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The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Certain genes control the color of human hair by affecting pigment production.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

High mTORC1 activity slows hair growth and causes it to lose color.

Cell-based models help test if cosmetic ingredients really work for hair growth and skin health.

Gray hair can potentially be reversed, leading to new treatments.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Hair color is determined by melanin produced and transferred in hair follicles.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

The Itpr3 gene causes a specific hair pattern in mice.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Cell aging can be both good and bad for tissue repair.

Hair color production in mice is closely linked to the hair growth phase and may also influence hair growth itself.

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Applying a specific inhibitor lightens skin and hair color.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Human skin's melanocytes respond to light by changing shape, producing pigments and hormones, which may affect sleep patterns.

Hair color is determined by different melanins and changes with age.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A mother's diet at conception can cause lasting genetic changes in her child.

New oral treatment, finasteride, effectively and safely treats common hair loss.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Male pattern baldness involves genetics, hormones, and needs better treatments.

The conclusion is that hair growth can be improved by activating hair cycles, changing the surrounding environment, healing wounds to create new hair follicles, and using stem cell technology.

The balance between androgen receptor and p53 is crucial for sebaceous gland differentiation.