Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and ADO[original query] |
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| eNOS 894T allele and coronary blood flow at rest and during adenosine-induced hyperemia. American journal of physiology. Heart and circulatory physiology 2001 Nov 281 (5): H1908-12. Naber C K, Baumgart D, Altmann C, Siffert W, Erbel R, Heusch |
| Simultaneous single-cell detection of two mutations for cystic fibrosis. Journal of assisted reproduction and genetics 2001 1 17 (9): 534-9. Drury K C, Liu M C, Zheng W, Kipersztok S, Williams R |
| Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003 Oct 18 (10): 1740-7. Frattini Annalisa, Pangrazio Alessandra, Susani Lucia, Sobacchi Cristina, Mirolo Massimiliano, Abinun Mario, Andolina Marino, Flanagan Adrienne, Horwitz Edwin M, Mihci Ercan, Notarangelo Luigi D, Ramenghi Ugo, Teti Anna, Van Hove Johan, Vujic Dragana, Young Terri, Albertini Alberto, Orchard Paul J, Vezzoni Paolo, Villa An |
| CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men. Bone 2008 Dec 43 (6): 995-8. Chu Kang, Koller Daniel L, Ichikawa Shoji, Snyder Richard, Curry Leah, Lai Dongbing, Austin Anthony, Xuei Xiaoling, Edenberg Howard J, Hui Siu L, Foroud Tatiana M, Peacock Munro, Econs Michael |
| Novel and known microsatellite markers within the ?-globin cluster to support robust preimplantation genetic diagnosis of ?-thalassemia and sickle cell syndromes. Hemoglobin 2011 1 35 (1): 56-66. Zachaki Sophia, Vrettou Christina, Destouni Aspasia, Kokkali Ggeorgia, Traeger-Synodinos Joanne, Kanavakis Emmanu |
| Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. American journal of human genetics 2015 Jul 97 (1): 22-34. Darabi Hatef, McCue Karen, Beesley Jonathan, Michailidou Kyriaki, Nord Silje, Kar Siddhartha, Humphreys Keith, Thompson Deborah, Ghoussaini Maya, Bolla Manjeet K, Dennis Joe, Wang Qin, Canisius Sander, Scott Christopher G, Apicella Carmel, Hopper John L, Southey Melissa C, Stone Jennifer, Broeks Annegien, Schmidt Marjanka K, Scott Rodney J, Lophatananon Artitaya, Muir Kenneth, Beckmann Matthias W, Ekici Arif B, Fasching Peter A, Heusinger Katharina, Dos-Santos-Silva Isabel, Peto Julian, Tomlinson Ian, Sawyer Elinor J, Burwinkel Barbara, Marme Frederik, Guénel Pascal, Truong Thérèse, Bojesen Stig E, Flyger Henrik, Benitez Javier, González-Neira Anna, Anton-Culver Hoda, Neuhausen Susan L, Arndt Volker, Brenner Hermann, Engel Christoph, Meindl Alfons, Schmutzler Rita K, , Arnold Norbert, Brauch Hiltrud, Hamann Ute, Chang-Claude Jenny, Khan Sofia, Nevanlinna Heli, Ito Hidemi, Matsuo Keitaro, Bogdanova Natalia V, Dörk Thilo, Lindblom Annika, Margolin Sara, , Kosma Veli-Matti, Mannermaa Arto, Tseng Chiu-Chen, Wu Anna H, Floris Giuseppe, Lambrechts Diether, Rudolph Anja, Peterlongo Paolo, Radice Paolo, Couch Fergus J, Vachon Celine, Giles Graham G, McLean Catriona, Milne Roger L, Dugué Pierre-Antoine, Haiman Christopher A, Maskarinec Gertraud, Woolcott Christy, Henderson Brian E, Goldberg Mark S, Simard Jacques, Teo Soo H, Mariapun Shivaani, Helland Åslaug, Haakensen Vilde, Zheng Wei, Beeghly-Fadiel Alicia, Tamimi Rulla, Jukkola-Vuorinen Arja, Winqvist Robert, Andrulis Irene L, Knight Julia A, Devilee Peter, Tollenaar Robert A E M, Figueroa Jonine, García-Closas Montserrat, Czene Kamila, Hooning Maartje J, Tilanus-Linthorst Madeleine, Li Jingmei, Gao Yu-Tang, Shu Xiao-Ou, Cox Angela, Cross Simon S, Luben Robert, Khaw Kay-Tee, Choi Ji-Yeob, Kang Daehee, Hartman Mikael, Lim Wei Yen, Kabisch Maria, Torres Diana, Jakubowska Anna, Lubinski Jan, McKay James, Sangrajrang Suleeporn, Toland Amanda E, Yannoukakos Drakoulis, Shen Chen-Yang, Yu Jyh-Cherng, Ziogas Argyrios, Schoemaker Minouk J, Swerdlow Anthony, Borresen-Dale Anne-Lise, Kristensen Vessela, French Juliet D, Edwards Stacey L, Dunning Alison M, Easton Douglas F, Hall Per, Chenevix-Trench Georg |
