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Research 691–720 of 1000+
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- Disease causing homozygous variants in the human hairless gene
- Antisense oligonucleotide targeting fibroblast growth factor receptor (FGFR)-1 stimulates cellular activity of hair follicles in an<i>in vitro</i>organ culture system
- 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
- Spironolactone May Reduce the Risk of Incident Rosacea
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Multimodal imaging of hair follicle bulge-derived stem cells in a mouse model of traumatic brain injury
- What’s New in the Histologic Evaluation of Alopecia and Hair-Related Disorders?
- Two Dogs with Juvenile-Onset Skin Diseases with Involvement of Extremities
- Footprints of the EADV: a meeting report from the 17th Congress of the European Academy of Dermatology and Venereology
- Hair growth-promoting effect of recombinant human sonic hedgehog proteins
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Production of a 135-residue long N-truncated human keratinocyte growth factor 1 in Escherichia coli
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Androgen Receptor Ligands: Agonists and Antagonists
- Antioxidant enzyme expression of mRNA and protein in the epididymis of finasteride-treated male rat offspring during postnatal development
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Actinic Keratosis: Risk Factors, Clinical, Diagnosis and Therapeutics Aspects. Part I
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study