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Research 421–450 of 1000+
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Human hair keratins
- Degradation of human hair keratin scaffold implanted for repairing injured skeletal muscles.
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Demethylation of methionine and keratin damage in human hair
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Production and characterization of human hair keratin bioplastic films with novel plasticizers
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas
- PLOS Science Wednesday: Hi Reddit, I'm Zhengquan Yu, here to talk about my recent PLOS Genetics paper that has identified the key role of a microRNA in hair loss. I'm joined by Maksim Plikus, who studi
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- 1301 STIM1, but not STIM2, is the calcium sensor critical for sweat secretion
- Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
- Leflunomide for the treatment of trichodysplasia spinulosa in a liver transplant recipient
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Alopecia totalis in an infant
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- Ectopic<i>Atoh1</i>expression drives Merkel cell production in embryonic, postnatal and adult epidermis
- Proteomic Characterization of Damaged Single Hairs Recovered after an Explosion for Protein-Based Human Identification