| The association between functional HLA-G 14bp insertion/deletion and +3142 C>G polymorphisms and susceptibility to multiple sclerosis. Immunology letters 2016 Oct . Ben Fredj Nadia, Sakly Kaouthar, Bortolotti Daria, Aissi Mouna, Frih-Ayed Mahbouba, Rotola Antonella, Caselli Elisabetta, Cura Franscesca, Sakly Nabil, Aouni Mahjoub, Di Luca Dario Di, Rizzo Rober |
| Serum KL-6 in pulmonary alveolar proteinosis: China compared historically with Germany and Japan. Journal of thoracic disease 2017 Feb 9 (2): 287-295. Guo Wen-Liang, Zhou Zi-Qing, Chen Lu, Su Zhu-Quan, Zhong Chang-Hao, Chen Yu, Li Shi-Y |
| Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility. Nature genetics 2017 Feb . Takeuchi Masaki, Mizuki Nobuhisa, Meguro Akira, Ombrello Michael J, Kirino Yohei, Satorius Colleen, Le Julie, Blake Mary, Erer Burak, Kawagoe Tatsukata, Ustek Duran, Tugal-Tutkun Ilknur, Seyahi Emire, Ozyazgan Yilmaz, Sousa Inês, Davatchi Fereydoun, Francisco Vânia, Shahram Farhad, Abdollahi Bahar Sadeghi, Nadji Abdolhadi, Shafiee Niloofar Mojarad, Ghaderibarmi Fahmida, Ohno Shigeaki, Ueda Atsuhisa, Ishigatsubo Yoshiaki, Gadina Massimo, Oliveira Sofia A, Gül Ahmet, Kastner Daniel L, Remmers Elaine |
| Association of LACC1, CEBPB-PTPN1, RIPK2 and ADO-EGR2 with ocular Behcet's disease in a Chinese Han population. The British journal of ophthalmology 2018 Jun . Wu Pengcheng, Du Liping, Hou Shengping, Su Guannan, Yang Lu, Hu Jiayue, Deng Jing, Cao Qingfeng, Yuan Gangxiang, Zhou Chunjiang, Kijlstra Aize, Yang Peize |
| Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives. BMC medical genomics 2020 8 13 (1): 117. Li Qing, Mao Yan, Li Shaoying, Du Hongzi, He Wenzhi, He Jianchun, Kong Lingyin, Zhang Jun, Liang Bo, Liu Jianqi |
| Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population. PloS one 2020 15 (5): e0233464. Sakono Takuto, Meguro Akira, Takeuchi Masaki, Yamane Takahiro, Teshigawara Takeshi, Kitaichi Nobuyoshi, Horie Yukihiro, Namba Kenichi, Ohno Shigeaki, Nakao Kumiko, Sakamoto Taiji, Sakai Tsutomu, Nakano Tadashi, Keino Hiroshi, Okada Annabelle A, Takeda Atsunobu, Ito Takako, Mashimo Hisashi, Ohguro Nobuyuki, Oono Shinichirou, Enaida Hiroshi, Okinami Satoshi, Horita Nobuyuki, Ota Masao, Mizuki Nobuhi |
| Trastuzumab emtansine for patients with non-small cell lung cancer positive for human epidermal growth factor receptor 2 exon-20 insertion mutations. European journal of cancer (Oxford, England : 1990) 2021 12 162 99-106. Iwama Eiji, Zenke Yoshitaka, Sugawara Shunichi, Daga Haruko, Morise Masahiro, Yanagitani Noriko, Sakamoto Tomohiro, Murakami Haruyasu, Kishimoto Junji, Matsumoto Shingo, Nakanishi Yoichi, Goto Koichi, Okamoto Isa |
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.
Arthritis & rheumatology (Hoboken, N.J.) 2021 Jan . Ortiz Fernández Lourdes, Coit Patrick, Yilmaz Vuslat, Yentür Sibel P, Alibaz-Oner Fatma, Aksu Kenan, Erken Eren, Düzgün Nursen, Keser Gokhan, Cefle Ayse, Yazici Ayten, Ergen Andac, Alpsoy Erkan, Salvarani Carlo, Casali Bruno, Kisacik Bünyamin, Kötter Ina, Henes Jörg, Çinar Muhammet, Schaefer Arne, Nohutcu Rahime M, Zhernakova Alexandra, Wijmenga Cisca, Takeuchi Fujio, Harihara Shinji, Kaburaki Toshikatsu, Messedi Meriam, Song Yeong-Wook, Kasifoglu Timuçin, Carmona F David, Guthridge Joel M, James Judith A, Martin Javier, González Escribano María Francisca, Saruhan-Direskeneli Güher, Direskeneli Haner, Sawalha Amr |
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