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Research 61–90 of 1000+
- Oestrogen functions in skin and skin appendages
- Significance of the polyglutamine tract polymorphism in the androgen receptor
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Lymphatic vessels interact dynamically with the hair follicle stem cell niche during skin regeneration <i>in vivo</i>
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Tailored chromatin modulation to promote tissue regeneration
- Transcriptional Profiling in Rat Hair Follicles following Simulated Blast Insult: A New Diagnostic Tool for Traumatic Brain Injury
- Gene Expression Analysis of Chondrogenic Markers in Hair Follicle Dermal Papillae Cells Under the Effect of Laser Photobiomodulation and the Synovial Fluid
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Molecular genetics of androgen insensitivity
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- LncRNA-000133 from secondary hair follicle of Cashmere goat: identification, regulatory network and its effects on inductive property of dermal papilla cells
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- ATP-dependent chromatin remodeling during mammalian development
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Biology and Genetics of Hair
- Learning from nudity: lessons from the nude phenotype
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Congenital hair loss disorders: Rare, but not too rare
- The nude gene and the skin
- Redefining hormone resistance in prostate cancer
- Diagnostic approach to low‐renin hypertension
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Genetic basis of polycystic ovary syndrome