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Research 931–960 of 1000+
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Miz1 is required for hair follicle structure and hair morphogenesis
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Generalised Glucocorticoid Resistance
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Persistent hair growth during treatment with the EGFR inhibitor erlotinib
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Thymic Mesenchymal Cells Have a Distinct Transcriptomic Profile
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- 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>)
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Keratin Gene Expression in Wool Fibre Development
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- TTNPB Promotes Human Pluripotent Stem Cell‐to‐Neural Stem Cell Transition via Modulation of Chromatin Accessibility and the S‐(5′‐adenosyl)‐L‐homocysteine/Choline Metabolic Network
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- 821 Pigmentation and autophagy in alopecia areata pathogenesis
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate