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Research 571–600 of 1000+
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Chemoprevention – History and general principles
- Advances in single-cell transcriptomics in animal research
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- Evaluation of noninvasive biospecimens for transcriptome studies
- The Wound Healing: A Mystery Still to Be Solved—What Is the Future?
- Human Epidermal Transglutaminase
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Alopecia: Association with Resistance to Thyroid Hormones
- Palatogenesis and cutaneous repair: A two‐headed coin
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Hair Follicle Pigmentation
- Structure of human type II 5 alpha-reductase gene.
- Androgenetic alopecia: An update
- Effects of autologous platelet‑rich plasma injections on facial skin rejuvenation
- Complex Changes in the Apoptotic and Cell Differentiation Programs during Initiation of the Hair Follicle Response to Chemotherapy
- Linking allergy to mercury to HLA and burning mouth syndrome
- Personalized Medicine in the Field of Inflammatory Skin Disorders
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- A Comprehensive Review of Current Anti-Aging Mechanisms and Therapeutic Approaches
- Evolution of long scalp hair in humans
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Psoriasis del cuero cabelludo etiología, diagnóstico y tratamiento
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Identification of the cell lineage at the origin of basal cell carcinoma
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration