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Research 391–420 of 1000+
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Microneedles mediated bioinspired lipid nanocarriers for targeted treatment of alopecia
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Anti-CXCL4 monoclonal antibody accelerates telogen to anagen transition and attenuates apoptosis of the hair follicle in mice
- Proline-rich protein-like PRPL1 controls elongation of root hairs in Arabidopsis thaliana
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Physiology of Male Gonadotropic Axis and Disorders of Sex Development
- Calreticulin: non‐endoplasmic reticulum functions in physiology and disease
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Efficacy of 1,550-nm Erbium-Glass Fractional Laser Treatment and Its Effect on the Expression of Insulin-Like Growth Factor 1 and Wnt/β-Catenin in Androgenetic Alopecia
- Effect of CUX1 on the Proliferation of Hu Sheep Dermal Papilla Cells and on the Wnt/β-Catenin Signaling Pathway
- Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Stage‐specific regulation of Gremlin1 on the differentiation and expansion of human urinary induced pluripotent stem cells into endothelial progenitors
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Proteomics Reveals the Role of PLIN2 in Regulating the Secondary Hair Follicle Cycle in Cashmere Goats
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development