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Research 361–390 of 806
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Myotonic Dystrophy—A Progeroid Disease?
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Analogs of human genetic skin disease in domesticated animals
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
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- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Congenital Adrenal Hyperplasia
- Decision letter: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Genetics of Inherited Ichthyoses and Related Diseases
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- WNT Signaling in Disease
- Regulatory T Cells: the Many Faces of Foxp3
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer