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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

Knocking out certain genes in mice helps understand skin and hair growth problems.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

NAG-1 may help prevent some metabolic issues related to PCOS.

Certain gene variations may increase the risk and severity of alopecia areata.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

PCOS shares similar genetic traits across different diagnosis criteria and is linked to other health conditions.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

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

Deleting TNFα gene reduces skin cancer risk in certain mice.

Higher free testosterone levels can increase bone density and decrease body fat but may raise the risk of prostate cancer, hair loss, and benign prostate enlargement.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

BMP signaling affects hair color by interacting with the MC-1R pathway.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Early over-expression of FoxN1 harms immune and skin development.

Understanding phenotypic plasticity is crucial for developing effective cancer therapies.

Gene expression, especially Dkk4, is key to cat color patterns.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.