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Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

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

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A mutation in the Sgkl gene causes defective hair growth in mice.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

p63 controls Satb1 to help skin develop properly.

A rare gene variant causes hair and nail issues in a family.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Three genes linked to the development of trichilemmal cysts were found.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

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

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Phospholipase C-δ1 is crucial for normal hair development.

CXCR2 in skin cells promotes tumor growth.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

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

Mutations in the KRT85 gene cause hair and nail problems.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

The HCR gene contributes to psoriasis risk.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.