Last Posted: Jan 22, 2020
- Assessment of HLA-A, HLA-DR, and HLA-DQ alleles in patients with pemphigus vulgaris from eastern of Turkey.
Dere Gokturk, et al. Journal of cosmetic dermatology 2020 1
- Correlation between polymorphisms of the NR3C1 gene and glucocorticoid effectiveness in patients with pemphigus vulgaris.
Fang Si-Yue, et al. Scientific reports 2017 0 (1) 11890
- Association of NFKB1 -94ATTG ins/del polymorphism (rs28362491) with pemphigus vulgaris.
Chatzikyriakidou Anthoula, et al. Experimental dermatology 2019 5
- Proinflammatory Cytokine Gene Polymorphisms in Bullous Pemphigoid.
Tabatabaei-Panah Pardis-Sadat, et al. Frontiers in immunology 2019 0 636
- High-resolution melting analysis to screen the ST18 gene functional risk variant for pemphigus vulgaris: The occasion to open a debate on its usefulness in clinical setting.
De Bonis Maria, et al. Experimental and molecular pathology 2019 3 57-63
- Region 1p13.2 including the RSBN1, PTPN22, AP4B1 and long non-coding RNA genes does not bear risk factors for endemic pemphigus foliaceus (fogo selvagem).
Lobo-Alves Sara Cristina, et al. International journal of immunogenetics 2019 3
- Subtype-specific inherited predisposition to pemphigus in the Chinese population.
Zhang S, et al. The British journal of dermatology 2018 9
- Investigation of the predisposing factor of pemphigus and its clinical subtype through a genome-wide association and next generation sequence analysis.
Sun Yonghu, et al. Journal of the European Academy of Dermatology and Venereology : JEADV 2018 8
- The p.Arg435His Variation of IgG3 With High Affinity to FcRn Is Associated With Susceptibility for Pemphigus Vulgaris-Analysis of Four Different Ethnic Cohorts.
Recke Andreas, et al. Frontiers in immunology 2018 0 1788
- Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population.
Gao Jinping, et al. The Journal of investigative dermatology 2018 5
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.