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Finasteride improves heart function and repairs damage after heart attack in mice.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

FOXN1 gene variants cause low T cells and immune issues from birth.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).

An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.

Alopecia areata in infants may be more common than previously thought.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

The review recommends hormone replacement therapy for women with premature ovarian insufficiency to manage symptoms and protect health, with specific approaches for different groups.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Mutant mice help researchers understand hair growth and related genetic factors.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

The document concludes that understanding hair follicle cell cycles is crucial for hair growth and alopecia research, and recommends specific techniques and future research directions.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Hair loss patients have different microbes in hair follicles, possibly affecting hair loss.

Different cell types work together to repair skin, and targeting them may improve healing and reduce scarring.

Dicer is crucial for hair growth in mice.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

CD2 might be a new treatment target for patchy alopecia areata.