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Research 271–300 of 1000+
- Aging and Anti-Aging in Hair and Hair Loss
- The role of protein lactylation in skin diseases: from molecular mechanisms to potential therapeutics
- <i>Malassezia</i> and the Asian menopausal skin
- Microgel emulsion loaded with recombinant oil body as a new drug delivery carrier to promote wound repair
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
- GPCRs as key regulators in wound healing
- Platelet‐rich plasma and regenerative dentistry
- Autophagy is essential for maintaining the growth of a human (mini-)organ: Evidence from scalp hair follicle organ culture
- The aetiopathogenesis of acne vulgaris - what's new?
- Red ginseng oil promotes hair growth and protects skin against UVC radiation
- Hyperadrenocorticism in Ferrets
- Construction strategies of skin organoids: A review
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Uncombable hair improved by biotin
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Converging physiological roles of the anthrax toxin receptors
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Two parietal cephaloceles in a female neonate
- Radiomics and radiogenomics in ovarian cancer: a review with a focus on ultrasound applications
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Exploring the Complexities of TGF-beta Signaling in Keloids: Beyond the Classical Smad Pathway
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome