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Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

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

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Heavy ion radiation has a more severe and long-lasting effect on mouse intestinal metabolites than gamma radiation.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

Haplogroup X found in Altaian population supports Amerindian origin.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Vitamin D receptor may help protect against UV-induced skin cancer.

Hair follicle stem cells can return to their original niche and help regenerate hair.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A gene called HDAC9 might be a new factor in male-pattern baldness.

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

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

HLA-DRB5 and other genes may be linked to alopecia universalis.