Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and TNFRSF13B[original query] |
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| Sequence analysis of TNFRSF13b, encoding TACI, in patients with systemic lupus erythematosus. Journal of clinical immunology 2007 Jul 27 (4): 372-7. Salzer Ulrich, Birmelin Jennifer, Bacchelli Chiara, Witte Torsten, Buchegger-Podbielski Ulrike, Buckridge Sylvie, Rzepka Rita, Gaspar H Bobby, Thrasher Adrian J, Schmidt Reinhold E, Melchers Inga, Grimbacher Bo |
| Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. Blood 2009 Feb 113 (9): 1967-76. Salzer Ulrich, Bacchelli Chiara, Buckridge Sylvie, Pan-Hammarström Qiang, Jennings Stephanie, Lougaris Vassilis, Bergbreiter Astrid, Hagena Tina, Birmelin Jennifer, Plebani Alessandro, Webster A David B, Peter Hans-Hartmut, Suez Daniel, Chapel Helen, McLean-Tooke Andrew, Spickett Gavin P, Anover-Sombke Stephanie, Ochs Hans D, Urschel Simon, Belohradsky Bernd H, Ugrinovic Sanja, Kumararatne Dinakantha S, Lawrence Tatiana C, Holm Are M, Franco Jose L, Schulze Ilka, Schneider Pascal, Gertz E Michael, Schäffer Alejandro A, Hammarström Lennart, Thrasher Adrian J, Gaspar H Bobby, Grimbacher Bo |
| An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. Genes and immunity 2009 Sep 10 (6): 566-78. Sazzini M, Zuntini R, Farjadian S, Quinti I, Ricci G, Romeo G, Ferrari S, Calafell F, Luiselli |
| Lymphocyte characteristics in children with common variable immunodeficiency. Clinical immunology (Orlando, Fla.) 2010 Apr 135 (1): 63-71. van de Ven Annick A J M, van de Corput Lisette, van Tilburg Cornelis M, Tesselaar Kiki, van Gent Rogier, Sanders Elisabeth A M, Boes Marianne, Bloem Andries C, van Montfrans Joris |
| Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency. Journal of clinical immunology 2012 Dec 32 (6): 1165-79. Kutukculer Necil, Gulez Nesrin, Karaca Neslihan E, Aksu Guzide, Berdeli Af |
Genome-wide association study of serum albumin:globulin ratio in Korean populations.
Journal of human genetics 2013 Mar 58 (3): 174-7. Hong Kyung-Won, Jin Hyun-Seok, Song Daesub, Kwak Hye-Kyoung, Kim Sung Soo, Kim Yeonju |
| Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders. Clinical immunology (Orlando, Fla.) 2015 Oct 160 (2): 301-14. van Schouwenburg Pauline A, Davenport Emma E, Kienzler Anne-Kathrin, Marwah Ishita, Wright Benjamin, Lucas Mary, Malinauskas Tomas, Martin Hilary C, , Lockstone Helen E, Cazier Jean-Baptiste, Chapel Helen M, Knight Julian C, Patel Smita |
| [Identification of mutations associated with coronary artery lesion susceptibility in Kawasaki disease by targeted enrichment of genomic region sequencing technique]. Zhonghua er ke za zhi = Chinese journal of pediatrics 2017 Jul 55 (7): 529-533. Zhu D Y, Song S R, Xie L J, Qiu F, Yang J, Xiao T T, Huang |
| Exome-wide association study identifies four novel loci for systemic lupus erythematosus in Han Chinese population. Annals of the rheumatic diseases 2018 03 77 (3): 417. Wen Leilei, Zhu Caihong, Zhu Zhengwei, Yang Chao, Zheng Xiaodong, Liu Lu, Zuo Xianbo, Sheng Yujun, Tang Huayang, Liang Bo, Zhou Yi, Li Pan, Zhu Jun, Ding Yantao, Chen Gang, Gao Jinping, Tang Lili, Cheng Yuyan, Sun Jingying, Elango Tamilselvi, Kafle Anjana, Yu Ruixing, Xue Ke, Zhang Yaohua, Li Feng, Li Zhanguo, Guo Jianping, Zhang Xuan, Zhou Chen, Tang Yuanjia, Shen Nan, Wang Meng, Yu Xueqing, Liu Shengxiu, Fan Xing, Gao Min, Xiao Fengli, Wang Peiguang, Wang Zaixing, Zhang Anping, Zhou Fusheng, Sun Liangdan, Yang Sen, Xu Jinhua, Yin Xianyong, Cui Yong, Zhang Xuej |
