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Research 271–300 of 440
- 1375 Cutaneous adnexal cysts revisited: A novel classification based on morphological and molecular features
- 1371 FGF7-dependent inhibition of human hair growth byan osteopontin-derived peptide: A novel solution for hirsutism and hypertrichosis?
- Carnosic acid in topical rosemary extract enhances skin repair via TRPA1 activation
- SnapshotDx Quiz: January 2021
- Expression of mesenchymal stem cell marker CD90 on dermal sheath cells of the anagen hair follicle in canine species
- Hair Regrowth with Cannabidiol (CBD)-rich Hemp Extract – A Case Series
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- 689 Cell-type-specific nascent transcriptomics through PRECISE-seq reveal molecular principles of tissue dynamics
- Transient stimulation of TRPMLs enhance the functionality of hDPCs and facilitate hair growth in mice
- A subpopulation of itch‐sensing neurons marked by Ret and somatostatin expression
- “Sebocytes’ makeup” - Novel mechanisms and concepts in the physiology of the human sebaceous glands
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Novel anti-aging gene NM_026333 contributes to proton-induced aging via NCX1-pathway
- Topical Administration of 15‐Deoxy‐<i>Δ</i><sup>12,14</sup>‐Prostaglandin J<sub>2</sub> Using a Nonionic Cream: Effect on UVB‐Induced Skin Oxidative, Inflammatory, and Histopathological Modifications in Mice
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Treatment of Hair Loss in the Trichorhinophalangeal Syndrome
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Recent advances in the epidermal growth factor receptor/ligand system biology on skin homeostasis and keratinocyte stem cell regulation
- Self-Activated Electrical Stimulation for Effective Hair Regeneration <i>via</i> a Wearable Omnidirectional Pulse Generator
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Mechanistic and therapeutic insight into the effects of cinnamon in polycystic ovary syndrome: a systematic review
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Forsythiasides: A review of the pharmacological effects
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice