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Research 241–270 of 342
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Biomedical applications of organoids in genetic diseases
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Recent Advances in Genome-Editing Technology with CRISPR/Cas9 Variants and Stimuli-Responsive Targeting Approaches within Tumor Cells: A Future Perspective of Cancer Management
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- The molecular basis of human keratin disorders
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- The Roles of EDA2R in Ageing and Disease
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Understanding human aging and the fundamental cell signaling link in age-related diseases: the middle-aging hypovascularity hypoxia hypothesis
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review