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Research 691–720 of 1000+
- Adenosine and Its Receptors in the Pathogenesis and Treatment of Inflammatory Skin Diseases
- Calcineurin/Nfatc1 signaling links skin stem cell quiescence to hormonal signaling during pregnancy and lactation
- Biology and Genetics of Hair
- Morphological Approach to Hair Disorders
- Acne in Dark Skin
- Racial and Gender Influences on Skin Disease
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- An overview of zinc and its importance in dermatology-Part II: The association of zinc with some dermatologic disorders
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- Expression patterns of the glial cell line–derived neurotrophic factor, neurturin, their cognate receptors GFRα-1, GFRα-2, and a common signal transduction element c-Ret in the human skin hair follicles
- Sex hormones and acne
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Aging of the hair follicle pigmentation system
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Current Genetics in Hair Diseases
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- Probiotics in Dermatology: An Evidence-based Approach
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Cutaneous Neuroimmune Interactions in Peripheral Neuropathic Pain States
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair