Search
for
Sort by
Research 571–600 of 1000+
- LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Sox13 is a novel early marker for hair follicle development
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Physiology of Testicular Function
- Effect of Fibroblast Growth Factor 10 and an Interacting Non-Coding RNA on Secondary Hair Follicle Dermal Papilla Cells in Cashmere Goats’ Follicle Development Assessed by Whole-Transcriptome Sequencing Technology
- Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Decay of Skin-Specific Gene Modules in Pangolins
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- The Effects of Single Testosterone Administration and Stress Induction on Steroid Hormone Levels in Hair
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Comprehensive analysis of the circular RNA expression profile and circRNA–miRNA–mRNA network in the goat skin with divergent wool curvature
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- mTOR signaling in hair follicle and hair diseases: recent progress
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds