Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Neoplasms and SAMHD1[original query] |
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| Identification of natural splice variants of SAMHD1 in virus-infected HCC. Oncology reports 2013 Dec . Shi Y, Lv G, Chu Z, Piao L, Liu X, Wang T, Jiang Y, Zhang P |
| Correction for Rentoft et al., Heterozygous colon cancer-associated mutations of SAMHD1 have functional significance. Proceedings of the National Academy of Sciences of the United States of America 2019 2 116 (10): 4744. Authors are not available |
| SAMHD1-deficient fibroblasts from Aicardi-Goutières Syndrome patients can escape senescence and accumulate mutations. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020 1 34 (1): 631-647. Franzolin Elisa, Coletta Sara, Ferraro Paola, Pontarin Giovanna, D'Aronco Giulia, Stevanoni Martina, Palumbo Elisa, Cagnin Stefano, Bertoldi Loris, Feltrin Erika, Valle Giorgio, Russo Antonella, Bianchi Vera, Rampazzo Chia |
| Precision oncology in AML: validation of the prognostic value of the knowledge bank approach and suggestions for improvement. Journal of hematology & oncology 2021 7 14 (1): 107. Bill Marius, Mrózek Krzysztof, Giacopelli Brian, Kohlschmidt Jessica, Nicolet Deedra, Papaioannou Dimitrios, Eisfeld Ann-Kathrin, Kolitz Jonathan E, Powell Bayard L, Carroll Andrew J, Stone Richard M, Garzon Ramiro, Byrd John C, Bloomfield Clara D, Oakes Christopher |
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia.
eLife 2022 1 11 . Chong Michael, Mohammadi-Shemirani Pedrum, Perrot Nicolas, Nelson Walter, Morton Robert, Narula Sukrit, Lali Ricky, Khan Irfan, Khan Mohammad, Judge Conor, Machipisa Tafadzwa, Cawte Nathan, O'Donnell Martin, Pigeyre Marie, Akhabir Loubna, Paré Guillau |
| SAMHD1 expression modulates innate immune activation and correlates with ovarian cancer prognosis. Frontiers in immunology 2023 2 14 1112761. Gutiérrez-Chamorro Lucía, Felip Eudald, Bernat-Peguera Adrià, Ezeonwumelu Ifeanyi Jude, Teruel Iris, Martínez-Cardús Anna, Clotet Bonaventura, Riveira-Muñoz Eva, Romeo Margarita, Margelí Mireia, Ballana Est |
| Causal inference of the effect of plasma proteins on the incidence of oral cancer: two-sample Mendelian randomization. BMC oral health 2024 9 24 (1): 1049. Tao Tian, Simin Li, Shaonan Hu, Yiwei Zhao, Gerhard Schmalz, Aneesha Acharya, Shaohong Hua |
| The landscape of rare genetic variants in familial Waldenström macroglobulinemia. Blood neoplasia 2024 7 1 (2): . Alexander Pemov, Jung Kim, Wen Luo, Jia Liu, Cole Graham, Kristine Jones, Delphine DeMangel, Neal D Freedman, Charles Dumontet, Bin Zhu, Mary L McMaster, Douglas R Stewa |
| Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases. medRxiv : the preprint server for health sciences 2024 5 . Jonathan Mitchell, Niedzica Camacho, Patrick Shea, Konrad H Stopsack, Vijai Joseph, Oliver Burren, Ryan Dhindsa, Abhishek Nag, Jacob E Berchuck, Amanda O'Neill, Ali Abbasi, Anthony W Zoghbi, Jesus Alegre-Díaz, Pablo Kuri-Morales, Jaime Berumen, Roberto Tapia-Conyer, Jonathan Emberson, Jason M Torres, Rory Collins, Quanli Wang, David Goldstein, Athena Matakidou, Carolina Haefliger, Lauren Anderson-Dring, Ruth March, Vaidehi Jobanputra, Brian Dougherty, Keren Carss, Slavé Petrovski, Philip W Kantoff, Kenneth Offit, Lorelei A Mucci, Mark Pomerantz, Margarete A Fab |
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