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Research 91–120 of 1000+
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Analysis of Lower-Limb Ulcers in Participants with Leprosy Sequelae Using Metabolomics and 16S Ribosomal DNA Sequencing
- Transcriptome Analysis Methods: From the Serial Analysis of Gene Expression and Microarray to Sequencing new Generation Methods
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Unraveling the Molecular Mechanism of Bider Marking Formation in Dun Mongolian Horses Through Transcriptome Sequencing
- CXCL12 Drives Reversible Fibroimmune Remodeling in Androgenetic Alopecia Revealed by Single-Cell RNA Sequencing
- Microbial dysbiosis and its diagnostic potential in androgenetic alopecia: insights from multi-kingdom sequencing and machine learning
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- ESDR303 – The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Systematic Analysis of Non-coding RNAs Involved in the Angora Rabbit (Oryctolagus cuniculus) Hair Follicle Cycle by RNA Sequencing
- Identification of key genes in type 2 diabetes‐induced erectile dysfunction rats with stem cell therapy through high‐throughput sequencing and bioinformatic analysis
- Exploring the Causal Relationship Between Plasma Proteins and Obstructive Sleep Apnea: A Study Using Genome-Wide Mendelian Randomization, Single-Cell RNA Sequencing Analysis, and Network Pharmacology
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Polymorphism in the A2M gene associated with high-quality milk in Murrah buffaloes (Bubalus bubalis)
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Multi-scale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Host-microbiome interactions and recent progress into understanding the biology of acne vulgaris
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Age-associated inflammation inhibits epidermal stem cell function
- Epithelial‐to‐mesenchymal transition in cutaneous wound healing: Where we are and where we are heading
- Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing
- Human epithelial hair follicle stem cells and their progeny: Current state of knowledge, the widening gap in translational research and future challenges
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Dissecting the microenvironment around biosynthetic scaffolds in murine skin wound healing