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Research 91–120 of 1000+
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Factors associated with early-onset androgenetic alopecia: A scoping review
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Clinical Snippets
- Australasian Society for Dermatology Research Meeting, May 2006
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Emerging nonmetabolic functions of skin fat
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Generalized atrophic benign epidermolysis bullosa.
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Le gène<i>hairless</i>de la souris
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Hairless: A nuclear receptor corepressor essential for skin function
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Sex differences in COVID-19: the role of androgens in disease severity and progression
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- The Challenging Consultation: Management of Melanoma
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Marie-unna hereditary hypotrichosis
- Clinical report of a Holstein's calf with ichthyosis.