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Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Rab5c is crucial for blood stem cell development by regulating Notch and AKT signals.

Actin and alpha-smooth muscle actin help skin heal in mouse fetuses.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

The Itpr3 gene causes a specific hair pattern in mice.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

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

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Keloid scars may form due to changes in skin cell characteristics and specific protein signaling.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Lack of KSR1 stops certain skin tumors in mice.

Efficient enzyme function relies on specific residue interactions and structural coordination.

EBF1 controls hair type and length.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Two specific genes are more active during hair growth in mice.

miR-370-3p slows sheep hair cell growth by blocking SMAD4.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

A gene mutation in mice causes skin defects and early death.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.