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Research 781–810 of 1000+
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- Quantification of mast cells in central centrifugal cicatricial alopecia
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Generalized Asymptomatic Cutaneous Pits and Comedones in a Young Woman
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- 1429 Proteomic analysis of cultured dermal papilla, dermal sheath and dermal fibroblast cells from female scalp highlights alterations in the cell populations with increasing age
- 567 Skin aging and carcinogenesis mechanisms by focusing on the stem cell competitive dynamics
- 565 hiPSC-derived skin organoids as tools for disease modelling: characterization of the epidermal-dermal junction
- 569 Hypoxic response of the expression of TGF-β2 and BMP4 in human dermal papilla cells
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- FGF5 is a crucial regulator of hair length in humans
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Diseases of Hair
- Diseases of Hair
- Pigmentary mosaicism: An update
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Poster Presentations
- A rare case of woolly hair with unusual associations
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Update on hidradenitis suppurativa: connecting the tracts