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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

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

Thiopurines help treat IBD but require genetic testing to avoid side effects.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

The research found that certain microRNAs are important for human hair growth and health.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Researchers found genes linked to hair loss in male giant pandas.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

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

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

Hormones and genes affect hair growth and male baldness.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Certain fungi protect skin health, but changes can allow harmful fungi to cause serious infections, needing more research for treatment and control.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

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

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Androgens can both increase and decrease hair growth in different parts of the body.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Chronic inflammatory skin diseases are caused by disrupted interactions between skin cells and immune cells.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.