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Research 661–690 of 1000+
- Association of the KAP 8.1 Gene Polymorphisms with Fibre Traits in Inner Mongolian Cashmere Goats
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Polymorphism of Exon V of prolactin gene and its association with Cashmere traits in Changthangi Pashmina goats
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Vitamin D activates type A natriuretic peptide receptor gene transcription in inner medullary collecting duct cells
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Development of a new therapeutic approach based on peptide nanoparticles delivering CRISPR-Cas9 for the specific targeting of KRAS mutations
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Calcium blockers protect against sensory epithelial damage and hearing loss in Cx26-cKO mice
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Epidermolysis Bullosa
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- FGF5 is a crucial regulator of hair length in humans
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Establishment of Tsc2-deficient rat embryonic stem cells
- Woodhouse-Sakati syndrome (WSS)
- An unusual presentation of X-linked adrenoleukodystrophy
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Bachmann–Bupp syndrome and treatment
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Birt–Hogg–Dubé syndrome
- BJD Editor's Choice
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility