Artículos de revistas sobre el tema "TGFBR1/2 polymorphisms"
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KAKLAMANI, VIRGINIA G., MAUREEN SADIM, YVONI KOUMANTAKI, PHEDON KAKLAMANIS y BORIS PASCHE. "Role of Polymorphisms in Adamantiades-Behçet’s Disease". Journal of Rheumatology 35, n.º 12 (diciembre de 2008): 2376–78. http://dx.doi.org/10.3899/jrheum.080676.
Texto completoGuhlich, Manuel, Laura Hubert, Caroline Patricia Nadine Mergler, Margret Rave-Fraenk, Leif Hendrik Dröge, Martin Leu, Heinz Schmidberger, Stefan Rieken, Andrea Hille y Markus Anton Schirmer. "Identification of Risk Loci for Radiotoxicity in Prostate Cancer by Comprehensive Genotyping of TGFB1 and TGFBR1". Cancers 13, n.º 21 (8 de noviembre de 2021): 5585. http://dx.doi.org/10.3390/cancers13215585.
Texto completoPuchenkova, Olesya A., Vladislav O. Soldatov, Andrei E. Belykh, OlgaYu Bushueva, Gennadii A. Piavchenko, Artem A. Venediktov, Nikolay K. Shakhpazyan, Alexey V. Deykin, Mikhail V. Korokin y Mikhail V. Pokrovskiy. "Cytokines in Abdominal Aortic Aneurysm: Master Regulators With Clinical Application". Biomarker Insights 17 (enero de 2022): 117727192210956. http://dx.doi.org/10.1177/11772719221095676.
Texto completoPuchenkova, Olesya A., Vladislav O. Soldatov, Andrei E. Belykh, OlgaYu Bushueva, Gennadii A. Piavchenko, Artem A. Venediktov, Nikolay K. Shakhpazyan, Alexey V. Deykin, Mikhail V. Korokin y Mikhail V. Pokrovskiy. "Cytokines in Abdominal Aortic Aneurysm: Master Regulators With Clinical Application". Biomarker Insights 17 (enero de 2022): 117727192210956. http://dx.doi.org/10.1177/11772719221095676.
Texto completoKirschneck, Margarita, Nermien Zbidat, Eva Paddenberg, Caio Luiz Bitencourt Reis, Isabela Ribeiro Madalena, Maria Angélica Hueb de Menezes-Oliveira, César Penazzo Lepri, Peter Proff, Christian Kirschneck y Erika Calvano Küchler. "Transforming Growth Factor Beta Receptor 2 (TGFBR2) Promoter Region Polymorphisms May Be Involved in Mandibular Retrognathism". BioMed Research International 2022 (15 de junio de 2022): 1–7. http://dx.doi.org/10.1155/2022/1503052.
Texto completoPauly, M., G. Mahon, M. A. Dicato, B. Metzger y A. Menzel. "Single Nucleotide Polymorphisms (SNP'S) in the P53, SMAD7 and TGFBR1 Genes Associated with Advanced Colorectal Cancer in Caucasian Patients Compared to Healthy Controls". Annals of Oncology 23 (septiembre de 2012): ix209. http://dx.doi.org/10.1016/s0923-7534(20)33231-2.
Texto completoKim, Dong Hwan (Dennis), Jina Yun, Jee Hyun Kong, Chul Won Jung, Ahmed Galal, Vikas Gupta, John Kuruvilla, Hans A. Messner y Jeffrey H. Lipton. "Single Nucleotide Polymorphism (SNP) Approach of Multiple Candidate Pathways Predicting the Risk of Acute / Chronic Graft-Versus-Host Disease or Transplant Outcomes Following Allogeneic Hematopoietic Stem Cell Transplantation: Potential Involvement of Nuclear Factor Kappa-B (NFKB), Platelet-Derived Growth Factor (PDGF) and Transforming Growth Factor-Beta (TGF-β) Pathway with Chronic Graft-Versus-Host Disease Graft-Versus-Host Disease." Blood 114, n.º 22 (20 de noviembre de 2009): 2221. http://dx.doi.org/10.1182/blood.v114.22.2221.2221.
