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Research 211–240 of 213
- Liposomal Helix aspersa Snail Mucus: A Biomacromolecular Platform for Attenuating Chronological Skin Aging Through Modulation of miR-34a-Associated Senescence and Extracellular Matrix Remodeling
- GLP-1 RAs and Skin Health: Exploring Dermatologic Side Effects and Therapeutic Interventions
- 612 Wnt signaling induces fibrotic fat loss via DPP4 in skin fibrosis
- Progeroide Syndrome
- BG02 A case of Werner syndrome: undiagnosed progeroid syndrome presenting as female pattern hair loss
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- 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
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging.
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Shared Phenotypes Among Segmental Progeroid Syndromes Suggest Underlying Pathways of Aging
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- 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
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China
- Impaired Lef1 activation accelerates iPSC-derived keratinocytes differentiation in Hutchinson-Gilford Progeria Syndrome
- 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 - A brief introduction
- Hutchinson-Gilford Progeria Syndrome: Premature Aging
- Ocular manifestations of Hutchinson-Gilford-Progeria syndrome: A rare presentation
- Molecular studies of Hutchinson-Gilford progeria syndrome
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Myotonic Dystrophy—A Progeroid Disease?
- For early diagnosis of young patients with Werner syndrome: Indication for genetic testing
- Premature aging syndromes: From patients to mechanism
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Endoplasmic reticulum stress at the crossroads of progeria and atherosclerosis