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Research 331–360 of 1000+
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Regulation of melanocyte stem cell behavior by the niche microenvironment
- The Genetics of Human Skin Disease
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Symmetry breaking of tissue mechanics in wound induced hair follicle regeneration of laboratory and spiny mice
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Retinoid Metabolism Is Altered in Human and Mouse Cicatricial Alopecia
- Is polycystic ovary syndrome a sexual conflict? A review
- Epigenetic regulation in adult stem cells and cancers
- Epimorphic regeneration in mice is p53-independent
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Regulation of pathophysiological and tissue regenerative functions of MSCs mediated via the WNT signaling pathway (Review)
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury