Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 114 Records) |
| Query Trace: Syndrome and INS[original query] |
|---|
| Preliminary Study Regarding the Association between Tumor Necrosis Factor Alpha Gene Polymorphisms and Childhood Idiopathic Nephrotic Syndrome in Romanian Pediatric Patients. Maedica 2017 Sep 12 (3): 164-168. Tieranu Ioana, Dutescu Monica I, Bara Constantin, Tieranu Cristian G, Balgradean Mihaela, Popa Olivia |
| Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals. BMC medicine 2017 12 15 (1): 213. Bansal Vikas, Gassenhuber Johann, Phillips Tierney, Oliveira Glenn, Harbaugh Rebecca, Villarasa Nikki, Topol Eric J, Seufferlein Thomas, Boehm Bernhard |
| Cytokine Gene Polymorphism in Children With Idiopathic Nephrotic Syndrome. Iranian journal of kidney diseases 2017 Nov 11 (6): 414-421. Midan Dina Abdel Razek, Elhelbawy Nesreen Gamal, Habib Mona Salah El-Din, Ahmedy Iman Aly, Noreldin Rasha Ibrah |
| The maternal 14 bp Ins/Del polymorphism in HLA-G is not associated with preeclampsia risk. International journal of immunogenetics 2017 Nov . Ferreira L C, Lopes T P B, Guimarães T B, Gomes C E M, Jeronimo S M |
| Genotype-based selection of treatment of patients with advanced colorectal cancer (SETICC): a pharmacogenetic-based randomized phase II trial. Annals of oncology : official journal of the European Society for Medical Oncology 2017 Nov . Abad A, Martínez-Balibrea E, Viéitez J M, Alonso-Orduña V, García Alfonso P, Manzano J L, Massutí B, Benavides M, Carrato A, Zanui M, Gallego J, Grávalos C, Conde V, Provencio M, Valladares-Ayerbes M, Salazar R, Sastre J, Montagut C, Rivera F, Aranda |
| Association of luteinizing hormone/choriogonadotropin receptor gene polymorphisms with polycystic ovary syndrome risk: a meta-analysis. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2018 Sep 1-5. Zou Ju, Wu Daichao, Liu Yan, Tan Sij |
| 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 |
| Heritability of metabolic traits associated with equine metabolic syndrome in Welsh ponies and Morgan horses. Equine veterinary journal 2018 Nov . Norton E M, Schultz N E, Rendahl A K, Mcfarlane D, Geor R J, Mickelson J R, McCue M |
| Cyfip1 Haploinsufficiency Does Not Alter GABA Receptor d-Subunit Expression and Tonic Inhibition in Dentate Gyrus PV Interneurons and Granule Cells. eNeuro 2019 Jun . Trent Simon, Hall Jeremy, Connelly William M, Errington Adam |
| The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease. Medicine 2019 Jun 98 (24): e15846. Guerini Franca R, Ripamonti Enrico, Costa Andrea S, Zanzottera Milena, Agliardi Cristina, Bolognesi Elisabetta, Clerici Mario, Racca Vittor |
| Plasma soluble HLA-G levels in a cohort of heart failure patients exposed to chemicals. Human immunology 2019 Dec . Bortolotti Daria, Vitali Emanuela, Stendardo Mariarita, Fucili Alessandro, Rizzo Roberta, Boschetto Pie |
| Evaluating the role of ENOSF1 and TYMS variants as predictors in fluoropyrimidine-related toxicities: An IPD meta-analysis. Pharmacological research 2019 Dec 104594. Hamzic Seid, Kummer Dominic, Froehlich Tanja K, Joerger Markus, Aebi Stefan, Palles Claire, Thomlinson Ian, Meulendijks Didier, Schellens Jan H M, García-González Xandra, López-Fernández Luis A, Amstutz Ursula, Largiadèr Carlo |
| The Apoptosis Pathway and CASP8 Variants Conferring Risk for Acute and Overuse Musculoskeletal Injuries. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2019 (3): 680-688. Seale Kirsten, Burger Marilize, Posthumus Michael, Häger Charlotte K, Stattin Evalena, Nilsson Kjell G, Collins Malcolm, September Alison |
| Association of endothelin receptor type A rs5333 gene polymorphism with steroid response in Egyptian children with idiopathic nephrotic syndrome. Pharmacogenomics 2019 Jan . Ezzat Ghada M, Ali Ahlam B, Mohamed Nahed A, Hetta Helal |
| Upward Gaze Palsy: a Valuable Sign to Distinguish Spinocerebellar Ataxias. Cerebellum (London, England) 2020 6 19 (5): 685-690. Franklin Gustavo L, Meira Alex T, Camargo Carlos H F, Nascimento Fábio A, Teive Hélio A |
| Polymorphisms in TYMS for Prediction of Capecitabine-Induced Hand-Foot Syndrome in Chinese Patients with Colorectal Cancer. Cancer research and treatment 2020 Dec . Dong Si-Qi, Wang Tong-Min, Zhang Jiang-Bo, He Yong-Qiao, Xue Wen-Qiong, Wu Zi-Yi, Yang Da-Wei, Cao Lian-Jing, Huang Jing-Wen, Li Xi-Zhao, Zhang Pei-Fen, Zheng Xiao-Hui, Jia Wei-H |
| Interleukin-4 and Interleukin-13 Gene Polymorphisms in Children With Idiopathic Nephrotic Syndrome. Frontiers in pediatrics 2020 12 8 591349. Al Rushood Maysoun, Al-Eisa Amal A, Haider Mohammad |
| Association of regulatory variants of dopamine ?-hydroxylase with cognition and tardive dyskinesia in schizophrenia subjects. Journal of psychopharmacology (Oxford, England) 2020 Jan 269881119895539. Punchaichira Toyanji J, Mukhopadhyay Anirban, Kukshal Prachi, Bhatia Triptish, Deshpande Smita N, Thelma B |
| Influence of DRD2 Polymorphisms on the Clinical Outcomes of Opioiddependent Patients on Methadone Maintenance Therapy. Journal of pharmacy & bioallied sciences 2021 4 12 (Suppl 2): S787-S803. Zahari Zalina, Lee Chee Siong, Ibrahim Muslih Abdulkarim, Musa Nurfadhlina, Mohd Yasin Mohd Azhar, Lee Yeong Yeh, Tan Soo Choon, Mohamad Nasir, Ismail Rus |
| Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants. Orphanet journal of rare diseases 2021 3 16 (1): 122. Zhu Hui, Yao Haijun, Xu Yue, Chen Yan, Han Bing, Wang Nan, Wang Hao, Zhang Qiang, Zhu Wenjiao, Shi Yuanping, Sun Hua, Zhao Shuangxia, Song Huaidong, Liu Yang, Qiao J |
| Association Between Macrophage Migration Inhibitory Factor -173 G>C Gene Polymorphism and Childhood Idiopathic Nephrotic Syndrome: A Meta-Analysis. Frontiers in pediatrics 2021 9 724258. Ying Daojing, Jiang Mengjie, Rong Liping, Zhuang Hongjie, Chen Lizhi, Xu Yuanyuan, Jiang Xiaoy |
| Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience. Hormone research in paediatrics 2021 1 93 (7-8): 423-432. Abali Zehra Yavas, De Franco Elisa, Karakilic Ozturan Esin, Poyrazoglu Sukran, Bundak Ruveyde, Bas Firdevs, Flanagan Sarah E, Darendeliler Fey |
| Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population. Laboratory medicine 2022 Aug . Shi Jianrong, Li Wei, Tao Ran, Zhou Dongming, Guo Yajun, Fu Haidong, Sun Anna, Zhang Junfeng, Mao Jianh |
| Influence of vascular endothelial growth factor on neutrophil activation in asthmatics. Postepy dermatologii i alergologii 2022 Apr 39 (2): 275-280. Gomu?ka Krzysztof, Liebhart Jerzy, Jasku?a Emilia, M?drala Wojcie |
| Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome. Iranian journal of immunology : IJI 2022 3 19 (1): 9. Li Wei, Li Lin, He Lin, Du Yun, Fu Hai-Dong, Peng Zhao-Yang, Xiang Wen-Qing, Mao Jian-H |
| Genetic Variants of Interleukin-4 in Romanian Patients with Idiopathic Nephrotic Syndrome. Medicina (Kaunas, Lithuania) 2022 2 58 (2): . Tieranu Ioana, Tieranu Cristian George, Dutescu Monica Irina, Berghea Camelia Elena, Balgradean Mihaela, Popa Olivia Mihae |
| Edema in childhood nephrotic syndrome: possible genes-hormones interplay. Journal, genetic engineering & biotechnology 2022 Feb 20 (1): 30. El-Halaby Hanan, Bakr Ashraf, Eid Riham, Abdalla Hussein Abdelaziz, Hamdy Nashwa, Shamekh Nora, Adel Amira, El-Husseiny Ahm |
| Toll-like receptor-2 (TLR-2) rs111200466 variant offers protection against SARS-CoV-2 infections and mortality: a worldwide epidemiological correlation analysis. Nucleosides, nucleotides & nucleic acids 2022 12 1-10. Nayak Nisha, Pati Abhijit, Nahak Suraj Kumar, Sarangi Surjyapratap, Pradhan Bidyutprabha, Padhi Sunali, Panda Aditya |
| Correlation between Toll-like Receptor Gene Polymorphisms and Idiopathic Nephrotic Syndrome in Chinese Children. Current medical science 2023 4 . Hui-Hui Gao, Wei Li, Xin-Yi Shou, Jian-Hua M |
| Tumor necrosis factor alpha gene polymorphism affects the pattern of idiopathic nephrotic syndrome in Kuwaiti Arab children. Journal of tropical pediatrics 2023 12 70 (1): . Amal A Al-Eisa, Maysoun Al Rushood, Sumedha Kashyap, Mohammad Z Haid |
- Page last reviewed:Feb 1, 2024
- Content source: