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Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Plant extracts may help prevent or reverse hair graying.

Editing the FGF5 gene in sheep increases fine wool growth.

Combination pharmacotherapy is generally more effective for treating keloids and hypertrophic scars.

Alopecia areata and vitiligo share immune system dysfunction but differ in specific immune responses and affected areas.

COVID-19 can lead to different skin symptoms and might trigger autoimmune diseases in genetically susceptible people.

Identified genes linked to male-pattern baldness may help develop new treatments.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

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

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Arsenic exposure from contaminated water severely damages the skin, causing hair loss, pigmentation changes, irritation, and can lead to skin cancer.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Human hair can almost fully recover its structure within about 1,000 minutes after being stretched.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

Two drugs, finasteride and minoxidil, are approved for hair loss treatment, but new therapies are being developed.

Biopolymers are increasingly used in cosmetics for their non-toxicity and skin benefits, with future biotech advancements likely to expand their applications.

Using existing drugs for new purposes could be a cost-effective way to treat chest pain and non-clogged heart arteries, with some drugs for lung blood pressure showing promise but needing more testing.

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

More research is needed to understand how testosterone is maintained in adult males.

Sex hormones affect hair growth and loss, and treatments for related hair diseases include various medications, hair transplantation, and light therapy.

Certain gene variations are linked to the thickness of cashmere goat hair.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

A child's hair loss after Kawasaki disease may help understand the disease's autoimmune causes.

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

People with chronic hair shedding had much lower vitamin D levels compared to healthy people.

Vitamin E affects liver metabolism, enhancing stress resistance, reducing blood clotting, and altering hormone processing.

Dr. Rodney Sinclair uses a detailed grading system to diagnose female pattern hair loss, recommends daily spironolactone and minoxidil for treatment, and believes genetics play a role in the condition.

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