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Research 721–750 of 1000+
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Restoration of hair follicle inductive properties by depletion of senescent cells
- Revival of generalized favus
- Biochemical Evidence That Small Proline-rich Proteins and Trichohyalin Function in Epithelia by Modulation of the Biomechanical Properties of Their Cornified Cell Envelopes
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Polyglandular autoimmune syndrome type 4 with GAD antibody and dystonia
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Efficacy and safety of SGLT2 inhibitor on insulin resistance and hyperglycemia in Werner syndrome—A case report
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- MicroRNA-302 Increases Reprogramming Efficiency via Repression of NR2F2
- A Subset of TREM2+ Dermal Macrophages Secretes Oncostatin M to Maintain Hair Follicle Stem Cell Quiescence and Inhibit Hair Growth
- PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment
- A complete guide to human microbiomes: Body niches, transmission, development, dysbiosis, and restoration
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp