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Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Polyamines help fix DNA damage accurately in cells.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Light therapy reduces scalp inflammation, boosts hair regrowth with Minoxidil 2%.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Immune cells are essential for early hair and skin development and healing.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

Light-based treatment, Photobiomodulation, shows promise for non-invasive skin therapy with few side effects.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Disabling the FGF5 gene in sheep leads to longer wool.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

Certain DNA regions in alpacas are linked to fiber diameter.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Three new types of a skin blistering disease were found, caused by specific gene mutations.