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Research 661–690 of 1000+
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- The FRZB gene regulates hair follicle development in rabbits via the Wnt/β-catenin signaling pathway
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Platelet-Rich Plasma Contains High Concentrations of DKK1, A Potent Inhibitor of Wnt Signaling that Limits Bone Regeneration and Hair Growth
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Clinical report of a Holstein's calf with ichthyosis.
- Inherited Epidermolysis Bullosa: A Clinical Case
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- The compatibility of Bacillus thuringiensis Cry protein-solubilizing buffers with the droplet feeding method in fall armyworm larvae
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- Regenerative Medicine of Epidermal Structures
- Evolution in action: highlighting a role for the Agouti gene in development?
- Main Plenary Sessions: Summaries of Papers
- Genetic basis of polycystic ovary syndrome
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- An Update of Congenital Adrenal Hyperplasia
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1
- Melanocytes: The new Black
- THE PATHOGENESIS OF ALOPECIA AREATA
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Nonclassic adrenal hyperplasia
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Congenital hair loss disorders: Rare, but not too rare