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Research 31–60 of 85
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- 078 The transmembrane protein LRIG1 regulates receptor tyrosine kinases in skin development and homeostasis
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Proteome Analysis of Human Hair Shaft
- KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- New clinico‐genetic classification of trichothiodystrophy
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- The Genetics of Human Skin Disease
- Transcriptomic landscape of early hair follicle and epidermal development
- 3D bioprinting of engineered exosomes secreted from M2-polarized macrophages through immunomodulatory biomaterial promotes in vivo wound healing and angiogenesis
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- New developments in the molecular treatment of ichthyosis: review of the literature
- Wound Regeneration Deficit in Rats Correlates with Low Morphogenetic Potential and Distinct Transcriptome Profile of Epidermis
- 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