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Research 31–60 of 1000+
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Genome-wide detection and sequence conservation analysis of long non-coding RNA during hair follicle cycle of yak
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Genetic and molecular aspects of androgenetic alopecia
- Physiological and transcriptomic analyses of brassinosteroid function in kiwifruit root
- Molecular Genetics of Alopecias
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- 546 Gene expression signatures and ALADIN score correlates with response of alopecia areata patients to treatment with JAK inhibitors
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- 9. Immunology and Genetics
- The Genetics of Human Skin Disease
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans