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Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Aromatase gene variation may increase female hair loss risk.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Activating TLR9 helps heal wounds and regrow hair by using specific immune cells.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

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

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

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

The study could not confirm if Victor Vinnetou was Mbuyisa Makhubu and suggested more evidence, like DNA tests, is needed.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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

More people, especially Hispanic/Latinx, in certain NYC communities experienced temporary hair loss during the COVID-19 pandemic.

Many males in Jordan misuse oral contraceptive pills for hair growth, muscle gain, and acne treatment.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.