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Research 121–150 of 495
- An <i>mTurq2-Col4a1</i> mouse model allows for live visualization of mammalian basement membrane development
- FGF5 is a crucial regulator of hair length in humans
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- The JAK/STAT signaling pathway: from bench to clinic
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Epigenetics of Colorectal Cancer
- TRP Channels in Skin Biology and Pathophysiology
- The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Aldo-Keto Reductase (AKR) 1C3 inhibitors: a patent review
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Vitamin D and skin diseases: A review
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- The developmental basis of fingerprint pattern formation and variation
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- Dutasteride reduces alcohol’s sedative effects in men in a human laboratory setting and reduces drinking in the natural environment
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep