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Research 601–630 of 1000+
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- The Effects of Single Testosterone Administration and Stress Induction on Steroid Hormone Levels in Hair
- Regulation of Hair Follicle Growth and Development by Different Alternative Spliceosomes of FGF5 in Rabbits
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Comprehensive analysis of the circular RNA expression profile and circRNA–miRNA–mRNA network in the goat skin with divergent wool curvature
- A missense mutation in Lama3 causes androgen alopecia
- Identification of N6-Methyladenosine-Related Factors and the Prediction of the Regulatory Mechanism of Hair Follicle Development in Rex and Hycole Rabbits
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Regulatory Effects of FGF9 on Dermal Papilla Cell Proliferation in Small-Tailed Han Sheep
- Endocrinology
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Generalised Glucocorticoid Resistance
- Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management
- Hair & Cutaneous Development
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Industry updates in advanced therapy medicinal products and regenerative medicine – March 2026
- Congenital Adrenal Hyperplasia
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- The JAK/STAT signaling pathway: from bench to clinic
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- NFATc1 Balances Quiescence and Proliferation of Skin Stem Cells
- Wnt Signaling, Lgr5, and Stem Cells in the Intestine and Skin
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities