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Research 721–750 of 1000+
- Disorders of Hair Pigmentation
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- FGF5 is a crucial regulator of hair length in humans
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Keratins: the hair shaft's backbone revealed
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles