The hair follicle (HF) is a highly conserved sensory organ associated with the immune
response against pathogens, thermoregulation, sebum production, angiogenesis …

Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare, uniformly fatal,
segmental “premature aging” disease in which children exhibit phenotypes that may give us …

Progeria: A Paradigm for Translational Medicine: Cell Skip to Main Content Advertisement Cell
This journal offers authors two options (open access or subscription) to publish research This …

Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare premature aging
disease presenting many features resembling the normal aging process. HGPS patients die …

Preservation of adult stem cells pools is critical for maintaining tissue homeostasis into old
age. Exhaustion of adult stem cell pools as a result of deranged metabolic signaling …

Alopecia is a common and distressing medical condition that has affected a majority of
people worldwide, which leads to great effects on the quality of life and self-esteem …

Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disease that causes
premature aging symptoms, such as vascular diseases, lipodystrophy, loss of bone mineral …

Lamin A-related progeroid syndromes are genetically determined, extremely rare and
severe. In the past ten years, our knowledge and perspectives for these diseases has widely …

The skin represents the first bearer of marks of time as well as an easily accessible model for
the assessment and determination of the involved molecular mechanisms. The deterioration …

Progerin expression disrupts critical adult stem cell functions involved in tissue repair - PMC
Back to Top Skip to main content NIH NLM Logo Access keys NCBI Homepage MyNCBI …