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Research 721–750 of 1000+
- Regulation of cashmere fineness traits by noncoding RNA in Jiangnan cashmere goats
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- Transcriptomic analysis of regulatory mechanisms in the telogen-anagen transition of ovine hair follicles
- Research Articles : New Evidence for the Involvement of the EGF Receptor Pathway in Hair Follicle Morphogenesis in uncv Mice
- Whole transcriptome sequencing of different hair types in inner Mongolian cashmere goats
- Integrated transcriptomic and proteomic analysis reveals molecular mechanisms of melatonin-regulated hair follicle growth in cashmere goats and comparative insights across goat breeds
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Integrative transcriptomic and metabolomic analyses reveal the role of melatonin in promoting secondary hair follicle development in cashmere goats
- The molecular anatomy of cashmere goat hair follicle during cytodifferentiation stage
- Die Patientenverfügung im rechtlichen Kontext und ihre praktische Anwendung
- Biology and Genetics of Hair
- 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
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- The Charnoly body as a universal biomarker of cell injury
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- 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
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- The Current Landscape for Direct-to-Consumer Genetic Testing: Legal, Ethical, and Policy Issues
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Role of thymosin beta 4 in hair growth
- 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
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Structural variation-driven FADS2P1 expression modulates hair trait diversity through unsaturated fatty acid metabolism in goats