Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 572 Records) |
| Query Trace: Disease and NOD2[original query] |
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| Identification of variants in genes associated with autoinflammatory disorders in a cohort of patients with psoriatic arthritis. RMD open 2022 9 8 (2): . Atschekzei Faranaz, Dubrowinskaja Natalia, Anim Manfred, Thiele Thea, Witte Torsten, Sogkas Georgi |
| Gut microbial DL-endopeptidase alleviates Crohn's disease via the NOD2 pathway. Cell host & microbe 2022 9 30 (10): 1435-1449.e9. Gao Jie, Zhao Xinmei, Hu Shixian, Huang Zhenhe, Hu Mengyao, Jin Shaoqin, Lu Bingyun, Sun Kai, Wang Zhang, Fu Jingyuan, Weersma Rinse K, He Xiaolong, Zhou Hongw |
| NOD2 in Crohn's disease- unfinished business. Journal of Crohn's & colitis 2022 8 . Ashton James J, Seaby Eleanor G, Beattie R Mark, Ennis Sar |
| It is not NOD2 - genetic and clinical risk factors for postoperative complications following ileocolic resection in Crohn's disease. International journal of colorectal disease 2022 Aug 37 (8): 1901-1908. Schardey Josefine, Zehl Sophie, Kappenberger Alina S, Zimmermann Petra, Beigel Florian, Schiergens Tobias S, Kasparek Michael S, Kühn Florian, Werner Jens, Wirth Ulri |
| Nucleotide oligomerization domain polymorphism confers no risk to Guillain-Barré syndrome. Acta neurologica Scandinavica 2022 Jun . Hayat Shoma, Asad Asaduzzaman, Hasan Imran, Jahan Israt, Papri Nowshin, Howlader Zakir Hossain, Islam Zhahir |
Identification of shared loci associated with both Crohn's disease and leprosy in East Asians.
Human molecular genetics 2022 May . Jung Seulgi, Park Dohoon, Lee Ho-Su, Kim Yongjae, Baek Jiwon, Hwang Sung Wook, Park Sang Hyoung, Yang Suk-Kyun, Ye Byong Duk, Han Buhm, Sun Yonghu, Liu Hong, Zhang Furen, Liu Jianjun, Song Kyuyou |
| Clinical Significance of Gene Mutations and Polymorphic Variants and their Association with Prostate Cancer Risk in Polish Men. Cancer control : journal of the Moffitt Cancer Center 2022 5 29 10732748211062342. Heise Marta, Jarzemski Piotr, Nowak Dagmara, B?k Aneta, Junkiert-Czarnecka Anna, Pilarska-Deltow Maria, Borysiak Maciej, Pilarska Beata, Haus Ol |
| Deciphering Genetic Susceptibility to Tuberculous Meningitis. Frontiers in neurology 2022 4 13 820168. Schurz Haiko, Glanzmann Brigitte, Bowker Nicholas, van Toorn Ronald, Solomons Regan, Schoeman Johan, van Helden Paul D, Kinnear Craig J, Hoal Eileen G, Möller Mar |
| Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis. Ophthalmology 2022 3 129 (7): 821-828. Zhong Zhenyu, Ding Jiadong, Su Guannan, Liao Weiting, Gao Yu, Zhu Yunyun, Deng Yang, Li Fuzhen, Du Liping, Gao Yuan, Yang Peize |
| Association of NOD1 and NOD2 Polymorphisms With Susceptibility to Subacute Sclerosing Panencephalitis. Journal of child neurology 2022 12 8830738221144081. Kocaaga Ayça, Cakmak Genc Gunes, Karakas Celik Sevim, Piskin ?brahim E, Calik Mustafa, Dursun Ahm |
| Polymorphisms in Pattern Recognition Receptor Genes Are Associated with Respiratory Disease Severity in Pig Farms. Animals : an open access journal from MDPI 2022 11 12 (22): . Suzuki Kasumi, Shinkai Hiroki, Yoshioka Gou, Matsumoto Toshimi, Takenouchi Takato, Tanaka Junji, Shimizu Masanori, Kitazawa Haruki, Uenishi Hirohi |
