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The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

VDR regulation varies by tissue and is crucial for its biological functions.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Cow placenta extract may help hair grow by increasing a growth factor but is less effective than minoxidil.

HB-EGF boosts the hair growth ability of stem cells, making it a potential hair loss treatment.

Cinnamomum osmophloeum leaf extract may help treat hair loss by promoting hair growth and increasing hair cell proliferation.

Blocking neurosteroid production can lead to more seizures and faster epilepsy onset in rats.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

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

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Cyanidin 3-O-arabinoside may help treat a common form of hair loss by protecting cells against aging and improving cell function.

Vanillic acid from wheat bran may promote hair growth by activating certain cell pathways and reversing hormone-related hair loss.

A specific gene mutation causes Olmsted syndrome.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Certain IL-18 gene variations may increase the risk of alopecia areata.

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

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

Udenafil may help hair grow by activating certain stem cells.