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MCHR2 gene duplications may be linked to alopecia areata.

Different prostate cancer treatments have similar risks of secondary cancers and related mortality when considering patient age and smoking history.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Skin changes can indicate a risk for breast cancer.

Robertsonian translocation can cause recurrent miscarriages.

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

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Localized breast cancer can affect skin and hair.

ESR2 gene linked to female-pattern hair loss.

Sun exposure and genetics increase skin cancer risk from precancerous lesions.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

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

Early baldness increases prostate cancer risk, radiotherapy and surgery have similar second cancer rates, and ALA may reduce prostate cancer risk.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Dabrafenib can cause skin growths and sometimes low-grade skin cancer.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

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

Radiotherapy affects mitochondrial-related genes in metastatic breast cancer cells.

Low-penetration genes might help personalize colorectal cancer prevention.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

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

Loss of TET2 increases the risk of skin and oral cancer.