Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Enhancing CD8+ T cell function to induce ferroptosis in tumor cells may help treat skin melanoma.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Two new gene clusters important for hair formation were found on human chromosome 11.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Hormone levels can help predict metformin treatment success in women with PCOS.

Inhibiting mTORC2 can reduce DNA repair and increase cancer cell death, suggesting potential for targeted brain cancer treatments.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

Caloric stress and differentiation increase IRES translation, affecting stem cell function and potential therapies.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Certain gene variations may increase the risk of PCOS in South Indian women.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Hair loss in certain mice is linked to changes in keratin-related genes.

Two new gene clusters important for hair formation were found on human chromosome 11.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

Matrix effects in LC-MS can be managed but not completely avoided.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Overactive signaling in hair follicles can lead to skin cancer.

Changing disulfide bonds in human hair affects its melting behavior and thermal stability.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

New biomarkers and targets for breast cancer treatment were identified to help prevent relapse and metastasis.

A genetic variant linked to hair thinning in Japanese women was found.