Search

everythinglearnresearchcommunity

for

Search:↓

Metformin is less effective in men with early-onset hair loss.

A new mutation in the HR gene causes hair loss in a specific family.

Ionizing radiation damages human hair follicles by stopping cell growth, causing cell death, disrupting color, and increasing stress and damage markers.

Examining scalp biopsies in different ways helps better diagnose hair loss types.

Adult skin cell-based early-stage skin substitutes improve wound healing and hair growth in mice.

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

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Telogen Effluvium is a common, usually reversible hair loss condition, often improved by removing the trigger and possibly treated with various products, though their effectiveness is uncertain.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

The document concludes that while some hair and scalp disorders can be treated, hair loss from destroyed follicles is permanent, and damaged hair can only regrow naturally.

Hair loss in children can be caused by fungal infections, trauma, autoimmune disorders, or stress, and treatments vary depending on the cause.

Arrector pili muscle regulates hair follicle stem cells, DNA methylation needed for hair cycling, and Wnt/B-catenin signaling starts hair growth.

Hypothyroidism harms rat skin, but topical triiodothyronine may help improve it.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

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

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

Hair transplantation is highly effective with careful technique and attention to patient needs.

Too much epidermal growth factor can cause hair loss.

The patient's long-term hair loss was caused by leukemia treatments and low estrogen levels, worsened by her genetic tendency for hair loss.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

The exact cause of growth hormone-responsive alopecia in dogs is unclear.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Topical calcitriol-analogs can reduce hair loss caused by chemotherapy.

Low zinc levels might contribute to early hair graying.

Getting a hyaluronic acid filler can sometimes cause temporary hair loss due to pressure on an artery, not blockage.

TGF-β1 increases androgen receptor activity in hair loss, but Hic-5/ARA55 can counter this effect.

Mutations in the LSS gene cause a rare type of hereditary hair loss.