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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

B-Raf and C-Raf are essential for maintaining melanocyte stem cells to prevent hair graying.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Matriptase is crucial for skin, hair, and immune cell health, and its imbalance can lead to cancer.

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Two new gene mutations cause a rare hair disorder.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Low-penetration genes might help personalize colorectal cancer prevention.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe symptoms and organ damage in mice.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

MEX3A is crucial for maintaining intestinal stem cells in mice.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.