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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Mrp3 may aid in wound healing and hair growth.

Activating PKM2 and Wnt/β-catenin signaling together can potentially enhance hair growth and could be a treatment for hair loss.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

Activating PKM2 and Wnt/β-catenin signaling speeds up wound healing.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

Mast cell and nerve fiber interactions in mouse skin change with the hair cycle.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

PKM2 is a promising target for heart repair and regeneration.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.

MPA increases cancer spread by boosting Eph A2 activity.

HoxC genes are crucial for normal hair and nail development.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

Removing Mediator 1 causes teeth cells to turn into hair cells.

A new mouse mutation causes skin and hair defects due to a gene change.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

Minoxidil sulfate and pinacidil promote hair growth likely by increasing blood flow, not by activating K channels.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A new mutation in mice causes crooked whiskers and messy hair.