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Moracin M boosts hair growth by activating key pathways and promoting cell growth.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

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

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

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

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

MED1 affects skin wound healing differently in young and old mice.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

MC4R gene variants not linked to female hair loss.

The research found that a protein called caveolin-1 is reduced in psoriasis, but reintroducing it can help alleviate some psoriasis symptoms.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Localized ROS production is essential for cell growth and movement in plants and animals.

CD98hc's role in skin health decreases with age.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

EdnrB signaling helps melanocyte stem cells regenerate and could be targeted to treat pigmentation issues.

Ceramide Synthase 4 is crucial for healthy skin barrier function.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

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

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.