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Research 301–330 of 1000+
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- Trichoscopy for common hair loss diseases: Algorithmic method for diagnosis
- Molecular pathology of skin adnexal tumours
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Treatment of Alopecia in Children
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Diffuse Hair Loss
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- An Approach to Detect Alopecia Areata Hair Disease Using Deep Learning
- Expert consensus on the management of telogen effluvium in India
- Scarring Alopecia in Pediatric Patients: A Narrative Review of Etiologies, Diagnosis, and Management Strategies
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Telogen Effluvium
- Keratins: the hair shaft's backbone revealed
- Alopecia in Belgian Blue crossbred calves: a case series
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The Requirement to Monitor Low-dose Oral Minoxidil in the Management of Hair Loss
- Effect of Oral Minoxidil on Monilethrix
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- Molecular Genetics of Human Hair Diseases
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Drug-Induced Hair Changes
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.