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Radiation therapy in breast cancer patients changes gene expression related to DNA damage, fibroblast growth, and hair follicle development, which could help improve treatment for radiation-induced fibrosis.

Higher TGF-β signaling may increase skin cancer risk in organ transplant recipients.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

The study found that analyzing certain cell signaling pathways is not a reliable method to tell apart two types of skin tumors.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

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

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

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

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

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

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

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

Targeting multiple pathways and understanding genetic mutations are crucial for effective melanoma therapy.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.