Search

everythinglearnresearchcommunity

for

Search:↓

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.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

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

A mutation in the human hairless gene causes alopecia universalis.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

The PML protein helps prevent skin cancer in mice.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

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

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

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

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Deleting TNFα gene reduces skin cancer risk in certain mice.

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

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

A unique gene mutation was found in a family with monilethrix.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Mutations in the SNRPE gene cause hereditary hair loss.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

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