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Research 271–300 of 303
- The Dickkopf Protein Family in Non-Neoplastic Disorders: Emerging Roles and Therapeutic Targeting
- Cannabidiol in Skin Health: A Comprehensive Review of Topical Applications in Dermatology and Cosmetic Science
- Exosome as a Therapeutic Agent in Cosmetic Dermatology
- Polydeoxyribonucleotide in Skincare and Cosmetics: Mechanisms, Therapeutic Applications, and Advancements Beyond Wound Healing and Anti-aging
- Vasoactive Intestinal Peptide Operates as a Negative Regulator of Human Hair Follicle Pigmentation Ex Vivo
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- The mechanical forces that shape our senses
- Engineering a New Mouse Model for Vitiligo
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Making the head: Caspases in life and death
- Use of chemotherapy during human pregnancy
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Congenital atrichia and hypotrichosis
- An Open-Label Comparative Study on the Effects of Platelet-Rich Plasma Therapy with Hydroquinone 4% Versus Hydroquinone 4% Alone in Melasma
- Evaluation of biophysical skin parameters and assessment of hair growth in patients with acne treated with isotretinoin
- Developmental Toxicity of Levo-Alpha-Acetylmethadol (LAAM) in Tolerant Rats
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- TONGUE, RED
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Bone morphogenetic protein (BMP) signaling controls hair pigmentation by means of cross-talk with the melanocortin receptor-1 pathway
- Tyrosine kinase inhibition and grey hair
- Sox2 in the dermal papilla regulates hair follicle pigmentation
- Pigmentary mosaicism: An update