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Research 361–390 of 1000+
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Study of seed hair growth in Populus tomentosa, an important character of female floral bud development
- Transient agonism of the sonic hedgehog pathway triggers a permanent transition of skin appendage fate in the chicken embryo
- Skin transcriptome reveals the periodic changes in genes underlying cashmere (ground hair) follicle transition in cashmere goats
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Role of regeneration in tissue repairing and therapies
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- The Genetics of Human Skin Disease
- Social selection favours offspring prone to the development of androgenetic alopecia.
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Evidence that Myc activation depletes the epidermal stem cell compartment by modulating adhesive interactions with the local microenvironment
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Control by a hair’s breadth: the role of microRNAs in the skin
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- Ageing processes influence keratin and KAP expression in human hair follicles
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Pyridoxine regulates hair follicle development via the PI3K/Akt, Wnt and Notch signalling pathways in rex rabbits
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- In Ovo Injection of CHIR-99021 Promotes Feather Follicle Development via Modulating the Wnt Signaling Pathway and Transcriptome in Goose Embryos (Anser cygnoides)
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Marie-unna hereditary hypotrichosis