Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 72 Records) |
| Query Trace: Disease and SP1[original query] |
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| A functional variant in the cystathionine ß-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population. Cell research 2012 Sep . Zhao Jian-Yuan, Yang Xue-Yan, Shi Kai-Hu, Sun Shu-Na, Hou Jia, Ye Zhi-Zhou, Wang Jue, Duan Wen-Yuan, Qiao Bin, Chen Yi-Jiang, Shen Hong-Bing, Huang Guo-Ying, Jin Li, Wang Hong-Y |
| Arachidonate 5-lipoxygenase gene variants affect response to fish oil supplementation by healthy African Americans. The Journal of nutrition 2012 Aug 142 (8): 1417-28. Armstrong Patrice, Kelley Darshan S, Newman John W, Staggers Frank E, Hartiala Janna, Allayee Hooman, Stephensen Charles |
| Association of Sp1 tandem repeat polymorphism of ALOX5 with coronary artery disease in Indian subjects. Clinical and translational science 2012 Oct 5 (5): 408-11. Todur Seema P, Ashavaid Tester |
| Association of collagen type I alpha 1 gene polymorphism with inguinal hernia. Hernia : the journal of hernias and abdominal wall surgery 2014 Aug 18 (4): 507-12. Sezer S, ?im?ek N, Celik H T, Erden G, Ozturk G, Düzgün A P, Ço?kun F, Demircan |
| Association of myeloperoxidase with ovarian cancer. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Jan 35 (1): 141-8. Castillo-Tong Dan Cacsire, Pils Dietmar, Heinze Georg, Braicu Ioana, Sehouli Jalid, Reinthaller Alexander, Schuster Eva, Wolf Andrea, Watrowski Rafal, Maki Richard A, Zeillinger Robert, Reynolds Wanda |
| The MDM2 285G-309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome. Familial cancer 2014 Mar 13 (1): 127-30. Renaux-Petel Mariette, Sesboüé Richard, Baert-Desurmont Stéphanie, Vasseur Stéphanie, Fourneaux Steeve, Bessenay Emilie, Frébourg Thierry, Bougeard Gaël |
| ALOX5 polymorphism associates with increased leukotriene production and reduced lung function and asthma control in children with poorly controlled asthma. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2013 May 43 (5): 512-20. Mougey E, Lang J E, Allayee H, Teague W G, Dozor A J, Wise R A, Lima J |
| Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease. Journal of Alzheimer's disease : JAD 2013 35 (3): 487-94. Villa Chiara, Ridolfi Elisa, Fenoglio Chiara, Ghezzi Laura, Vimercati Roberto, Clerici Francesca, Marcone Alessandra, Gallone Salvatore, Serpente Maria, Cantoni Claudia, Bonsi Rossana, Cioffi Sara, Cappa Stefano, Franceschi Massimo, Rainero Innocenzo, Mariani Claudio, Scarpini Elio, Galimberti Danie |
| Matrix metalloproteinase-2 (-1306 c>t) promoter polymorphism and risk of colorectal cancer in the Saudi population. Asian Pacific journal of cancer prevention : APJCP 2013 14 (10): 6025-30. Saeed Hesham Mahmoud, Alanazi Mohammad Saud, Parine Narasimha Reddy, Shaik Jilani, Semlali Abdelhabib, Alharbi Othman, Azzam Nahla, Aljebreen Abdulrahman, Almadi Majid, Shalaby Manal A |
| Polymorphism of DEFA in Chinese Han population with IgA nephropathy. Human genetics 2014 Oct 133 (10): 1299-309. Xu Ricong, Feng Shaozhen, Li Zhijian, Fu Yonggui, Yin Peiran, Ai Zhen, Liu Wenting, Yu Xueqing, Li Mi |
| Association of collagen I, IX and vitamin D receptor gene polymorphisms with radiological severity of intervertebral disc degeneration in Southern European Ancestor. European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society 2015 Sep . Tokta? Zafer Orkun, Ek?i Murat ?akir, Y?lmaz Baran, Demir Mustafa Kemal, Özgen Serdar, K?l?ç Türker, Konya Den |
| Matrix metalloproteinase-2 -1306 C>T gene polymorphism is associated with reduced risk of cancer: a meta-analysis. Asian Pacific journal of cancer prevention : APJCP 2015 16 (3): 889-96. Haque Shafiul, Akhter Naseem, Lohani Mohtashim, Ali Arif, Mandal Raju |
| Risk factors for symptomatic osteonecrosis in childhood ALL: A retrospective study of a Slovenian pediatric ALL population between 1970 and 2004. Experimental and therapeutic medicine 2016 Aug 12 (2): 840-846. Karas-Kuželi?ki Nataša, Mencej-Bedra? Simona, Jazbec Janez, Marc Janja, Mlinari?-Raš?an Ire |
| Polymorphisms of collagen 1A1 (COL1A1) gene and their relation to bone mineral density in postmenopausal women. Ginekologia polska 2015 Dec 86 (12): 907-14. Majchrzycki Marian, Bartkowiak-Wieczorek Joanna, Wolski Hubert, Drews Krzysztof, Bogacz Anna, Czerny Bogus?aw, Zagrodnik-U?an Edyta, Seremak-Mrozikiewicz Agniesz |
| Relevance of Sp Binding Site Polymorphism in WWOX for Treatment Outcome in Pancreatic Cancer. Journal of the National Cancer Institute 2016 May 108 (5): . Schirmer Markus A, Lüske Claudia M, Roppel Sebastian, Schaudinn Alexander, Zimmer Christian, Pflüger Ruben, Haubrock Martin, Rapp Jacobe, Güngör Cenap, Bockhorn Maximilian, Hackert Thilo, Hank Thomas, Strobel Oliver, Werner Jens, Izbicki Jakob R, Johnsen Steven A, Gaedcke Jochen, Brockmöller Jürgen, Ghadimi B Micha |
| Serum Paraoxonase activity in relation to lipid profile in Age-related Macular Degeneration patients. Experimental eye research 2016 Sep 152 100-112. AnandBabu Kannadasan, Bharathidevi S R, Sripriya Sarangapani, Sen Parveen, Prakash Vadivelu Jaya, Bindu Appukuttan, Viswanathan Natarajan, Angayarkanni Narayanasa |
| Degenerated intervertebral disc prolapse and its association of collagen I alpha 1 Spl gene polymorphism: A preliminary case control study of Indian population. Indian journal of orthopaedics 0 49 (6): 589-94. Anjankar Shailendra D, Poornima Subhadra, Raju Subodh, Jaleel M A, Bhiladvala Dilnavaz, Hasan Qurratula |
| Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. Diabetes 2015 Dec . Porta Massimo, Toppila Iiro, Sandholm Niina, Hosseini S Mohsen, Forsblom Carol, Hietala Kustaa, Borio Lorenzo, Harjutsalo Valma, Klein Barbara E, Klein Ronald, Paterson Andrew D, , Groop Per-Henrik, |
| CTLA-4 Genetic Variants (rs11571317 and rs3087243): Role in Susceptibility and Progression of Breast Cancer. World journal of oncology 2017 Oct 8 (5): 162-170. Goske Maruthi, Ramachander V R Vinish, Komaravalli Prasanna Latha, Rahman P Fazul, Rao Chandrasekhar, Jahan Parve |
| Effect of genetic variants of OPTN in the pathophysiology of Paget's disease of bone. Biochimica et biophysica acta. Molecular basis of disease 2017 Oct . Silva Iris A L, Conceição Natércia, Gagnon Édith, Caiado Helena, Brown Jacques P, Gianfrancesco Fernando, Michou Laëtitia, Cancela M Leon |
| Functional analysis of a novel ENG variant in a patient with hereditary hemorrhagic telangiectasia (HHT) identifies a new Sp1 binding-site. Gene 2018 1 647 85-92. Plumitallo Sara, Ruiz-Llorente Lidia, Langa Carmen, Morini Jacopo, Babini Gabriele, Cappelletti Donata, Scelsi Laura, Greco Alessandra, Danesino Cesare, Bernabeu Carmelo, Olivieri Car |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy. Molecular neurodegeneration 2024 8 19 (1): 61. 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, Maria Stamelou, Thomas Arzberger, Sigrun Roeber, Ulrich Müller, Franziska Hopfner, 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, Edward B Lee, 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, , Clifton Dalgard, Dennis W Dickson, Günter U Höglinger, Gerard D Schellenberg, Daniel H Geschwind, Wan-Ping L |
| 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 |
- Page last reviewed:Feb 1, 2024
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