Search Results - "PEUCHMAUR, Michel"
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1
Whole-Exome Sequencing of Cell-Free DNA Reveals Temporo-spatial Heterogeneity and Identifies Treatment-Resistant Clones in Neuroblastoma
Published in Clinical cancer research (15-02-2018)“…Neuroblastoma displays important clinical and genetic heterogeneity, with emergence of new mutations at tumor progression. To study clonal evolution during…”
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2
Ontogeny of human mucosal-associated invariant T cells and related T cell subsets
Published in The Journal of experimental medicine (05-02-2018)“…Mucosal-associated invariant T (MAIT) cells are semi-invariant Vα7.2 CD161 CD4 T cells that recognize microbial riboflavin precursor derivatives such as…”
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3
Emergence of new ALK mutations at relapse of neuroblastoma
Published in Journal of clinical oncology (01-09-2014)“…In neuroblastoma, the ALK receptor tyrosine kinase is activated by point mutations. We investigated the potential role of ALK mutations in neuroblastoma clonal…”
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4
Activated ALK signals through the ERK–ETV5–RET pathway to drive neuroblastoma oncogenesis
Published in Oncogene (01-03-2018)“…Activating mutations of the ALK receptor occur in a subset of neuroblastoma tumors. We previously demonstrated that Alk mutations cooperate with MYCN…”
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5
Genomic Copy Number Profiling Using Circulating Free Tumor DNA Highlights Heterogeneity in Neuroblastoma
Published in Clinical cancer research (15-11-2016)“…The tumor genomic copy number profile is of prognostic significance in neuroblastoma patients. We have studied the genomic copy number profile of cell-free DNA…”
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6
Clinical and histological differences between adults and children in new onset IgA nephropathy
Published in Pediatric nephrology (Berlin, West) (01-10-2020)“…Background Previous reports suggest initial presentation of IgA nephropathy (IgAN) in children is different from adults. No systematic comparison of clinical,…”
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7
Overall Genomic Pattern Is a Predictor of Outcome in Neuroblastoma
Published in Journal of clinical oncology (01-03-2009)“…For a comprehensive overview of the genetic alterations of neuroblastoma, their association and clinical significance, we conducted a whole-genome DNA copy…”
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8
Radiogenomics of neuroblastomas: Relationships between imaging phenotypes, tumor genomic profile and survival
Published in PloS one (25-09-2017)“…This study investigated relationships between neuroblastomas (NBs) imaging phenotypes, tumor genomic profile and patient outcome. This IRB-approved…”
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9
Small bowel stenosis: a manifestation of chronic graft-versus-host disease in children?
Published in Human pathology (01-02-2018)“…Digestive graft-versus-host disease (GVHD) is a frequent complication after bone marrow transplantation, but small bowel obstruction is an extremely rare…”
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10
Neonatal cancer
Published in The lancet oncology (01-12-2013)“…Summary Neonatal cancer is rare and comprises a heterogeneous group of neoplasms with substantial histological diversity. Almost all types of paediatric cancer…”
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11
Calretinin immunohistochemistry: a simple and efficient tool to diagnose Hirschsprung disease
Published in Modern pathology (01-10-2009)“…Diagnosis of Hirschsprung disease (HD) is quite entirely based on the histopathological analysis of suction rectal biopsies. This hematoxylin and eosin…”
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12
CCR1 inhibition ameliorates the progression of lupus nephritis in NZB/W mice
Published in The Journal of immunology (1950) (01-02-2014)“…Systemic lupus erythematosus is a chronic inflammatory autoimmune disease, the development of which is characterized by a progressive loss of renal function…”
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13
Immunosuppressive Treatment in Children With IgA Nephropathy and the Clinical Value of Podocytopathic Features
Published in Kidney international reports (01-07-2018)“…There is a need for treatment guidelines and prognostic factor identification in children with primary IgA nephropathy. We analyzed the causative effect of…”
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14
LOCALIZATION AND mRNA EXPRESSION OF CYP3A AND P-GLYCOPROTEIN IN HUMAN DUODENUM AS A FUNCTION OF AGE
Published in Drug metabolism and disposition (01-11-2005)“…Cytochromes P450 3A (CYP3A) and P-glycoprotein (P-gp) are mainly located in enterocytes and hepatocytes. The CYP3A/P-gp system contributes to the first-pass…”
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15
A variant of ASIC2 mediates sodium retention in nephrotic syndrome
Published in JCI insight (09-08-2021)“…Idiopathic nephrotic syndrome (INS) is characterized by proteinuria and renal sodium retention leading to edema. This sodium retention is usually attributed to…”
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16
Inflammatory alterations in mesenteric adipose tissue in Crohn's disease
Published in Gastroenterology (New York, N.Y. 1943) (01-07-1999)“…Background & Aims: Abnormalities of fat in the mesentery including adipose tissue hypertrophy and fat wrapping have been long recognized on surgical specimens…”
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17
Transformation of a low-grade follicular lymphoma into a composite lymphoma combining a high-grade B-cell lymphoma and a lymphoblastic neoplasm expressing Terminal deoxynucleotidyl Transferase: a case report
Published in Journal of medical case reports (27-07-2020)“…High-grade B-cell lymphoma with rearrangements of MYC and BCL2 and/or BCL6 is an aggressive mature B-cell neoplasm, whereas B-lymphoblastic lymphoma is…”
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18
Synthesis of glucocorticoid-induced leucine zipper (GILZ) by macrophages: an anti-inflammatory and immunosuppressive mechanism shared by glucocorticoids and IL-10
Published in Blood (15-01-2003)“…Glucocorticoids and interleukin 10 (IL-10) prevent macrophage activation. In murine lymphocytes, glucocorticoids induce expression of glucocorticoid-induced…”
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19
Clinical characteristics and outcome of patients with neuroblastoma presenting genomic amplification of loci other than MYCN
Published in PloS one (11-07-2014)“…Somatically acquired genomic alterations with MYCN amplification (MNA) are key features of neuroblastoma (NB), the most common extra-cranial malignant tumour…”
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20
Mast Cells and MCPT4 Chymase Promote Renal Impairment after Partial Ureteral Obstruction
Published in Frontiers in immunology (04-05-2017)“…Obstructive nephropathy constitutes a major cause of pediatric renal progressive disease. The mechanisms leading to disease progression are still poorly…”
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