Human T-cell Leukemia Virus Type 3
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Last Posted: Mar 07, 2023
- [Genetic analysis and its clinical implication in adult T-cell leukemia/lymphoma].
Kogure Yasunori, et al. [Rinsho ketsueki] The Japanese journal of clinical hematology 2018 0 (10) 2127-2135 - Mutational Intratumor Heterogeneity is a Complex and Early Event in the Development of Adult T-cell Leukemia/Lymphoma.
Farmanbar Amir, et al. Neoplasia (New York, N.Y.) 2018 0 (9) 883-893 - Association of the rs4143815 polymorphism of PDL1 gene with HTLV-1 infection and proviral load in asymptomatic blood donors in northeast Iran.
Hezave Yalda Amiri, et al. Microbiology and immunology 2022 0 (6) 324-329 - Genetic Alterations in Adult T-Cell Leukemia/Lymphoma: Novel Discoveries with Clinical and Biological Significance.
Sakihama Shugo, et al. Cancers 2022 0 (10) - The association of polymorphisms (rs2227981 and rs10204525) of PDCD1 gene with susceptibility to human T-cell leukemia virus type 1.
Hezave Yalda Amiri, et al. Microbial pathogenesis 2021 6 105049 - Possible mechanisms underlying the association between human T-cell leukemia virus type 1 (HTLV-1) and hypertension in elderly Japanese population.
Shimizu Yuji, et al. Environmental health and preventive medicine 2021 1 (1) 17 - Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma.
Kataoka Keisuke, et al. Blood 2017 10 - Human T-cell leukemia virus type I Tax genotype analysis in Okinawa, the southernmost and remotest islands of Japan: Different distributions compared with mainland Japan and the potential value for the prognosis of aggressive adult T-cell leukemia/lymphoma.
Sakihama Shugo, et al. Leukemia research 2017 8 18-24 - Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load.
Sanabani SS, et al. BMC infectious diseases 2012 12 (1) 1 - In contrast to HIV, KIR3DS1 does not influence outcome in HTLV-1 retroviral infection.
O'Connor Geraldine M, et al. Human immunology 2012 8 (8) 783-7
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 08, 2024
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