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Research 721–750 of 1000+
- Signalling couples hair follicle stem cell quiescence with reduced histone H3 K4/K9/K27me3 for proper tissue homeostasis
- <i>Hedychium spicatum</i>: a systematic review on traditional uses, phytochemistry, pharmacology and future prospectus
- Nonclassic congenital adrenal hyperplasia
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Management of CAH during pregnancy
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Androgen receptor gene CAG and GGN polymorphisms in infertile Nigerian men
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Relationship of Early-Onset Baldness to Prostate Cancer in African-American Men
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Is there any relationship between decreased AgNOR protein synthesis and human hair loss?
- LncRNA-000133 from secondary hair follicle of Cashmere goat: identification, regulatory network and its effects on inductive property of dermal papilla cells
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- Synchronous profiling and analysis of mRNAs and ncRNAs in the dermal papilla cells from cashmere goats
- Genetics of Structural Hair Disorders
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Establishment of keratinocyte cell lines from human hair follicles
- A Systematic Approach to Afro-Textured Hair Disorders
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- “Cold” X5 Hairlaser™ used to treat male androgenic alopecia and hair growth: an uncontrolled pilot study
- A genomic approach to susceptibility and pathogenesis leads to identifying potential novel therapeutic targets in androgenetic alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Clinico-investigative profile of patients of hirsutism in a tertiary level institution
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development