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Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

Oxidative stress worsens PCOS by damaging cells and disrupting metabolism, suggesting antioxidant treatments might help.

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.

Manipulating cell cleanup processes could help treat hair loss.

Lack of sleep in mice leads to prostatitis by reducing certain hormones and activating an inflammatory pathway, which can be temporarily fixed with normal sleep.

Smoking reduces antioxidants and causes DNA damage in hair follicles.

Bezafibrate treatment improved skin and spleen health in aging mice but didn't extend lifespan.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Rapamycin treatment helps reduce brain inflammation and symptoms of mitochondrial disease by blocking specific pathways in mice.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Non-surgical procedures can help reduce wrinkles and stimulate skin repair by understanding skin aging at the molecular level.

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

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Oxidative stress and immune dysfunction are linked to both Hashimoto's thyroiditis and polycystic ovary syndrome, with diet and specific treatments important for managing these conditions.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Cyanidin 3-O-arabinoside may help treat a common form of hair loss by protecting cells against aging and improving cell function.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

Apoptosis, not oxidative stress, is linked to aging in mice with mtDNA mutations.

Some HIV treatments can harm mitochondria, potentially causing side effects like lactic acidosis and nerve damage.