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Research 121–150 of 193
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Homozygous K5Cre transgenic mice have wavy hair and accelerated malignant progression in a murine model of skin carcinogenesis
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
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- APECED: JAK Inhibition in an Adult Case with Long-Term Follow-up
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Low Heterozygosity and Historical Bottleneck Effect Depicted From the Genome Assembly of the Indus River Dolphin (<i>Platanista minor</i>)
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Defective trophoblast function in mice with a targeted mutation of Ets2
- A protein kinase target of a PDK1 signalling pathway is involved in root hair growth in Arabidopsis
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Genetic hair and nail disorders
- 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
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Parsing patterns: Emerging roles of tissue self-organization in health and disease