663 results on '"Verkarre, Virginie"'
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102. IL-15 triggers an antiapoptotic pathway in human intraepithelial lymphocytes that is a potential new target in celiac disease--associated inflammation and lymphomagenesis
103. MYO5B and Bile Salt Export Pump Contribute to Cholestatic Liver Disorder in Microvillous Inclusion Disease
104. Un léiomyome utérin particulier
105. Using Contrast-Enhanced Ultrasound in Addition to Cross-Sectional Imaging for Indeterminate Renal Cysts May Lead to Overclassification in Bosniak III Category: A Case-Control Study
106. Germline MET pathogenic variants in papillary renal cell carcinomas type I: specific phenotype in French population and novel germline pathogenic variant MET c.3389T>C, p.(Leu1130Ser)
107. Overexpression of miR‐483‐5p is confined to metastases and linked to high circulating levels in patients with metastatic pheochromocytoma/paraganglioma
108. Inhibition of TGF-β Signaling by IL-15: A New Role for IL-15 in the Loss of Immune Homeostasis in Celiac Disease
109. Intracellular Factor H Drives Tumor Progression Independently of the Complement Cascade
110. Complement C1s and C4d as Prognostic Biomarkers in Renal Cancer: Emergence of Noncanonical Functions of C1s
111. Molecular Mechanisms and Clinical Pathophysiologies of Focal ATP-Sensitive Potassium Channel Hyperinsulinism and Beckwith-Wiedemann Syndrome
112. Comprehensive study of nine novel cases of TFEB‐amplified renal cell carcinoma: an aggressive tumour with frequent PDL1 expression.
113. Glucose Metabolism in 105 Children and Adolescents After Pancreatectomy for Congenital Hyperinsulinism
114. Diagnostic approach in TFE3-rearranged renal cell carcinoma: a multi-institutional international survey
115. The Immunoscore in Localized Urothelial Carcinoma Treated with Neoadjuvant Chemotherapy: Clinical Significance for Pathologic Responses and Overall Survival
116. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma
117. Familial Focal Congenital Hyperinsulinism
118. Les cancers héréditaires et le pathologiste
119. Apport du pathologiste dans les prédispositions héréditaires aux paragangliomes et phéochromocytomes
120. Les cancers du rein héréditaires vus par le pathologiste en 2020
121. Clear Cell Papillary Renal Cell Carcinoma: A Recent Entity With Distinct Imaging Patterns
122. Functional Imaging of the Pancreas: The Role of [ 18 F]Fluoro- L -DOPA PET in the Diagnosis of Hyperinsulinism of Infancy
123. Capsular involvement in patients undergoing partial nephrectomy for localized renal cell carcinoma: an adverse pathological finding?
124. Low-grade oncocytic renal tumor (LOT): mutations in mTOR pathway genes and low expression of FOXI1.
125. Brief Communication: The Relationship of Regression of Cirrhosis to Outcome in Chronic Hepatitis C
126. FIB-4: An inexpensive and accurate marker of fibrosis in HCV infection. comparison with liver biopsy and fibrotest
127. Nodular regenerative hyperplasia is a new cause of chronic liver disease in HIV-infected patients
128. Congenital Hyperinsulinism: Pancreatic [18F]Fluoro-l-Dihydroxyphenylalanine (DOPA) Positron Emission Tomography and Immunohistochemistry Study of DOPA Decarboxylase and Insulin Secretion
129. Relationship of HLA-DQ8 and severity of celiac disease: Comparison of New York and Parisian cohorts
130. A Direct Role for NKG2D/MICA Interaction in Villous Atrophy during Celiac Disease
131. Using Contrast-Enhanced Ultrasound in Addition to Cross-Sectional Imaging for Indeterminate Renal Cysts May Lead to Overclassification in Bosniak III Category: A Case-Control Study.
132. Interleukin 15: a key to disrupted intraepithelial lymphocyte homeostasis and lymphomagenesis in celiac disease
133. Recurrent partial trisomy 1q22-q44 in clonal intraepithelial lymphocytes in refractory celiac sprue
134. iPSC-Derived Embryoid Bodies as Models of c-Met-Mutated Hereditary Papillary Renal Cell Carcinoma
135. Abstract 3688: iPSC-derived cancer organoids recapitulate genomic and phenotypic alterations of c-Met-mutated hereditary kidney cancer
136. Tumor Cells Hijack Macrophage-Produced Complement C1q to Promote Tumor Growth
137. Congenital hyperinsulinism: current trends in diagnosis and therapy
138. ICAM-3 and E-selectin endothelial cell expression differentiate two phases of angiogenesis in infantile hemangiomas
139. Paternal Mutation of the Sulfonylurea Receptor (SUR1) Gene and Maternal Loss of 11p15 Imprinted Genes Lead to Persistent Hyperinsulinism in Focal Adenomatous Hyperplasia
140. The surgical management of atypical forms of congenital hyperinsulinism
141. Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism: Association with a Reduction to Homozygosity of a Mutation in ABCC8 or KCNJ11
142. MET alterations in biphasic squamoid alveolar papillary renal cell carcinomas and clinicopathological features.
143. Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1(+) Tim-3(+) CD8(+) T Cells
144. Telomerase Activation and ATRX Mutations Are Independent Risk Factors for Metastatic Pheochromocytoma and Paraganglioma
145. iPSC-derived Cancer Organoids Recapitulate Genomic and Phenotypic Alterations of c-met-mutated Hereditary Kidney Cancer
146. NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: a CELAC study
147. Sunitinib Prior to Planned Nephrectomy in Metastatic Renal Cell Carcinoma: Angiogenesis Biomarkers Predict Clinical Outcome in the Prospective Phase II PREINSUT Trial
148. Integrative analysis of dysregulated microRNAs and mRNAs in multiple recurrent synchronized renal tumors from patients with von Hippel-Lindau disease
149. MP28-17 NON-TYPE 1 PAPILLARY RENAL CELL CARCINOMA IS ASSOCIATED WITH A WORST ONCOLOGICAL OUTCOME IN PATIENTS TREATED SURGICALLY
150. LBA29 COMPLEMENT ACTIVATION ORCHESTRATED BY CANCER CELLS AND C1Q-PRODUCING TUMOR ASSOCIATED MACROPHAGES HAS A DELETERIOUS IMPACT ON PATIENT’S PROGNOSIS IN CLEAR CELL RENAL CELL CANCER.
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