Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 678 Records) |
Query Trace: NOD2[original query] |
---|
Polymorphisms in the Genes Coding for TLRs, NLRs and RLRs Are Associated with Clinical Parameters of Patients with Acute Myeloid Leukemia. International journal of molecular sciences 2022 Aug 23 (17): . Wicherska-Paw?owska Katarzyna, Bogunia-Kubik Katarzyna, Kuszczak Bart?omiej, ?acina Piotr, Dratwa Marta, Ja?wiec Bo?ena, Wróbel Tomasz, Rybka Justy |
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 |
Bladder cancer survival in patients with NOD2 or CDKN2A variants. Oncotarget 2022 4 13 628-640. Z?owocka-Per?owska El?bieta, van de Wetering Thierry, To?oczko-Grabarek Aleksandra, Scott Rodney J, Lubi?ski J |
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 |
Genomic and RNA-Seq profiling of patients with HFrEF unraveled OAS1 mutation and aggressive expression. International journal of cardiology 2022 11 375 44-54. Li Xin, Shen Yanying, Xu Xiang, Guo Ge, Chen Yibing, Wei Qingxia, Li Hanlu, He Kunlun, Liu Chunl |
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 |
NOD2 Signaling Circuitry during Allergen Sensitization Does Not Worsen Experimental Neutrophilic Asthma but Promotes a Th2/Th17 Profile in Asthma Patients but Not Healthy Subjects. International journal of molecular sciences 2022 10 23 (19): . Bouté Mélodie, Ait Yahia Saliha, Fan Ying, Alvarez-Simon Daniel, Vorng Han, Balsamelli Joanne, Nanou Julie, de Nadai Patricia, Chenivesse Cécile, Tsicopoulos An |
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 |
Presence of NOD2 mutations is not associated with hepatic or systemic hemodynamic abnormalities of cirrhosis. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2023 6 . Robin Greinert, Alexander Zipprich, Markus Casper, Matthias Christian Reichert, Frank Lammert, Cristina Ripo |
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 |
Correction: Association of NOD2 and IFNG single nucleotide polymorphisms with leprosy in the Amazon ethnic admixed population. PLoS neglected tropical diseases 2023 3 17 (3): e0011228. Leturiondo André Luiz, Noronha Ariani Batista, Mendonça Carla Yael Ribeiro, Ferreira Cynthia de Oliveira, Alvarado-Arnez Lucia Elena, Manta Fernanda Saloum de Neves, Bezerra Ohanna Cavalcanti de Lima, Carvalho Elizeu Fagundes de, Moraes Milton Ozório, Rodrigues Fabíola da Costa, Talhari Caroli |
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 |
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 |
The Immunometabolic Gene N-Acetylglucosamine Kinase Is Uniquely Involved in the Heritability of Multiple Sclerosis Severity. International journal of molecular sciences 2024 4 25 (7): . Serge Nataf, Marine Guillen, Laurent Pa |
Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata. Frontiers in endocrinology 2024 1 14 1309620. Xue-Yong Zheng, Yan-Ping Ma, Bo Zhang, Yan-Xin Chen, Lei Tang, Xiao-Hua Tai, Jia-Hao C |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: