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A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

BAF200 is essential for proper heart and coronary artery formation.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

FOXO3 is essential for proper feather development in goose embryos.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

TSPO might help treat anxiety and depression.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

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

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Deleting part of a gene in mice causes wavy hair and high pup loss.

New pyrazole-based inhibitors show promise for treating metabolic diseases and other conditions.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

MLO proteins are crucial for root hair growth by regulating calcium and ROS levels.

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

A specific mutation in PA-PLA1α causes abnormal hair growth.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

CDP is crucial for lung and hair follicle cell development.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.