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Research 181–210 of 268
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Spatiotemporal Labeling of Melanocytes in Mice
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model
- Regenerative Medicine
- Cellular senescence and polycystic ovary syndrome: mechanisms and therapeutic strategies from a new perspective
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- RAGE and Its Ligands in Melanoma
- Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- TLR9 activation in large wound induces tissue repair and hair follicle regeneration via γδT cells
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- The Role of BMP7 in the Proliferation of Hu Sheep Dermal Papilla Cells Is Influenced by DNA Methylation
- Regulating the Wnt/β-catenin Signaling Pathway Promotes Repigmentation in Vitiligo Using Fire Needle Therapy
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Vaccines, adjuvants and autoimmunity
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Nanoparticle-Based Targeting of Vaccine Compounds to Skin Antigen-Presenting Cells By Hair Follicles and their Transport in Mice
- Toll-Like Receptor Function in Acute Wounds
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Transcriptional Characteristics Showed That miR-144-y/FOXO3 Participates in Embryonic Skin and Feather Follicle Development in Zhedong White Goose
- Myotonic Dystrophy—A Progeroid Disease?
- A kindred with mutant IKAROS and autoimmunity
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients