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Research 61–90 of 724
- 0977 Pathogenic hallmarks of primary lymphocyte-mediated scarring alopecia revealed by single nuclear and spatial multiomics
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- 1452 Noncoding dsRNA stimulates exosome biosynthesis to regulate skin regeneration
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Label-free proteomics to identify keratins and keratin-associated proteins and their effects on the fleece traits of Inner Mongolia Cashmere Goats
- 723 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and three-dimensional chromatin topology in lineage-specific loci to control hair growth
- 731 Generation of a laser capture microdissection and RNAseq-based human anagen hair follicle transcriptome atlas
- 603 Pathological modeling of epidermolysis bullosa simplex (EBS) using induced pluripotent stem cells (iPSC)
- Few Simple Sequence Repeats in Human Hair
- Clinical Snippets
- Differential expression of type I IRS keratin genes in three breeds of sheep
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- The formulation and in‐vitro evaluation of WS Biotin, a novel encapsulated form of D‐Biotin with improved water solubility for hair and skin treatment applications
- Molecular stratification of the human fetal vaginal epithelium by spatial transcriptome analysis
- iTRAQ-based quantitative proteomics revealing the therapeutic mechanism of a medicinal and edible formula YH0618 in reducing doxorubicin-induced alopecia by targeting keratins and TGF-β/Smad3 pathway
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Ageing processes influence keratin and KAP expression in human hair follicles
- Construction of transcriptome atlas of white yak hair follicle during anagen and catagen using single-cell RNA sequencing
- Revealing biological mechanisms of skin pigment recovery during treatment in vitiligo patients: A proteomic analysis
- Bacteria induce skin regeneration via IL-1β signaling
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Evaluation of Gene Expression Patterns in Micrografts Demonstrate Induction of Catagen-Like Processes During Storage
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- A curated catalog of canine and equine keratin genes
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Meta-Analysis of Gene Expression Reveals the Core Transcriptomic Profile of Lesional Scalp in Alopecia Areata
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Hair regrowth in a male patient with extensive androgenetic alopecia on estrogen therapy