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Research 421–450 of 1000+
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Systemic humoral activation facilitates tissue regeneration by D-chiral biomaterial scaffolds
- Techniques for Creating Inconspicuous Face-lift Scars
- Scalp micropigmentation: a promising camouflage modality
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- The JAK/STAT signaling pathway: from bench to clinic
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Biotin and biotinidase deficiency
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Evaluation of noninvasive biospecimens for transcriptome studies
- Frontiers in Topical Photoprotection
- Hypertension's 3 Dilemmas and 3 Solutions: Pharmacology of the Kidney in Hypertension
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- The vitamin B5/coenzyme A axis: A target for immunomodulation?
- In vitro strategies for mimicking dynamic cell–ECM reciprocity in 3D culture models
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Millets as a dietary supplement for managing chemotherapy induced side effects
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Comparative Study of Trichoscopic Features of Alopecia Areata between Adults and Children and between Different Body Parts (Scalp, Beard, Eyebrow, and Moustache)
- Nanogenerators in Biomedical Frontiers: Revolutionizing Self-Powered Healthcare Systems
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- Secondary Cicatricial Scalp Alopecia Caused by Brunsting-Perry Pemphigoid: A Case Report
- Subject Index
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs