus Rizal Ardy Hariandy Hamid, Akmal Taher und Nur Rasyid. „Genetic polymorphisms as prognostic factors for recurrent kidney stones: A systematic review and meta-analysis“. PLOS ONE 16, Nr. 5 (06.05.2021): e0251235. http://dx.doi.org/10.1371/journal.pone.0251235.
Ward, Roger. „Genetic polymorphisms and additive genetic models“. Behavior Genetics 15, Nr. 6 (November 1985): 537–48. http://dx.doi.org/10.1007/bf01065449.
Calvano Küchler, E., J. Arid, M. Palinkas, M. Ayumi Omori, RM de Lara, LM Napolitano Gonçalves, SC Hallak Regalo, C. Paes Torres Mantovani, A. Rezende Vieira und K. Diaz-Serrano. „Genetic Polymorphisms in ACTN3 Contribute to the Etiology of Bruxism in Children“. Journal of Clinical Pediatric Dentistry 44, Nr. 3 (01.01.2020): 180–84. http://dx.doi.org/10.17796/1053-4625-44.3.8.
Novaković, Ivana, Nela Maksimović, Slobodan Cvetković und Dragana Cvetković. „Gene Polymorphisms as Markers of Disease Susceptibility“. Journal of Medical Biochemistry 29, Nr. 3 (01.07.2010): 135–38. http://dx.doi.org/10.2478/v10011-010-0022-y.
Singh, Shweta, Gourdas Choudhuri und Sarita Agarwal. „Frequency of CFTR, SPINK1, and Cathepsin B Gene Mutation in North Indian Population: Connections between Genetics and Clinical Data“. Scientific World Journal 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/763195.
Celec, Peter, Daniela Ostatníková, Zuzana Holešová, Gabriel Minárik, Andrej Ficek, Silvia Kelemenová, Zdeněk Putz und Matúš Kúdela. „Spatial Abilities in Prepubertal Intellectually Gifted Boys and Genetic Polymorphisms Related to Testosterone Metabolism“. Journal of Psychophysiology 23, Nr. 1 (Januar 2009): 1–6. http://dx.doi.org/10.1027/0269-8803.23.1.1.
Yvert, Thomas, Catalina Santiago, Elena Santana-Sosa, Zoraida Verde, Felix Gómez-Gallego, Luis Lopez-Mojares, Margarita Pérez, Nuria Garatachea und Alejandro Lucia. „Physical-Capacity-Related Genetic Polymorphisms in Children with Cystic Fibrosis“. Pediatric Exercise Science 27, Nr. 1 (Februar 2015): 102–12. http://dx.doi.org/10.1123/pes.2014-0050.
SHIN, HYOUNG DOO, IL KIM, CHAN-BUM CHOI, SOO OK LEE, HYE WON LEE und SANG-CHEOL BAE. „Different Genetic Effects of Interferon Regulatory Factor 5 (IRF5) Polymorphisms on Systemic Lupus Erythematosus in a Korean Population“. Journal of Rheumatology 35, Nr. 11 (November 2008): 2148–51. http://dx.doi.org/10.3899/jrheum.080124.
Shalimova, Anna, Galyna Fadieienko, Olena Kolesnikova, Anna Isayeva, Vira Zlatkina, Valeriya Nemtsova, Kostyantyn Prosolenko, Valentyna Psarova, Natalia Kyrychenko und Maryna Kochuieva. „The Role of Genetic Polymorphism in the Formation of Arterial Hypertension, Type 2 Diabetes and their Comorbidity“. Current Pharmaceutical Design 25, Nr. 3 (30.05.2019): 218–27. http://dx.doi.org/10.2174/1381612825666190314124049.
Kuramochi, Hidekazu, Hitoshi Kanno, Tomotaka Uchiyama, Go Nakajima, Kayoko Saito und Kazuhiko Hayashi. „Comprehensive analysis of genetic polymorphisms and irinotecan-induced adverse events in Japanese gastrointestinal cancer patients: A DMET microarray profiling study.“ Journal of Clinical Oncology 30, Nr. 15_suppl (20.05.2012): e21108-e21108. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.e21108.
Diao, Hong-Mei, Zheng-Feng Song und Hai-Dong Xu. „Association between MTHFR genetic polymorphism and Parkinson’s disease susceptibility: a meta-analysis“. Open Medicine 14, Nr. 1 (17.08.2019): 613–24. http://dx.doi.org/10.1515/med-2019-0069.
Chumakova, G. A., A. P. Momot, A. A. Kozarenko und N. G. Veselovskaya. „Genetic predisposition to atherothromboses in patients with severe angina pectoris“. CardioSomatics 1, Nr. 1 (15.03.2010): 80–83. http://dx.doi.org/10.26442/cs44989.
Ayesh, Hazem, Sajida S. Ayesh, Azizullah Beran und Suhail Ayesh. „Association of NOS3 and TNF Genetic Polymorphisms With the Predisposition to Elevated Cholesterol, Retrospective Study“. Journal of the Endocrine Society 5, Supplement_1 (01.05.2021): A33. http://dx.doi.org/10.1210/jendso/bvab048.064.
