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FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

Foxn1 is important for fat development, metabolism, and wound healing in skin.

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

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

TNFα helps grow and maintain liver cells in 3D culture for a long time.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

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

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

Sebaceous glands help study fatty acid transporters and binding proteins.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Nod factor can trigger changes in legume root hairs with just one molecule.

Nanofat shows promise for facial rejuvenation and treating skin issues but needs more research for long-term safety.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Fatp4 is crucial for healthy skin development and function.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.