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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.

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

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Researchers developed a new method to identify animal hair in textiles, which is effective for various fibers and more reliable than previous methods.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Certain metabolites are lower in women with PCOS and could be potential markers for the condition.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

S100A3 protein is crucial for hair shaft formation in mice.

Cysteine-rich keratins evolved independently in mammals, reptiles, and birds for hard skin structures like hair, claws, and feathers.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Finasteride reduces alcohol withdrawal severity in male mice but increases it in female mice.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

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

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.

The conclusion is that future hair loss treatments should target the root causes of hair thinning, not just promote hair growth.

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 research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

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

Men with baldness at the front and top of their head at age 45 may have a higher risk of aggressive prostate cancer.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

People with alopecia areata often have higher rates of allergies and autoimmune diseases.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

In situ DNA labeling in hair can help predict forensic DNA analysis success.