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5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Glucosylceramides are essential for healthy skin and proper wound healing.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

A gene mutation in Lama3 is linked to a common type of hair loss.

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

The study found that aging hair follicle stem cells change behavior, leading to hair loss, but drugs targeting these cells may help restore hair growth.

p120-catenin helps control skin inflammation by regulating cadherin levels.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

Autophagy helps delay aging in mouse glands, maintains fat balance, and controls scent production.

Zebrafish with mutations similar to human Cantú Syndrome have heart cells with altered channel properties, making them a good model to study the condition.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Hox genes control hair follicle stem cell regeneration in different body regions.

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

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Wnt ligands, produced by dermal papilla cells, are essential for adult hair growth and regeneration.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Blocking mTORC1 reduces skin tumor growth in mice.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

The Hairless gene is crucial for healthy skin and hair growth.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

SOX4 is crucial for the development of melanoma.

Hair loss in certain mice is linked to changes in keratin-related genes.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.