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Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Nelfb is essential for dermal fat development and survival.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Lack of Fgf21 slows hair growth by affecting gene interactions.

NIPP1 is important for healthy skin and could help treat skin inflammation.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A low-protein diet with methionine is cost-effective and supports normal growth and high-quality pelts in blue foxes.

Targeting regulatory T cells may help treat age-related diseases.

Too much Sonic Hedgehog protein stops hair growth in embryos.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Fatp4 is crucial for healthy skin development and function.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

PBX1 helps reduce aging and cell death in hair follicle stem cells by decreasing DNA damage, not by improving DNA repair.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Researchers found a way to make rat hair follicle cells start turning into motor neuron-like cells, but couldn't fully turn them into working motor neurons.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A woman with Fox-Fordyce disease had symptom relief using tretinoin cream.

Lef1 helps adult skin cells maintain their ability to heal wounds and regenerate hair, but the study's methods and conclusions have been questioned.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

Blocking EGFR in mice causes hair loss and skin changes.

Sox9 is important in the development of tumors in domestic animals.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A specific gene mutation causes long hair in Angora rabbits.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.