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Research 151–180 of 1000+
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Integration Analysis of Transcriptome Sequencing and Whole-Genome Resequencing Reveal Wool Quality-Associated Key Genes in Zhexi Angora Rabbits
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Comparative Analysis of Chloroplast Genomes in Sansevieria Reveals Phylogenetic Relationships and High Variability Molecular Markers
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Differential plasma proteome analysis reveals key proteins associated with insulin resistance in acne vulgaris patients
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Diphenyl cresyl phosphate [MAK Value Documentations, 2003]
- Machine learning driven multi-omics analysis of the genetic mechanisms behind the double-coat fleece formation in Hetian sheep
- FGF5 is a crucial regulator of hair length in humans
- Cantú Syndrome Is Caused by Mutations in ABCC9