| A novel signature based on pyroptosis-related genes for predicting prognosis and treatment response in prostate cancer patients. Frontiers in genetics 2022 11 13 1006151. Xiao Xi, Li Jianpeng, Wan Shun, Wu Mingzhe, Li Zonglin, Tian Junqiang, Mi J |
| NOD2c.3019-3020insC AND c.2104C>T GENE VARIANTS AMONG PATIENTS FROM WESTERN UKRAINE WITH CROHN'S DISEASE AND COLORECTAL CANCER. Experimental oncology 2022 05 44 (1): 52-59. Lozynska L, Pinyazhko R, Lozynska M, Plawski A, Makukh H, Lukavetskyy O, Grzegotsky M, Pinyazhko |
| Genetic Polymorphisms of NOD2 and ATG16L1 in Different Types of Digestive Tract Inflammation. Archives of Razi Institute 2023 6 78 (1): 493-498. N Mushtaq Hashim Al-Bderee, N Faaz Nassir Al-Saad, M Jawad Al-Imari, S Mudhaher Habbeb, A Mizal Az |
| Genetic architecture of the inflammatory bowel diseases across East Asian and European ancestries. Nature genetics 2023 5 55 (5): 796-806. Zhanju Liu, Ruize Liu, Han Gao, Seulgi Jung, Xiang Gao, Ruicong Sun, Xiaoming Liu, Yongjae Kim, Ho-Su Lee, Yosuke Kawai, Masao Nagasaki, Junji Umeno, Katsushi Tokunaga, Yoshitaka Kinouchi, Atsushi Masamune, Wenzhao Shi, Chengguo Shen, Zhenglin Guo, Kai Yuan, , , , Shu Zhu, Dalin Li, Jianjun Liu, Tian Ge, Judy Cho, Mark J Daly, Dermot P B McGovern, Byong Duk Ye, Kyuyoung Song, Yoichi Kakuta, Mingsong Li, Hailiang Hua |
| NOD2 polymorphisms may direct a Crohn's disease phenotype in patients with Very EarlyOnset Inflammatory Bowel Disease. Journal of pediatric gastroenterology and nutrition 2023 5 . Ashleigh Watson, Lisa Forbes Satter, Ashley Reiland Sauceda, Richard Kellermayer, Lina B Kar |
| Chronic inflammatory intestinal disorders in hidradenitis suppurativa. Dermatology (Basel, Switzerland) 2023 4 . Réka Palatka, Janka Eszter Anna, Soltész Lilla, Szabó Imre L?rinc, Kapitány Anikó, Dajnoki Zsolt, Emri Gabriella, Nagy Gábor, Palatka Károly, Zouboulis Christos C, Szegedi Andrea, Gáspár Kriszti |
| Association of the rs2111234, rs3135499, rs8057341 polymorphisms in the NOD2 gene with leprosy: A case-control study in the Norte de Santander, Colombia population. PloS one 2023 3 18 (3): e0281553. Bustos Mónica Alexandra, Castañeda-Castañeda Luz Dary, Acosta Carmen Rosa, García Diana, Bohada Diana Patricia, Rodríguez Raúl, Guerrero Martha Iníri |
| Variants of NOD2 in Leishmania guyanensis-infected patients with cutaneous leishmaniasis and correlations with plasma circulating pro-inflammatory cytokines. PloS one 2023 2 18 (2): e0281814. Mesquita Tirza Gabrielle Ramos de, Junior José do Espírito Santo, Souza Josué Lacerda de, Silva Lener Santos da, Nascimento Tuanny Arruda do, Souza Mara Lúcia Gomes de, Guerra Marcus Vinitius de Farias, Ramasawmy Rajendrana |
| Implications of combined NOD2 and other gene mutations in autoinflammatory diseases. Frontiers in immunology 2023 11 14 1265404. Hafsa Nomani, Zuoming Deng, Brianne Navetta-Modrov, Jie Yang, Mark Yun, Olga Aroniadis, Peter Gorevic, Ivona Aksentijevich, Qingping Y |
| No role of common NOD2 gene variants in predicting sepsis related outcomes in Indian patients undergoing hematopoietic stem cell transplant. Medical journal, Armed Forces India 2023 11 79 (6): 689-693. Aditya Jandial, Shano Naseem, Alka Khadwal, Neelam Varma, Pallab Ray, Charanpreet Singh, Arihant Jain, Deepesh Lad, Pankaj Malhotra, Gaurav Praka |
| The role of admixture in the rare variant contribution to inflammatory bowel disease. Genome medicine 2023 11 15 (1): 97. Courtney Astore, Shivam Sharma, Sini Nagpal, , David J Cutler, John D Rioux, Judy H Cho, Dermot P B McGovern, Steven R Brant, Subra Kugathasan, I King Jordan, Greg Gibs |
| Body impedance analysis to estimate malnutrition in inflammatory bowel disease patients - A cross-sectional study. Journal of digestive diseases 2023 1 . Reiner Johannes, Koch Kristina, Woitalla Julia, Huth Astrid, Bannert Karen, Sautter Lea, Jaster Robert, Witte Maria, Lamprecht Georg, Schäffler Holg |
| Genetic variants in patients with recurrent pericarditis. Journal of cardiovascular medicine (Hagerstown, Md.) 2024 9 25 (11): 799-804. Massimo Imazio, Flavio Faletra, Jessica Zucco, Catia Mio, Matteo Carraro, Alberto Maria Gava, Marzia De Biasio, Giuseppe Damante, Valentino Colli |
| A Systemic Review and Meta-analysis on Natural Resistance-associated Macrophage Protein 1 (3'-Untranslated Region) and Nucleotide-binding Oligomerization Domain-2 (rs8057341) Polymorphisms and Leprosy Susceptibility in Asian and Caucasian Populations. International journal of mycobacteriology 2024 6 13 (2): 115-125. Bibin Savio Antony, Chitra Nagarajan, Danis Vijay Devaraj, Gowtham Kumar Subbar |
| Germline polymorphisms of the NOD2 pathway may predict the effectiveness of radioiodine in differentiated thyroid cancer treatment. Journal of endocrinological investigation 2024 5 . M Borowczyk, M Kaczmarek-Ry?, S Hryhorowicz, M Sypniewski, D Filipowicz, P Dobosz, M Oszywa, M Rucha?a, K Ziemnic |
| Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes 2024 4 15 (4): . Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, On Behalf Of The Rare Genomes Project Consortium, Társis Paiva Vieira, Carlos Eduardo Stein |
| Impaired reprogramming of the autophagy flux in maturing dendritic cells from crohn disease patients with core autophagy gene-related polymorphisms. Autophagy 2024 4 1-17. Gaëlle Quiniou, Leslie Andromaque, Rémi Duclaux-Loras, Océane Dinet, Ornella Cervantes, Mallorie Verdet, Camille Meunier, Gilles Boschetti, Christophe Viret, Stéphane Nancey, Mathias Faure, Aurore Rozièr |
| Comprehensive clinical phenotype, genotype and therapy in Yao syndrome. Frontiers in immunology 2024 10 15 1458118. Hafsa Nomani, Song Wu, Ashmia Saif, Frank Hwang, Jane Metzger, Brianne Navetta-Modrov, Peter D Gorevic, Ivona Aksentijevich, Qingping Y |
| The known genetic variants of BRCA1, BRCA2 and NOD2 in pancreatitis and pancreatic cancer risk assessment. Scientific reports 2025 1 15 (1): 1791. Jaros?aw Matykiewicz, Wioletta Adamus-Bia?ek, Monika Wawszczak-Kasza, Bartosz Molasy, Magdalena Ko?oma?ska, Rus?an Oblap, ?ukasz Madej, Dorota Kozie?, Stanis?aw G?usz |
- Page last reviewed:Feb 1, 2024
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