Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Inflammation and NOTCH4[original query] |
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| Genetic association of sequence variants near AGER/NOTCH4 and dementia. Journal of Alzheimer's disease : JAD 2011 24 (3): 475-84. Bennet Anna M, Reynolds Chandra A, Eriksson Ulrika K, Hong Mun-Gwan, Blennow Kaj, Gatz Margaret, Alexeyenko Andrey, Pedersen Nancy L, Prince Jonathan |
Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.
The Journal of allergy and clinical immunology 2013 Aug 132 (2): 313-20.e15. Li Xingnan, Hawkins Gregory A, Ampleford Elizabeth J, Moore Wendy C, Li Huashi, Hastie Annette T, Howard Timothy D, Boushey Homer A, Busse William W, Calhoun William J, Castro Mario, Erzurum Serpil C, Israel Elliot, Lemanske Robert F, Szefler Stanley J, Wasserman Stephen I, Wenzel Sally E, Peters Stephen P, Meyers Deborah A, Bleecker Eugene |
| Polymorphic Variations Associated With Doxorubicin-Induced Cardiotoxicity in Breast Cancer Patients. Oncology research 2017 Mar . Todorova Valentina K, Makhoul Issam, Dhakal Ishwori, Wei Jeanne, Stone Annjanette, Carter Weleetka, Owen Aaron, Klimberg V Suzan |
| A Notch4 missense mutation is associated with susceptibility to tuberculosis in Chinese population. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2019 Dec 78 104145. Zhang Jingwei, Jiao Lin, Bai Hao, Wu Qian, Wu Tao, Liu Tangyuheng, Hu Xuejiao, Song Jiajia, Ying Bin |
| The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children. The Journal of clinical investigation 2022 10 133 (1): . Benamar Mehdi, Chen Qian, Chou Janet, Julé Amélie M, Boudra Rafik, Contini Paola, Crestani Elena, Lai Peggy S, Wang Muyun, Fong Jason, Rockwitz Shira, Lee Pui, Chan Tsz Man Fion, Altun Ekin Zeynep, Kepenekli Eda, Karakoc-Aydiner Elif, Ozen Ahmet, Boran Perran, Aygun Fatih, Onal Pinar, Sakalli Ayse Ayzit Kilinc, Cokugras Haluk, Gelmez Metin Yusuf, Oktelik Fatma Betul, Cetin Esin Aktas, Zhong Yuelin, Taylor Maria Lucia, Irby Katherine, Halasa Natasha B, Mack Elizabeth H, , Signa Sara, Prigione Ignazia, Gattorno Marco, Cotugno Nicola, Amodio Donato, Geha Raif S, Son Mary Beth, Newburger Jane, Agrawal Pankaj B, Volpi Stefano, Palma Paolo, Kiykim Ayca, Randolph Adrienne G, Deniz Gunnur, Baris Safa, De Palma Raffaele, Schmitz-Abe Klaus, Charbonnier Louis-Marie, Henderson Lauren A, Chatila Talal |
| Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. European heart journal 2023 4 . Chen Hao Yu, Dina Christian, Small Aeron M, Shaffer Christian M, Levinson Rebecca T, Helgadóttir Anna, Capoulade Romain, Munter Hans Markus, Martinsson Andreas, Cairns Benjamin J, Trudsø Linea C, Hoekstra Mary, Burr Hannah A, Marsh Thomas W, Damrauer Scott M, Dufresne Line, Le Scouarnec Solena, Messika-Zeitoun David, Ranatunga Dilrini K, Whitmer Rachel A, Bonnefond Amélie, Sveinbjornsson Garðar, Daníelsen Ragnar, Arnar David O, Thorgeirsson Gudmundur, Thorsteinsdottir Unnur, Gudbjartsson Daníel F, Hólm Hilma, Ghouse Jonas, Olesen Morten Salling, Christensen Alex H, Mikkelsen Susan, Jacobsen Rikke Louise, Dowsett Joseph, Pedersen Ole Birger Vesterager, Erikstrup Christian, Ostrowski Sisse R, , O'Donnell Christopher J, Budoff Matthew J, Gudnason Vilmundur, Post Wendy S, Rotter Jerome I, Lathrop Mark, Bundgaard Henning, Johansson Bengt, Ljungberg Johan, Näslund Ulf, Le Tourneau Thierry, Smith J Gustav, Wells Quinn S, Söderberg Stefan, Stefánsson Kári, Schott Jean-Jacques, Rader Daniel J, Clarke Robert, Engert James C, Thanassoulis Geor |
| NOTCH4 Single-Nucleotide Polymorphism Is Associated with Brain Arteriovenous Malformation in a Chinese Han Population. European neurology 2023 2 86 (2): 107-115. Zhong Ming, Zhang Jianbo, Li Zhenjun, Liu Ziying, Fan Haiyan, Su Hengxian, Meng Hongliang, Zhang Xin, Li Xifeng, Duan Chuan-Zhi, He Xuyi |
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