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Research 451–480 of 1000+
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Role of vitamin D in skin and hair biology
- KATP Channels in Zebrafish Cardiovascular System: A Model to Study Cantú Syndrome
- Gene that causes woolly hair revealed
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Keratin gene mutations in disorders of human skin and its appendages
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Hair follicle regeneration suppresses Ras-driven oncogenic growth
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- The Naked (N) Mutation, Chromosome 15
- In vivo Alteration of the Keratin 17 Gene in Hair Follicles by Oligonucleotide-directed Gene Targeting
- Trichothiodystrophy hair shafts display distinct ultrastructural features
- Ligand-Independent Actions of the Vitamin D Receptor Maintain Hair Follicle Homeostasis
- Genetically separable determinants of hair keratin gene expression
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Porokeratotic eccrine and hair follicle nevus: a report of two cases and review of the literature
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation