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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

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

Women with greater androgen sensitivity respond better to finasteride for hair loss.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

Ducks can get the Rous sarcoma virus if infected shortly after birth, leading to tumors and disease spread.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Researchers found a genetic region that influences the number of coat layers in dogs.

The modified Direct Hair Transplantation method is effective for treating baldness with better graft survival and less damage than standard techniques.

The yeast found in a sea lion's skin lesion was almost identical to that on healthy skin, suggesting environmental factors may affect fungal growth and the cause of the lesion is unclear.

Finding functions for unknown GPCRs is hard but key for making new drugs.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

Mammals might fail to regenerate not because they lack the right cells, but because of how cells respond to their surroundings, and changing this environment could enhance regeneration.

The document concludes that good cosmetic outcomes in hair transplantation depend on the surgeon's artistic skill and careful planning.