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Research 211–240 of 569
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Analogs of human genetic skin disease in domesticated animals
- Utility of trichoscopy
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Lysophospholipid Mediators in Health and Disease
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Evaluation of the Safety and Effectiveness of Oral Minoxidil in Children: A Systematic Review
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Hidradenitis suppurativa: A folliculotropic disease of innate immune barrier dysfunction?
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Canine alopecia X
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- THE WATER SOLUBLE VITAMINS
- Modelling androgen synthesis and action during human sexual differentiation
- Pain in Multiple Sclerosis: Understanding Pathophysiology, Diagnosis, and Management Through Clinical Vignettes
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Dysfunction of keratinocyte adhesion
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Genetics of Alopecia
- Topical Treatment for Scarring and Non-Scarring Alopecia: An Overview of the Current Evidence
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Integrating stem cell biology and organoid technology for skin regenerative therapies