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Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Understanding genes and mutations can lead to new treatments for hair loss disorders.

Diet changes can protect against harmful environmental effects on fetal development.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Genetic factors can help predict male pattern baldness risk.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

The package offers tools for exploring potential miRNA changes in female hair loss.

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

Certain genes influence wool, growth, and reproduction traits in Uruguayan Merino sheep.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Rodent spiny hair traits are due to genetic factors other than the Edar gene.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Robertsonian translocation can cause recurrent miscarriages.

Genetic factors can predict male pattern baldness risk.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

The study found potential new DNA patterns in fertility genes, but further testing is needed.

New genes linked to male pattern baldness were found on chromosome 20p11.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Key genes and pathways influence wool traits in Merino sheep.