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Research 841–870 of 1000+
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- White piedra and pediculosis capitis in the same patient
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- The inheritance of common baldness: Two B or not two B ?
- Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- 14-3-3σ Is Required for Club Hair Retention
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- 519 Phase I/IIa clinical trial for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.