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Research 721–750 of 1000+
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Timely Wound Healing Is Dependent on Endothelial but Not on Hair Follicle Stem Cell Toll-Like Receptor 2 Signaling
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea
- Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Role of anabolic agents in colorectal carcinogenesis: Myths and realities (Review)
- An important role of podoplanin in hair follicle growth
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Differential Expression of Proteins Associated with the Hair Follicle Cycle - Proteomics and Bioinformatics Analyses
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene