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Research 931–960 of 998
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- Discovery of an Androgen Receptor Degrader Featuring a Pyridazinyl Glutarimide CRBN-Binding Motif for Transdermal Treatment of Androgenetic Alopecia
- Compare the Efficacy of PRP Intervention VS Exosomes for Hair loss, a Case Series Study
- Overview of the Circadian Clock in the Hair Follicle Cycle
- Hair in the Wrong Place
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Ambassadors in Dermatology and Venereology: An interview with Professor Fabio Ayala
- A UTILIZAÇÃO DE PLASMA RICO EM PLAQUETAS COMO POTENCIALIZADOR DO REJUVENESCIMENTO FACIAL EM PROCEDIMENTOS ESTÉTICOS
- Red nail bands in conjunction with telogen effluvium as a post‐COVID‐19 phenomenon
- Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- Zeb2 recruits HDAC–NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- Targeting Wnt/β-catenin signaling and its interplay with TGF-β and Notch signaling pathways for the treatment of chronic wounds
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Ornithine decarboxylase is upregulated by the androgen receptor in skeletal muscle and regulates myoblast proliferation
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Malt1 Protease Is Critical in Maintaining Function of Regulatory T Cells and May Be a Therapeutic Target for Antitumor Immunity
- Update on hidradenitis suppurativa: connecting the tracts
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Techniques for Creating Inconspicuous Face-lift Scars
- Novel ECM Patch Combines Poly(vinyl alcohol), Human Fibroblast-Derived Matrix, and Mesenchymal Stem Cells for Advanced Wound Healing
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases
- Effects of mitotane treatment on human steroid metabolism: implications for patient management
- Quaternary ammonium iminofullerenes improve root growth of oxidative-stress maize through ASA-GSH cycle modulating redox homeostasis of roots and ROS-mediated root-hair elongation
- A randomized placebo-controlled study on the effects of pioglitazone on cortisol metabolism in polycystic ovary syndrome
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>