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FERONIA regulates plant growth, pollen interactions, and sugar signaling.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

NFIC helps rat dental cells grow and turn into bone-like cells.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Id2 gene helps keep hair follicle stem cells inactive.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

4-octyl itaconate may prevent hearing loss caused by the drug cisplatin by activating certain cell protection pathways.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Fgfr2b helps maintain healthy skin and prevent cancer.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Ift20 is essential for hair follicle function and skin cell movement.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

The vector successfully directed specific gene expression in hair follicles.

Far-infrared radiation improves stem cell growth and movement, helping heart therapy.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

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

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

NFIB and STAT5 work together to control specific genetic programs in cells.