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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

The Gsdma3 gene is essential for normal hair development in mice.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

FGF signaling is crucial for starting feather development in chicken embryos.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

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A genetic change in the FGF5 gene affects hair growth in cashmere goats.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

NFIB and STAT5 work together to control specific genetic programs in cells.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

FLCN helps control iron levels in cells.

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

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

A new gene mutation is linked to monilethrix in the studied family.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

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.