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Certain gene variations might increase the risk of a hair loss condition in Koreans.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A specific gene mutation causes congenital hair loss.

Finasteride increases CD8+ T cells in BPH tissues.

A20 protein is crucial for normal skin and hair development.

Agalsidase alfa helps treat Fabry's disease but needs more research for long-term benefits.

The FDA did not approve certain drugs for prostate cancer prevention due to concerns about their effectiveness and potential risks.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Certain gut bacteria can lower androgen levels in male mice.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

A parasite molecule can speed up skin healing and reduce scarring.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

IGFBP5 may be a potential target for Parkinson's treatment by reducing neuron death.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.