Last Posted: Feb 21, 2023
- High Frequency of Cryptosporidium hominis Infecting Infants Points to A Potential Anthroponotic Transmission in Maputo, Mozambique.
Cossa-Moiane Idalécia, et al. Pathogens (Basel, Switzerland) 2021 0 (3)
- An evaluation of molecular diagnostic tools for the detection and differentiation of human-pathogenic Cryptosporidium spp.
Jiang Jianlin, et al. The Journal of eukaryotic microbiology 2004 0 542-7
- Toll-Like Receptors and Mannose Binding Lectin Gene Polymorphisms Associated with Cryptosporidial Diarrhea in Children in Southern India.
Liakath Farzana Begum, et al. The American journal of tropical medicine and hygiene 2021 9
- Autophagy - related 16 - like 1 single nucleotide gene polymorphism increases the risk and severity of Cryptosporidium parvum infection.
El-Refai Samar A, et al. Molecular and biochemical parasitology 2021 8 111407
- Genome-Wide Association Study of Cryptosporidiosis in Infants Implicates PRKCA.
Wojcik Genevieve L, et al. mBio 2020 2 (1)
- Genetic diversity of Cryptosporidium identified in clinical samples from cities in Brazil and Argentina.
Peralta Regina Helena Saramago, et al. Memo?rias do Instituto Oswaldo Cruz 2016 1 (1) 30-6
- Molecular seasonal, age and gender distributions of Cryptosporidium in diarrhoeic Egyptians: distinct endemicity.
El-Badry A A, et al. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 2015 10
- A review of the global burden, novel diagnostics, therapeutics, and vaccine targets for cryptosporidium.
Checkley William et al. Lancet Infect Dis 2015 Jan (1) 85-94
- Comparative genomic analysis reveals occurrence of genetic recombination in virulent Cryptosporidium hominis subtypes and telomeric gene duplications in Cryptosporidium parvum.
Guo Yaqiong et al. BMC Genomics 2015 320
- Cryptosporidium infections: molecular advances.
Lendner Matthias et al. Parasitology 2014 Sep (11) 1511-32
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
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- 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:Jun 02, 2023
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