Last Posted: May 26, 2021
- Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans.
Schwarm Christian, et al. Orphanet journal of rare diseases 2021 5 (1) 228
- COL17A1 gene polymorphisms are frequent in bullous pemphigoid.
Tabatabaei-Panah P-S, et al. Journal of the European Academy of Dermatology and Venereology : JEADV 2021 4
- Dipeptidyl peptidase-4 inhibitor-related bullous pemphigoid: A comparative study of 100 patients with bullous pemphigoid and diabetes mellitus.
Chanprapaph Kumutnart, et al. The Journal of dermatology 2021 2
- TH17/IL23 cytokine gene polymorphisms in bullous pemphigoid.
Tabatabaei-Panah Pardis-Sadat, et al. Molecular genetics & genomic medicine 2020 12 e1519
- Association between TH2 Cytokine Gene Polymorphisms and Risk of Bullous Pemphigoid.
Tabatabaei-Panah Pardis-Sadat, et al. Immunological investigations 2020 10 1-13
- Proinflammatory Cytokine Gene Polymorphisms in Bullous Pemphigoid.
Tabatabaei-Panah Pardis-Sadat, et al. Frontiers in immunology 2019 0 636
- Biological predictors shared by dementia and bullous pemphigoid patients point out a cross-antigenicity between BP180/BP230 brain and skin isoforms.
Julio Tamiris A, et al. Immunologic research 2018 9
- 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
- TNF-a -308G/A gene polymorphism in bullous pemphigoid and alopecia areata.
Moravvej Hamideh, et al. Human antibodies 2018 5
- HLA-C*17, DQB1*03:01, DQA1*01:03 and DQA1*05:05 Alleles Associated to Bullous Pemphigoid in Brazilian Population.
Chagury Azis Arruda, et al. Annals of dermatology 2018 2 (1) 8-12
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.