Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: THPO[original query] |
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Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes. Journal of medical genetics 2004 May 41 (5): 334-41. McCarthy J J, Parker A, Salem R, Moliterno D J, Wang Q, Plow E F, Rao S, Shen G, Rogers W J, Newby L K, Cannata R, Glatt K, Topol E J, |
Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias. International journal of hematology 2015 Jul 102 (1): 140-3. Houwing Maite E, Koopman-Coenen Eva A, Kersseboom Rogier, Gooskens Saskia, Appel Inge M, Arentsen-Peters Susan T C J M, de Vries Andrica C H, Reinhardt Dirk, Stary Jan, Baruchel André, de Haas Valerie, Blink Marjolein, Lopes Cardozo Rob H, Pieters Rob, Michel Zwaan C, van den Heuvel-Eibrink Marry |
Association of BAK1 single nucleotide polymorphism with a risk for dengue hemorrhagic fever. BMC medical genetics 2016 17 (1): 43. Dang Tran Ngoc, Naka Izumi, Sa-Ngasang Areerat, Anantapreecha Surapee, Wichukchinda Nuanjun, Sawanpanyalert Pathom, Patarapotikul Jintana, Tsuchiya Naoyuki, Ohashi J |
Molecular Profiling for Predictors of Radiosensitivity in Patients with Breast or Head-and-Neck Cancer. Cancers 2020 4 12 (3): . Drobin Kimi, Marczyk Michal, Halle Martin, Danielsson Daniel, Papiez Anna, Sangsuwan Traimate, Bendes Annika, Hong Mun-Gwan, Qundos Ulrika, Harms-Ringdahl Mats, Wersäll Peter, Polanska Joanna, Schwenk Jochen M, Haghdoost Siam |
Multiplex Protein Biomarker Profiling in Patients with Familial Hypercholesterolemia. Genes 2021 10 12 (10): . Dlouha Dana, Blaha Milan, Rohlova Eva, Hubacek Jaroslav A, Lanska Vera, Visek Jakub, Blaha Vladim |
Novel THPO variant in hereditary thrombocytopenia: A potential candidate variant for predisposition to myeloid neoplasm. PloS one 2022 12 17 (12): e0271624. Kwon Seok Ryun, Kim Man Jin, Lee Young-Eun, Yun Jiwon, Jeong Da-Jeong, Park Jae Hyeon, Kwon Sunghoon, Lee Dong So |
Genomic Variation Affecting MPV and PLT Count in Association with Development of Ischemic Stroke and Its Subtypes. Molecular neurobiology 2023 7 . Abhilash Ludhiadch, Sulena, Sandeep Singh, Sudip Chakraborty, Dixit Sharma, Mahesh Kulharia, Paramdeep Singh, Anjana Muns |
Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia. Hematology (Amsterdam, Netherlands) 2023 3 28 (1): 2187155. Hantaweepant Chattree, Suktitipat Bhoom, Pithukpakorn Manop, Chinthammitr Yingyong, Limwongse Chanin, Tansiri Nawaporn, Sawatnatee Surasak, Takpradit Chayamon, Rotchanapanya Wannaphorn, Pongudom Saranya, Charoenprasert Kanyaporn, Paiboonsukwong Kittiphong, Thamprasert Wichuda, Nolwachai Narumol, Rattanasawat Wanlapa, Sae-Aeng Busakorn, Khorwanichakij Nisachon, Saetow Putchong, Saengboon Supawee, Kamjornpreecha Krittichat, Pholmoo Wikanda, Dujjawan Boonyanuch, Siritanaratkul Noppad |
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- Page last updated:Mar 25, 2024
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