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Research 901–930 of 1000+
- Pyruvate Kinase M2 Role in Cardiovascular Repair
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Differential transcriptome study on the damage of testicular tissues caused by chronic infection of T. gondii in mice
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Co-expression of PADI isoforms during progenitor differentiation enables functional diversity
- 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
- Characters of KRT80 and its roles in neoplasms diseases
- Expression profile of long non-coding RNA in inner Mongolian cashmere goat with putative roles in hair follicles development
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Anabolic and Metabolic Effects of Testosterone and Other Androgens: Direct Effects and Role of Testosterone Metabolic Products
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Autophagy critically controls skin inflammation and apoptosis-induced stem cell activation
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- The Roles of EDA2R in Ageing and Disease
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Decay of Skin-Specific Gene Modules in Pangolins
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- Antiandrogenic activity of Riboflavin 5′-phosphate (FMN) in 22Rv1 and LNCaP human prostate cancer cell lines
- Acne Syndromes and Mosaicism
- Current Genetics in Hair Diseases
- Modeling animal genomics in mice: An authentic approach for the functional interrogation of evolutionarily and agriculturally critical variants