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Research 481–510 of 1000+
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Discovery and Functional Analysis of Secondary Hair Follicle miRNAs during Annual Cashmere Growth
- The Rho guanosine nucleotide exchange factors Vav2 and Vav3 modulate epidermal stem cell function
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Harnessing Microbiome, Bacterial Extracellular Vesicle, and Artificial Intelligence for Polycystic Ovary Syndrome Diagnosis and Management
- ISX-9 Promotes KGF Secretion From MSCs to Alleviate ALI Through NGFR-ERK-TAU-β-Catenin Signaling Axis
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Role of the SOX family in cancer immune evasion: Emerging player and promising therapeutic opportunities
- The Role of MicroRNA, Long Non-Coding RNA and Circular RNA in the Pathogenesis of Polycystic Ovary Syndrome: A Literature Review
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Hair and Nail Manifestations of Systemic Disease
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Skin Stearoyl-CoA Desaturase Genes
- Alopecia management from a comparative perspective: pharmacological and pharmaceutical insights in humans, dogs, and cats
- Trichological disorders in Organ Transplant Recipients - case report and literature review.
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- Telitacicept for systemic lupus erythematosus with post‑surgical papillary thyroid carcinoma: A case report
- Diagnostic Signs and Symptoms of Cyanocobalamin Deficiency at Rural Setting in India: Novel Method of Supplementation
- Genetic Differences between Male and Female Pattern Hair Loss in a Korean Population
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits