Pages that link to "Q38270425"

The following pages link to The fragile site WWOX gene and the developing brain (Q38270425):

Displaying 11 items.

• Pleiotropic Functions of Tumor Suppressor WWOX in Normal and Cancer Cells (Q28080922) (← links)
• W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report (Q36096253) (← links)
• WWOX dysfunction induces sequential aggregation of TRAPPC6AΔ, TIAF1, tau and amyloid β, and causes apoptosis (Q37167514) (← links)
• WWOX modulates the ATR-mediated DNA damage checkpoint response (Q39996960) (← links)
• Tumor Suppressor WWOX inhibits osteosarcoma metastasis by modulating RUNX2 function (Q41991686) (← links)
• Current questions and controversies in chromosome fragile site research: does WWOX, the gene product of common fragile site FRA16D, have a passive or active role in cancer? (Q42367791) (← links)
• Phosphorylation/de-phosphorylation in specific sites of tumor suppressor WWOX and control of distinct biological events (Q47878130) (← links)
• Severe CNS involvement in WWOX mutations: Description of five new cases. (Q52919014) (← links)
• WWOX Phosphorylation, Signaling, and Role in Neurodegeneration (Q58777445) (← links)
• A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay (Q88887070) (← links)
• The WWOX Gene Influences Cellular Pathways in the Neuronal Differentiation of Human Neural Progenitor Cells (Q90206210) (← links)