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Research 181–210 of 1000+
- Pili trianguli et canaliculi as a phenotypic subtype in patients with central centrifugal cicatricial alopecia: A scanning electron microscopy study
- Aging, alopecia, and stem cells
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Keratin Gene Expression Differences in Wool Follicles and Sequence Diversity of High Glycine-Tyrosine Keratin-Associated Proteins (Kaps) in Magra Sheep of India
- Woodhouse-Sakati syndrome (WSS)
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Forensic DNA Phenotyping
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Recent advances in treatment for Benign Prostatic Hyperplasia
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Identification of the cell lineage at the origin of basal cell carcinoma
- Biochemical and trichological characterization of diffuse alopecia in women
- The riddle of genuine skin microrelief and wrinkles
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Female pattern hair loss
- High‐Sulfur Protein Gene Expression in a Transgenic Mouse
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)
- Hormonal and Surgical Treatment Options for Transgender Women and Transfeminine Spectrum Persons
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- P-12 ACTH-INDEPENDENT CUSHING SYNDROME WITH INCONCLUSIVE ADRENAL CT SCAN RESULTS
- Lupus erythematosus: systemic and cutaneous manifestations
- SEXUAL DIMORPHISM IN MAMMALS
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis