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Research 211–240 of 1000+
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Evaluating the Role of Thyroid Stimulating Hormone and Ferritin Levels with Hair Loss among Patients with COVID-19: Case-Control Study
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Alopecia por diluição da cor em uma cadela Staffordshire Bull Terrier azul: Relato de caso
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hair Loss in Children
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- Fondation René Touraine
- Modelling androgen synthesis and action during human sexual differentiation
- Australasian Society for Dermatology Research Meeting, May 2007
- BH07: Testosterone deficiency in men with female pattern hair loss
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Structural changes in hair follicles and sebaceous glands of hairless mice following exposure to sulfur mustard
- Small extracellular vesicles from menstrual blood-derived mesenchymal stem cells (MenSCs) as a novel therapeutic impetus in regenerative medicine
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Keratins: the hair shaft's backbone revealed
- Cellular senescence in skin‐related research: Targeted signaling pathways and naturally occurring therapeutic agents
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Trichodysplasia of immunosuppression treated with oral valganciclovir
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair shaft disorders in children – An update
- Sox9 expression in canine epithelial skin tumors
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease