Silicosis
What's New
Last Posted: Jan 18, 2025
- Novel functional eQTL-SNPs associated with susceptibility to occupational pulmonary fibrosis: A multi-stage study.
Rui Zhao, et al. Ecotoxicology and environmental safety 2025 0 117679 - Candidate gene polymorphisms associated with silicosis and coal workers' pneumoconiosis: a systematic review and meta-analysis.
Yingying Zhang, et al. BMC pulmonary medicine 2024 0 (1) 580 - Multi-omics and multi-stages integration identified a novel variant associated with silicosis risk.
Chunmeng Jin, et al. Archives of toxicology 2024 0 - Telomerase gene variants and telomere shortening in patients with silicosis or asbestosis.
Fan Yali, et al. Occupational and environmental medicine 2020 0 - Genetic damage in coal and uranium miners.
da Silva Flavio Manoel Rodrigues, et al. Mutation research. Genetic toxicology and environmental mutagenesis 2021 0 503348 - Genetic polymorphisms and their effects on the severity of silicosis in workers exposed to silica in Brazil.
Castro Marcos César Santos de, et al. Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia 2022 0 (5) e20220167 - Genetic susceptibility in pneumoconiosis in China: a systematic review.
Chair Sek Ying, et al. International archives of occupational and environmental health 2022 0 (1) 45-56 - The single nucleotide polymorphism rs1814521 in long non-coding RNA ADGRG3 associates with the susceptibility to silicosis: a multi-stage study.
Wang Wei, et al. Environmental health and preventive medicine 2022 0 (0) 5 - Functional variant of the carboxypeptidase M (CPM) gene may affect silica-related pneumoconiosis susceptibility by its expression: a multistage case-control study.
Chu Minjie, et al. Occupational and environmental medicine 2019 0 (3) 169-174 - TP53 p.R72P genotype is a marker of poor prognosis in lung cancer.
Neumann Mirko Peter, et al. Cancer biomarkers : section A of Disease markers 2017 0 (4) 747-754
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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 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
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