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TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

The development of breeding tubercles in male zebrafish relies on a specific enzyme that processes hormones.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Different keratins have unique expression patterns in mouse skin cells.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

A specific gene mutation causes a severe skin disorder in a family.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Tanshinone IIA helps protect skin tissue from low oxygen damage by boosting certain cell markers.

Smad2 and Smad3 are essential for normal skin development, and their absence causes severe skin issues and cancer.

Steroid sulfatase inhibitors could help treat hormone-related disorders and cancers.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

A fungal enzyme was used to make compounds more soluble, aiding drug discovery and crop protection.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

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

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Sebaceous glands help study fatty acid transporters and binding proteins.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

rRSPO1 protein boosts hair growth by activating a key signaling pathway.

ILC1-like cells can cause alopecia areata by themselves.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.