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Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

Blocking YAP/TAZ could be a new way to treat skin cancer.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Inhibiting Bmp signaling disrupts hair growth and differentiation.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

BMPR1a-ECD reduces wrinkles much more effectively than retinoic acid.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Modulating the BTNL2 pathway can prevent hair loss in mice.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Hoxc13 gene is essential for hair, nail, and papilla development.

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

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

Akt2 protein is essential for normal cell division in early mouse embryos.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Bezafibrate treatment improved skin and spleen health in aging mice but didn't extend lifespan.