Publications by authors named "Le-shi Wang"
[Gardner syndrome with chronic osteomyelitis of the jaw: a case report].
Hua Xi Kou Qiang Yi Xue Za Zhi
August 2018
Article Synopsis
- Gardner syndrome is a rare genetic disorder that is passed down through families and has an autosomal dominant inheritance pattern.
- The condition is characterized by various symptoms, including numerous intestinal polyps, soft tissue tumors, dental issues, bone growths called osteomas, and eye disorders related to the retinal pigment.
- A case study is presented involving a patient suffering from Gardner syndrome along with chronic osteomyelitis in the jaw, emphasizing the significant complications that can arise from the disease.
Breast cancer is the most common cancer and the second leading cause of mortality for women worldwide. It is necessary to identify valuable molecular markers to predict breast cancer progression in patients and treatment effect. Serine-arginine protein kinase 1 (SRPK1), a member of SR kinase family, phosphorylates the SR splicing factors which plays essential roles in normal cell development and multiple human diseases.
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