Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: Syndrome and CTLA4[original query] |
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Influence of CTLA4 haplotypes on susceptibility and some extraglandular manifestations in primary Sjögren's syndrome. Arthritis and rheumatism 2006 Aug 54 (8): 2434-40. Downie-Doyle Sarah, Bayat Noushin, Rischmueller Maureen, Lester Sus |
Cytotoxic T lymphocyte antigen-4 Ala17 polymorphism is a genetic marker of autoimmune adrenal insufficiency: Italian association study and meta-analysis of European studies. European journal of endocrinology / European Federation of Endocrine Societies 2010 Feb 162 (2): 361-9. Brozzetti Annalisa, Marzotti Stefania, Tortoioli Cristina, Bini Vittorio, Giordano Roberta, Dotta Francesco, Betterle Corrado, De Bellis Annamaria, Arnaldi Giorgio, Toscano Vincenzo, Arvat Emanuela, Bellastella Antonio, Mantero Franco, Falorni Alberto, |
Clinical and genetic characteristics of autoimmune polyglandular syndrome type 3 variant in the Japanese population. The Journal of clinical endocrinology and metabolism 2012 Jun 97 (6): E1043-50. Horie Ichiro, Kawasaki Eiji, Ando Takao, Kuwahara Hironaga, Abiru Norio, Usa Toshiro, Yamasaki Hironori, Ejima Eri, Kawakami Atsus |
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients. Human immunology 2012 Jul 73 (7): 740-6. Fourati Hajer, Bouzid Dorra, Abida Olfa, Kharrat Najla, Mnif Fatma, Haddouk Samy, Fesel Constantin, Costa João, Ben Ayed Mourad, Abid Mohamed, Rebai Ahmed, Penha-Gonçalves Carlos, Masmoudi Hat |
Pharmacogenetics of efficacy and safety of HCV treatment in HCV-HIV coinfected patients: significant associations with IL28B and SOCS3 gene variants. PloS one 2012 7 (11): e47725. Vidal Francesc, López-Dupla Miguel, Laguno Montserrat, Veloso Sergi, Mallolas Josep, Murillas Javier, Cifuentes Carmen, Gallart Lluis, Auguet Teresa, Sampériz Gloria, Payeras Antoni, Hernandez Pilar, Arnedo Mireia, Gatell Josep Ma, Richart Cristób |
Genetic variations of immunoregulatory genes associated with Rasmussen syndrome. Epilepsy research 2013 Oct . Takahashi Y, Mogami Y, Mine J, Imai K, Koide Y, Matsuda K, Akasaka N, Konishi T, Imamura A, Inoue Y |
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations. Nature medicine 2014 Dec 20 (12): 1410-6. Schubert Desirée, Bode Claudia, Kenefeck Rupert, Hou Tie Zheng, Wing James B, Kennedy Alan, Bulashevska Alla, Petersen Britt-Sabina, Schäffer Alejandro A, Grüning Björn A, Unger Susanne, Frede Natalie, Baumann Ulrich, Witte Torsten, Schmidt Reinhold E, Dueckers Gregor, Niehues Tim, Seneviratne Suranjith, Kanariou Maria, Speckmann Carsten, Ehl Stephan, Rensing-Ehl Anne, Warnatz Klaus, Rakhmanov Mirzokhid, Thimme Robert, Hasselblatt Peter, Emmerich Florian, Cathomen Toni, Backofen Rolf, Fisch Paul, Seidl Maximilian, May Annette, Schmitt-Graeff Annette, Ikemizu Shinji, Salzer Ulrich, Franke Andre, Sakaguchi Shimon, Walker Lucy S K, Sansom David M, Grimbacher Bo |
ATPase4A Autoreactivity and Its Association With Autoimmune Phenotypes in the Type 1 Diabetes Genetics Consortium Study. Diabetes care 2015 Oct 38 Suppl 2 S29-36. Wenzlau Janet M, Fain Pamela R, Gardner Thomas J, Frisch Lisa M, Annibale Bruno, Hutton John |
Genetics of Autoimmune Thyroiditis in Type 1 Diabetes Reveals a Novel Association With DPB1*0201: Data From the Type 1 Diabetes Genetics Consortium. Diabetes care 2015 Oct 38 Suppl 2 S21-8. Kahles Heinrich, Fain Pamela R, Baker Peter, Eisenbarth George, Badenhoop Kla |
Association of TNF-a, CTLA4, and PTPN22 polymorphisms with type 1 diabetes and other autoimmune diseases in Brazil. Genetics and molecular research : GMR 2015 14 (4): 18936-44. Tavares N A C, Santos M M S, Moura R, Araújo J, Guimarães R L, Crovella S, Brandão L A |
Increased Risk for Malignancies in 131 Affected CTLA4 Mutation Carriers. Frontiers in immunology 2018 9 9 2012. Egg David, Schwab Charlotte, Gabrysch Annemarie, Arkwright Peter D, Cheesman Edmund, Giulino-Roth Lisa, Neth Olaf, Snapper Scott, Okada Satoshi, Moutschen Michel, Delvenne Philippe, Pecher Ann-Christin, Wolff Daniel, Kim Yae-Jean, Seneviratne Suranjith, Kim Kyoung-Mee, Kang Ji-Man, Ojaimi Samar, McLean Catriona, Warnatz Klaus, Seidl Maximilian, Grimbacher Bo |
Cytotoxic T- Lymphocyte Antigen-4 (CTLA4) Gene Expression and Urinary CTLA4 Levels in Idiopathic Nephrotic Syndrome. Indian journal of pediatrics 2018 Jul . Mishra Om P, Chhabra Prashant, Narayan Gopeshwar, Srivastava Pradeep, Prasad Rajniti, Singh Ankur, Abhinay Abhishek, Batra Vineeta |
Genetic association of CTLA4 gene with polycystic ovary syndrome in the Chinese Han population. Medicine 2018 Jul 97 (29): e11422. Su Jing, Li Yan, Su Guanglong, Wang Jing, Qiu Ting, Ma Rong, Zhao L |
Association of CD28 and CTLA4 haplotypes with susceptibility to primary Sjögren's syndrome in Mexican population. Journal of clinical laboratory analysis 2018 Jul e22620. López-Villalobos Erika Fabiola, Carrillo-Ballesteros Francisco Josué, Muñoz-Valle José Francisco, Palafox-Sánchez Claudia Azucena, Valle Yeminia, Orozco-Barocio Gerardo, Oregon-Romero Edi |
Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations. Clinical immunology (Orlando, Fla.) 2018 1 188 52-57. Besnard Caroline, Levy Eva, Aladjidi Nathalie, Stolzenberg Marie-Claude, Magerus-Chatinet Aude, Alibeu Olivier, Nitschke Patrick, Blanche Stéphane, Hermine Olivier, Jeziorski Eric, Landman-Parker Judith, Leverger Guy, Mahlaoui Nizar, Michel Gérard, Pellier Isabelle, Suarez Felipe, Thuret Isabelle, de Saint-Basile Geneviève, Picard Capucine, Fischer Alain, Neven Bénédicte, Rieux-Laucat Frédéric, Quartier Pierre, |
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes. Blood 2019 Apr . Hadjadj Jérôme, Aladjidi Nathalie, Fernandes Helder, Leverger Guy, Magérus-Chatinet Aude, Mazerolles Fabienne, Stolzenberg Marie-Claude, Jacques Sidonie, Picard Capucine, Rosain Jérémie, Fourrage Cécile, Hanein Sylvain, Zarhrate Mohammed, Pasquet Marlène, Abou Chahla Wadih, Barlogis Vincent, Bertrand Yves, Pellier Isabelle, Colomb Bottollier Elodie, Fouyssac Fanny, Blouin Pascale, Thomas Caroline, Cheikh Nathalie, Dore Eric, Pondarre Corinne, Plantaz Dominique, Jeziorski Eric, Millot Frédéric, Garcelon Nicolas, Ducassou Stéphane, Perel Yves, Leblanc Thierry, Neven Bénédicte, Fischer Alain, Rieux-Laucat Frédéric, |
Autoimmunity-Related Risk Variants in PTPN22 and CTLA4 Are Associated With ME/CFS With Infectious Onset. Frontiers in immunology 2020 11 578. Steiner Sophie, Becker Sonya C, Hartwig Jelka, Sotzny Franziska, Lorenz Sebastian, Bauer Sandra, Löbel Madlen, Stittrich Anna B, Grabowski Patricia, Scheibenbogen Carm |
Association of Polygenetic Risk Scores Related to Immunity and Inflammation with Hyperthyroidism Risk and Interactions between the Polygenetic Scores and Dietary Factors in a Large Cohort.
Journal of thyroid research 2021 2021 7664641. Song Mi Young, Park Sunm |
High mutation burden in the checkpoint and micro-RNA processing genes in myelodysplastic syndrome. PloS one 2021 3 16 (3): e0248430. Moiseev Ivan Sergeevich, Tcvetkov Nikolay Yurevich, Barkhatov Ildar Munerovich, Barabanshikova Maria Vladimirovna, Bug Dmitrii Sergeevich, Petuhova Natalya Vitalievna, Tishkov Artem Valerievich, Bakin Evgenyi Alexandrovich, Izmailova Ekaterina Andreevna, Shakirova Alena Igorevna, Kulagin Alexandr Dmitrievich, Morozova Elena Vladislavov |
Prediction of Tacrolimus Dose/Weight-Adjusted Trough Concentration in Pediatric Refractory Nephrotic Syndrome: A Machine Learning Approach. Pharmacogenomics and personalized medicine 2022 3 15 143-155. Mo Xiaolan, Chen Xiujuan, Wang Xianggui, Zhong Xiaoli, Liang Huiying, Wei Yuanyi, Deng Houliang, Hu Rong, Zhang Tao, Chen Yilu, Gao Xia, Huang Min, Li Jia |
Tacrolimus pharmacokinetics in pediatric nephrotic syndrome: A combination of population pharmacokinetic modelling and machine learning approaches to improve individual prediction. Frontiers in pharmacology 2022 12 13 942129. Huang Qiongbo, Lin Xiaobin, Wang Yang, Chen Xiujuan, Zheng Wei, Zhong Xiaoli, Shang Dewei, Huang Min, Gao Xia, Deng Hui, Li Jiali, Zeng Fangling, Mo Xiaol |
Insilico prediction and functional analysis of nonsynonymous SNPs in human CTLA4 gene. Scientific reports 2022 11 12 (1): 20441. Irfan Muhammad, Iqbal Talha, Hashmi Sakina, Ghani Uzma, Bhatti Att |
BRAF V600E/RAS Mutations and Lynch Syndrome in Patients With MSI-H/dMMR Metastatic Colorectal Cancer Treated With Immune Checkpoint Inhibitors. The oncologist 2023 4 . Colle Raphael, Lonardi Sara, Cachanado Marine, Overman Michael J, Elez Elena, Fakih Marwan, Corti Francesca, Jayachandran Priya, Svrcek Magali, Dardenne Antoine, Cervantes Baptiste, Duval Alex, Cohen Romain, Pietrantonio Filippo, André Thier |
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- Page last updated:Apr 22, 2024
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