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Groundbreaking research unveils genetic characteristics and improved prognosis of triple negative apocrine carcinoma

Researchers identified distinct genomic characteristics that impact prognosis for patients with triple negative apocrine carcinoma. The study confirmed a five-year disease-free survival rate of 92.2% for these patients, significantly higher than those diagnosed with other types of TNBC.

Oncotarget: Cutaneous apocrine sweat gland carcinoma

Researchers analyzed DNA repair targeting in cutaneous apocrine sweat gland carcinoma (CAC) cells with a PALB2 aberration. They found sensitivities to BET-bromodomain inhibition and modest sensitivity to DNA-PKi, ATRi, WEE1i, and PARPi. The study also identified a potential therapeutic opportunity for targeting PALB2 deficient cells th...

SourceImpact Journals LLC·JournalOncotarget·DateJul 19, 2021

Perspiration problems? No sweat!

Osaka University researchers have generated immortalized human eccrine sweat gland myoepithelial cells (iEM cells), which can be cultured for over ten generations. This achievement has the potential to develop next-generation antiperspirants and promote research on sweat dysfunction and regeneration.

Scientists unravel the mystery of a rare sweating disorder

A rare genetic disorder called anhidrosis has been linked to a mutation in the ITPR2 gene, which controls calcium release in sweat glands. The study, led by Katsuhiko Mikoshiba and Niklas Dahl, found that a single nucleotide change in the DNA code impairs sweat production, leading to hyperthermia risk.

SourceRIKEN·JournalJournal of Clinical Investigation·DateOct 20, 2014

First animal model of recent human evolution

A team of researchers created an animal model of recent human evolution, revealing a single mutation that produced several traits common in East Asian peoples. The study found that the mutation arose around 30,000 years ago in central China and is linked to thicker hair, denser sweat glands, and other skin features.

SourceHarvard Medical School·JournalCell·DateFeb 14, 2013

Mutation linked with the absence of fingerprints

Scientists have identified a rare genetic mutation that underlies adermatoglyphia, a condition characterized by the complete absence of fingerprints. The study provides valuable insight into the genetics of fingerprint formation and highlights the usefulness of rare genetic mutations in understanding human biology.

SourceCell Press·JournalAmerican Journal of Human Biology·DateAug 4, 2011