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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Some women with PCOS have rare genetic variants linked to the condition.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Thymic peptides can either promote or inhibit human hair growth.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

CD2 might be a new treatment target for patchy alopecia areata.

Researchers found potential urine markers for polycystic ovary syndrome, including testosterone-glucuronide and 11α-hydroxyprogesterone, which may help diagnose the condition.

Specific gene variants affect wool traits in Chinese Tan sheep.