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Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

FGF13 gene changes cause excessive hair growth in a rare condition.

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

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

EDA2R gene linked to hair loss.

COX2 and ATP synthase control the size of hedgehog spines.

Mesenchymal MEIS2 is essential for whisker development without needing sensory nerves.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

Lack of cystatin M/E causes thin hair and dry skin.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

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

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Increasing SSAT makes skin more prone to cancer.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

A specific genetic variation affects wool quality in sheep.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.