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Research 361–390 of 1000+
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Genetically Induced Cell Death in Bulge Stem Cells Reveals Their Redundancy for Hair and Epidermal Regeneration
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Congenital atrichia with papular lesions
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Generation of the Krt24-CreERT2 Mouse Line Targeting Outer Bulge Hair Follicle Cells
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Genetics of Diabetes in Childhood
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Expression profile analysis of microRNAs during hair follicle development in the sheep foetus
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Polycystic Ovary Syndrome Phenotypes and Infertility Treatment
- 453 Signaling by Senescent Melanocytes Induces New Hair Growth and Informs Hair Growth-Activating Injectable for Androgenetic Alopecia
- Bicalutamide: A review
- Minoxidil may suppress androgen receptor-related functions
- Runx1 transcription factor is involved in the regulation of KAP5 gene expression in human hair follicles
- 한국인의 두피모발 특성과 남성형탈모증
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Analysis of differential expression of hair follicle tissue transcriptome in Hetian sheep undergoing different periodic changes
- Caída capilar: nuevos factores causales y nuevos principios activos para un abordaje más integral con complementos alimenticios
- Hox genes in development and beyond
- The palette of techniques for cell cycle analysis
- The Implication of Neuroactive Steroids in Tourette's Syndrome Pathogenesis: A Role for 5α‐Reductase?
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica