Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: SAMHD1[original query] |
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Polymorphisms of the SAMHD1 gene are not associated with the infection and natural control of HIV type 1 in Europeans and African-Americans. AIDS research and human retroviruses 2012 Dec 28 (12): 1565-73. Coon Sirena, Wang Danxin, Wu |
Increased expression of intrinsic antiviral genes in HLA-B*57-positive individuals. Journal of leukocyte biology 2013 Nov 94 (5): 1051-9. Raposo Rui André Saraiva, Abdel-Mohsen Mohamed, Holditch Sara J, Kuebler Peter J, Cheng Rex G, Eriksson Emily M, Liao Wilson, Pillai Satish K, Nixon Douglas |
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 |
Analysis of Immunological, Viral, Genetic, and Environmental Factors That Might Be Associated with Decreased Susceptibility to HIV Infection in Serodiscordant Couples in Florianópolis, Southern Brazil. AIDS research and human retroviruses 2015 Sep . Santos Íris M, da Rosa Elis A, Gräf Tiago, Ferreira Luiz G E, Petry Andrea, Cavalheiro Fernanda, Reiche Edna M, Zanetti Carlos R, Pinto Aguinaldo |
Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL. Blood 2015 Aug . Guièze Romain, Robbe Pauline, Clifford Ruth, de Guibert Sophie, Pereira Bruno, Timbs Adele, Dilhuydy Marie-Sarah, Cabes Maite, Ysebaert Loïc, Burns Adam, Nguyen-Khac Florence, Davi Frédéric, Véronèse Lauren, Combes Paricia, Le Garff-Tavernier Magali, Leblond Véronique, Merle-Béral Hélène, Alsolami Reem, Hamblin Angela, Mason Joanne, Pettitt Andrew, Hillmen Peter, Taylor Jenny, Knight Samantha J L, Tournilhac Olivier, Schuh An |
SAMHD1 Gene Mutations Are Associated with Cerebral Large-Artery Atherosclerosis. BioMed research international 2015 2015 739586. Li Wei, Xin Baozhong, Yan Junpeng, Wu Ying, Hu Bo, Liu Liping, Wang Yilong, Ahn Jinwoo, Skowronski Jacek, Zhang Zaiqiang, Wang Yongjun, Wang He |
Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing. PloS one 2016 11 (12): e0167641. Kim Jung-Ah, Hwang Byungjin, Park Si Nae, Huh Sunghoon, Im Kyongok, Choi Sungbin, Chung Hye Yoon, Huh JooRyung, Seo Eul-Ju, Lee Je-Hwan, Bang Duhee, Lee Dong So |
SAMHD1 Mutations Are Also Responsible for Aicardi-Goutières in the Cree Population. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2017 8 44 (6): 749-751. Kharrat Ashraf, MacKenzie Jennifer, Venkateswaran Suni |
ERRATUM: SAMHD1 Polymorphisms were Significantly Correlated with HIV/SIV Virus Load in PBMC from Chinese Rhesus Macaques and Cynomolgus Macaques. Current HIV research 2017 12 15 (5): 382. Authors are not available |
Association of genetic polymorphisms in genes involved in Ara-C and dNTP metabolism pathway with chemosensitivity and prognosis of adult acute myeloid leukemia (AML). Journal of translational medicine 2018 Apr 16 (1): 90. Zhu Ke-Wei, Chen Peng, Zhang Dao-Yu, Yan Han, Liu Han, Cen Li-Na, Liu Yan-Ling, Cao Shan, Zhou Gan, Zeng Hui, Chen Shu-Ping, Zhao Xie-Lan, Chen Xiao-Pi |
Combination of exome sequencing and immune testing confirms Aicardi-Goutières syndrome type 5 in a challenging pediatric neurology case. Cold Spring Harbor molecular case studies 2018 10 4 (5): . Haskell Gloria T, Mori Mari, Powell Cynthia, Amrhein Timothy J, Rice Gillian I, Bailey Lauren, Strande Natasha, Weck Karen E, Evans James P, Berg Jonathan S, Kishnani Pri |
Pharmacogenetic variation influences sensory neuropathy occurrence in Southern Africans treated with stavudine-containing antiretroviral therapy. PloS one 2018 13 (10): e0204111. Moketla Marvin Blessings, Wadley Antonia L, Kamerman Peter, de Assis Rosa Deb |
Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review. Journal of clinical medicine 2019 5 8 (5): . Garau Jessica, Cavallera Vanessa, Valente Marialuisa, Tonduti Davide, Sproviero Daisy, Zucca Susanna, Battaglia Domenica, Battini Roberta, Bertini Enrico, Cappanera Silvia, Chiapparini Luisa, Crasà Camilla, Crichiutti Giovanni, Dalla Giustina Elvio, D'Arrigo Stefano, De Giorgis Valentina, De Simone Micaela, Galli Jessica, La Piana Roberta, Messana Tullio, Moroni Isabella, Nardocci Nardo, Panteghini Celeste, Parazzini Cecilia, Pichiecchio Anna, Pini Antonella, Ricci Federica, Saletti Veronica, Salvatici Elisabetta, Santorelli Filippo M, Sartori Stefano, Tinelli Francesca, Uggetti Carla, Veneselli Edvige, Zorzi Giovanna, Garavaglia Barbara, Fazzi Elisa, Orcesi Simona, Cereda Cristi |
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 |
The SAMHD1 rs6029941 (A/G) Polymorphism Seems to Influence the HTLV-1 Proviral Load and IFN-Alpha Levels. Frontiers in cellular and infection microbiology 2020 7 10 246. Queiroz Maria Alice Freitas, Amoras Ednelza da Silva Graça, Moura Tuane Carolina Ferreira, da Costa Carlos Araújo, de Sousa Maisa Silva, Lima Sandra Souza, Ishak Ricardo, Vallinoto Antonio Carlos Rosár |
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 |
Targeted copy number variant identification across the neurodegenerative disease spectrum. Molecular genetics & genomic medicine 2022 Jun e1986. Dilliott Allison A, Zhang Kristina K, Wang Jian, Abrahao Agessandro, Binns Malcolm A, Black Sandra E, Borrie Michael, Dowlatshahi Dar, Finger Elizabeth, Fischer Corinne E, Frank Andrew, Freedman Morris, Grimes David, Hassan Ayman, Jog Mandar, Kumar Sanjeev, Lang Anthony E, Mandzia Jennifer, Masellis Mario, Pasternak Stephen H, Pollock Bruce G, Rajji Tarek K, Rogaeva Ekaterina, Sahlas Demetrios J, Saposnik Gustavo, Sato Christine, Seitz Dallas, Shoesmith Christen, Steeves Thomas D L, Swartz Richard H, Tan Brian, Tang-Wai David F, Tartaglia Maria C, Turnbull John, Zinman Lorne, , Hegele Robert |
Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number.
HGG advances 2022 10 4 (1): 100147. Pillalamarri Vamsee, Shi Wen, Say Conrad, Yang Stephanie, Lane John, Guallar Eliseo, Pankratz Nathan, Arking Dan |
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 2022 10 12 (10): . Tesolin Paola, Bertinetto Francesca Eleonora, Sonaglia Arianna, Cappellani Stefania, Concas Maria Pina, Morgan Anna, Ferrero Norma Maria, Zabotti Alen, Gasparini Paolo, Amoroso Antonio, Quartuccio Luca, Girotto Giorg |
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 |
SAMHD1 Single Nucleotide Polymorphisms Impact Outcome in Children with Newly Diagnosed Acute Myeloid Leukemia. Blood advances 2023 1 . Marrero Richard James, Cao Xueyuan, Wu Huiyun, Elsayed Abdelrahman H, Klco Jeffery M, Ribeiro Raul C, Rubnitz Jeffrey E, Ma Xiaotu, Meshinchi Soheil, Aplenc Richard, Kolb E Anders, Ries Rhonda E, Alonzo Todd, Pounds Stanley B, Lamba Jatinder Ka |
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- Page last updated:Apr 22, 2024
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