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ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Blocking Oncostatin M's role in the JAK-STAT pathway can stimulate hair growth in mice.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

HoxC genes are crucial for normal hair and nail development.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The Hippo signaling pathway helps control organ size during regeneration by regulating gene expression.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

The FOS gene helps hair growth in Tan sheep.

PLIN2 affects hair growth in cashmere goats, potentially improving cashmere quality.

FoxN1 overexpression in young mice harms immune cell and skin development.

Activated protein C helps protect mice from radiation damage.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Certain genes help dermal papillae cells in hair follicles grow and group together.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A new keratin gene was found in mice, explaining hair growth.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Certain gene variations are found in people with polycystic ovary syndrome.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.