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Certain gene combinations may affect prostate cancer risk, and GSTP1 methylation is linked to tumor aggressiveness.

GLI2 increases follistatin production in human skin cells.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

FGF5 gene mutations cause long hair in domestic cats.

Childhood growth hormone deficiency can be accurately diagnosed using gene expression data and random forest analysis.

Graying hair is caused by changes in gene expression affecting cell functions.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Mutations in the hairless protein gene cause hair loss.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Enhancing CD8+ T cell function to induce ferroptosis in tumor cells may help treat skin melanoma.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Melatonin receptor genes likely play an important role in the development of goose feather follicles.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Mutation in hairless gene may increase hair loss risk.

Fox genes are important for hair growth and development in cashmere goats.

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

Antizyme slows skin tumor growth by reducing cell growth in mice.

Melatonin shortens the hair growth cycle by increasing PDGFA gene expression.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.