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Research 31–60 of 1000+
- Androgens Affect the Activity of Human Sebocytes in Culture in a Manner Dependent on the Localization of the Sebaceous Glands and Their Effect Is Antagonized by Spironolactone
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Peer Review #1 of "Secreted Frizzled-related protein 4 inhibits the regeneration of hair follicles (v0.1)"
- 18β‐Glycyrrhetinic acid: its core biological properties and dermatological applications
- Clouston’s Syndrome-A Case Report
- The role of PPAR<i>γ</i>-mediated signalling in skin biology and pathology: new targets and opportunities for clinical dermatology
- Developmental signals in skin morphogenesis
- The Antiandrogenic Action of 4–Androsten–3–one–17β– Carboxylic Acid and Its Methyl Ester on Hamster Flank Organ1
- Activation of temperature-sensitive Ca2+-permeable TRPV3 channels by natural ï¡-hydroxyl acids causes exfoliation for skin-resurfacing
- Epidermolysis Bullosa
- Buschke-Ollendorff syndrome
- Ichthyosis
- Cutaneous Manifestations of Mucopolysaccharidoses
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- プログラミング開発環境の変化と対策 (プログラム作りの環境 ) -- (実例:各社はこんな環境で生産性向上を図っている)
- Vitiligo
- Canine Zinc-Responsive Dermatosis
- Clinical Case Notes. Tamoxifen optic neuropathy
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- The CAP1/Prss8 catalytic triad is not involved in PAR2 activation and protease nexin‐1 (PN‐1) inhibition
- A Hot New Twist to Hair Biology
- A University Center for the Performing Arts
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Sterol Intermediates of Cholesterol Biosynthesis Inhibit Hair Growth and Trigger an Innate Immune Response in Cicatricial Alopecia
- Mimosine Dipeptide Enantiomsers: Improved Inhibitors against Melanogenesis and Cyclooxygenase
- Cutaneous gene therapy
- A Case of Acrodermatitis Enteropathica
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Spontaneous hair hyperpigmentation in response to vitamin intake in pregnancy—A clue for homocystinuria
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa