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Research 211–240 of 1000+
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- Resident macrophages of the lung and liver: The guardians of our tissues
- Cells, growth factors and biomaterials used in tissue engineering for hair follicles regeneration
- Auditory Threshold Variability in the SAMP8 Mouse Model of Age-Related Hearing Loss: Functional Loss and Phenotypic Change Precede Outer Hair Cell Loss
- Repurposing Auranofin for Oncology and Beyond: A Brief Overview of Clinical Trials as Mono- and Combination Therapy
- Molecular Morbidity Score–Can MicroRNAs Assess the Burden of Disease?
- Self-Assembled Peptide Hydrogels in Regenerative Medicine
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Premature aging syndromes: From patients to mechanism
- Nucleocytoplasmic Communication in Progeria
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Incidence of liver toxicity associated with the use of flutamide in prostate cancer patients
- Toxicologic studies with the hypotensive agent minoxidil
- Epidermal Stem Cells Manipulated by pDNA-VEGF165/CYD-PEI Nanoparticles Loaded Gelatin/β-TCP Matrix as a Therapeutic Agent and Gene Delivery Vehicle for Wound Healing
- A patient with combined polycystic ovary syndrome and autoimmune polyglandular syndrome type 2
- Progeroide Syndrome
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- CFTR potentiator ivacaftor protects against noise-induced hair cell loss by increasing Nrf2 and reducing oxidative stress
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor