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The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Disabling the FGF5 gene in sheep leads to longer wool.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Chemotherapy-induced hair loss is partly due to decreased laminin-511 and increased laminin-332.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

FGF5 gene mutations cause long hair in domestic cats.

Sebaceous glands can heal and regenerate after injury using their own stem cells and help from hair follicle cells.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

Taking an amino acid supplement improved skin, hair, and nail health in women.

Hoxc13 is linked to seasonal hair growth in Cashmere goats and is affected by melatonin.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Twist2 is essential for proper skin healing and hair growth in developing mice.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Feather growth and regeneration involve complex patterns, stem cells, and evolutionary insights.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Lack of cystatin M/E causes thin hair and dry skin.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Some herbal ingredients like linalool and tea tree oil have anti-dandruff properties and are safe for use in shampoos.