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Research 181–210 of 183
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Male Pattern Baldness – Symptoms, Causes, and Treatments
- Oral Presentations
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Endoplasmic reticulum stress at the crossroads of progeria and atherosclerosis
- Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging.
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Genetics of Progeria and Aging
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Ocular manifestation in progeria: A case report
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Impaired Lef1 activation accelerates iPSC-derived keratinocytes differentiation in Hutchinson-Gilford Progeria Syndrome
- Hutchinson-Gilford progeria syndrome - A brief introduction
- 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
- Nucleocytoplasmic Communication in Progeria
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China
- A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)
- Hutchinson-Gilford Progeria Syndrome: Premature Aging
- Ocular manifestations of Hutchinson-Gilford-Progeria syndrome: A rare presentation
- Molecular studies of Hutchinson-Gilford progeria syndrome
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria
- Premature aging syndromes: From patients to mechanism
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Geriatric Dermatology: Overview
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations