HuGE Literature Finder
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| 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 |
| Polymorphisms in TYMS for Prediction of Capecitabine-Induced Hand-Foot Syndrome in Chinese Patients with Colorectal Cancer. Cancer research and treatment : official journal of Korean Cancer Association 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 |
| Association of regulatory variants of dopamine ß-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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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, Geor R J, Mickelson J R, McCue M |
| 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 |
| 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 |
| 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, Orduña V A, García Alfonso P, Manzano J L, Massutí B, Benavides M, Carrato A, Zanui M, Gallego J, Grávalos C, Conde V, Provencio M, Valladares M, Salazar R, Sastre J, Montagut C, Rivera F, Aranda |
| 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 |
| 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 |
| Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome. Pediatric nephrology (Berlin, Germany) 2017 Sep . Demircioglu K?l?c Beltinge, Buyukcelik Mithat, Oguzkan Balc? Sibel, Pehlivan Sacide, Kul Seval, Col Nilgun, Balat Ay |
| A PRISMA-compliant meta-analysis of MDR1 polymorphisms and idiopathic nephrotic syndrome: Susceptibility and steroid responsiveness. Medicine 2017 Jun 96 (24): e7191. Han Shi-Sheng, Xu Yan-Qiu, Lu Yan, Gu Xiang-Chen, Wang |
| Angiotensin-Converting Enzyme Gene Polymorphism in Children with Idiopathic Nephrotic Syndrome, Effect on Biopsy Findings. Fetal and pediatric pathology 2017 May 1-11. Monajemzadeh Maryam, Hesami Mahshid, Shahsiah Reza, Vasei Mohammad, Hooshmand Safoora, Tanzifi Parin, Hajizadeh Niloofar, Ataei Neamatollah, Mehrkash Mehryar, Javadi Larijani Faezeh, Moghtaderi Mastaneh, Bazargani Behnaz, Khorvash Reza, Soleimanifar Narj |
| Single-nucleotide polymorphism of INS, INSR, IRS1, IRS2, PPAR-G and CAPN10 genes in the pathogenesis of polycystic ovary syndrome. Journal of genetics 2017 Mar 96 (1): 87-96. Thangavelu Maheswari, Godla Usha Rani, Paul Solomon F D, Maddaly Ra |
| ABCB1 polymorphisms and steroid treatment in children with idiopathic nephrotic syndrome. British journal of biomedical science 2016 Oct 1-6. Safan Manal A, Elhelbawy Nesreen G, Midan Dina A, Khader Heba |
| HCV-related liver and lymphoproliferative diseases: association with polymorphisms of IL28B and TLR2. Oncotarget 2016 May . De Re Valli, De Zorzi Mariangela, Caggiari Laura, Lauletta Gianfranco, Tornesello Maria Lina, Fognani Elisa, Miorin Marta, Racanelli Vito, Quartuccio Luca, Gragnani Laura, Russi Sabino, Pavone Fabio, Ghersetti Michela, Costa Elena Garlatti, Casarin Pietro, Bomben Riccardo, Mazzaro Cesare, Basaglia Giancarlo, Berretta Massimiliano, Vaccher Emanuela, Izzo Francesco, Buonaguro Franco Maria, De Vita Salvatore, Zignego Anna Linda, De Paoli Paolo, Dolcetti Riccar |
| Association between DßH 5'-insertion/deletion polymorphism and cognition in patients with chronic schizophrenia. The Journal of clinical psychiatry 2016 Mar 77 (3): 379-85. Hui Li, Han Mei, Huang Xu Feng, Ye Min Jie, Zhang Xuan, He Jin Cai, Lv Meng Han, Soares Jair C, Zhang Xiang Ya |
| Paraoxnase1 Gene Polymorphism in Childhood Idiopathic Nephrotic Syndrome. Nephron 2016 Jan . Al-Eisa Amal A, Sukumaran Vazhappilly J, Haider Mohammad |
| Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children. Clinical and experimental nephrology 2016 Jan . Dhandapani Mohanapriya Chinambedu, Venkatesan Vettriselvi, Rengaswamy Nammalwar Bollam, Gowrishankar Kalpana, Ekambaram Sudha, Sengutavan Prabha, Perumal Venkatachal |
| Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome. International journal of nephrology 2016 2016 1417456. Suvanto Maija, Jahnukainen Timo, Kestilä Marjo, Jalanko Han |
| Vitamin D receptor gene TaqI and Apal polymorphisms and steroid responsiveness in childhood idiopathic nephrotic syndrome. International journal of nephrology and renovascular disease 2016 9 187-92. Al-Eisa Amal A, Haider Mohammad |
| Association between genes encoding components of the Leutinizing hormone/Luteinizing hormone-choriogonadotrophin receptor pathway and polycystic ovary syndrome in Egyptian women. IUBMB life 2015 Dec . El-Shal Amal S, Zidan Haidy E, Rashad Nearmeen M, Abdelaziz Ahmed M, Harira Mervat |
| 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 |
| Pathway Analysis Based on a Genome-Wide Association Study of Polycystic Ovary Syndrome. PloS one 2015 10 (8): e0136609. Shim Unjin, Kim Han-Na, Lee Hyejin, Oh Jee-Young, Sung Yeon-Ah, Kim Hyung-L |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 28, 2022
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