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Research 61–90 of 1000+
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- Effect of Fibroblast Growth Factor 10 and an Interacting Non-Coding RNA on Secondary Hair Follicle Dermal Papilla Cells in Cashmere Goats’ Follicle Development Assessed by Whole-Transcriptome Sequencing Technology
- Whole transcriptome sequencing of different hair types in inner Mongolian cashmere goats
- Genome-wide detection and sequence conservation analysis of long non-coding RNA during hair follicle cycle of yak
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- ESDR303 – The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- 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
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- 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
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- 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