Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 276 Records) |
Query Trace: SP1[original query] |
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Association of SP1 rs1353058818 and STAT3 rs1053004 gene polymorphisms with human tongue squamous cell carcinoma. Bioscience reports 2019 Jul . Lai Heqing, Xu Guochao, Meng Haifeng, Zhu Haiyi |
A novel mutation (-195C>A) in the promoter region of CFTR gene is associated with Chinese Congenital Bilateral Absence of Vas Deferens (CBAVD). Gene 2019 Jul 144007. Feng Jiarong, Wu Xiao, Zhang Yanan, Yang Xiaojian, Ma Gongchao, Chen Shitao, Luo Shaoge, Zhang Y |
A substitution in the pre-S1 promoter region is associated with the viral regulation of hepatitis B virus. Virology journal 2019 5 16 (1): 59. Ogura Suguru, Tameda Masahiko, Sugimoto Kazushi, Ikejiri Makoto, Usui Masanobu, Ito Masaaki, Takei Yoshiyu |
Sp1 Binding Site Polymorphism at COL1A1 Gene and Its Relation to Bone Mineral Density for Osteoporosis Risk Factor Among the Sikkimese Men and Women of Northeast India. Indian journal of clinical biochemistry : IJCB 2019 Apr 34 (2): 230-233. Soibam Deepa, Singh T A, Nandy Parvati, Dewan Sunder Kishore, Baruah Ank |
Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13.
BMC medical genomics 2019 Dec 12 (1): 196. Chen Zhongzhong, Lin Xiaoling, Lei Yunping, Chen Haitao, Finnell Richard H, Wang Yaping, Xu Jianfeng, Lu Daru, Xie Hua, Chen Fa |
Mutation and methylation status of KIT and TP in canine cutaneous and subcutaneous mast cell tumours. Veterinary and comparative oncology 2019 Oct . Vozdova Miluse, Kubickova Svatava, Fictum Petr, Cernohorska Halina, Fröhlich Jan, Rubes Ji |
Association of the MDM2 SNP285 and SNP309 Genetic Variants with the Risk, Age at Onset and Prognosis of Breast Cancer in Central European Women: A Hospital-Based Case-Control Study. International journal of molecular sciences 2019 1 20 (3): . Miedl Heidi, Lebhard Jürgen, Ehart Lisa, Schreiber Mart |
Fish Oil Supplementation in Overweight/Obese Patients with Uncontrolled Asthma. A Randomized Trial. Annals of the American Thoracic Society 2019 1 16 (5): 554-562. Lang Jason E, Mougey Edward B, Hossain Md Jobayer, Livingston Floyd, Balagopal P Babu, Langdon Scott, Lima John |
The 17?-estradiol induced upregulation of the adhesion G-protein coupled receptor (ADGRG7) is modulated by ESR? and SP1 complex. Biology open 2019 1 8 (1): . Hassan Amani, Bagu Edward T, Levesque Mathieu, Patten Shunmoogum A, Benhadjeba Samira, Edjekouane Lydia, Villemure Isabelle, Tremblay André, Moldovan Flori |
COLIA1?+?1245 G?>?T Sp1 Binding Site Polymorphism is Not Associated with ACL Injury Risks Among Indian Athletes. Indian journal of orthopaedics 2020 Sep 54 (5): 647-654. Shukla Manish, Gupta Rahul, Pandey Vivek, Tiwari Pramod Kumar, Amrathlal Rabbind Sin |
Polymorphisms in the CTLA4 promoter sequence are associated with canine hypoadrenocorticism. Canine medicine and genetics 2020 8 7 2. Boag Alisdair M, Short Andrea, Kennedy Lorna J, Syme Hattie, Graham Peter A, Catchpole Bri |
Systematic Review and Meta-Analysis of Candidate Gene Association Studies With Fracture Risk in Physically Active Participants. Frontiers in genetics 2020 7 11 551. Ryan-Moore Edward, Mavrommatis Yiannis, Waldron Ma |
Genetic variation implicates plasma angiopoietin-2 in the development of acute kidney injury sub-phenotypes. BMC nephrology 2020 Jul 21 (1): 284. Bhatraju Pavan K, Cohen Max, Nagao Ryan J, Morrell Eric D, Kosamo Susanna, Chai Xin-Ya, Nance Robin, Dmyterko Victoria, Delaney Joseph, Christie Jason D, Liu Kathleen D, Mikacenic Carmen, Gharib Sina A, Liles W Conrad, Zheng Ying, Christiani David C, Himmelfarb Jonathan, Wurfel Mark |
Functional COL1A1 variants are associated with the risk of acute musculoskeletal soft tissue injuries. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2020 Feb . Gibbon Andrea, Raleigh Stuart M, Ribbans William J, Posthumus Michael, Collins Malcolm, September Alison |
Tumor necrosis factor (TNF)-?- 308 G/A gene polymorphism (rs1800629) in Egyptian patients with alopecia areata and vitiligo, a laboratory and in silico analysis. PloS one 2020 15 (12): e0240221. Abd El-Raheem Talal, Mahmoud Rania H, Hefzy Enas M, Masoud Mohamed, Ismail Reham, Aboraia Nesreen M |
Comprehensive assessment of PD-L1 and PD-L2 dysregulation in gastrointestinal cancers. Epigenomics 2020 12 12 (24): 2155-2171. Zhao Qijie, Guo Jinan, Zhao Yueshui, Shen Jing, Kaboli Parham Jabbarzadeh, Xiang Shixin, Du Fukuan, Wu Xu, Li Mingxing, Wan Lin, Li Xiang, Wen Qinglian, Li Jing, Zou Chang, Xiao Zhanga |
BAX -248 G>A and BCL2 -938 C>A Variant Lowers the Survival in Patients with Nasopharyngeal Carcinoma and Could be Associated with Tissue-Specific Malignancies: A Multi-Method Approach. Asian Pacific journal of cancer prevention : APJCP 2021 Apr 22 (4): 1171-1181. Chatterjee Koustav, De Saikat, Deb Roy Sankar, Sahu Sushil Kumar, Chakraborty Arindom, Ghatak Sandeep, Das Nilanjana, Mal Sudipa, Roy Chattopadhyay Nabanita, Das Piyanki, Reddy R Rajendra, Mukherjee Syamantak, Das Ashok Kumar, Puii Zoreng, Zomawia Eric, Singh Yengkhom Indibor, Tsering Sam, Riba Komri, Rajasubramaniam Shanmugam, Suryawanshi Amol Ratnakar, Choudhuri Tathaga |
Single Nucleotide Polymorphisms Associated with Metformin and Sulphonylureas' Glycaemic Response among South African Adults with Type 2 Diabetes Mellitus. Journal of personalized medicine 2021 Feb 11 (2): . Masilela Charity, Pearce Brendon, Ongole Joven Jebio, Adeniyi Oladele Vincent, Benjeddou Mon |
The IL-22 gene rs2227478 polymorphism significantly decreases the risk of colorectal cancer in a Han Chinese population. Pathology, research and practice 2021 11 228 153690. Jin Yuchen, Meng Linghan, Yang Haoyi, Cheng Sirui, Xiao Yiting, Wang Xingru, Feng Xianhong, Xiong Qiantao, Chen Bife |
Association between polymorphisms of collagen genes and susceptibility to intervertebral disc degeneration: a meta-analysis. Journal of orthopaedic surgery and research 2021 10 16 (1): 616. Xie Guohui, Liang Chunhong, Yu Honglin, Zhang Q |
Functional regulatory variants implicate distinct transcriptional networks in dementia. Science (New York, N.Y.) 2022 08 377 (6608): eabi8654. Cooper Yonatan A, Teyssier Noam, Dräger Nina M, Guo Qiuyu, Davis Jessica E, Sattler Sydney M, Yang Zhongan, Patel Abdulsamie, Wu Sarah, Kosuri Sriram, Coppola Giovanni, Kampmann Martin, Geschwind Daniel |
Pharmacogenomics of Leukotriene Modifiers: A Systematic Review and Meta-Analysis. Journal of personalized medicine 2022 Jun 12 (7): . Zhao Yuxuan, Zhang Xinyi, Han Congxiao, Cai Yuchun, Li Sicong, Hu Xiaowen, Wu Caiying, Guan Xiaodong, Lu Christine, Nie Xiaoy |