Texto completoChen, Ruo-Xi, Wen-Min Lu, Mei-Ping Lu, Mei-Lin Wang, Xin-Jie Zhu, Zhong-Fei Wu, Hui-Qin Tian, Lu-Ping Zhu, Zheng-Dong Zhang y Lei Cheng. "Polymorphisms in MicroRNA Target Sites of TGF-β Signaling Pathway Genes and Susceptibility to Allergic Rhinitis". International Archives of Allergy and Immunology 182, n.º 5 (2021): 399–407. http://dx.doi.org/10.1159/000511975.
Texto completoKim, Dennis Dong Hwan, Hong-Hee Won, Wei Xu, Jieun Uhm, Vikas Gupta, John Kuruvilla, Hans A. Messner y Jeffrey H. Lipton. "The Risk of Organ Specific Graft-Versus-Host Disease Can Be Predicted by the Multiple Single Nucleotide Polymorphism Based Predictive Models." Blood 120, n.º 21 (16 de noviembre de 2012): 3056. http://dx.doi.org/10.1182/blood.v120.21.3056.3056.
Texto completoThorne, Jacob W., Reid Redden, Scott A. Bowdridge, Gabrielle M. Becker, Morgan R. Stegemiller y Brenda M. Murdoch. "PSV-B-21 Genome-Wide Analysis of Sheep Artificially or Naturally Infected with Gastrointestinal Nematodes". Journal of Animal Science 100, Supplement_3 (21 de septiembre de 2022): 307–8. http://dx.doi.org/10.1093/jas/skac247.560.
Texto completoWeener, M. E., N. A. Bakunina, J. M. Salmasi, G. V. Poryadin, D. Barh, Yu D. Kuznetsova y L. M. Balashova. "Genetic testing of ocular manifestations of proliferative syndrome to provide pathophysiology-oriented treatment". Russian Journal of Clinical Ophthalmology 22, n.º 1 (2022): 16–22. http://dx.doi.org/10.32364/2311-7729-2022-22-1-16-22.
Texto completoOmori, A., C. Stephens, J. Cooc, P. V. Danenberg, K. Danenberg, H. Lenz y B. Pasche. "Microarray analysis of formalin-fixed paraffin-embedded specimens shows distinct gene expression patterns in tumors containing the transforming growth factor beta receptor 6A polymorphism (TGFBR1*6A)". Journal of Clinical Oncology 25, n.º 18_suppl (20 de junio de 2007): 4111. http://dx.doi.org/10.1200/jco.2007.25.18_suppl.4111.
Texto completoAlves, Ana Paula V. D., Amanda B. Freitas, José Eduardo Levi, Antonio G. Amorim Filho, Lucas A. M. Franco, Mara Sandra Hoshida, Elizabeth G. Patiño, Rossana P. V. Francisco y Mario Henrique B. Carvalho. "COL1A1, COL4A3, TIMP2 and TGFB1 polymorphisms in cervical insufficiency". Journal of Perinatal Medicine 49, n.º 5 (8 de febrero de 2021): 553–58. http://dx.doi.org/10.1515/jpm-2020-0320.
Texto completoAl-Harbi, Najla M., Sara S. Bin Judia, Krishna N. Mishra, Mohamed M. Shoukri y Ghazi A. Alsbeih. "Genetic Predisposition to Cervical Cancer and the Association With XRCC1 and TGFB1 Polymorphisms". International Journal of Gynecologic Cancer 27, n.º 9 (noviembre de 2017): 1949–56. http://dx.doi.org/10.1097/igc.0000000000001103.
Texto completoZakrzewski, Piotr K., Ewa Forma, Adam I. Cygankiewicz, Magdalena Bryś, Katarzyna Wójcik-Krowiranda, Andrzej Bieńkiewicz, Andrzej Semczuk y Wanda M. Krajewska. "Betaglycan Gene (TGFBR3) Polymorphism Is Associated with Increased Risk of Endometrial Cancer". Journal of Clinical Medicine 9, n.º 10 (24 de septiembre de 2020): 3082. http://dx.doi.org/10.3390/jcm9103082.
Texto completoFlanagan, Jonathan M., Denise M. Frohlich, Thad A. Howard, William H. Schultz, Catherine Driscoll, Ramamoorthy Nagasubramanian, Nicole A. Mortier et al. "Genetic predictors for stroke in children with sickle cell anemia". Blood 117, n.º 24 (16 de junio de 2011): 6681–84. http://dx.doi.org/10.1182/blood-2011-01-332205.
Texto completoLee, Eunyoung, Yun-Gyoo Lee, Inho Kim, Ji-Hyun Kwon, Dong-Yeop Shin, Ji-Yeon Bae, Sung-Soo Yoon et al. "Impact of Cytokine Gene Polymorphisms on Risk and Treatment Outcomes of Aplastic Anemia". Blood 118, n.º 21 (18 de noviembre de 2011): 4369. http://dx.doi.org/10.1182/blood.v118.21.4369.4369.
Texto completoGritsenko, O. V., G. A. Chumakova, O. V. Gruzdeva, A. V. Ponasenko y O. L. Barbarash. "Profibrotic genetic polymorphisms as possible risk factors for the development of diastolic dysfunction in patients with epicardial adiposity". Russian Journal of Cardiology 27, n.º 10 (5 de septiembre de 2022): 5208. http://dx.doi.org/10.15829/1560-4071-2022-5208.
Texto completoGonçalves Junior, Roberto, Aristides da Rosa Pinheiro, José Jorge Schoichet, Carlos Henrique Ramirez Nunes, Rackel Gonçalves, Leticia Ladeira Bonato, Valquiria Quinelato et al. "MMP13, TIMP2 and TGFB3 Gene Polymorphisms in Brazilian Chronic Periodontitis and Periimplantitis Subjects". Brazilian Dental Journal 27, n.º 2 (abril de 2016): 128–34. http://dx.doi.org/10.1590/0103-6440201600601.
Texto completoBerro, Mariano, Virginia Palau, Maria Marta Rivas, Maria Cecilia Foncuberta, Adriana Vitriu, Guillermina Remaggi, Gregorio Jaimovich et al. "TGFB1 Functional Polymorphisms in Sibling HSCT. "Tto be or Not Tto be"". Blood 126, n.º 23 (3 de diciembre de 2015): 4275. http://dx.doi.org/10.1182/blood.v126.23.4275.4275.
Texto completoBerro, Mariano, Louise Cooke, Neema P. Mayor, Gustavo Kusminsky, Steven G. E. Marsh, J. Alejandro Madrigal y Bronwen E. Shaw. "TGFB1 Functional Polymorphisms: Impact on Outcome in Allogeneic Unrelated Donor Haematopoietic Stem Cell Transplantation". Blood 112, n.º 11 (16 de noviembre de 2008): 3011. http://dx.doi.org/10.1182/blood.v112.11.3011.3011.
Texto completoLi, Xiang-Ting, Chang-Qing Shen, Rui Zhang, Ji-Kui Shi, Zong-Hong Li, Hong-Yu Liu, Bo Sun, Kai Wang y Li-Ru Yan. "Association of TGFBR2 rs6785358 Polymorphism with Increased Risk of Congenital Ventricular Septal Defect in a Chinese Population". Pediatric Cardiology 36, n.º 7 (30 de mayo de 2015): 1476–82. http://dx.doi.org/10.1007/s00246-015-1189-2.
Texto completoDriscoll, M. Catherine, Joseph Devaney, Heather Gordish, Caterina Minniti y Eric P. Hoffman. "Genetic Modifiers of Cerebrovascular Large Vessel Stenosis in Sickle Cell Anemia." Blood 104, n.º 11 (16 de noviembre de 2004): 1658. http://dx.doi.org/10.1182/blood.v104.11.1658.1658.
Texto completoMooney, Rachel E., Gerry J. Linden, Lewis Winning, Katie Linden, Frank Kee, Pascal P. McKeown, Jayne V. Woodside, Christopher C. Patterson y Gareth J. McKay. "Association of TGFB1 rs1800469 and BCMO1 rs6564851 with coronary heart disease and IL1B rs16944 with all-cause mortality in men from the Northern Ireland PRIME study". PLOS ONE 17, n.º 8 (22 de agosto de 2022): e0273333. http://dx.doi.org/10.1371/journal.pone.0273333.
Texto completoYuan, Xianglin, Zhongxing Liao, Zhensheng Liu, Li-E. Wang, Susan L. Tucker, Li Mao, Xin Shelley Wang et al. "Single Nucleotide Polymorphism at rs1982073:T869C of the TGFβ1 Gene Is Associated With the Risk of Radiation Pneumonitis in Patients With Non–Small-Cell Lung Cancer Treated With Definitive Radiotherapy". Journal of Clinical Oncology 27, n.º 20 (10 de julio de 2009): 3370–78. http://dx.doi.org/10.1200/jco.2008.20.6763.
Texto completoFlanagan, Jonathan Michael, Thad A. Howard, Denise M. Frohlich, William Herbert Schultz, Catherine Driscoll, Ramamoorthy Nagasubramanian, Nicole A. Mortier et al. "Validation of Genetic Predictors for Stroke In Children with Sickle Cell Anemia". Blood 116, n.º 21 (19 de noviembre de 2010): 2639. http://dx.doi.org/10.1182/blood.v116.21.2639.2639.
Texto completoOnyeneho, Karyn. "Genetic Determinants of Type 2 Diabetes Mellitus in Adults of African Ancestry: Identification of the Associated Factors". Current Developments in Nutrition 6, Supplement_1 (junio de 2022): 1121. http://dx.doi.org/10.1093/cdn/nzac078.015.
Texto completoPark, Eunkyung, Song Joo Yang, Inho Kim, Eun Hyung Jeon y Seonyang Park. "Genome-Wide Association Study for Determinants of Acute Graft Vs Host Disease (aGVHD) After Allogeneic Hematopoietic Stem Cell Transplantation: Development of 7 SNP Model Predicting aGVHD". Blood 118, n.º 21 (18 de noviembre de 2011): 1010. http://dx.doi.org/10.1182/blood.v118.21.1010.1010.
Texto completoChen, Rong-Fu, Lin Wang, Jiin-Tsuey Cheng, Hau Chuang, Jen-Chieh Chang, Jien-Wei Liu, I.-Chun Lin y Kuender D. Yang. "Combination of CTLA-4 and TGFβ1 gene polymorphisms associated with dengue hemorrhagic fever and virus load in a dengue-2 outbreak". Clinical Immunology 131, n.º 3 (junio de 2009): 404–9. http://dx.doi.org/10.1016/j.clim.2009.01.015.
Texto completoSebastiani, Paola, Ling Wang, Thomas Perls, Dellara F. Terry, Monty Montano, Clinton T. Baldwin y Martin H. Steinberg. "A Repertoire of Genes Modifying the Risk of Death in Sickle Cell Anemia." Blood 110, n.º 11 (16 de noviembre de 2007): 150. http://dx.doi.org/10.1182/blood.v110.11.150.150.
Texto completoLaky, Karen, Jessica Kinard, Anthony Guerrerio y Pamela Frischmeyer-Guerrerio. "Altered TGFβ signaling in non-hematopoietic cells leads to eosinophilic esophagitis." Journal of Immunology 200, n.º 1_Supplement (1 de mayo de 2018): 104.11. http://dx.doi.org/10.4049/jimmunol.200.supp.104.11.
Texto completoSchipp, Cyrill, Arndt Borkhardt, Polina Stepensky y Ute Fischer. "Identifying Possible Candidate Factors Influencing the Penetrance of Heterozygous NFKB1 Loss of Function Mutations By Whole Exome Sequencing". Blood 128, n.º 22 (2 de diciembre de 2016): 3706. http://dx.doi.org/10.1182/blood.v128.22.3706.3706.
