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Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Finasteride may help treat childhood brain tumors by activating certain genes.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

CDK4 levels affect the number of hair follicle stem cells in mice.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Certain genetic markers may increase or decrease prostate cancer risk.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Certain genetic variants increase the risk of aggressive prostate cancer.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

A truncated protein linked to breast cancer may change cell adhesion.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A gene mutation in mice causes permanent hair loss and skin issues.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

There are two ways to start hair growth: one needs Stat3 and the other does not, but both need PI3K activation.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Alpha mangostin may protect certain breast cancer cells by activating the p53 pathway.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

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