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Research 451–480 of 1000+
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Compound glycyrrhizin promotes hair growth in C57BL/6 mice by regulating the Wnt/β-catenin pathway
- P-Phenylenediamine-Induced Angioedema-like Facies: A Case Report and Review of Pathomechanisms
- An off-the-shelf bioactive EV delivering cryogel orchestrating immunomodulatory reprogramming and angiogenesis for diabetic ulcer healing
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Emerging Role of Dermal White Adipose Tissue in Modulating Hair Follicle Development During Aging
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Biology, diagnosis and treatment of <i>Malassezia</i> dermatitis in dogs and cats
- Multi-functional nanozyme-integrated astragalus polysaccharide hydrogel for targeted phased therapy in diabetic wound healing
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Dermal Blimp1 Acts Downstream of Epidermal TGFβ and Wnt/β-Catenin to Regulate Hair Follicle Formation and Growth
- Opposing impacts on healthspan and longevity by limiting dietary selenium in telomere dysfunctional mice
- Nanofiber-mediated sequential photothermal antibacteria and macrophage polarization for healing MRSA-infected diabetic wounds
- Understanding the Role of Type I Interferons in Cutaneous Lupus and Dermatomyositis: Toward Better Therapeutics
- Systemic Lupus Erythematosus: What Every Clinician Needs to Know
- Influence of Atopic Dermatitis on the Dermoscopic Phenotype of Positive Patch Test Reactions: A Prospective Comparative Study
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Retinoic acid drives hair follicle stem cell activation via Wnt/β‐catenin signalling in androgenetic alopecia
- A Chronic Contact Eczema Impedes Migration of Antigen-Presenting Cells in Alopecia Areata
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Aesthetically relevant symptoms of menopause transition: Impact and approach to management
- THE INFLUENCE OF SKIN MICROBIOME IMBALANCE ON SPECIFIC PATHOLOGICAL SKIN CONDITIONS
- Neuroimmunomodulation in chronic wounds: an opinion
- Brain and muscle Arnt-like protein-1 (BMAL1) controls circadian cell proliferation and susceptibility to UVB-induced DNA damage in the epidermis
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Ontogenetic Transition in Fetal Wound Transforming Growth Factor-β Regulation Correlates with Collagen Organization
- Controlled Delivery of T-box21 Small Interfering RNA Ameliorates Autoimmune Alopecia (Alopecia Areata) in a C3H/HeJ Mouse Model