Texto completoMartinez-Castaldi, Carolina, Vikki G. Nolan, Clinton T. Baldwin, Lindsay A. Farrer, Martin H. Steinberg y Elizabeth S. Klings. "Association of Genetic Polymorphisms in the TGF-β Pathway with the Acute Chest Syndrome of Sickle Cell Anemia." Blood 110, n.º 11 (16 de noviembre de 2007): 2247. http://dx.doi.org/10.1182/blood.v110.11.2247.2247.
Texto completoKrela-Kaźmierczak, I., M. Michalak, A. Wawrzyniak, A. Szymczak, P. Eder, L. Łykowska-Szuber, M. Kaczmarek-Ryś et al. "The c.29T>C polymorphism of the transforming growth factor beta-1 (TGFB1) gene, bone mineral density and the occurrence of low-energy fractures in patients with inflammatory bowel disease". Molecular Biology Reports 44, n.º 6 (9 de octubre de 2017): 455–61. http://dx.doi.org/10.1007/s11033-017-4131-2.
Texto completoSaidakramovich, Khasanov Ulugbek y Sharipov Sanjar Salomovich*. "Analysis of Associative Relationship of Allelic and Genotypical Variants of Polymorphism Rs 2010963 of the VEGFA Gene with Formation and Development of Ronchopathy". International Journal of Advanced Dental Sciences and Technology 1, n.º 2 (10 de agosto de 2021): 1–5. http://dx.doi.org/10.35940/ijadst.b1002.081221.
Texto completoSaidakramovich, Khasanov Ulugbek y Sharipov Sanjar Salomovich. "Analysis of Associative Relationship of Allelic and Genotypical Variants of Polymorphism Rs 2010963 of the VEGFA Gene with Formation and Development of Ronchopathy". International Journal of Advanced Dental Sciences and Technology 1, n.º 2 (10 de agosto de 2021): 1–5. http://dx.doi.org/10.54105/ijadst.b1002.081221.
Texto completoConcas, Maria Pina, Anna Morgan, Fabrizio Serra, Andries Paul Nagtegaal, Berthe C. Oosterloo, Sudha Seshadri, Nancy Heard-Costa et al. "Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability". Genes 12, n.º 8 (10 de agosto de 2021): 1228. http://dx.doi.org/10.3390/genes12081228.
Texto completoAyala de Miguel, Pablo, María Valle Enguix-Riego, Jon Cacicedo, Blas David Delgado, Marco Pérez, Juan Manuel Praena-Fernández, Laura Quintana Cortés, Pablo Borrega, Eleonor Rivin del Campo y Jose Lopez Guerra. "Prognostic value of the TGFß1 rs4803455 single nucleotide polymorphism and its association with prophylactic cranial irradiation in small cell lung cancer." Journal of Clinical Oncology 38, n.º 15_suppl (20 de mayo de 2020): e21038-e21038. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e21038.
Texto completoAdewoye, Adeboye H., Vikki G. Nolan, Clinton T. Baldwin, Diego F. Wyszynski, Qian-Li Ma, John J. Farrell, Alice Bisbee et al. "Association of Polymorphisms of the Transforming Growth Factor-β/Bone Morphogenetic Protein (TGF-β/BMP) Pathway with Sickle Cell Bacteremia." Blood 106, n.º 11 (16 de noviembre de 2005): 3170. http://dx.doi.org/10.1182/blood.v106.11.3170.3170.
Texto completoAshley-Koch, Allison E., Laura M. De Castro, Felicia Lennon-Graham, Jude Jonassaint, Terry L. Jackson, Jennifer Price, Jason Galloway et al. "Priapism in SCD: Clinical and Genetic Correlations." Blood 106, n.º 11 (16 de noviembre de 2005): 3174. http://dx.doi.org/10.1182/blood.v106.11.3174.3174.
