Search
for
Sort by
Research 751–780 of 1000+
- Whole-transcriptome analysis reveals the profiles and roles of coding and non-coding RNAs during hair follicle cycling in Rex rabbits
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- The molecular anatomy of cashmere goat hair follicle during cytodifferentiation stage
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- Chi-miR-30b-5p inhibits dermal papilla cells proliferation by targeting CaMKIIδ gene in cashmere goat
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Characterization and functional analysis of Krtap11-1 during hair follicle development in Angora rabbits (Oryctolagus cuniculus)
- Research Articles : New Evidence for the Involvement of the EGF Receptor Pathway in Hair Follicle Morphogenesis in uncv Mice
- Die Patientenverfügung im rechtlichen Kontext und ihre praktische Anwendung
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Untargeted metabolomic approach to study the serum metabolites in women with polycystic ovary syndrome
- Screening of microRNA and mRNA related to secondary hair follicle morphogenesis and development and functional analysis in cashmere goats
- <i>De Novo</i>Transcriptome Assembly and Differential Gene Expression Profiling of Three<i>Capra hircus</i>Skin Types during Anagen of the Hair Growth Cycle
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Chi-miR-130b-3p regulates Inner Mongolia cashmere goat skin hair follicles in fetuses by targeting<i>Wnt family member 10A</i>
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Hair follicle gene expression profiling in the SubPopulations and InteRmediate Outcome Measures in COPD Study (SPIROMICS)
- Role of thymosin beta 4 in hair growth
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Structural variation-driven FADS2P1 expression modulates hair trait diversity through unsaturated fatty acid metabolism in goats
- Regulation of melanin synthesis in goat hair follicles by melatonin through the Wnt/β-catenin pathway
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Discovery Potential Hub Genes and Pathways in Keloid Fibroblast Development Based on Bioinformatics Analysis
- High-Throughput Sequencing Reveals miRNAs Affecting Follicle Development in Chicken