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Research 721–750 of 1000+
- Siberian cats help in solving part of the mystery surrounding golden cats
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- The role of <i>Atg5</i> gene in tumorigenesis under autophagy deficiency conditions
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Involvement of DKK1 secreted from adipose‐derived stem cells in alopecia areata
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Review: Evolution and diversification of corneous beta‐proteins, the characteristic epidermal proteins of reptiles and birds
- Exosomes mediate sensory hair cell protection in the inner ear
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- An important role of podoplanin in hair follicle growth
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Witnessed trauma exposure induces fear in mice through a reduction in endogenous neurosteroid synthesis
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- TGFβ‐mediated inhibition of hypodermal adipocyte progenitor differentiation promotes wound‐induced skin fibrosis
- Tissue Regeneration, Stem Cells, and Wound Healing