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Research 601–630 of 1000+
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Dual-Reporter Gene-Based Multimodal Imaging for Tracking Mesenchymal Stem Cells in Diabetic Skin Wound Repair
- Alopecia areta: a review
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Follicular Stem Cells in Androgenetic Alopecia
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Androgens and androgen receptor action in skin and hair follicles
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Learning from nudity: lessons from the nude phenotype
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- What causes hidradenitis suppurativa ?—15 years after
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Concerted gene duplications in the two keratin gene families
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Chrousos syndrome: from molecular pathogenesis to therapeutic management