Academic literature on the topic 'Polymorphism of the TLR4 gene'

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Journal articles on the topic "Polymorphism of the TLR4 gene"

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Salamaikina, S. A., V. I. Korchagin, K. O. Mironov, and M. A. Karnaushkina. "Association of Toll-like receptor polymorphism and gene expression level with the risk of developing chronic obstructive pulmonary disease (COPD) and its severity." Bulletin of Siberian Medicine 24, no. 1 (2025): 77–85. https://doi.org/10.20538/1682-0363-2025-1-77-85.

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Aim. Determine the influence of genetic factors of innate immunity on the risk of development and severity of COPD. Materials and methods. The study included 103 patients diagnosed with chronic obstructive pulmonary disease and 47 conditionally healthy people without any chronic bronchopulmonary pathologies. The expression level of TLR genes and alleles of rs5743551 (TLR1), rs5743708 (TLR2), rs3804100 (TLR2), rs3806790 (TLR4), rs5743810 (TLR6), rs3804880 (TLR8) single nucleotide polymorphisms were analyzed via real-time polymerase chain reaction (PCR). Results. Several tendencies were observed
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Liu, Fengjing, Weixin Lu, Qiaohui Qian, Weigang Qi, Jifan Hu, and Bo Feng. "Frequency of TLR 2, 4, and 9 Gene Polymorphisms in Chinese Population and Their Susceptibility to Type 2 Diabetes and Coronary Artery Disease." Journal of Biomedicine and Biotechnology 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/373945.

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Toll-like receptors (TLRs) are pivotal components of the innate immune response. Activation of the innate immune system and subsequent chronic low-grade inflammation are thought to be involved in the pathogenesis of atherosclerosis and type 2 diabetes. In the study, we genotyped TLRs gene polymorphisms, including TLR2 Arg677Trp and Arg753Gln, TLR4 Asp299Gly and Thr399Ile, TLR9-1486T/C and -1237T/C. The frequencies of TT, TC and CC genotype of TLR9-1486T/C mutation were 39.6%, 45.8% and 14.6%, respectively; the frequencies of T allele and C allele were 62.5% and 37.5%. However, neither of these
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Shevchenko, A. V., V. F. Prokofiev, V. I. Konenkov, V. V. Chernykh, and A. N. Trunov. "Features of toll-like receptor genes (TLR-2, TLR-3, TLR-4 and TLR-6) polymorphism in open-angle glaucoma patients." Vavilov Journal of Genetics and Breeding 29, no. 1 (2025): 128–34. https://doi.org/10.18699/vjgb-25-15.

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Modern research shows that innate immunity plays an important role in the pathogenesis of primary open-angle glaucoma (POAG). An increase in the content of toll-like receptors (TLR) in the glaucomatous retina of the human eye was revealed. TLRs can modulate the immune response in glaucoma; provide early recognition of damaging agents, activation of signaling pathways and effector mechanisms of the nonspecific immune defense system aimed at restoring homeostasis. The TLR-encoding genes’ polymorphism alters the amino acid structure of the receptors, which leads to changes in their immune functio
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Khaled, Bedewy M., Abou Seada M. Noha, Antonios A. M. Manal, and Saleh M. Engy. "Role of Toll-Like Receptors 2 and 4 Genes Polymorphisms in Neonatal Sepsis in a Developing Country: A Pilot Study." Journal of Pediatric Infectious Diseases 15, no. 06 (2020): 276–82. http://dx.doi.org/10.1055/s-0040-1714710.

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Abstract Objective Toll-like receptors (TLR) are one of the key molecules that alert the immune system to the presence of microbial infections. This study attempts to elucidate the role of TLR2 and TLR4 polymorphisms in neonatal sepsis. Methods A case–control study including 30 neonates with confirmed sepsis compared with 20 neonates in a control group. TLR2 and TLR24 gene polymorphisms were confirmed by polymerase chain reaction. Results The majority of infections were attributed to gram-negative organisms (72.5%) namely Klebsiella pneumoniae, Pseudomonas aeruginosa, and Escherichia coli. Res
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Dorofeyev, Andriy E., Anna A. Dorofeyeva, Elena A. Kiriyan, Olga A. Rassokhina, and Yulia Z. Dynia. "GENETIC POLYMORPHISM IN PATIENTS WITH EARLY AND LATE ONSET OF ULCERATIVE COLITIS." Wiadomości Lekarskie 73, no. 1 (2020): 87–90. http://dx.doi.org/10.36740/wlek202001116.

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The aim was to investigate SNPs of TLR-2,3,4, NOD2/CARD15, JAK-2, and IL-10 in patients with the early and late UC onset. Matherials and methods: 126 patients with UC were investigated. To assess the predisposition of the early and late UC onset the incidence of the following SNPs: Arg753Gln TLR2 gene, Phe412Leu TLR3 gene, Asp299Gly and Thr399Ile TLR4 gene, C-819T, G-1082A and C-592A gene IL-10, Val617Phe gene JAK2, Gly908Arg gene NOD2/CARD15 were analyzed. Results: 76 patients had early disease onset and 50 had a late one. SNPs of TLR3 were observed in 50.8% cases. TLR4 polymorphism was more
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Kesici, Gülin Gökçen, Selda Kargın Kaytez, Talih Özdaş, and Sibel Özdaş. "Association of Toll-Like Receptor Polymorphisms With Nasal Polyposis." Ear, Nose & Throat Journal 100, no. 1 (2019): NP26—NP32. http://dx.doi.org/10.1177/0145561319859305.

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Nasal polyposis is a disease characterized with chronic inflammation of the nasal mucosa. Toll-like receptors (TLRs) are defined as essential receptors of the innate immune system and may play in the development of nasal polyposis. A total of 71 patients with nasal polyposis and 74 healthy controls were included in this study. Three single-nucleotide polymorphisms (SNPs); TLR2 (2258 A>G), TLR4 (896 A>G), and TLR4 (1196 C>T) were analyzed in all patients. The degree of pair-wise linkage disequilibrium and the genotype and haplotype analyses were conducted using regression in this logis
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Shi, Jimin, Haowen Xiao, Yi Luo, et al. "Relationship between Gene Polymorphism of Recipient/ Donor Immune Pathway and Invasive Fungal Infection after Allogeneic Hematopoietic Stem Cell Transplantation." Blood 124, no. 21 (2014): 3871. http://dx.doi.org/10.1182/blood.v124.21.3871.3871.

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Abstract Invasive fungal infections are a major cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation(allo-HSCT). During the past 2 decades, changes in transplantation practices and strategies to diagnose and treat IFI have likely impacted the epidemiology of IFI. Polymorphism of genes, which take part in the allogeneic immune response after allo-HSCT, lead to allograft immunoreactivity differences between individuals. It also may affect IFI after transplantation. Methods: We analyzed allo-HSCT recipients at our center during the period January 2001 through
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Svitich, O. A., O. Yu Olisova, E. A. Meremianina, N. D. Rasskazova, V. A. Fomina, and M. B. Potapova. "Association of single nucleotide polymorphisms of <i>TLR2</i>, <i>TLR4</i> and <i>TLR9</i> with atopic dermatitis." Medical Immunology (Russia) 25, no. 5 (2023): 1043–48. http://dx.doi.org/10.15789/1563-0625-aos-2807.

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Toll-like receptors (TLRs) are the most studied among all Pattern Recognition Receptors, the main function of which is to initiate innate immune response by recognizing pathogen-associated molecular patterns of various microorganisms on the skin surface. TLR-mediated recognition plays an important role in linking innate and adaptive immunity that ultimately leads to the production of key cytokines, chemokines and antimicrobial peptides. Today, there is growing interest in research on single nucleotide polymorphisms (SNPs) in TLR genes and its influence on susceptibility to inflammatory disease
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Sinitskaya, A. V., M. V. Khutornaya, O. N. Khryachkova, et al. "Associations of <i>TLR</i> gene polymorphism with the risk of rheumatic heart disease." Сибирский научный медицинский журнал 43, no. 6 (2024): 177–84. http://dx.doi.org/10.18699/ssmj20230622.

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Aim of the study was to investigate the associations between TLR gene polymorphism and the risk of rheumatic heart disease (RHD).Material and methods. 251 RHD patients (190 females and 61 males) and 300 healthy donors (190 females and 110 males), whose age was 57 [29; 77] and 53 [21; 80] years (median [lower quartile; upper quartile]), respectively, were recruited in the presented study. Eight polymorphic variants in the TLR gene were genotyped by realtime PCR.Results. We found no statistically significant differences in the frequency of eight polymorphic variants in the TLR1, TLR2, TLR4 and T
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Wu, Hongjiao, Hui Gao, Ang Li, et al. "Impact of Genetic Variation in TLR4 3′UTR on NSCLC Genetic Susceptibility." Journal of Oncology 2020 (April 9, 2020): 1–7. http://dx.doi.org/10.1155/2020/7593143.

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Toll-like receptors (TLRs) are expressed not only in immune cells but also in a variety of tumor cells. Single-nucleotide polymorphisms (SNPs) located in the TLRs’ promoter or the 3′ untranslated region may affect gene expression by affecting the activity of the promoter or regulating the binding of mRNA to miRNA. This study aimed to investigate the association of the SNPs in TLR genes with the susceptibility to NSCLC. This case-control study involved 700 lung cancer patients and 700 healthy controls. All individuals were genotyped for all selected SNPs in TLR genes using polymerase chain reac
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Dissertations / Theses on the topic "Polymorphism of the TLR4 gene"

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Бевз, Т., Г. Мартинюк, С. Куляс, О. Попович та Л. Медведєва. "Особливості клінічного перебігу та прогнозу хронічного гепатиту С при поліморфізмі гену TLR4". Thesis, Сумський державний університет, 2017. http://essuir.sumdu.edu.ua/handle/123456789/65455.

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Згідно офіційної статистики, в Україні станом на 1 січня 2014 р. близько 3% наслення хворі на ВГС. Приблизно у 85% всіх інфікованих розвивається хронічний гепатит С, що призводить до розвитку цирозу печінки у 20% (протягом 20 років) і гепатоцелюлярної карциноми у 7% пацієнтів. Відсутність специфічної імунопрофілактики; побічні ефекти та стійкість до лікування, яке є високовартісним – все це диктує необхідність пошуку нових шляхів оптимізації діагностики та лікування хворих на хронічний вірусний гепатит С.<br>The clinical investigation discusses the connection between TLR4-polymorphysm
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Lundberg, Anna. "Immune responses to lipopolysaccharide in relation to allergic disease : a TLR4 gene polymorphism and endotoxin exposure." Doctoral thesis, Linköpings universitet, Pediatrik, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-16783.

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Background: Allergic diseases have increased during the last decades, particularly in affluent countries, possibly due to a reduced and/or altered microbial exposure during infancy. Activation of the immune system by microbes early in life is probably required for accurate maturation of the immune system and tolerance development. It is not fully understood how microbial exposure is associated with the development of allergic diseases, however. Genetic factors may influence microbial induced immune responses. A certain polymorphism, in the gene coding for the Toll-like receptor 4, i.e. (TLR4 A
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Бевз, Т., Г. Мартинюк, С. Куляс, О. Попович та Л. Медведєва. "Особливості клінічного перебігу та прогнозу хронічного гепатиту С при поліморфізмі гену TLR4". Thesis, Сумський державний університет, 2017. http://essuir.sumdu.edu.ua/handle/123456789/64380.

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Згідно офіційної статистики, в Україні станом на 1 січня 2014 р. близько 3% наслення хворі на ВГС. Приблизно у 85% всіх інфікованих розвивається хронічний гепатит С, що призводить до розвитку цирозу печінки у 20% (протягом 20 років) і гепатоцелюлярної карциноми у 7% пацієнтів. Відсутність специфічної імунопрофілактики; побічні ефекти та стійкість до лікування, яке є високовартісним – все це диктує необхідність пошуку нових шляхів оптимізації діагностики та лікування хворих на хронічний вірусний гепатит С.<br>The clinical investigation discusses the connection between TLR4-polymorphys
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Roldan, Montes Valentina. "Estudo de polimorfismos do gene TLR4 e suas associações com características de importância econômica em búfalas leiteiras /." Jaboticabal, 2016. http://hdl.handle.net/11449/144661.

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Orientador: Humberto Tonhati<br>Coorientador: Gregório Miguel Ferreira de Camargo<br>Coorientador: Naudin Alejandro Hurtado Lugo<br>Banca: Lenira El Faro Zadra<br>Banca: Henrique Nunes de Oliveira<br>Resumo: Considerando a importância das doenças que afetam o desempenho produtivo dos animais na indústria leiteira em todo o mundo é necessário implementar ferramentas moleculares que auxiliem na identificação e controle destas doenças. Quando ocorre alguma infecção em um organismo superior, existe aumento do número de células de defesa e o sistema imune inato proporciona uma linha de defesa contr
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Neto, Lídio Gonçalves Lima. "Polimorfismo dos genes CD14, TLR2, TLR4, IL6 e sua associação com o infarto do miocárdio em adultos jovens." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/9/9136/tde-18022014-101606/.

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O objetivo deste estudo foi avaliar a possível associação entre os polimorfismos -260C/T do gene CD14, Arg753Gln do gene TLR2, Asp299Gli e Thr39911e do gene TLR4 e -174G/C do gene IL6 com o infarto do miocárdio em adultos jovens. Para isso, foi realizado um estudo caso controle, sendo o grupo de estudo constituído por 102 pacientes que tiveram de infarto do miocárdio (34,5 ± 5 anos) e o grupo controle (35,1±8,7 anos) por 108 indivíduos sem histórico de doenças cardiovasculares. A genotipagem foi realizada pela PCRRFLP. Houve ausência de associação entre a distribuição dos genótipos dos SNPs -2
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Prioli, Renato Alves [UNESP]. "Caracterização da variabilidade de genes relacionados à fisiologia do sistema imune em equinos da raça mangalarga." Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/92578.

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Made available in DSpace on 2014-06-11T19:26:06Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-02-08Bitstream added on 2014-06-13T19:33:16Z : No. of bitstreams: 1 prioli_ra_me_jabo.pdf: 689132 bytes, checksum: 17eaeca002f2374370af36bb9266bcc4 (MD5)<br>Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)<br>Os objetivos deste trabalho foram a padronização de metodologia alternativa de genotipagem do SNP AY_731081:g.1900T>C do gene CD14 equino por PCR-RFLP, bem como a caracterização em equinos da raça Mangalarga deste e de outros dois polimorfismos, o AY_005808: c.1530A>G do T
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Pakalnienė, Jolita. "Genų, koduojančių penktą chemokino ir trečią Toll-like receptorius, polimorfizmų reikšmė erkinio encefalito viruso infekcijos metu." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2014. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2014~D_20140930_085230-33015.

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Erkinis encefalitas (EE) – pati dažniausia ir sunkiausia virusinė nervų sistemos infekcija Lietuvoje, kuria per metus vidutiniškai suserga 400 žmonių. Užsikrėtus EE virusu (EEV), galima besimptomė arba klinikinius požymius sukelianti ligos eiga, turinti platų požymių spektrą – nuo lengvos, meningitinės ligos formos iki sunkaus encefalito. Nors mirštamumas nuo EE yra nedidelis, svarbiausia problema – ilgai trunkantis sveikimo laikotarpis ir ilgalaikiai liekamieji reiškiniai, kurie būdingi 26–46 proc. persirgusiųjų. Neaišku, kodėl užsikrėtę identiško virulentiškumo virusu, vieni žmonės perserga
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Salimu, Josephine. "Tumour antigen cross-presentation from irradiated tumour cells and the role of tlr4 polymorphism." Thesis, Cardiff University, 2014. http://orca.cf.ac.uk/64217/.

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Immune responses contribute to the success of radiation therapy of solid tumours; however, the mechanism of triggering CD8+ T cell responses is poorly understood. Antigen cross-presentation from tumour cells by dendritic cells (DC) is a likely dominant mechanism to achieve CD8+ T cell stimulation. We established a cross-presentation model in prostate cancer in which DC present a naturally expressed oncofetal tumour antigen (5T4) from irradiated DU145 tumour cells to 5T4-specific T cells. Ionising radiation (12 Gy) caused G2/M cell cycle arrest and cell death, increased cellular 5T4 and high-mo
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Tellier, Aurélien. "A theory of polymorphism in gene-for-gene interactions." Thesis, University of East Anglia, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439932.

