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Research 301–330 of 1000+
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- 14. Wound Healing; Cutaneous Therapy; Hair
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Tissue engineering of human hair follicles using a biomimetic developmental approach
- An Update of Congenital Adrenal Hyperplasia
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Diagnostic approach to low‐renin hypertension
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases
- Alopecia Areata
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- In vitro hair follicle growth model for drug testing
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Exploring the association between alopecia areata and thyroid dysfunction: A review