learn Osteopontin signaling protein that, when suppressed, may grow hair by reducing inflammation and stem cell loss
research A Syndromic Extreme Insulin Resistance Caused by Biallelic POC1A Mutations in Exon 10 7 citations, August 2017 in “European journal of endocrinology” Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.
research Atrichia With Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review 3 citations, January 2013 in “Dermatology” New genetic mutations causing hair loss were found in a Chinese family.
research Analysis of the Relationship Between the Mutation Site of the SLC39A4 Gene and Acrodermatitis Enteropathica: A Case Report and Literature Review 11 citations, January 2020 in “BMC pediatrics” New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.
research Hutchinson-Gilford Progeria Syndrome: Current Status and Prospects for Gene Therapy Treatment 39 citations, January 2019 in “Cells” Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.
research Hutchinson-Gilford Syndrome: History, Causes, Phenotype and Research Advances June 2023 in “GSC Advanced Research and Reviews” Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.