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Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.

A specific gene variation in goats is linked to better growth traits.

TIP39 and PTH2R help control calcium levels and skin cell development.

Inhibiting ODC can prevent UV-induced skin cancer.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

pCLCA2 protein may help maintain skin structure and function.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

miR-199a-3p controls hair growth and is linked to alopecia areata.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Gene variation affects prostate issues and hair loss.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

The HCR gene contributes to psoriasis risk.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

Mutations in the KRT85 gene cause hair and nail problems.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

New genetic mutations causing hair loss were found in a Chinese family.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Specific keratin gene mutations can cause monilethrix.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.