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The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

New genetic mutations causing hair loss were found in a Chinese family.

A mother's diet at conception can cause lasting genetic changes in her child.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Understanding phenotypic plasticity is crucial for developing effective cancer therapies.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

The SOSTDC1 gene is crucial for determining sheep wool type.

Minoxidil promotes hair growth by increasing cell division and DNA synthesis.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

DNA methylation changes are linked to hair growth cycles in goats.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

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

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.