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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

The method allows for 3D tracking of hair follicle stem cells and shows they can regenerate hair for up to 180 days.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Rac1 is essential for proper hair structure and color.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Ptprq has multiple forms that change during inner ear development.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Finasteride exposure affects gene expression and anogenital distance in male rat fetuses.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Effective, well-tolerated, and affordable treatments are needed for recurrent ischemic priapism.

Finasteride caused blisters on hands and feet.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

HPV genes and estradiol increase a cancer-related signaling pathway, which may be targeted for cervical cancer treatment.

HO-1 helps skin health and healing but can worsen melanoma; it's a potential treatment target for skin diseases.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Dutasteride works better than finasteride for preventing and treating prostate cancer.

MC4R gene variants not linked to female hair loss.

ILK is essential for skin development, pigmentation, and healing.

The document suggests a rare skin condition might be caused by a genetic phenomenon.