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Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

FLRG and follistatin have different roles in wound healing.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

We need more research to better understand human hair follicle stem cells for improved treatments for hair loss and skin cancer.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

FGF5s can block the effects of FGF5, which may help control hair growth in cashmere goats.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Gene mutations can cause problems in male genital development.

Annurca apple supplement safely increases hair growth and keratin in humans.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

Kojyl cinnamate ester derivatives can promote hair growth by increasing adiponectin production in fat tissues.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Certain gene variations increase the risk of alopecia areata in Koreans.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.