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Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

Protein Kinase C shows promise for cancer treatment, but more research is needed to develop effective inhibitors.

DA-9401 helps protect rat testis from finasteride damage.

Scientists discovered two versions of a new human hair keratin gene.

YAP1 helps fat cell formation by influencing the Hippo pathway.

A specific gene change is linked to severe hair loss.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Runx1 helps control the KAP5 gene in human hair follicles.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

TRPV4 slows hair growth by affecting hair follicle cells.

Gene variations may increase oxidative stress in male pattern baldness.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

A new treatment using nanoparticles can effectively prevent and reduce hair loss caused by chemotherapy.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Keratins are crucial for cell structure, growth, and disease risk.

A new mutation in the HR gene causes hair loss in a specific family.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Epristeride's metabolism in zebrafish helps improve doping detection methods.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Blocking mTORC1 reduces skin tumor growth in mice.

Androgens may increase arrhythmias in Brugada Syndrome, while Finasteride could reduce them.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.