Search

everythinglearnresearchcommunity

for

Search:↓

A new DSG4 gene mutation causes hair defects in a young girl.

The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

A specific gene mutation causes congenital hair loss.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

KRT72 gene helps form hair.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

cDermo-1 causes dense skin, feathers, and scales in chickens.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Two gene areas linked to male pattern baldness found, more research needed.

A new gene mutation is linked to monilethrix in the studied family.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

Some people have a genetic variation that makes them less effective at breaking down drugs.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Gene therapy in mice increased lifespan and improved health without causing cancer.

The EDAR gene greatly affects hair thickness in Asian populations.

The research helps in creating genetically modified animals to study hair growth.