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Research 571–600 of 1000+
- Comparison of allogeneic stem cell transplant conditioning regimens in AML, MDS and CLL
- 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
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Evolutionary Divergence of Fibroblast Growth Factors Across Species: Insight into Functional Diversification
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Distinct stem cells contribute to mammary gland development and maintenance
- <i>Hoxc13</i> mutant mice lack external hair
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Dermatologic manifestations of endocrine disorders
- Ferreting out stem cells from their niches
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Non polycystic ovary syndrome–related endocrine disorders associated with hirsutism
- 5-Alpha reductase deficiency
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
- Interventions for female pattern hair loss
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- INTERFERONS IN DERMATOLOGY
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A preliminary study of differentially expressed genes in expanded skin and normal skin: implications for adult skin regeneration
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Molecular Genetics of Alopecias
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates