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Research 61–90 of 1000+
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Relationship between the bacterial community structures on human hair and scalp
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Intermittent nitrate transdermal therapy
- First Report of ‘<i>Candidatus</i> Phytoplasma aurantifolia’ Associated with the Invasive Weed <i>Eclipta prostrata</i> in Taiwan
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Neurosarcoidosis Occurring 6 Years after Onset of Vogt-Koyanagi-Harada Disease
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Identification of the causative dermatophyte of tinea capitis in children attending Mbarara Regional Referral Hospital in Uganda by PCR-ELISA and comparison with conventional mycological diagnostic methods
- Identification of Trichophyton rubrum by Nested PCR Analysis from Paraffin Embedded Specimen in Trichophytia Profunda Acuta of the Glabrous Skin
- Authentication of herbs by physiological & morphological studies through HPTLC, ICP-MS, UV Spectroscopy, Genetic Engineering & PCR
- Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method
- Standard DNA Methylation Analysis in Mouse Epidermis: Bisulfite Sequencing, Methylation-Specific PCR, and 5-Methyl-Cytosine (5mC) Immunological Detection