Last Posted: Oct 05, 2021
- The application of radiomics in laryngeal cancer.
Rajgor Amarkumar Dhirajlal et al. The British journal of radiology 2021 20210499
- DIAPH2, PTPRD and HIC1 Gene Polymorphisms and Laryngeal Cancer Risk.
?nit Miros?aw, et al. International journal of environmental research and public health 2021 7 (14)
- Survival of Laryngeal Cancer Patients Depending on Zinc Serum Level and Oxidative Stress Genotypes.
Lubiński Jakub, et al. Biomolecules 2021 6 (6)
- Full-coverage TP53 deep sequencing of recurrent head and neck squamous cell carcinoma facilitates prognostic assessment after recurrence.
Kobayashi Kenya, et al. Oral oncology 2020 11 105091
- Prognostic Significance of Oxidation Pathway Mutations in Recurrent Laryngeal Squamous Cell Carcinoma.
Heft Neal Molly E, et al. Cancers 2020 10 (11)
- Genotype of Null Polymorphisms in Genes GSTM1, GSTT1, CYP1A1, and CYP1A1*2A (rs4646903 T>C)/CYP1A1*2C (rs1048943 A>G) in Patients with Larynx Cancer in Southeast Spain.
Sánchez-Siles Mariano, et al. Cancers 2020 9 (9)
- An autophagy-related model of 4 key genes for predicting prognosis of patients with laryngeal cancer.
Luo Meng-Si et al. Medicine 2020 Jul 99(30) e21163
- A six-gene expression signature related to angiolymphatic invasion is associated with poor survival in laryngeal squamous cell carcinoma.
Metzger Karl et al. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2020 Jul
- Transforming growth factor-ß1 gene polymorphism as a potential risk factor in Turkish patients with laryngeal squamous cell carcinoma.
Abakay Candan Demiröz, et al. Journal of cancer research and therapeutics 0 0 (1) 144-149
- Genetic polymorphisms as non-modifiable susceptibility factors to laryngeal cancer.
Escalante Paula, et al. Bioscience reports 2020 4
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
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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.