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Atan, Deniz. "Cytokine gene polymorphism in non-infectious uveitis." Thesis, University of Bristol, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492470.

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Non-infectious uveitis is a blinding intraocular inflammatory disorder with an autoimmune pathogenesis. Like other autoimmune diseases, uveitis has multifactorial and polygenic aetiology. The results of this study have shown that polymorphisms of the ILIO and TNF genes influence the susceptibility and seventy of uveitis. These polymorphisms were either known to correlate with altered transcription levels, or linked with other polymorphisms positioned within regulatory conserved non-coding sequences. Thus the identification of specific genetic variants that confer susceptibility or resistance t
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Books on the topic "Polymorphism of the TLR4 gene"

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Koen, Vandenbroeck, ed. Cytokine gene polymorphisms in multifactorial conditions. CRC Taylor & Francis, 2006.

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Farhan, Ayar Jawi. T cell receptor gene polymorphism and usage in rheumatoid arthritis. University of Manchester, 1997.

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Masatoshi, Nei, ed. Humanpolymorphic genes. Oxford University Press, 1988.

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Ellegren, Hans. Genome analysis with microsatellite markers. Dept. of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, 1993.

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Roychoudhury, Arun K. Human polymorphic genes: World distribution. Oxford University Press, 1988.

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Liu, Zhanjiang. Next generation sequencing and whole genome selection in aquaculture. Wiley-Blackwell, 2011.

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George, Stamatoyannopoulos, and Nienhuis Arthur W, eds. Experimental approaches for the study of hemoglobin switching: Proceedings of the Fourth Conference on Hemoglobin Switching, October 1-3, 1984. A.R. Liss, 1985.

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de Luis Roman, Daniel-Antonio, and Ana B. Crujeiras, eds. Gene Polymorphism and Nutrition: Relationships with Chronic Disease. MDPI, 2023. http://dx.doi.org/10.3390/books978-3-0365-7771-5.

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Vandenbroeck, Koen. Cytokine Gene Polymorphisms in Multifactorial Conditions. Taylor & Francis Group, 2006.

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Vandenbroeck, Koen. Cytokine Gene Polymorphisms in Multifactorial Conditions. Taylor & Francis Group, 2006.

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Book chapters on the topic "Polymorphism of the TLR4 gene"

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Crute, Ian R. "Gene-for-gene recognition in plant—pathogen interactions." In Infection, Polymorphism and Evolution. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-0077-6_8.

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Hamon, Martial, and Carole Amant. "Gene Polymorphism and Restenosis." In Arterial Remodeling: A Critical Factor in Restenosis. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6079-1_26.

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Rich, Alexander. "Conformational Polymorphism in DNA." In Evolutionary Tinkering in Gene Expression. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5664-6_1.

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Kutikhin, Anton G., and Arseniy E. Yuzhalin. "Structural Genomic Variation in TLR4 Gene and Cancer." In Genomics of Pattern Recognition Receptors. Springer Basel, 2013. http://dx.doi.org/10.1007/978-3-0348-0688-6_3.

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Cook, L. M., and R. S. Callow. "Gene interplay models for polymorphism." In Genetic and Evolutionary Diversity. Garland Science, 2023. http://dx.doi.org/10.1201/9781003421887-15.

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Vinall, Lynne E., Wendy S. Pratt, and Dallas M. Swallow. "Detection of Mucin Gene Polymorphism." In Glycoprotein Methods and Protocols. Humana Press, 2000. http://dx.doi.org/10.1385/1-59259-048-9:337.

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Trowsdale, John. "Polymorphism in the HLA-D Region." In Regulation of Immune Gene Expression. Humana Press, 1986. http://dx.doi.org/10.1007/978-1-4612-5014-2_5.

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Mondal, Muhammad Shafiul Alam, and Yearul Kabir. "Host Immune Gene Polymorphism and Cancer." In Handbook of Cancer and Immunology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-80962-1_48-1.

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Akhtar, Kulsum, Ishrat Parveiz Bhat, Syed Sameer Aga, Syed Douhath Yousuf, and Syed Mudassar. "Cytokine Gene Polymorphisms and Their Role in Autoimmune Diseases." In Genetic Polymorphism and Disease. CRC Press, 2022. http://dx.doi.org/10.1201/9781003246244-23.

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Ferns, G. A. A., S. C. Shelley, A. Rees, J. Stocks, and D. J. Galton. "An Apoprotein AII Gene Polymorphism and Hyperlipidaemia." In Human Apolipoprotein Mutants. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4615-9474-1_16.

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Conference papers on the topic "Polymorphism of the TLR4 gene"

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Rask-Andersen, A., DC Rennie, L. Bharadwaj, DA Schwartz, Y. Chen, and JA Dosman. "High Risk for Atopic Asthma in Subjects with Polymorphism of TLR4 and Farm Exposure – A Gene-Environment Interaction." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a3655.

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Didkovsky, Nikolay, Irina Malashenkova, Daniil Ogurtsov, et al. "IL1B T-31C AND TLR3 LEU412PHE GENE POLYMORPHISMS IN PATIENTS WITH ALKOHOLISM." In XVIII INTERNATIONAL INTERDISCIPLINARY CONGRESS NEUROSCIENCE FOR MEDICINE AND PSYCHOLOGY. LCC MAKS Press, 2022. http://dx.doi.org/10.29003/m2745.sudak.ns2022-18/125-126.

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KHRABROVA, Lyudmila A., Sergey I. SOROKIN, Nina V. BLOKHINA, and Tatyana V. KALASHNIKOVA. "Myostatin Gene Polymorphism in Local Horse Breeds." In XVIII International Scientific and Practical Conference "Modern Trends in Agricultural Production in the World Economy". Sibac, 2020. http://dx.doi.org/10.32743/kuz.agri.2020.27-33.

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Hlapčić, Iva, Marija Grdić Rajković, Andrea Hulina-Tomašković, Sanja Popović-Grle, Margareta Radić Antolic, and Lada Rumora. "Gene expression and genetic variations of HSP70TLR2 and TLR4 in COPD." In ERS International Congress 2021 abstracts. European Respiratory Society, 2021. http://dx.doi.org/10.1183/13993003.congress-2021.pa2384.

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Ahasic, Amy, Yang Zhao, Li Su, B. T. Thompson, and David Christiani. "Leptin Receptor Gene (LEPR) Polymorphism And ARDS Susceptibility." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a2099.

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Perrot-Andre, S., A. Ramouneau-Pigot, Y. Fontana, J. Sany, JF Eliaou, and B. Combe. "SAT0023 Hla gene polymorphism in psoriatic arthritis (psa)." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.375.

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Telepneva, R., G. Evseeva, E. Nagovitsyna, E. Suprun, S. Suprun, and O. Lebedko. "ADRB2 Gene Polymorphism in Children with Bronchial Asthma." In American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a1789.

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Alwiyah, Alwiyah, Nuraini H, Agung PP, and Jakaria Jakaria. "Polymorphism Diacylglycerol Acyltransferase 1 (DGAT1) Gene in Bali Cattle." In Smart Livestock Management to Support Breeding Stock Availability Toward Modern Agriculture. Indonesian Center for Animal Research and Development (ICARD), 2018. http://dx.doi.org/10.14334/proc.intsem.lpvt-2018-p.32-39.

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Rufino, M. C., T. Bartholo, A. P. Viana, B. Chaves, V. D´Elia, and C. Costa. "SERPINA1 Gene Polymorphism: Analysis of Patients Over 2 Years." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a3785.

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Boujelbene, Nadia, Ines Zemni, Wafa Babay, et al. "240 TGF-beta gene polymorphism and ovarian cancer susceptibility." In ESGO 2024 Congress Abstracts. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/ijgc-2024-esgo.599.

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Reports on the topic "Polymorphism of the TLR4 gene"

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Iyshwarya, B. K., Ilibagiza Regine, and Ramakrishnan Veerabathiran. Association of MTHFR Gene Polymorphism in Diabetic Nephropathy. Peeref, 2022. http://dx.doi.org/10.54985/peeref.2207p7008018.

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ZHENG, Jiansheng, and Tang ZHU. Polymorphism of fucosyltransferase 3 (FUT3) gene is associated with inflammatory bowel disease (IBD) — a systematic review and Meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.3.0001.

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Review question / Objective: Polymorphism of fucosyltransferase 3 (FUT3) gene is associated with inflammatory bowel disease (IBD) — a systematic review and Meta-analysis. Condition being studied: This study collected relevant literatures and analyzed the relationship between the polymorphism of the FUT3 genes at rs3745635, rs3894326, and rs28362459 to the IBD with Meta-analysis, in order to further explore the possible mechanism of the polymorphism of the FUT3 gene and IBD.
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Torrungruang, Kitti, Soranun Chantarangsu, and Thanyachai Sura. Association between vitamin D receptor gene polymorphisms and chronic periodontitis in Thais. Chulalongkorn University, 2015. https://doi.org/10.58837/chula.res.2015.18.

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Polymorphisms of the vitamin D receptor (VDR) gene have been implicated in the susceptibility to infections and bone-related diseases. However, their relationship with periodontal disease remains unclear. This cross-sectional study investigated whether the susceptibility to chronic periodontitis in a Thai population is associated with VDR polymorphisms. Genomic DNA was obtained from 1,460 subjects, aged 39-65 years. Genotyping of VDR polymorphisms (FokI, BsmI, ApaI, and TaqI) was performed using real-time polymerase chain reaction. Subjects were categorized into three groups; no/mild, moderate
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Dimitrova, Ivona, Milena Bozhilova-Sakova, Maya Ignatova, and Nikolay Petrov. Polymorphism of FABP3 Gene in Some Merino and Local Sheep Breeds in Bulgaria. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2020. http://dx.doi.org/10.7546/crabs.2020.05.18.

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Hu, Yinan, Zhen Li, and Yanhong Ren. Association of FAM13A gene polymorphism and interstitial lung disease susceptibility: A meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.2.0122.

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Xu, Sen, Jielei Zhou та Yunzhu Zhang. Quantitative assessment of the association between TNF-α gene polymorphism and angina risk. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2024. http://dx.doi.org/10.37766/inplasy2024.7.0120.

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Li, Qian, Menglu Chen, Wen Li, Yihui Chai, Liancheng Guan, and Yunzhi Chen. Association of vitamin D receptor gene polymorphism with the risk of sepsis: a meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2023. http://dx.doi.org/10.37766/inplasy2023.4.0045.

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Wongpiyabovorn, Jongkonnee, Nattiya Hirankarn, Yingyos Avihingsanon, Tewin Tencomnao, Yong Poovorawan, and Kriangsak Ruchusatsawat. The association between immunogenetics and genetic susceptibility of psoriasis in Thai population. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.27.

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Psoriasis is T-cell-mediated skin autoimmunity, required environmental triggers and genetic susceptibility factors to become manifested. Psoriasis is a chronic skin disease characterized by the abnormal hyperproliferation and differentiation of the epidermis, elongated and prominent blood vessels and a thick perivascular lymphocytic infiltrate. Vascular endothelial growth factor (VEGF) gene play important role in pathogenesis of various diseases with angiogenic basis such as breast cancer and autoimmune disease including psoriasis. Many studies analyzed the association of VEGF gene polymorphis
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Kadiyska, Tanya, Maria Glushkova, and Lyudmil Lazarov. Role of the PPARG Gene Polymorphism RS1801282 in Bulgarian Obese Adults in the Development of Prediabetes. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2018. http://dx.doi.org/10.7546/crabs.2018.11.14.

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Kadiyska, Tanya, Maria Glushkova, Ivan Lyudmil, Lyudmil Lazarov, and Ivan Tourtourikov. Role of the TCF7L2 Gene Polymorphism rs7903146 in Bulgarian Obese Adults in Response to a Low-calorie Diet. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2019. http://dx.doi.org/10.7546/crabs.2019.12.13.

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