Ito, Soichiro, Takeshi Hirota, Miyu Yanai, Mai Muto, Eri Watanabe, Yuki Taya und Ichiro Ieiri. „Effects of Genetic Polymorphisms of Cathepsin A on Metabolism of Tenofovir Alafenamide“. Genes 12, Nr. 12 (20.12.2021): 2026. http://dx.doi.org/10.3390/genes12122026.
Miyairi, Isao, und John P. DeVincenzo. „Human Genetic Factors and Respiratory Syncytial Virus Disease Severity“. Clinical Microbiology Reviews 21, Nr. 4 (Oktober 2008): 686–703. http://dx.doi.org/10.1128/cmr.00017-08.
Cordeiro, Quirino, Ricardo Noguti, Cássio M. C. Bottino und Homero Vallada. „Study of association between genetic polymorphisms of phospholipase A2 enzymes and Alzheimer's disease“. Arquivos de Neuro-Psiquiatria 68, Nr. 2 (April 2010): 189–93. http://dx.doi.org/10.1590/s0004-282x2010000200007.
Naranjo-Galvis, C. A., A. de-la-Torre, L. E. Mantilla-Muriel, L. Beltrán-Angarita, X. Elcoroaristizabal-Martín, R. McLeod, N. Alliey-Rodriguez et al. „Genetic Polymorphisms in Cytokine Genes in Colombian Patients with Ocular Toxoplasmosis“. Infection and Immunity 86, Nr. 4 (05.02.2018): e00597-17. http://dx.doi.org/10.1128/iai.00597-17.
Zhang, Guoqiang, und Maohe Jin. „Genetic associations between CYP24A1 polymorphisms and predisposition of cancer: A meta-analysis“. International Journal of Biological Markers 35, Nr. 4 (14.10.2020): 71–79. http://dx.doi.org/10.1177/1724600820944408.
Traspov, AA, MM Minashkin, SV Poyarkov, AG Komarov, IA Shtinova, GI Speshilov, IA Karbyshev, NV Pozdniakova und MA Godkov. „The rs17713054 and rs1800629 polymorphisms of genes LZTFL1 and TNF are associated with COVID-19 severity“. Bulletin of Russian State Medical University, Nr. 2022(6) (Dezember 2022): 92–97. http://dx.doi.org/10.24075/brsmu.2022.065.
Gimelfarb, A. „Pleiotropy and multilocus polymorphisms.“ Genetics 130, Nr. 1 (01.01.1992): 223–27. http://dx.doi.org/10.1093/genetics/130.1.223.
Beletskaya, Inessa S., Sergey Yu Astakhov, Tatiana L. Karonova, Olga V. Galkina, Evdokia O. Bogdanova, Evgeniy L. Akopov und Alexandra A. Kozyreva. „Pseudoexfoliative glaucoma and molecular genetic characteristics of vitamin D metabolism“. Ophthalmology journal 11, Nr. 2 (15.06.2018): 19–28. http://dx.doi.org/10.17816/ov11219-28.
Sufiawati, Irna, Risti Saptarini und Eriska Riyanti. „HUBUNGAN POLIMORFISME GEN RESEPTOR ESTROGEN ALFA DENGAN JUMLAH SEL T CD4+ PADA ANAK TERINFEKSI HIV“. ODONTO : Dental Journal 4, Nr. 2 (01.12.2017): 94. http://dx.doi.org/10.30659/odj.4.2.94-100.
Gade-Andavolu, Radhika, David E. Comings, James MacMurray, Ravi K. Vuthoori, Wallace W. Tourtellotte, Rashed M. Nagra und Lawrence A. Cone. „RANTES: a genetic risk marker for multiple sclerosis“. Multiple Sclerosis Journal 10, Nr. 5 (Oktober 2004): 536–39. http://dx.doi.org/10.1191/1352458504ms1080oa.
Khayrutdinov, V. R., und V. R. Khairutdinov. „Genetic profile of psoriasis patients“. Vestnik dermatologii i venerologii 87, Nr. 4 (15.08.2011): 14–19. http://dx.doi.org/10.25208/vdv1027.
Shimada, Tadanaga, Taka-aki Nakada und Shigeto Oda. „Genetic polymorphisms in sepsis“. Nihon Kyukyu Igakukai Zasshi 24, Nr. 1 (2013): 1–11. http://dx.doi.org/10.3893/jjaam.24.1.
Altshuler, David, Leonid Kruglyak und Eric Lander. „Genetic Polymorphisms and Disease“. New England Journal of Medicine 338, Nr. 22 (28.05.1998): 1626. http://dx.doi.org/10.1056/nejm199805283382214.
Arcaroli, John, Michael B. Fessler und Edward Abraham. „GENETIC POLYMORPHISMS AND SEPSIS“. Shock 24, Nr. 4 (Oktober 2005): 300–312. http://dx.doi.org/10.1097/01.shk.0000180621.52058.e1.