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The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The treatment improved survival and controlled cancer spread but required managing side effects like rashes.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Boron/nitrogen-doped carbon nano-onions improve targeted breast cancer treatment by enhancing drug delivery and reducing side effects.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

TICE salvage chemotherapy is effective for treating germ-cell tumors with poor prognosis.

Combining genetic models helps improve heat tolerance in beef cattle.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Netherton's disease causes multiple hair defects.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

CTP-543 is generally safe for treating alopecia areata.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Seven new genetic risk areas for prostate cancer were found.