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Research 331–360 of 1000+
- Dermatological complications due to post‑COVID‑19 syndrome: A systematic review
- GRowing an Epidermal Tumor
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Regenerative Potential of Adipose Tissue–Derived Exosomes in Treating Hair Shaft Abnormalities: A Case Report
- TONGUE, RED
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Cases Report the Cronkhite-Canada Syndrome
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- WNT Signaling in Disease
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Animal and in vitro Models for the Study of Hair Follicles
- The developmental basis of fingerprint pattern formation and variation
- Keratins: the hair shaft's backbone revealed
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Nutritional Disorders of the Hair and Their Management
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Trichothiodystrophy: Current Concepts
- Diphenylcyclopropenone-Induced Vitiligo in a Patient with Alopecia Universalis
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves