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Research 31–60 of 1000+
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Eziopatogenesi e terapia dell'acne:studio epidemiologico delle caratteristiche cliniche di una popolazione di pazienti affetti da acne e analisi dei polimorfismi del gene codificante per il recettore degli androgeni e del gene codificante per il citocromo P-450 1A1
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Variation in the ovine trichohyalin gene and its association with wool curvature
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Ulcerative colitis and total alopecia in a mother and her son
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Polarized microscopy in genetic hair disorders: case series
- Lab Quality Management and Methodology
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Cardiac biopsy in myocarditis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Modelling androgen synthesis and action during human sexual differentiation
- Exploring the therapeutic potential of naturally occurring taxifolin, a dietary flavonoid: an updated comprehensive review
- Exosomes and Their Bioengineering Strategies in the Cutaneous Wound Healing and Related Complications: Current Knowledge and Future Perspectives
- Advanced nanocarrier- and microneedle-based transdermal drug delivery strategies for skin diseases treatment
- Silk Fibroin and Its Nanocomposites for Wound Care: A Comprehensive Review
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population