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Research 211–240 of 1000+
- Culturing of Melanocytes from the Equine Hair Follicle Outer Root Sheath
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- The Role of Vitamin D3 Deficiency and Colonization of the Oral Mucosa by Candida Yeast-like Fungi in the Pathomechanism of Psoriasis
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Androgens and Hirsutism in a Large Cohort of Portuguese Women
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Dermatologic care of patients with differences of sex development
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs