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Research 24
- Genetics of Structural Hair Disorders
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- The Genetics of Human Skin Disease
- Identifying molecular targets for reverse aging using integrated network analysis of transcriptomic and epigenomic changes during aging
- Mechanisms of Puerariae Lobatae Radix in regulating sebaceous gland secretion: insights from network pharmacology and experimental validation
- Genetic Defects of Female Sexual Differentiation
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Sox13 is a novel early marker for hair follicle development
- Deletion of the <i>Sox21</i> gene drastically affects hair lipids
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Comparison of CD146 +/− mesenchymal stem cells in improving premature ovarian failure
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- Fibroblast bioelectric signaling drives hair growth
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Role of the SOX family in cancer immune evasion: Emerging player and promising therapeutic opportunities
- The Potential Reversible Transition between Stem Cells and Transient-Amplifying Cells: The Limbal Epithelial Stem Cell Perspective
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- TTNPB Promotes Human Pluripotent Stem Cell‐to‐Neural Stem Cell Transition via Modulation of Chromatin Accessibility and the S‐(5′‐adenosyl)‐L‐homocysteine/Choline Metabolic Network
- Growth hormone deficiency with late-onset hypothalamic hypoadrenocorticism associated with respiratory and renal dysfunction: a case report
- Induction of Pluripotent Stem Cells Via Wnt Signaling Pathway.