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Research 391–420 of 866
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- 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
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Genetics of Inherited Ichthyoses and Related Diseases
- 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
- 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
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Clinical biochemistry of dihydrotestosterone
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Genetic Hair Disorders: A Review
- Skin Development and Disease: A Molecular Perspective
- Converging physiological roles of the anthrax toxin receptors