research Medical and Professional Ethics
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research MAGİSTRAL AVTOMOBİL YOLLARI. TARIXİ, TORPAQ SAHƏSİ, MÜASİR VƏZİYYƏTİ, PROBLEMLƏRİ
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research INTELIGÊNCIA EMOCIONAL E EMPREENDEDORISMO FEMININO
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research Notes from the Editor Emeritus, 1999–2001: The Buyer’s Remorse Dilemma
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research [Comments on the paper: “Studies on the etiology of androgenetic alopecia in the female” by E. Vadász and M. Debreczeni (Hautarzt 18, 454-456, 1967)].
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research Prevalensi Dermatitis Seboroik Di Poli Kulit Dan Kelamin Rsud Meuraxa Kota Banda Aceh Periode Tahun 2016-2019
Seborrheic dermatitis was most common in late adults and toddlers from 2016 to 2019.
research Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.
research Co-Editors' Messages
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research International Journal of Aesthetic and Restorative Surgery
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research Homeostasis of the sebaceous gland and mechanisms of acne pathogenesis
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research Get the essential small equipment you need fast!
Buy the basic tools you need quickly.
research Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
Defective protein folding due to a mutation is key in ANE syndrome.
research Med Check
Horizant has risks like other seizure drugs, Johnson & Johnson misled about Risperdal, and Quanterix found a possible link between brain oxygen loss and Alzheimer's markers.
research Issue Information
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research 41949 Raman spectroscopy of alopecia drugs to assess their potential for laser-assisted drug delivery
Raman spectroscopy is promising for measuring and enhancing drug delivery in alopecia treatments.
research Errata
The document corrects errors in previous articles, including a reversed term, updated subject weights, hair count data, and reference numbering.
research Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.
research Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
A new genetic mutation was found causing hair and eye issues in a boy.
research Fermented rice bran extract delays skin aging by increasing the synthesis of collagen and elastin
Fermented rice bran extract helps delay skin aging by boosting collagen and elastin.
research 11 Ways to Completely Ruin Your cheap college football jerseys design online
research Use of rotary echoes in 2 H
A new method accurately measures molecular movement without complex modeling.
research 42736 Safety Assessments in the Multinational Phase 3 THRIVE-AA1 Trial with CTP-543 (Deuruxolitinib) in Adult Patients with Moderate to Severe Alopecia Areata
research Risk of age-related macular degeneration in men receiving 5α-reductase inhibitors: a population-based cohort study
Men taking dutasteride may have a higher risk of age-related macular degeneration.
research Guided Superficial Enhanced Fluid Fat Injection (SEFFI) Procedures for Facial Rejuvenation: An Italian Multicenter Retrospective Case Reports
SEFFI is a safe and effective anti-aging treatment with few complications.
research Faculty Opinions recommendation of Identification of drug-specific public TCR driving severe cutaneous adverse reactions.
Researchers found a specific T cell receptor linked to severe drug reactions like Stevens-Johnson syndrome when patients take carbamazepine.
research Potentiometric determination of minoxidil in topical use pharmaceutical samples
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research ISID0652 – Efficacy comparison of photobiomodulation devices in the treatment of androgenetic alopecia
research Self-Assembled Berberine-Sinapic Acid Nanomedicine for Synergistic Chemotherapy
BBR-SA nanomedicine is a safe and effective treatment for breast cancer.
research Hair restoration
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research A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.