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Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

Reducing SOX2 in colorectal cancer cells decreases tumor growth and self-renewal.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

p63 controls Satb1 to help skin develop properly.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

A specific gene change in APCDD1 increases the risk of hair loss.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

A specific gene mutation causes woolly hair and hair loss.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

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

Overexpressing COX-2 in mice skin reduces skin tumor development.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A gene mutation causes curly hair and hair loss in rats.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Higher levels of the protein Pannexin-1 may play a role in hair loss in women with PCOS.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

The E2 protein affects gene activity in hair follicles of mice.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.