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UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

New genetic mutations linked to rare skin disorders were found in three newborns.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Hedgehog signaling in certain cells is crucial for hair growth during wound healing.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Vitamin C deficiency changes gene expression, affecting skin and hair health.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Mice with alopecia areata had wider lymphatic vessels in their skin.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Zinc is crucial for skin health and treating various skin disorders.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

White blood cells and their traps can slow down the process of new hair growth after a wound.

The KRTAP21-2 gene affects wool length and quality in sheep.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Special proteins are important for skin balance, healing, and aging, and affect skin stem cells.

Autophagy helps control skin inflammation and cancer responses and regulates hair growth by affecting stem cell activity.