Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: EPHB4[original query] |
---|
EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. Circulation. Cardiovascular genetics 2009 Oct 2 (5): 476-82. Weinsheimer Shantel, Kim Helen, Pawlikowska Ludmila, Chen Yongmei, Lawton Michael T, Sidney Stephen, Kwok Pui-Yan, McCulloch Charles E, Young William |
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 |
Phase II study of the multitargeted tyrosine kinase inhibitor XL647 in patients with non-small-cell lung cancer. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2012 May 7 (5): 856-65. Pietanza M Catherine, Gadgeel Shirish M, Dowlati Afshin, Lynch Thomas J, Salgia Ravi, Rowland Kendrith M, Wertheim Michael S, Price Katharine A, Riely Gregory J, Azzoli Christopher G, Miller Vincent A, Krug Lee M, Kris Mark G, Beumer Jan H, Tonda Margaret, Mitchell Ben, Rizvi Naiyer |
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- |
Reduced blood pressure after smooth muscle EFNB2 deletion and the potential association of EFNB2 mutation with human hypertension risk. European journal of human genetics : EJHG 2016 Aug . Wang Yujia, Hamet Pavel, Thorin Eric, Tremblay Johanne, Raelson John, Wu Zenghui, Luo Hongyu, Jin Wei, Lavoie Julie L, Peng Junzheng, Marois-Blanchet Francois-Christophe, Tahir Muhammad Ramzan, Chalmers John, Woodward Mark, Harrap Stephen, Qi Shijie, Li Charles Yibin, Wu Jiangpi |
Right- vs. Left-Sided Metastatic Colorectal Cancer: Differences in Tumor Biology and Bevacizumab Efficacy. International journal of molecular sciences 2017 Jun 18 (6): . Ulivi Paola, Scarpi Emanuela, Chiadini Elisa, Marisi Giorgia, Valgiusti Martina, Capelli Laura, Casadei Gardini Andrea, Monti Manlio, Ruscelli Silvia, Frassineti Giovanni Luca, Calistri Daniele, Amadori Dino, Passardi Alessand |
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 |
Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia. Molecular genetics & genomic medicine 2018 May 6 (3): 350-356. Pawlikowska Ludmila, Nelson Jeffrey, Guo Diana E, McCulloch Charles E, Lawton Michael T, Kim Helen, Faughnan Marie E, |
Genomic alterations of ground-glass nodular lung adenocarcinoma. Scientific reports 2018 5 8 (1): 7691. Lee Hyun, Joung Je-Gun, Shin Hyun-Tae, Kim Duk-Hwan, Kim Yujin, Kim Hojoong, Kwon O Jung, Shim Young Mog, Lee Ho Yun, Lee Kyung Soo, Choi Yoon-La, Park Woong-Yang, Hayes D Neil, Um Sang-W |
RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation. Journal of medical genetics 2019 7 57 (1): 48-52. Revencu Nicole, Fastre Elodie, Ravoet Marie, Helaers Raphaël, Brouillard Pascal, Bisdorff-Bresson Annouk, Chung Clara W T, Gerard Marion, Dvorakova Veronika, Irvine Alan D, Boon Laurence M, Vikkula Miik |
Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)? Genetics in medicine : official journal of the American College of Medical Genetics 2019 Feb . Wooderchak-Donahue Whitney L, Akay Gulsen, Whitehead Kevin, Briggs Eric, Stevenson David A, O'Fallon Brendan, Velinder Matthew, Farrell Andrew, Shen Wei, Bedoukian Emma, Skrabann Cara M, Antaya Richard J, Henderson Kate, Pollak Jeffrey, Treat James, Day Ronald, Jacher Joseph E, Hannibal Mark, Bontempo Kelly, Marth Gabor, Bayrak-Toydemir Pinar, McDonald Jam |
Capillary malformation-arteriovenous malformation syndrome: a multicentre study. Clinical and experimental dermatology 2020 8 46 (2): 300-305. Valdivielso-Ramos M, Martin-Santiago A, Azaña J M, Hernández-Nuñez A, Vera A, Perez B, Tercedor J, Feito M, Vicente A, Prat C, Lopez-Gutierrez J C, Garnacho G, Baselga E, Roe E, Palencia S, Cordero P, Moreno R, Agudo A, de la Cueva P, Torrelo |
The expressions of EphB4 and ephrinB2 in lung adenocarcinomas: a high level of the EphB4 protein is associated with lymph node metastasis. International journal of clinical and experimental pathology 2020 1 12 (9): 3447-3452. Li Ji, Sun Yuejun, Wang Xiaoxia, Wang Jiandong, Zhu Yeha |
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 as a Novel Target for the EGFR-Independent Suppressive Effects of Osimertinib on Cell Cycle Progression in Non-Small Cell Lung Cancer. International journal of molecular sciences 2021 8 22 (16): . Nanamiya Ren, Saito-Koyama Ryoko, Miki Yasuhiro, Inoue Chihiro, Asavasupreechar Teeranut, Abe Jiro, Sato Ikuro, Sasano Hirono |
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 |
Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to Phenotype. Frontiers in pediatrics 2022 5 10 871565. Tas Berivan, Starnoni Daniele, Smajda Stanislas, Vivanti Alexandre J, Adamsbaum Catherine, Eyries Mélanie, Melki Judith, Tawk Marcel, Ozanne Augustin, Revencu Nicole, Soubrier Florent, Siala Selima, Vikkula Miikka, Deiva Kumaran, Saliou Guillau |
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 |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: