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Using finasteride with TIP extends time off period for prostate cancer patients.

Skin organoids are a promising new model for studying human skin development and testing treatments.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

BMP2 needs periosteal tissue to help regenerate mouse middle finger bones within a specific time.

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Placental growth factor may help treat hair loss.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

People with Seasonal Affective Disorder have different brain activity in certain areas when resting.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

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

Stress activates a special function of the Vitamin D receptor with the help of c-Jun, which can also prevent cell death.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Activating NRF2 might help treat hair disorders by improving antioxidant defenses.

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.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

South Asian women with PCOS present with different symptoms compared to White women, influenced by ethnicity, obesity, and age.

Injecting alpha-melanocyte-stimulating hormone in mice improved skin healing and reduced scarring.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Eating isoflavone can help mice grow hair by increasing a growth factor.

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The Cross-section Trichometer is a new tool that can measure hair quantity and detect hair loss and growth.

DNA methylation changes are linked to hair growth cycles in goats.

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

Removing vitamin D and calcium receptors in mice skin cells slows down skin wound healing.