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Research 301–330 of 1000+
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- Evaluation of Gene Expression Patterns in Micrografts Demonstrate Induction of Catagen-Like Processes During Storage
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- 1358 PRC1 fine-tunes gene repression and activation to safeguard skin epithelium development and stem cell specification
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Complex Regional Pain Syndrome Type I : measurements and treatment
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
- 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
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Disease causing homozygous variants in the human hairless gene
- Effects of Guasha on histomorphology of scraped skins and on expression of calcitonin gene-related peptide and substance P in rats
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Comparative gene expression analysis of nestin-expressing hair follicle-derived cells
- Comparison of MMP1 gene expression and collagen percentage in response to polydioxanone, poly-L-lactic acid and polycaprolactone thread implantation in ageing rat skin
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient