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Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

QLT0267 stops hair follicle cell growth and movement.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

The Shh gene controls cell growth and death in cashmere goat hair follicles, affecting hair growth.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.

Hairless gene not strongly linked to baldness.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Substances from human hair cells can affect hair loss-related genes, potentially leading to new treatments for baldness.

Blocking CXCR4 may help treat hidradenitis suppurativa.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Sgk3 kinase is essential for normal hair growth in mice.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

PDGFC gene may help select goats with desirable curly wool traits.

Hox genes are crucial for development and tissue maintenance, affecting structures and functions throughout life.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Key genes and pathways influence wool traits in Merino sheep.

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

A specific gene mutation causes sparse, brittle hair in a family.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

The model can effectively test gene functions and drug responses in human skin.