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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Male pattern hair loss may be linked to the developmental origins of hair follicles.

Collagen VI is crucial for nerve function and affects wound-induced hair regrowth.

Meniran leaf extract pomade with 10% concentration effectively stimulates hair growth in rabbits.

Men's and women's pattern hair loss progress differently, with men showing more hair thinning and women having more widespread hair loss.

Genetic factors play a major role in acne.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

Targeted anticancer therapies can cause severe side effects similar to traditional chemotherapy, but with different types.

ERG increases SOX9, promoting prostate cancer growth and invasion.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Cannabinoids may help treat various skin conditions.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

Calcineurin inhibitors, used in kidney transplants, can cause a wide range of side effects including kidney damage and other health issues.

FGF5 gene mutations cause long hair in domestic cats.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Forensic DNA Phenotyping can help predict physical traits from crime scene DNA to identify suspects.

Methotrexate is not proven to maintain remission in ulcerative colitis.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Significant progress was made in understanding PXE, but effective treatments are still needed.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.