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Research 121–150 of 1000+
- SkIndia Quiz 24: Itchy papules over face
- Keratinization and its Disorders
- Organization and Expression of Hair Follicle Genes.
- Research Snippets
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Electrophoretic variation of hair proteins.
- Integration Analysis of Transcriptome and Proteome Reveal the Mechanisms of Goat Wool Bending
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Atrichia and Papular Lesions: Report of a Case
- Desmosomes in Developing Human Epidermis
- From molecular biology to therapeutics
- Alopecia totalis in an infant
- Hair Anomalies in a 6-Year-Old Girl
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Characterisation of low abundance wool proteins through novel differential extraction techniques
- <i>De novo</i> mutations in monilethrix
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Unexpected Autocrine Role of Vascular Endothelial Growth Factor in Squamous Cell Carcinoma
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- Congenital hair loss disorders: Rare, but not too rare
- Molecular changes in skin predict predisposition to breast cancer
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Ha 1 and Ha 4-Trichocytic Cytokeratin Subunits Expression during Hair Development in Rat Embryonal Skin
- Morphological Study on the Coat Hair in Golden Takin
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Loose anagen syndrome in one identical twin girl