Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and XIAP[original query] |
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| Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease. Journal of inherited metabolic disease 2010 Dec 33 Suppl 3 S233-40. Weiss Karl Heinz, Runz Heiko, Noe Barbara, Gotthardt Daniel Nils, Merle Uta, Ferenci Peter, Stremmel Wolfgang, Füllekrug Joach |
| Distribution of coding apoptotic gene polymorphisms in women with extreme phenotypes of breast cancer predisposition and tolerance. Tumori 0 97 (2): 248-51. Ulybina Yulia M, Kuligina Ekatherina S, Mitiushkina Nathalia V, Sherina Nathalia Y, Baholdin Dmitry V, Voskresenskiy Dmitry A, Polyakov Igor S, Togo Alexandr V, Semiglazov Vladimir F, Imyanitov Evgeny |
| XIAP variants in male Crohn's disease. Gut 2015 Jan 64 (1): 66-76. Zeissig Yvonne, Petersen Britt-Sabina, Milutinovic Snezana, Bosse Esther, Mayr Gabriele, Peuker Kenneth, Hartwig Jelka, Keller Andreas, Kohl Martina, Laass Martin W, Billmann-Born Susanne, Brandau Heide, Feller Alfred C, Röcken Christoph, Schrappe Martin, Rosenstiel Philip, Reed John C, Schreiber Stefan, Franke Andre, Zeissig Sebasti |
| Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis. International journal of hematology 2017 Mar . Mukda Ekchol, Trachoo Objoon, Pasomsub Ekawat, Tiyasirichokchai Rawiphorn, Iemwimangsa Nareenart, Sosothikul Darintr, Chantratita Wasun, Pakakasama Sama |
| Genetic profile of patients with early onset inflammatory bowel disease. Gene 2017 12 645 18-29. Girardelli Martina, Basaldella Federica, Paolera Sara Della, Vuch Josef, Tommasini Alberto, Martelossi Stefano, Crovella Sergio, Bianco Anna Moni |
| Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: Molecular analyses of PRF1, UNC13D, STX11, STXBP2, SH2D1A, and XIAP. Clinical genetics 2018 Apr . Chen X, Wang F, Zhang Y, Teng W, Wang M, Nie D, Zhou X, Wang D, Zhao H, Zhu P, Liu |
| Analysis of Genes Associated With Monogenic Primary Immunodeficiency Identifies Rare Variants in XIAP in Patients With Crohn's Disease. Gastroenterology 2018 Feb . Amininejad Leila, Charloteaux Benoit, Theatre Emilie, Liefferinckx Claire, Dmitrieva Julia, Hayard Pierre, Muls Vincianne, Maisin Jean-Marc, Schapira Michael, Ghislain Jean-Michel, Closset Pierre, Talib Mehdi, Abramowicz Marc, Momozawa Yukihide, Deffontaine Valerie, Crins François, Mni Myriam, Karim Latifa, Cambisano Nadine, Ornemese Sandra, Zucchi Alessandro, Minsart Charlotte, Deviere Jacques, Hugot Jean-Pierre, De Vos Martine, Louis Edouard, Vermeire Severine, Van Gossum Andre, Coppieters Wouter, Twizere Jean-Claude, Georges Michel, Franchimont Denis, |
| Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders. Blood advances 2020 Jun 4 (12): 2578-2594. Gadoury-Levesque Vanessa, Dong Lei, Su Rui, Chen Jianjun, Zhang Kejian, Risma Kimberly A, Marsh Rebecca A, Sun Mi |
| Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center. Gastroenterology 2020 2 158 (8): 2208-2220. Crowley Eileen, Warner Neil, Pan Jie, Khalouei Sam, Elkadri Abdul, Fiedler Karoline, Foong Justin, Turinsky Andrei L, Bronte-Tinkew Dana, Zhang Shiqi, Hu Jamie, Tian David, Li Dalin, Horowitz Julie, Siddiqui Iram, Upton Julia, Roifman Chaim M, Church Peter C, Wall Donna A, Ramani Arun K, Kotlarz Daniel, Klein Christoph, Uhlig Holm, Snapper Scott B, Gonzaga-Jauregui Claudia, Paterson Andrew D, McGovern Dermot P B, Brudno Michael, Walters Thomas D, Griffiths Anne M, Muise Aleixo |
| Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease. Nature communications 2020 Feb 11 (1): 995. Serra Eva Gonçalves, Schwerd Tobias, Moutsianas Loukas, Cavounidis Athena, Fachal Laura, Pandey Sumeet, Kammermeier Jochen, Croft Nicholas M, Posovszky Carsten, Rodrigues Astor, Russell Richard K, Barakat Farah, Auth Marcus K H, Heuschkel Robert, Zilbauer Matthias, Fyderek Krzysztof, Braegger Christian, Travis Simon P, Satsangi Jack, Parkes Miles, Thapar Nikhil, Ferry Helen, Matte Julie C, Gilmour Kimberly C, Wedrychowicz Andrzej, Sullivan Peter, Moore Carmel, Sambrook Jennifer, Ouwehand Willem, Roberts David, Danesh John, Baeumler Toni A, Fulga Tudor A, Carrami Eli M, Ahmed Ahmed, Wilson Rachel, Barrett Jeffrey C, Elkadri Abdul, Griffiths Anne M, , , , , , , Snapper Scott B, Shah Neil, Muise Aleixo M, Wilson David C, Uhlig Holm H, Anderson Carl |
| Treosulfan-Based Conditioning in Matched Family, Unrelated and Haploidentical Hematopoietic Stem Cell Transplantation for Genetic Hemophagocytic Lymphohistiocytosis: Experience and Outcomes over 10 Years from India. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 2 38 (1): 84-91. Swaminathan Venkateswaran Vellaichamy, Uppuluri Ramya, Meena Satish Kumar, Varla Harika, Chandar Rumesh, Ramakrishnan Balasubramaniam, Jayakumar Indira, Raj Revat |
| Primary Immunodeficiencies Associated With Early-Onset Inflammatory Bowel Disease in Southeast and East Asia. Frontiers in immunology 2022 1 12 786538. Sasahara Yoji, Uchida Takashi, Suzuki Tasuku, Abukawa Dai |
| Severe adult haemophagocytic lymphohistiocytosis (HLHa) correlates with HLH-related gene variants. The Journal of allergy and clinical immunology 2023 9 . Coralie Bloch, Jean Philippe Jais, Marine Gil, Marouane Boubaya, Yves Lepelletier, Brigitte Bader-Meunier, Nizar Mahlaoui, Nicolas Garcelon, Olivier Lambotte, David Launay, Claire Larroche, Estibaliz Lazaro, Francois Liffermann, Olivier Lortholary, Marc Michel, Jean-Marie Michot, Pierre Morel, Morgane Cheminant, Felipe Suarez, Louis Terriou, Geoffrey Urbanski, Jean-Francois Viallard, Alexandre Alcais, Alain Fischer, Geneviève de Saint Basile, Olivier Hermine, |
| Clinical Features and Genetic Analysis of Taiwanese Primary Immunodeficiency Patients with Prolonged Diarrhea and Monogenetic Inflammatory Bowel Disease. Journal of clinical immunology 2023 5 . Wen-I Lee, Chien-Chang Chen, Shih-Hsiang Chen, Wan-Tz Lai, Tang-Her Jaing, Liang-Shiou Ou, Chi-Jou Liang, Chen-Chen Kang, Jing-Long Hua |
| MicroRNA?24 alleviates colorectal cancer progression via a rs28382740 single nucleotide polymorphism in the long noncoding region of X?linked inhibitor of apoptosis protein. Oncology letters 2024 10 28 (6): 591. Yu-Feng Tian, Chi-Jung Huang, Chih-Yi Liu, Shung-Haur Yang, Chih-Sheng Hung, Kai-Yuan Lin, Ching-Long Lai, Chun-Chao Cha |
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