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Research 661–690 of 1000+
- Exosomal miRNA-218–5p derived from low-passage dermal papilla cells modulates hair follicle growth and development
- Influence of NUDT15 Genotyping on Dose Intensity of Thiopurine Administration and Long-Term Clinical Outcomes (Hospitalization and Surgery)
- Additional file 2 of Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Hard Keratin IF and Associated Proteins
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- The Tumor Suppressor Actions of the Vitamin D Receptor in Skin
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Sox13 is a novel early marker for hair follicle development
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- DKK4 as a novel candidate marker for Zhexi Angora rabbit wool quality
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- P78 Acrodermatitis enteropathica in children: clinical cases
- Generalised Glucocorticoid Resistance
- Chitin and Chitosans: Characteristics, Eco-Friendly Processes, and Applications in Cosmetic Science