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Research 30 of 42
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.
- Novel insights into cardiocutaneous syndromes
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- De Novo-Designed Bifunctional Proteins for Targeted Protein Degradation
- De novo designed bifunctional proteins for targeted protein degradation
- <i>De novo</i> designed bifunctional proteins for targeted protein degradation
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Transcriptome sequencing reveals the expression profiles of lncRNAs and mRNAs in goat skin tissues with different types of wool coats
- Inherited Epidermolysis Bullosa: A Clinical Case
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Detecting the Mechanism behind the Transition from Fixed Two-Dimensional Patterned Sika Deer (Cervus nippon) Dermal Papilla Cells to Three-Dimensional Pattern
- Hair Dermal papilla maintain its hair inducing characteristics via autocrine exosomal miR-23a-3p
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- Genetic Defects of Female Sexual Differentiation
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- 1445 UVA-induced senescence in human skin ex vivo leads to impaired wound healing
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Skin Development and Disease: A Molecular Perspective
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages