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Research 571–600 of 1000+
- Sex Hormones and Related Compounds, Including Hormonal Contraceptives
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Animals in Dermatology
- Patient Satisfaction and Quality of Life Among Adult Women with Androgenetic Alopecia Using 5% Topical Minoxidil.
- Parsing patterns: Emerging roles of tissue self-organization in health and disease
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Squamous epithelial proliferation induced by walleye dermal sarcoma retrovirus cyclin in transgenic mice
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Alopecia Universalis Associated with Ulcerative Colitis and The Role of Azathioprine
- Resolution of advanced conjunctival squamous cell carcinoma with cemiplimab immunotherapy, IFNα-2b, and retinoic acid treatment over 2 years of follow-up
- The anatomical distribution of lentiginous melanoma (lentigo maligna and lentigo maligna melanoma): Differences according to sex
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Value of dermoscopy for the diagnosis of monilethrix
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Diagnostic Signs and Symptoms of Cyanocobalamin Deficiency at Rural Setting in India: Novel Method of Supplementation
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Ptosis in childhood
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Sox9 expression in canine epithelial skin tumors