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.