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DNA changes in tetraploid wheat improve root growth and nitrogen use.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The study mapped yak skin cells to understand hair growth better.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

Blocking neurosteroid production can lead to more seizures and faster epilepsy onset in rats.

Fox genes are important for hair growth and development in cashmere goats.

The new wound dressing speeds up healing of infected wounds safely and effectively.

Bone marrow stem cells and their medium help hair regrowth.

Capsaicin offers health benefits and flavor but faces challenges in food use.

The nervous system helps control stem cell behavior and immune responses, affecting tissue repair and maintenance.

Microneedles with traditional Chinese medicine can help regrow hair in androgenic alopecia.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Galectin-1 helps in RNA processing in cell nuclei.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Two new gene mutations cause a rare hair disorder.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

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

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.