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Research 151–180 of 491
- Formation of the iε-(γ-glutamyl)lysine crosslink in hair proteins. Investigation of transamidases in hair follicles
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- iε-(γ<sup>-Glutamyl</sup>) lysine cross-linkage in citrulline-containing protein fractions from hair
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Genetically null mice reveal a central role for epidermal growth factor receptor in the differentiation of the hair follicle and normal hair development.
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Case 21-2012
- Variation in the ovine trichohyalin gene and its association with wool curvature
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Hair Follicle Culture
- Wnt signaling in skin organogenesis
- Management of congenital ichthyoses: European guidelines of care, part two
- Defining Hair Follicles in the Age of Stem Cell Bioengineering
- The Genetics of Human Skin Disease
- 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 Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Homeodynamic Rejuvenation: an adaptive framework for resetting skin aging
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures