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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

UC.145 may be a new biomarker for predicting gastric cancer.

RXR agonists may promote hair growth in humans.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

The gene Prss53 affects hair shape and bone development in rabbits.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

ΔNp63α helps control a protein that stops cancer cells from spreading.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

KRT72 gene helps form hair.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

RANK-RANKL signaling is essential for hair growth and skin health.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

A protein complex called mTORC1 likely affects when hair growth starts in mice.

The hairless protein is important for skin, hair, and may influence cancer development.

Krtap11-1 is important for hair strength and structure.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Targeting the TNFRSF1B gene may help treat hair loss.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

The FRZB gene slows hair growth in rabbits.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

The Celsr1 gene is crucial for normal hair patterning in mice.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.