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Research 331–360 of 1000+
- Epidemiological Transition and Forecasting of Diabetes Burden in Saudi Arabia: A Comprehensive Analysis From the Global Burden of Disease Study 1990–2023
- A COMPREHENSIVE REVIEW ON TRIDAX PROCUMBENS LIN
- Evaluation of anti-Zika virus activities of broad-spectrum antivirals and NIH clinical collection compounds using a cell-based, high-throughput screen assay
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- S100A6: molecular function and biomarker role
- PROTACs: A novel strategy for cancer drug discovery and development
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- Primary High‐Grade Ovarian Sertoli–Leydig Cell Tumor With Bilateral Adnexal Involvement in a Patient Diagnosed With Peutz–Jeghers Syndrome
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- Gonadal Suppressive and Cross‐Sex Hormone Therapy for Gender Dysphoria in Adolescents and Adults
- Multiple Autoimmune Syndrome type 3- Thyroiditis, Vitiligo and Alopecia Areata
- S100A6 Protein—Expression and Function in Norm and Pathology
- Discovery of COVID-19 Inhibitors Targeting the SARS-CoV2 Nsp13 Helicase
- 66-Year-Old Woman With Painless Vesicular Lesions
- Endocrine Management of Adult Gender-Dysphoric/Gender-Incongruent Persons: A Clinical Practice Guideline from Endocrine Society of India
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Two cases of low-prostate-specific antigen localized prostate cancer incidentally detected by computed tomography
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Cold thermal injury from cold caps used for the prevention of chemotherapy-induced alopecia
- Adenovirus-Mediated Wnt5a Expression Inhibits the Telogen-To-Anagen Transition of Hair Follicles in Mice
- Metabolic syndrome in androgenic alopecia
- Recent Advances in Peptide Drug Discovery: Novel Strategies and Targeted Protein Degradation
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Female pattern hair loss: A retrospective study in a tertiary referral center
- Female pattern hair loss