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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

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New compounds were made that effectively block a specific enzyme related to androgen conditions.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

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Vepdegestrant may become the first FDA-approved PROTAC degrader, marking a new era in drug development.

HA-P5 effectively treats acne without causing side effects seen in other treatments.

A specific gene mutation causes woolly hair and hair loss.

The 1540nm fractional erbium-glass laser helps treat hair loss caused by hormones.

A girl had rickets due to a gene mutation affecting vitamin D response.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

TH07 is a topical combination of finasteride, latanoprost, and minoxidil, and shows promise.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

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

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

A new method to make finasteride for hair loss treatment was developed.

5ARI treatment improves PSA test accuracy for prostate cancer diagnosis.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.