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The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Certain transporters are found in human hair follicles and may affect hair growth and loss.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

The study found new details about human hair growth and suggests that preventing a specific biological pathway could potentially treat hair graying.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Pregnancy can cause specific skin conditions that need correct diagnosis and treatment to protect both mother and baby.

Pregnancy can cause skin changes and affect existing skin conditions, with limited treatment options due to the need for fetal safety.

Most pregnant women experience skin changes like darkening and itching, while serious skin conditions are rare but need early treatment.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

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

Disrupted cholesterol production impairs hair follicle stem cells, leading to hair loss.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Low IGF-1 and high HDL cholesterol levels are linked to more hair loss in middle-aged women.

Insulin helps heal corneal wounds and nerves in diabetic mice by activating the Wnt signaling pathway.

Certain vitamins and their derivatives can help hair grow longer by activating specific growth signals.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

Early onset female hair loss is linked to lower hair density, scalp issues, and certain genetic factors.

Jieduquyuziyin prescription helps treat SLE with atherosclerosis by improving cholesterol removal and reducing inflammation.

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

Skin-derived precursors in hair follicles come from different origins but function similarly.

Erbium glass laser treatment may help with skin remodeling, reduce inflammation, and improve skin cell maturation.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.