Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and EPHB4[original query] |
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| XL647--a multitargeted tyrosine kinase inhibitor: results of a phase II study in subjects with non-small cell lung cancer who have progressed after responding to treatment with either gefitinib or erlotinib. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2012 Jan 7 (1): 219-26. Pietanza M Catherine, Lynch Thomas James, Lara Primo N, Cho John, Yanagihara Ronald H, Vrindavanam Nandagopal, Chowhan Naveed Mahfooz, Gadgeel Shirish M, Pennell Nathan A, Funke Roel, Mitchell Ben, Wakelee Heather A, Miller Vincent |
| EphB4 gene polymorphism and protein expression in non-small-cell lung cancer. Molecular medicine reports 2012 Aug 6 (2): 405-8. Zheng Ming-Feng, Ji Yong, Wu Xiao-Bo, Ye Shu-Gao, Chen Jing- |
| Clinical and genetic findings in children with central nervous system arteriovenous fistulas. Annals of neurology 2017 11 82 (6): 972-980. Saliou Guillaume, Eyries Mélanie, Iacobucci Marta, Knebel Jean-François, Waill Marie-Christine, Coulet Florence, Ozanne Augustin, Soubrier Flore |
| Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation. Molecular genetics & genomic medicine 2021 Sep e1794. Choksi Foram, Weinsheimer Shantel, Nelson Jeffrey, Pawlikowska Ludmila, Fox Christine K, Zafar Atif, Mabray Marc C, Zabramski Joseph, Akers Amy, Hart Blaine L, Morrison Leslie, McCulloch Charles E, Kim Hel |
| EPHB4 mutation causes adult and adolescent-onset primary lymphedema. American journal of medical genetics. Part A 2021 7 185 (12): 3810-3813. Greene Arin K, Brouillard Pascal, Sudduth Christopher L, Smits Patrick J, Konczyk Dennis J, Vikkula Miik |
| Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19. medRxiv : the preprint server for health sciences 2021 4 . Klaric Lucija, Gisby Jack S, Papadaki Artemis, Muckian Marisa D, Macdonald-Dunlop Erin, Zhao Jing Hua, Tokolyi Alex, Persyn Elodie, Pairo-Castineira Erola, Morris Andrew P, Kalnapenkis Anette, Richmond Anne, Landini Arianna, Hedman Åsa K, Prins Bram, Zanetti Daniela, Wheeler Eleanor, Kooperberg Charles, Yao Chen, Petrie John R, Fu Jingyuan, Folkersen Lasse, Walker Mark, Magnusson Martin, Eriksson Niclas, Mattsson-Carlgren Niklas, Timmers Paul R H J, Hwang Shih-Jen, Enroth Stefan, Gustafsson Stefan, Vosa Urmo, Chen Yan, Siegbahn Agneta, Reiner Alexander, Johansson Åsa, Thorand Barbara, Gigante Bruna, Hayward Caroline, Herder Christian, Gieger Christian, Langenberg Claudia, Levy Daniel, Zhernakova Daria V, Smith J Gustav, Campbell Harry, Sundstrom Johan, Danesh John, Michaëlsson Karl, Suhre Karsten, Lind Lars, Wallentin Lars, Padyukov Leonid, Landén Mikael, Wareham Nicholas J, Göteson Andreas, Hansson Oskar, Eriksson Per, Strawbridge Rona J, Assimes Themistocles L, Esko Tonu, Gyllensten Ulf, Baillie J Kenneth, Paul Dirk S, Joshi Peter K, Butterworth Adam S, Mälarstig Anders, Pirastu Nicola, Wilson James F, Peters James |
| Methodological quality assessment of genetic studies on brain arteriovenous malformation related hemorrhage: A cross-sectional study. Frontiers in genetics 2023 4 14 1123898. Jiang Junhao, Qin Zhuo, Yan Junxia, Liu Jun |
| Variations in RASA1 and EPHB4 in Chinese patients with capillary malformation-arteriovenous malformation. The Journal of dermatology 2024 11 . Qin Zeng, Wenmin Lu, Ying Ye, Ming Li, Hongsong Ge, Qiaoyu Cao, Wei He, Cheng Zhang, Wei So |
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