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Research 181–210 of 1000+
- Skin aging: mechanisms, evaluation, and rejuvenation
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Research progress on mechanisms of skin aging and anti-aging strategies
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- Rhamnose-mediated modulation of hair follicle growth: insights from chemical genomics
- LncRNAs regulate the cyclic growth and development of hair follicles in Dorper sheep
- 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
- Identification of Biomarkers in Affected Hair Follicles from Chronic Discoid LupusErythematosus by Weighted Gene Co-Expression Network Analysis
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Two females with hair loss
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Weakly supervised learning of biomedical information extraction from curated data
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- The dermatological consequences of obesity
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis