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Research 181–210 of 1000+
- TARANTULAS DO NOT SHOOT SILK FROM FEET
- Clinical study on 88 cases of Korean 20-nail dystrophy
- Нарушения фосфорно-кальциевого обмена у детей с хронической болезнью повек
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Changes in the nail plate of the elderly
- Effects of Testosterone+Finasteride on Bone After Spinal Cord Injury: A Randomized, Double-Blind, Placebo-Controlled Pilot Study
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Loss of Vascular Endothelial Growth Factor in Human Alopecia Hair Follicles
- Cicatricial (Scarring) Alopecias
- Principles of Hair Cycle Control
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Diagnostic Exercise: Severe Bilaterally Symmetrical Alopecia in a Horse
- Psoriatic onychopachydermoperiostitis: improvement with etanercept
- Reversible Myopathy and Ophthalmoparesis After Low-Dose Finasteride Administration for Androgenic Alopecia
- Re: The Efficacy of Dihydrotestosterone Transdermal Gel Before Primary Hypospadias Surgery: A Prospective, Controlled, Randomized Study
- Trelles-Jaeger Lid Plate
- Letters to the Editor
- Metabolic Syndrome Prevalence in Psoriasis
- <i>Hoxc13</i> mutant mice lack external hair
- Hair follicle differentiation and regulation.
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Alopecia areata
- The mesenchymal component of hair follicle neogenesis: background, methods and molecular characterization
- Morpho-Regulation of Ectodermal Organs
- The structural and functional aspects of hair cell regeneration in the chick as a result of exposure to intense sound
- The role of lymphocytes in the development and treatment of alopecia areata
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Absorption sites of orally administered drugs in the small intestine
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene