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Research 361–390 of 592
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- NEDD4 and NEDD4L regulate Wnt signalling and intestinal stem cell priming by degrading LGR5 receptor
- Dermatologic adverse events associated with afatinib: an oral ErbB family blocker
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Hox genes in development and beyond
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- The molecular basis of human keratin disorders
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Prostate Cancer Early Detection, Version 2.2015
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Lineage Analysis of Epidermal Stem Cells
- Advancements and challenges in stem cell transplantation for regenerative medicine
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Feline dermatophytosis
- Follicular mucinosis: A detailed morphologic and immunopathologic study
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- Myotonic Dystrophy—A Progeroid Disease?
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Malt1 Protease Is Critical in Maintaining Function of Regulatory T Cells and May Be a Therapeutic Target for Antitumor Immunity
- Regeneration Genetics
- Recently Identified Forms of Epidermolysis Bullosa
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Targeting Wnt Signaling for Gastrointestinal Cancer Therapy: Present and Evolving Views