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Certain changes to the B-ring of androgen receptor ligands can increase their effectiveness for potential treatments of muscle and bone conditions.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Asparagus racemosus root extract reduced sebum and pore size in men but not in women.

HEY2+ cells help regenerate skin during wound healing.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A girl had two rare hair conditions that helped understand their overlap.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

rRSPO1 protein boosts hair growth by activating a key signaling pathway.

Different keratins have unique expression patterns in mouse skin cells.

The composite sponge helps heal diabetic wounds by reducing inflammation and promoting new blood vessel growth.

Gene variation affects prostate issues and hair loss.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Blocking SEPT4 might help heal wounds and regrow hair faster.

Specialized ribosomes affect aging in human skin cells.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

The condition might be caused by genetic changes after birth.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

KLHL24-mutant stem cells help understand skin and heart disease.

RCS-01 is safe and may help rejuvenate aging skin.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

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

The technique effectively shows how human skin and hair cells form into ball-like structures.

Human hair follicles have a scent receptor that can influence hair growth.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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