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Research 481–510 of 1000+
- Bipolar Patients and Bullous Pemphigoid after Risperidone Long-Acting Injectable: A Case Report and a Review of the Literature
- Combination Therapy for Extensive Tumoral Calcinosis in Juvenile Dermatomyositis
- Bazi Bushen capsule alleviates skin photoaging by targeting the KEAP1–NRF2 pathway
- Zoonotic Majocchi's Granuloma of the Vulva.
- Coexistence of dermatomyositis and alopecia areata: Insight into pathogenesis
- A novel monoclonal antibody to the outer root sheath cells
- A concomitant diagnosis of COVID‐19 infection and systemic lupus erythematosus complicated by a macrophage activation syndrome: A new case report
- The use of dihydroxyacetone for photoprotection in variegate porphyria
- Desmoplastic tricholemmoma in a dog
- Engineering a 3D wounded skin equivalent to study early inflammatory and regenerative responses in vitro
- Bullous lesions in patients with cutaneous lupus erythematosus: A clinicopathologic study
- A Case of Linear Alopecia of the Scalp
- Four murine monoclonal antibodies specific for the inner root sheath in the human hair follicle
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- A case of sarcoidal foreign body reaction to permanent makeup: the involvement of M2 macrophages
- The Case Files
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Caspase-3 Regulates YAP-Dependent Cell Proliferation and Organ Size
- Primary Involvement of NADPH Oxidase 4 in Hypoxia-Induced Generation of Reactive Oxygen Species in Adipose-Derived Stem Cells
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- New-onset systemic lupus erythematosus beginning as class V lupus nephritis after COVID-19 vaccination
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Ornithine Decarboxylase Expression Leads to Translocation and Activation of Protein Kinase CK2 in Vivo
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Epigen Transgenic Mice Develop Enlarged Sebaceous Glands
- Clinical features of primary cicatricial alopecia in Chinese patients
- Dendritic epidermal T cells secreting exosomes promote the proliferation of epidermal stem cells to enhance wound re-epithelialization