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SIPHL1 from tomato enhances plants' response to low phosphate levels.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

CTIP2 may help in skin development and maintenance.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

The E2 protein affects gene activity in hair follicles of mice.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

Targeting mTOR in myeloid cells may help reduce psoriasis symptoms.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

The PML protein helps prevent skin cancer in mice.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Chronic T. gondii infection may harm male fertility.

LGD1069 effectively prevents breast tumors in mice without toxicity.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Fluorescent proteins in mouse models effectively visualize tumor blood vessel growth.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Researchers developed a mouse model that tracks hair growth using bioluminescence, improving accuracy in studying hair cycles.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

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