research Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features
A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.
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research First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.
research P22-023-23 Pilot Study Protocol on Application of Non-Invasive Vitamin D Hair Test and Screening E-Tool for Indigenous Populations in the Great Northern Plains
research In Vivo Follicular Unit Multiplication: Is It Possible to Harvest an Unlimited Donor Supply?
It's not possible to get unlimited hair for transplants from the same donor area.
research 575 INTASYL self-delivering RNAi: A flexible platform to treat dermatological malignancies
INTASYL is a promising, adaptable RNAi technology for treating skin cancers.
research VAGINAL KERATINIZATION IN VITRO*
research Computer aided classification of female androgenetic alopecia-an image processing and analysis system
research Report on the Toronto Meeting
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research The Skin
research Throwing Caution to the Wind?
The document's conclusion cannot be summarized because the content is not available.
research Arthritic Lifestyles
research Response of the Skin of Mice to Methyl Ether of Vitamin A and Vitamin A Palmitate1
research NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.
research Plastic Needle Shield: A Two-in-One Solution
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research Hear from the Assistants
research Heterogeneity of ornithine decarboxylase expression in 12-O-tetradecanoylphorbol-13-acetate-treated mouse skin and in epidermal tumors
ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.
research Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.
research Notes From the Floor: A Report of the Nashville Meeting
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research Abhrs Recognition
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research The Third Annual ASHRS Conference – Rancho Mirage, California
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research Hard Keratin IF and Associated Proteins
research 710 BIOMARKERS OF SUNITNIB CLINICAL RESPONSE IN METASTATIC RENAL CLEAR CELL CARCINOMA PATIENTS
research Poster Exhibits
research Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
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research 17beta Hydroxysteroid Dehydrogenase Type 3 Inhibitors
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research Cloning and Characterization of a Mouse Type I Hair Keratin cDNA
research THE GRAYING OF HAIR
research Scalp Reduction: Mirror, Mirror on the Wall
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research Co-editors' Messages
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research Insight into the pathogensis of polycystic ovarian syndrome
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