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Research 61–90 of 1000+
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- scMC learns biological variation through the alignment of multiple single-cell genomics datasets
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Transforming 300 billion points of data into diagnostics, therapeutics and new insights into disease
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Exploiting molecular genetic diagnoses of polycystic ovary syndrome to achieve better patient outcome
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Comparative Analysis of Chloroplast Genomes in Sansevieria Reveals Phylogenetic Relationships and High Variability Molecular Markers
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Discovery of differentially expressed genes in cashmere goat (Capra hircus) hair follicles by RNA sequencing
- Differences in cell subsets between sun-exposed and unexposed skin: preliminary single-cell sequencing and biological analysis from a single case
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Genome-wide association study of skin complex diseases
- Transcriptome sequencing and identification of cytochrome P450 monooxygenases involved in the biosynthesis of maslinic acid and corosolic acid in <i>Avicennia marina</i>
- Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen