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Research 31–60 of 1000+
- Functional Genome and Proteome Analyses of Cutaneous Autoimmune Diseases
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Evaluation of noninvasive biospecimens for transcriptome studies
- 0748 Synergy of TP53 and non-canonical sonic hedgehog pathway in the development of complex basal cell carcinoma
- Combined transcriptomics and proteomics forecast analysis for potential genes regulating the Columbian plumage color in chickens
- CSI on steroids
- Construction of a cDNA library and identification of genes from Liaoning cashmere goat
- Selection signatures for fiber production in commercial species: A review
- Single-Cell Omics Advances in Understanding Tissue Development and Complex Trait Formation in Sheep and Goats
- Research Progress on the Molecular Mechanism of Poultry Feather Follicle Development
- MULTIOMICS – A NEW EXCITING ERA OF RESEARCH
- An in silico approach to the identification of potential proteomic and genomic diagnostic biomarkers for primary cicatricial alopecia
- Tackling underrepresentation to aid understanding of Parkinson’s disease: Progress and further opportunities
- An Approach to Identify Targets of Breast Cancer Stem Cells
- The Rotterdam Study: 2016 objectives and design update
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Transcriptional profiling in alopecia areata defines immune and cell cycle control related genes within disease-specific signatures
- Profiling Chromatin Accessibility at Single-Cell Resolution
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative study on seasonal hair follicle cycling by analysis of the transcriptomes from cashmere and milk goats
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Gene Expression in Rat Dermal Papilla Cells: Analysis of 2529 ESTs
- A genomic approach to susceptibility and pathogenesis leads to identifying potential novel therapeutic targets in androgenetic alopecia
- Single-cell sequencing reveals the new existence form of dermal papilla cells in the hair follicle regeneration of cashmere goats
- Melatonin promotes the proliferation of dermal papilla cells in cashmere goats via activation of chi-let-7d-5p/WNT2 axis
- Melatonin promotes proliferation of Inner Mongolia cashmere goat hair follicle papilla cells through Wnt10b