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miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Using deep learning to predict gene expression from images could help assess colorectal cancer metastasis.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

CDP is crucial for lung and hair follicle cell development.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Certain miRNAs may influence cashmere fiber traits in goats by affecting hair follicle activities.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

ASLNC168501 can help treat hair loss by restoring hair follicle stem cell function.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

Specific genes influence hair and cashmere growth in Laiwu black goats.

ILC1-like cells can cause alopecia areata by themselves.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Defective protein folding due to a mutation is key in ANE syndrome.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

A truncated protein linked to breast cancer may change cell adhesion.