Kaposi Sarcoma
What's New
Last Posted: Apr 20, 2024
- Molecular Features of HHV8 Monoclonal Microlymphoma Associated with Kaposi Sarcoma and Multicentric Castleman Disease in an HIV-Negative Patient.
Evelina Rogges, et al. International journal of molecular sciences 2024 0 (7) - Role of the Killer Immunoglobulin-like Receptor and Human Leukocyte Antigen I Complex Polymorphisms in Kaposi Sarcoma-Associated Herpesvirus Infection.
Xin Zhang, et al. Open forum infectious diseases 2023 0 (8) ofad435 - Anaplastic Kaposi Sarcoma: A Clinicopathologic and Molecular Genetic Analysis.
Grant M Fischer, et al. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2023 0 100191 - No Association of IFNL4 Genotype With Opportunistic Infections and Cancers Among Men With Human Immunodeficiency Virus 1 Infection.
Fang Michelle Z, et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2022 0 (3) 521-527 - Inhibitory KIR2DL2 receptor and HHV-8 in classic or endemic Kaposi sarcoma.
Bortolotti Daria, et al. Clinical and experimental medicine 2022 0 - Genetic landscape of indolent and aggressive Kaposi sarcomas.
Malouf Gabriel G, et al. Journal of the European Academy of Dermatology and Venereology : JEADV 2022 7 - Environmental risk factors and genetic markers of Kaposi's sarcoma-associated herpesvirus infection among Uygur population in Xinjiang, China.
Zhang Xin, et al. Journal of medical virology 2022 1 - Telomerase promoter mutations in human immunodeficiency virus-related conjunctiva neoplasia.
Starita Noemy, et al. Journal of translational medicine 2018 3 (1) 77 - Association of genetic variations in miR-146a rs2910164 and miR-149 rs11614913 with the development of classic Kaposi sarcoma.
Yang H, et al. Genetics and molecular research : GMR 2016 11 (4) - Risk of Classic Kaposi Sarcoma With Combinations of Killer Immunoglobulin-Like Receptor and Human Leukocyte Antigen Loci: A Population-Based Case-control Study.
Goedert J J, et al. The Journal of infectious diseases 2015 8
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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:Apr 29, 2024
- Content source: