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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Exosomes show promise for tissue repair and regeneration with advantages over traditional cell therapies.

Targeting ornithine decarboxylase can help prevent skin cancer.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Four new genes related to sheep wool were discovered, showing genetic diversity.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Hoxc13 is essential for hair growth and follicle development.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

LGD1069 effectively prevents breast tumors in mice without toxicity.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

IGN genes may regulate hair growth and could be targeted for hair-loss treatments.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

The study identified key genes involved in goat hair growth.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Exosomes from dermal papilla cells can help grow hair and might treat hair loss.

EGFRi/MEKi treatments cause hair follicles to lose some immune protection, leading to inflammation.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Exosomes protect ear hair cells from damage by controlling cell waste removal, potentially helping treat hearing loss.

EGFR helps hair follicles transition properly by controlling Stathmin levels.