| TNFRSF13B/TACI Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency. Avicenna journal of medical biotechnology 2018 8 10 (3): 192-195. Karaca Neslihan Edeer, Severcan Ezgi Ulusoy, Guven Burcu, Azarsiz Elif, Aksu Guzide, Kutukculer Nec |
| The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). Scientific reports 2021 Apr 11 (1): 8308. Bisgin Atil, Sonmezler Ozge, Boga Ibrahim, Yilmaz Musta |
| Protein and functional isoform levels and genetic variants of the BAFF and APRIL pathway components in systemic lupus erythematosus. Scientific reports 2022 7 12 (1): 11219. Ortiz-Aljaro Pilar, Montes-Cano Marco Antonio, García-Lozano José-Raúl, Aquino Virginia, Carmona Rosario, Perez-Florido Javier, García-Hernández Francisco José, Dopazo Joaquín, González-Escribano María Francis |
| Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Patients with Myeloma? Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 Jun . Macauda Angelica, Clay-Gilmour Alyssa, Hielscher Thomas, Hildebrandt Michelle A T, Kruszewski Marcin, Orlowski Robert Z, Kumar Shaji K, Ziv Elad, Orciuolo Enrico, Brown Elizabeth E, Försti Asta, Waller Rosalie G, Machiela Mitchell J, Chanock Stephen J, Camp Nicola J, Rymko Marcin, Ra?ny Ma?gorzata, Cozen Wendy, Várkonyi Judit, Piredda Chiara, Pelosini Matteo, Belachew Alem A, Subocz Edyta, Hemminki Kari, Rybicka-Ramos Malwina, Giles Graham G, Milne Roger L, Hofmann Jonathan N, Zaucha Jan Maciej, Vangsted Annette Juul, Goldschmidt Hartmut, Rajkumar S Vincent, Tomczak Waldemar, Sainz Juan, Butrym Aleksandra, Watek Marzena, Iskierka-Jazdzewska El?bieta, Buda Gabriele, Robinson Dennis P, Jurczyszyn Artur, Dudzi?ski Marek, Martinez-Lopez Joaquin, Sinnwell Jason P, Slager Susan L, Jamroziak Krzysztof, Reis Rui Manuel Vieira, Weinhold Niels, Bhatti Parveen, Carvajal-Carmona Luis G, Zawirska Daria, Norman Aaron D, Mazur Grzegorz, Berndt Sonja I, Campa Daniele, Vachon Celine M, Canzian Federi |
| TNFRSF13B is a potential contributor to prostate cancer. Cancer cell international 2022 May 22 (1): 180. Li Chia-Yang, Huang Shu-Pin, Chen Yei-Tsung, Wu Hsin-En, Cheng Wei-Chung, Huang Chao-Yuan, Yu Chia-Cheng, Lin Victor C, Geng Jiun-Hung, Lu Te-Ling, Bao Bo-Yi |
| Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study. Frontiers in immunology 2022 1 12 786516. Rojas-Restrepo Jessica, Caballero-Oteyza Andrés, Huebscher Katrin, Haberstroh Hanna, Fliegauf Manfred, Keller Baerbel, Kobbe Robin, Warnatz Klaus, Ehl Stephan, Proietti Michele, Grimbacher Bo |
| Multiple genetic variants involved in both autoimmunity and autoinflammation detected in Chinese patients with sporadic Meniere's disease: a preliminary study. Frontiers in neurology 2023 6 14 1159658. Jing Zou, Guoping Zhang, Hongbin Li, Zikai Zhao, Qing Zhang, Ilmari Pyykkö, Antti Mäkit |
| Genetic testing of Behçet's disease using next-generation sequencing to identify monogenic mimics and HLA-B*51. Rheumatology (Oxford, England) 2023 11 . Alice Burleigh, Ebun Omoyinmi, Charalampia Papadopoulou, Eslam Al-Abadi, Ying Hong, Fiona Price-Kuehne, Elena Moraitis, Hannah Titheradge, Francesca Montesi, Diane Xu, Despina Eleftheriou, Paul Brog |
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