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Research 691–720 of 1000+
- Skin burn wound healing in rabbits treated with autologous platelet-rich fibrin
- Líquen plano pilar e alopecia frontal fibrosante: correlação dos achados clínicos e dermatoscópicos com o grau de inflamação do exame histopatológico
- Dermatologia e Procedimentos Estéticos Ed. XVIII
- Hyperactivation of sympathetic nerves drives depletion of melanocyte stem cells
- The Molecular Revolution in Cutaneous Biology: Noncoding RNAs: New Molecular Players in Dermatology and Cutaneous Biology
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Tumor suppressor identity can contribute to heterogeneity of phenotype in hair follicle stem cell‐induced squamous cell carcinoma
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- CD34 <sup>+</sup> cell–derived fibroblast-macrophage cross-talk drives limb ischemia recovery through the OSM-ANGPTL signaling axis
- Derivation of Stem Cell-like Cells From Spherical Culture of Astrocytes for Enhanced Neural Repair After Middle Cerebral Artery Occlusion
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population
- A new type of pachyonychia congenita.
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].
- The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Zebrafish Model of Hereditary Pigmentary Disorders
- 436 Allergic contact dermatitis stimulates hair follicle stem cells via macrophage-mediated regulation
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Investigating the mechanisms underlying age-related dysfunctions in skin and hair follicle regeneration
- Green Synthesis of Silver Nanoparticles by Using<i>Ziziphus nummularia</i>Leaves Aqueous Extract and Their Biological Activities
- Developmental genetics of color pattern establishment in cats
- CD49fhigh Defines a Distinct Skin Mesenchymal Stem Cell Population Capable of Hair Follicle Epithelial Cell Maintenance
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models