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Research 61–90 of 1000+
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- The Skin Microbiome: Current Landscape and Future Opportunities
- Shape Variability and Classification of Human Hair: A Worldwide Approach
- The biology of hair shape
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- THE INFLUENCE OF SKIN MICROBIOME IMBALANCE ON SPECIFIC PATHOLOGICAL SKIN CONDITIONS
- A human prenatal skin cell atlas reveals immune cell regulation of skin morphogenesis
- Keratin expression in the hair of different racial groups
- Montagna Symposium 2015: Harnessing Stem Cells to Reveal Novel Skin Biology and Disease Treatments
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- Human hair melanins: what we have learned and have not learned from mouse coat color pigmentation
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Alopecia Areata in Skin of Color Patients: New Considerations Sparked by the Approval of Baricitinib
- Indian Hair
- Low Heterozygosity and Historical Bottleneck Effect Depicted From the Genome Assembly of the Indus River Dolphin (<i>Platanista minor</i>)
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Transcriptomic analyses of regenerating adult feathers in chicken
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Spectrum of Phenotypes Associated with Human MC1R Variations