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Research 541–570 of 1000+
- Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Single-Nucleus and Bulk RNA Sequencing Reveals the Involvement of Natural Killer and CD8+ T Cells in the Progression of Androgenetic Alopecia
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Platelet-Rich Plasma for Treatment of Hair Loss Improves Patient-Reported Quality of Life
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Competitive balance of intrabulge BMP/Wnt signaling reveals a robust gene network ruling stem cell homeostasis and cyclic activation
- WNT Signaling in Disease
- Long-Term Effects of COVID-19
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- Epidermal Deletion of Rac1 Causes Stem Cell Depletion, Irrespective of whether Deletion Occurs during Embryogenesis or Adulthood
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Secondary Metabolites with Antifungal Activities from Mangrove Derived Fungus Monascus purpureus WMD2424
- Androgen Receptor–Mediated Paracrine Signaling Induces Regression of Blood Vessels in the Dermal Papilla in Androgenetic Alopecia
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Ptch2 is a Potential Regulator of Mesenchymal Stem Cells
- Recent Advances in the Electro-Active Therapeutic Phytochemical-Based Sensors
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle