Anthrax
What's New
Last Posted: Mar 01, 2023
- Retrospective Analysis of the Relationship between Two Anthrax Outbreaks in Kazakhstan Based on Genomic Data.
Shevtsov Alexandr, et al. Microbiology resource announcements 2020 0 (50) - Public Discussion of Anthrax on Twitter: Using Machine Learning to Identify Relevant Topics and Events.
Miller Michele et al. JMIR public health and surveillance 2021 7(6) e27976 - Protective effect of anthrax toxin receptor 2 polymorphism rs4333130 against the risk of ankylosing spondylitis.
Xu Haitao, et al. Medicine 2020 7 (28) e19942 - As D.I.Y. Gene Editing Gains Popularity, 'Someone Is Going to Get Hurt'
E Baumgaertner, NY Times, May 14, 2018 - A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.
Vathipadiekal Vinod, et al. American journal of hematology 2016 8 - Gene control of tyrosine kinase TIE2 and vascular manifestations of infections.
Ghosh Chandra C, et al. Proceedings of the National Academy of Sciences of the United States of America 2016 2 - CDC Anthrax Information
- A complex role of anthrax toxin receptor 2 polymorphisms and capillary morphogenesis protein 2 in ankylosing spondylitis pathogenesis.
Zhang Zhijian, et al. Clinical rheumatology 2016 1 - Determination of IL1 R2, ANTXR2, CARD9, and SNAPC4 single nucleotide polymorphisms in Iranian patients with ankylosing spondylitis.
Momenzadeh Parisa, et al. Rheumatology international 2015 11 - Anthrax toxin receptor 2 gene (ANTXR2) rs4333130 is associated with ankylosing spondylitis.
Ou Yanjuan, et al. International journal of clinical and experimental medicine 2015 0 (5) 7679-83
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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 the CDC Office of Public Health Genomics 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, 2023
- Page last updated:Mar 22, 2023
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