Clonally Expanded T Cells Reveal Immunogenicity of Rhabdoid Tumors

Amaury Leruste, Jimena Tosello, Rodrigo Nalio Ramos, +28

Cancer Cell

Cancer ImmunosurveillanceRhabdoid TumorsImmunologyTumor ImmunityImmunotherapy +2

Mycophenolate Mofetil in Pregnancy After Renal Transplantation: A Case of Major Fetal Malformations

Camille Le Ray, Aurore Coulomb, Élisabeth Éléfant, +2

Obstetrics and Gynecology

Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study

Tasnim Chagtai, Christina Zill, Linda Dainese, +23

Journal of Clinical Oncology

Langerhans cell histiocytosis: therapeutic strategy and outcome in a 30‐year nationwide cohort of 1478 patients under 18 years of age

Charlotte Rigaud, Mohamed Barkaoui, Caroline Thomas, +22

British Journal of Haematology

Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island

Alice Hadchouel, Thomas Wieland, Matthias Griese, +16

The American Journal of Human Genetics

Biallelic MutationsAdvanced Lung DiseaseMethionyl-trna Synthetase CauseGeneticsPulmonary Alveolar Proteinosis +7

Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children

Florence Flamein, Laure Riffault, Céline Muselet-Charlier, +18

Human Molecular Genetics

Inflammatory Lung DiseaseAdvanced Lung DiseaseLung InflammationGeneticsImmunology +16

Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios

Mireille Lacoste, Yi Cai, Liliane Guicharnaud, +24

Journal of the American Society of Nephrology

Renal PathologyPathologyCongenital Heart AnomalyEmbryologyRenal Function +16

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

Graciana Jaureguiberry, Muriel de La Dure‐Molla, David Parry, +67

Nephron Physiology

Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form

Julie Salomon, Olivier Goulet, Danielle Canioni, +23

Human Genetics

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPathology +6

Repopulation of Athymic Mouse Liver by Cryopreserved Early Human Fetal Hepatoblasts

D. Mahieu‐Caputo, Jean-Étienne Allain, Julie Branger, +9

Human Gene Therapy