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Research 31–60 of 215
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Geriatric Dermatology: Overview
- Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Nucleocytoplasmic Communication in Progeria
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- STRESS AND AGING*
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- How to diagnose a lipodystrophy syndrome
- Syndromes of Severe Insulin Resistance (SSIRs)
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Scleroderma and L-tryptophan: A possible explanation of the eosinophilia-myalgia syndrome
- Werner′s syndrome
- Early Onset Werner Syndrome
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Efficacy and safety of SGLT2 inhibitor on insulin resistance and hyperglycemia in Werner syndrome—A case report
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- Male fertility and skin diseases
- Congenital atrichia and hypotrichosis
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- The Ayurvedic Management in Graying of Hair
- Hair Loss in Children
- Acquired Uncombable Hair
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family