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

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Chemokine signaling is important for hair development.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Non-ablative and ablative fractional lasers helped hair growth in some cases without major side effects, but didn't work for all hair disorders.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

Taking too many vitamin and mineral supplements can cause serious health problems.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

Different skin diseases show unique patterns of skin cell separation, cell death, and granular layer changes.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

A gene mutation in mice causes permanent hair loss and skin issues.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Stem cells can help regenerate hair follicles.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

Dermatologists play a key role in identifying and documenting signs of abuse and injury for forensic investigations.

Thermoresponsive nanogels show promise for delivering medicine through the skin but need more safety testing and regulatory approval before clinical use.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Cell therapy shows promise for treating severe psoriasis but needs more research to confirm safety and effectiveness.