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Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

Tanning ability is linked to specific DNA changes in skin genes.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

Injury boosts normal skin cell growth, reducing cancer cell advantage.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

CCCA can affect both genders and all ages, and it has a genetic component.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

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

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Mutations in the hHb6 gene cause the hair disorder monilethrix.