Search
for
Sort by
Research 871–900 of 1000+
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Novel insights into cardiocutaneous syndromes
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- BJD Editor's Choice
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Role of vitamin D in skin and hair biology
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- 890 Development of pigmented reconstructed human epidermis model containing human melanoblasts from keratinocyte culture
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Cellular heterogeneity and microenvironmental control of skin cancer
- Epidermolysis Bullosa in Calves in the United Kingdom
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- IL-17 axis is a significant driver of skin inflammation in Card14 mutant pityriasis rubra pilaris model mice
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation
- Deletion of an enhancer in FGF5 is associated with ectopic expression in goat hair follicles and the cashmere growth phenotype
- Red Blood Cells Folate Level in Patients with Alopecia Areata
- A BIOCHEMICAL MARKER IN A DOMINANT MOUSE TRAIT
- 0748 Synergy of TP53 and non-canonical sonic hedgehog pathway in the development of complex basal cell carcinoma