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Long-term use of dutasteride for enlarged prostate may worsen blood sugar, cholesterol, and erectile dysfunction.

Whale genes show changes that help them live in water, like less hair and better flippers.

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

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Gene therapy shows promise for enhancing physical traits but faces ethical, safety, and regulatory challenges.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Mutation in hairless gene may increase hair loss risk.

A genetic marker linked to a type of hair loss was found in most patients studied.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Mutation in hairless gene may increase hair loss risk.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new gene mutation causes insulin resistance in a girl and her mother.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.