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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Mesothelioma of the tunica vaginalis testis is rare, often high-grade, and has a median survival of about 24 months.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Maternal melatonin improves offspring hair growth by affecting specific proteins and pathways.

A gene mutation causes monilethrix in a Chinese family.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

MCHR2 gene duplications may be linked to alopecia areata.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

5% topical minoxidil improves hair density and quality in monilethrix patients.

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

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

A gene mutation causes curly hair and hair loss in rats.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

FOXN1 gene variants cause low T cells and immune issues from birth.

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.