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Research 391–420 of 1000+
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals
- Disease causing homozygous variants in the human hairless gene
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Expression of lipid-protein gene PLP2 in Liaoning cashmere goat
- Feather arrays are patterned by interacting signalling and cell density waves
- Keratin disorders: from gene to therapy
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Evidence for Masculinization of Adipokine Gene Expression in Visceral and Subcutaneous Adipose Tissue of Obese Women With Polycystic Ovary Syndrome (PCOS)
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Characterization of <i>BMP</i>2 gene expression in embryonic and adult Inner Mongolia Cashmere goat (<i>Capra hircus</i>) hair follicles
- Proprietary Herbal Extract Downregulates the Gene Expression of Il-1 and #945; in HaCaT Cells: Possible Implications Against Nonscarring Alopecia
- Androgen receptor gene CAG and GGN polymorphisms in infertile Nigerian men
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- A role of melatonin in neuroectodermal‐mesodermal interactions: the hair follicle synthesizes melatonin and expresses functional melatonin receptors
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- The Modulatable Stem Cell Niche: Tissue Interactions during Hair and Feather Follicle Regeneration
- Study on the zona pellucida 4 (ZP4) gene sequence and its expression in the ovaries of patients with polycystic ovary syndrome
- Advanced glycation end-products inhibit mesenchymal-epidermal interaction by up-regulating proinflammatory cytokines in hair follicles
- JAK-centric explainable few-shot gene-expression diagnosis framework for alopecia via MultiPLIER priors and relation-style set-to-set comparison
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium