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A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Blocking the prolactin receptor might help treat various diseases, but more research is needed.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Researchers found two new genetic variants linked to Alzheimer's disease.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

No clear link between specific gene and hair loss in Mexican brothers.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Researchers found 15 new genetic links to skin traits in Japanese women.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Some early COVID-19 mutations in patients predicted future common virus mutations.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

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

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new AI model diagnoses hair and scalp disorders with 92% accuracy, better than previous models.

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

Hormones and genes affect hair growth and male baldness.

Selective breeding caused the unique curly hair in Mangalitza pigs.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

The document concludes that diagnosing and treating Human African Trypanosomiasis is challenging, but new treatments like fexinidazole are promising.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.