ObjectiveThis study aimed to study the role of PALB2 on the prognosis of skull base chordoma patients and the proliferation, migration, and invasion of chordoma cells. Methods187 patients with primary skull base chordoma were involved in the study. Immunohistochemical analysis was used to measure the PALB2 protein expression. Kaplan-Meier analysis, univariate and multivariate Cox analysis were used to evaluate the impact of PALB2 on patient prognosis. A nomogram was established for predicting the progression free survival of chordoma patients. Cell counting kit-8, colony formation, transwell migration, and invasion assays were used to assess the proliferation, migration, and invasion of chordoma cells with PALB2 knockdown. TIMER 2.0 was use...
Introduction: The loss of SMARCB1/INI1 protein has been recently described in poorly differentiated ...
BackgroundChordoma is a slow-growing but malignant subtype of bone sarcoma with relatively high recu...
Chordoma is a rare malignant bone tumour, showing notochordal differentiation, which occurs in the a...
ObjectiveThis study aimed to study the role of PALB2 on the prognosis of skull base chordoma patient...
BackgroundThe prognostic factors of skull base chordoma associated with outcomes of patients after s...
-BACKGROUND: A chordoma is a slow-growing, invasive neoplasm in the neuraxis that is thought to aris...
Background: The recurrence rate of chordoma is high, and the prognosis is poor. Methods: Differen...
Chordomas are tumors that arise at vertebral bodies and the base of the skull. Although rare in inci...
OBJECTIVE: Despite refinement of surgical techniques and adjuvant radiotherapy, the prognosis for pa...
Chordomas are rare embryogenetic tumors, arising from remnants of the notochord, characterized by lo...
OBJECTIVE: Despite refinement of surgical techniques and adjuvant radiotherapy, the prognosis for pa...
OBJECTIVE: Skull base chordomas (SBCs) are rare dysembryogenetic invasive tumors with a variable ten...
Chordomas are slow-growing malignant neoplasms. Determination of histopathologic prognostic factors ...
Objectives Skull base chordomas are locally aggressive malignant tumors derived from the notochord ...
Prognosis of chordomas is difficult to predict based solely on histological findings. The purpose of...
Introduction: The loss of SMARCB1/INI1 protein has been recently described in poorly differentiated ...
BackgroundChordoma is a slow-growing but malignant subtype of bone sarcoma with relatively high recu...
Chordoma is a rare malignant bone tumour, showing notochordal differentiation, which occurs in the a...
ObjectiveThis study aimed to study the role of PALB2 on the prognosis of skull base chordoma patient...
BackgroundThe prognostic factors of skull base chordoma associated with outcomes of patients after s...
-BACKGROUND: A chordoma is a slow-growing, invasive neoplasm in the neuraxis that is thought to aris...
Background: The recurrence rate of chordoma is high, and the prognosis is poor. Methods: Differen...
Chordomas are tumors that arise at vertebral bodies and the base of the skull. Although rare in inci...
OBJECTIVE: Despite refinement of surgical techniques and adjuvant radiotherapy, the prognosis for pa...
Chordomas are rare embryogenetic tumors, arising from remnants of the notochord, characterized by lo...
OBJECTIVE: Despite refinement of surgical techniques and adjuvant radiotherapy, the prognosis for pa...
OBJECTIVE: Skull base chordomas (SBCs) are rare dysembryogenetic invasive tumors with a variable ten...
Chordomas are slow-growing malignant neoplasms. Determination of histopathologic prognostic factors ...
Objectives Skull base chordomas are locally aggressive malignant tumors derived from the notochord ...
Prognosis of chordomas is difficult to predict based solely on histological findings. The purpose of...
Introduction: The loss of SMARCB1/INI1 protein has been recently described in poorly differentiated ...
BackgroundChordoma is a slow-growing but malignant subtype of bone sarcoma with relatively high recu...
Chordoma is a rare malignant bone tumour, showing notochordal differentiation, which occurs in the a...