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Research 481–510 of 1000+
- Viewpoint 4
- γδ17 T cell-stromal networks modulate matrix composition and vascularity in foreign body response
- Abstracts of 42nd National Conference of Association of Clinical Biochemists of India (ACBICON 2015)
- Hair Changes Caused by Aging
- Piecing together the pigment-type switching puzzle
- CD201+ fascia progenitors choreograph injury repair
- POLY CYSTIC OVARIAN SYNDROME: AN UPDATED REVIEW
- ALOPECIA DE PADRÃO FEMININO: ATUALIZAÇÃO DIAGNÓSTICA E TERAPÊUTICA
- Effects and Mechanism of Nutrients on Root Hair Growth
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Hair through the female life cycle
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Sculpting with stiffness: rigidity as a regulator of morphogenesis
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Forensic DNA Phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Selection signatures in goats reveal a novel deletion mutant underlying cashmere yield and diameter
- Genotypic and Phenotypic Study of PDCD4 gene Concerning micro RNA-21 and micro RNA-449b Polymorphism in Breast Cancer
- W locus alleles of the KIT Gene in Turkish Van Cats and Their Association with Certain Phenotypes
- Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- The developmental basis of fingerprint pattern formation and variation
- Central centrifugal cicatricial alopecia: challenges and solutions
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- The role of WNT10B in physiology and disease: A 10-year update
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome