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Estrogen increases blood vessel growth factor production, while testosterone blocks this increase.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Hairless gene not strongly linked to baldness.

About half the patients treated with capecitabine and docetaxel developed severe hand-foot syndrome.

Minoxidil foam helps hair growth by increasing good proteins and decreasing bad pathways in men with hair loss.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

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.

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

Longer CAG repeats in gene linked to more severe hair loss in females.

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

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

Mutation in hairless gene may increase hair loss risk.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.