A Novel SNP in the Promoter Region of IGF1 Associated With Yunshang Black Goat Kidding Number via Promoting Transcription Activity by SP1. Frontiers in cell and developmental biology 2022 6 10 873095. Li Kunyu, Liu Yufang, He Xiaoyun, Tao Lin, Jiang Yanting, Lan Rong, Hong Qionghua, Chu Mingxi |
Developing a novel DNA methylation risk score for survival and identification of prognostic gene mutations in endometrial cancer: a study based on TCGA data. Japanese journal of clinical oncology 2022 5 52 (9): 992-1000. Shen Po-Chien, Wang Ying-Fu, Chang Hao-Chih, Huang Wen-Yen, Lo Cheng-Hsiang, Su Yu-Fu, Yang Jen-Fu, Lin Chun-Shu, Dai Yang-Ho |
Network analysis reveals dysregulated functional patterns in type II diabetic skin. Scientific reports 2022 4 12 (1): 6889. Liu Chunan, Ram Sudha, Hurwitz Bonnie |
Bone-related polymorphisms and dental status in older men and women. Results of the longitudinal Pro.V.A. study. Journal of dental sciences 2022 1 17 (1): 528-534. Musacchio Estella, Binotto Pierluigi, Silva-Netto Fatima, Perissinotto Egle, Sartori Leonar |
Role of clusterin gene 3'-UTR polymorphisms and promoter hypomethylation in the pathogenesis of pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Biochimica et biophysica acta. Gene regulatory mechanisms 2023 8 1866 (4): 194980. Ramani Shyam Kapuganti, Lipsa Sahoo, Pranjya Paramita Mohanty, Bushra Hayat, Sucheta Parija, Debasmita Pankaj Alo |
Thalassaemia Patients with Polymorphism of <em>COL1A1</em> Sp1 are at Greater Risk of Spine Degenerative Changes. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2023 12 33 (12): 1379-1384. Sadia Hassan, Osheen Sajjad, Tehreem Fatima, Bushra Irum, Saqib Mehmood, Uruj Zeh |
Genetic polymorphisms in CYP2B6 may be associated with lung cancer risk in the Chinese Han population. Expert review of respiratory medicine 2024 1 1-9. Xiaoya Ma, Xufeng Zang, Leteng Yang, Wenqian Zhou, Yujie Li, Jie Wei, Jinping Guo, Junhui Han, Jing Liang, Tianbo J |
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. medRxiv : the preprint server for health sciences 2024 1 . Hui Wang, Timothy S Chang, Beth A Dombroski, Po-Liang Cheng, Vishakha Patil, Leopoldo Valiente-Banuet, Kurt Farrell, Catriona Mclean, Laura Molina-Porcel, Alex Rajput, Peter Paul De Deyn, Nathalie Le Bastard, Marla Gearing, Laura Donker Kaat, John C Van Swieten, Elise Dopper, Bernardino F Ghetti, Kathy L Newell, Claire Troakes, Justo G de Yébenes, Alberto Rábano-Gutierrez, Tina Meller, Wolfgang H Oertel, Gesine Respondek, Thomas Arzberger, Sigrun Roeber, Pau Pastor, Alexis Brice, Alexandra Durr, Isabelle Le Ber, Thomas G Beach, Geidy E Serrano, Lili-Naz Hazrati, Irene Litvan, Rosa Rademakers, Owen A Ross, Douglas Galasko, Adam L Boxer, Bruce L Miller, Willian W Seeley, Vivanna M Van Deerlin, Charles L White, Huw Morris, Rohan de Silva, John F Crary, Alison M Goate, Jeffrey S Friedman, Yuk Yee Leung, Giovanni Coppola, Adam C Naj, Li-San Wang, Dennis W Dickson, Günter U Höglinger, Gerard D Schellenberg, Daniel H Geschwind, Wan-Ping L |
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- Page last updated:Apr 22, 2024
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