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Research 61–90 of 1000+
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Polarized microscopy in genetic hair disorders: case series
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Deletion of the epidermis derived laminin γ1 chain leads to defects in the regulation of late hair morphogenesis
- The nude gene and the skin
- AN UPDATE OF HAIR SHAFT DISORDERS
- Genetic Hair Disorders: A Review
- Comparative study of male and female human hair: A microscopic analysis.
- Hair Shaft Disorders
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Hair Loss in Children
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Regenerative Potential of Adipose Tissue–Derived Exosomes in Treating Hair Shaft Abnormalities: A Case Report
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Cosmetic Approach for Healthy and Damaged Hair
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Hair aging and anti-aging
- A rare pediatric case of loose anagen hair syndrome
- <i>Hoxc13</i> mutant mice lack external hair
- Effect of shampoo, conditioner and permanent waving on the molecular structure of human hair
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- Nε-(carboxymethyl) lysine represses hair follicle formation by inhibiting Sonic hedgehog expression in a NF-κB-independent manner
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- The dermatoscope in the hair clinic: Trichoscopy of scarring and nonscarring alopecia