Texto completoMartin-Antonio, Beatriz, Rocio Cardesa, Isabel Álvarez, Francisco Márquez-Malaver, Alicia Báez, Magdalena Carmona, Jose Falantes et al. "Genetic Variability In the Transcriptional Factor EP300 Strongly Influences the Clinical Outcome of Allogeneic Stem Cell Transplantation (Allo-SCT)". Blood 116, n.º 21 (19 de noviembre de 2010): 527. http://dx.doi.org/10.1182/blood.v116.21.527.527.
Texto completoGiraud, Sophie, Claire Bardel, Sophie Dupuis-Girod, Marie-France Carette, Brigitte Gilbert-Dussardier, Sophie Riviere, Jean-Christophe Saurin et al. "Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia". Orphanet Journal of Rare Diseases 15, n.º 1 (22 de septiembre de 2020). http://dx.doi.org/10.1186/s13023-020-01533-2.
Texto completoZhang, Xiaoying, Shasha Yu, Wencai Chen, Jianfei Ren y Xiaofeng Chen. "Abstract 246: TGF-β1 and TGFBR2 Polymorphisms With ISH". Arteriosclerosis, Thrombosis, and Vascular Biology 37, suppl_1 (mayo de 2017). http://dx.doi.org/10.1161/atvb.37.suppl_1.246.
Texto completoVarghese, Sindhu y Subbaraj Gowtham Kumar. "Role of eNOS and TGFβ1 gene polymorphisms in the development of diabetic nephropathy in type 2 diabetic patients in South Indian population". Egyptian Journal of Medical Human Genetics 23, n.º 1 (12 de enero de 2022). http://dx.doi.org/10.1186/s43042-022-00216-w.
Texto completoHassab, Hoda, Marwa Hanafi, Ahmed Elbeheiry, Mona Hassan y Yasmine El Chazli. "Does TGFBR3 Polymorphism Increase the Risk of Silent Cerebral Infarction in Egyptian Children with Sickle Cell Disease?" Indian Journal of Pediatrics, 4 de julio de 2022. http://dx.doi.org/10.1007/s12098-022-04181-5.
Texto completoCorredor, Zuray, Miguel Inácio da Silva Filho, Lara Rodríguez-Ribera, Antonia Velázquez, Alba Hernández, Calogerina Catalano, Kari Hemminki et al. "Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population". Scientific Reports 10, n.º 1 (10 de enero de 2020). http://dx.doi.org/10.1038/s41598-019-56695-2.
Texto completoLee, Daniel, Clement K. Chan, Prema Abraham y David Sarraf. "Post-hoc analysis of single nucleotide polymorphism profile for eyes with vascularized pigment epithelial detachment due to ARMD". European Journal of Ophthalmology, 24 de junio de 2020, 112067212093282. http://dx.doi.org/10.1177/1120672120932829.
Texto completo"Preliminary results of the investigations regarding the association of transforming growth factor- beta1 (TGFB1) gene polymorphism to metabolic syndrome in a Romanian patients group". Biointerface Research in Applied Chemistry 9, n.º 3 (15 de junio de 2019): 3974–78. http://dx.doi.org/10.33263/briac93.974978.
Texto completoMališić, Emina, Nina Petrović, Muriel Brengues, David Azria, Ivana Z. Matić, Ivana Srbljak Ćuk, Katarina Kopčalić, Tatjana Stanojković y Marina Nikitović. "Association of polymorphisms in TGFB1, XRCC1, XRCC3 genes and CD8 T-lymphocyte apoptosis with adverse effect of radiotherapy for prostate cancer". Scientific Reports 12, n.º 1 (9 de diciembre de 2022). http://dx.doi.org/10.1038/s41598-022-25328-6.
Texto completoYu, Guopeng, Bo Liang, Keneng Yin, Ming Zhan, Xin Gu, Jiangyi Wang, Shangqing Song et al. "Identification of Metabolism-Related Gene-Based Subgroup in Prostate Cancer". Frontiers in Oncology 12 (16 de junio de 2022). http://dx.doi.org/10.3389/fonc.2022.909066.
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