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A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Skin RAGE levels are linked to inflammation and cell death.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Young donor, early passage stem cells have the highest stemness.

Pioglitazone may help treat lichen planopilaris, but more research is needed.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Lysophospholipids can act as anti-inflammatory agents through specific receptors, but more research is needed.

ZPK helps skin cells mature and may affect skin health.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

The research found that a protein called PPARg is important for the formation and healing of sebaceous glands, which can regenerate independently from hair follicles.

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.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

Nelfb is essential for dermal fat development and survival.

Dermal EZH2 controls skin cell development and hair growth in mice.

Sgk3 kinase is essential for normal hair growth in mice.

Glucocorticoids reduce fat production in liver cells, while androgens increase it in females; manipulating certain enzymes can influence these effects.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Gene therapy with a vitamin D receptor gene improved hair growth in rats with a type of rickets-related baldness.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.