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Research 151–180 of 1000+
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Attenuated Total Reflection Fourier Transform Infrared Spectroscopy Analysis of Human Hair Fiber Structure
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Supplementary material from "Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair"
- Histological features of melasma lesions and the expression of keratin 10
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Downregulation of mRNAs Encoding Keratin-Associated Proteins in the Tongue of Mice Fed a High-Fat Diet
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Affects Keratin 1 and Keratin 17 Gene Expression and Differentially Induces Keratinization in Hairless Mouse Skin
- [Studies on monilethrix].
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation
- [Nevus comedonicus. A rare skin disease of the hair follicles].
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Loose anagen syndrome in one identical twin girl.
- Current Genetics in Hair Diseases
- Atrichia with papular lesions
- Ichthyosis hystrix
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Trichofolliculoma: a rare variant of hair follicle hamartoma
- Alopezien und Hypotrichosen im Kindesalter
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Trichothiodystrophy hair shafts display distinct ultrastructural features
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Trichohyalin is a Potential Major Autoantigen in Human Alopecia Areata
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- <i>Hoxc13</i> and the development of hair follicle