Ayelet Erez


Ontology type: schema:Person     


Person Info

NAME

Ayelet

SURNAME

Erez

Publications in SciGraph latest 50 shown

  • 2018-12 Novel antibiofilm chemotherapies target nitrogen from glutamate and glutamine in SCIENTIFIC REPORTS
  • 2018-12 MTCH2-mediated mitochondrial fusion drives exit from naïve pluripotency in embryonic stem cells in NATURE COMMUNICATIONS
  • 2018-11-09 Mutant p53-dependent mitochondrial metabolic alterations in a mesenchymal stem cell-based model of progressive malignancy in CELL DEATH & DIFFERENTIATION
  • 2018-10 Rewiring urea cycle metabolism in cancer to support anabolism in NATURE REVIEWS CANCER
  • 2018-08 Author Correction: BCAT1 restricts αKG levels in AML stem cells leading to IDHmut-like DNA hypermethylation in NATURE
  • 2017-11 BCAT1 restricts αKG levels in AML stem cells leading to IDHmut-like DNA hypermethylation in NATURE
  • 2016-04 Corrigendum: PAR1 signaling regulates the retention and recruitment of EPCR-expressing bone marrow hematopoietic stem cells in NATURE MEDICINE
  • 2015-11 PAR1 signaling regulates the retention and recruitment of EPCR-expressing bone marrow hematopoietic stem cells in NATURE MEDICINE
  • 2015-11 Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis in NATURE
  • 2015-07 Metabolic dysregulation in monogenic disorders and cancer — finding method in madness in NATURE REVIEWS CANCER
  • 2015-01 Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-04 Argininosuccinic aciduria: from a monogenic to a complex disorder in GENETICS IN MEDICINE
  • 2013-03 Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-11 Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function in NEUROGENETICS
  • 2012-06 Response to Srilatha et al. in GENETICS IN MEDICINE
  • 2012-05 Argininosuccinate lyase deficiency in GENETICS IN MEDICINE
  • 2012-02 Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-12 Requirement of argininosuccinate lyase for systemic nitric oxide production in NATURE MEDICINE
  • 2011-05 Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females in GENETICS IN MEDICINE
  • 2011-03 Phenotypic manifestations of copy number variation in chromosome 16p13.11 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-03 Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-10 Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder in NEUROGENETICS
  • 2009-05 Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2004-07 Sil overexpression in lung cancer characterizes tumors with increased mitotic activity in ONCOGENE
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