Pages that link to "Q56448767"
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The following pages link to Geertruy Te Kronnie (Q56448767):
Displaying 50 items.
- Antibodies covalently immobilized on actin filaments for fast myosin driven analyte transport (Q27316404) (← links)
- Functional protein network activation mapping reveals new potential molecular drug targets for poor prognosis pediatric BCP-ALL (Q28475897) (← links)
- Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia (Q28943326) (← links)
- A leukemia-enriched cDNA microarray platform identifies new transcripts with relevance to the biology of pediatric acute lymphoblastic leukemia. (Q30790942) (← links)
- New data on robustness of gene expression signatures in leukemia: comparison of three distinct total RNA preparation procedures (Q31116667) (← links)
- CRLF2 overexpression identifies an unfavourable subgroup of adult B-cell precursor acute lymphoblastic leukemia lacking recurrent genetic abnormalities (Q33429079) (← links)
- MLL rearrangements in pediatric acute lymphoblastic and myeloblastic leukemias: MLL specific and lineage specific signatures (Q33473001) (← links)
- Molecular mechanisms of HIF-1alpha modulation induced by oxygen tension and BMP2 in glioblastoma derived cells (Q33480001) (← links)
- Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation (Q33691942) (← links)
- Low PKCα expression within the MRD-HR stratum defines a new subgroup of childhood T-ALL with very poor outcome (Q34221792) (← links)
- The effects of siRNA-mediated inhibition of E2A-PBX1 on EB-1 and Wnt16b expression in the 697 pre-B leukemia cell line. (Q34537277) (← links)
- The MLL recombinome of acute leukemias in 2013. (Q34651113) (← links)
- Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias (Q34973772) (← links)
- Notch3/Jagged1 circuitry reinforces notch signaling and sustains T-ALL (Q35022504) (← links)
- Epigenetic silencing of TFPI-2 in canine diffuse large B-cell lymphoma (Q35138335) (← links)
- Targeting of hyperactivated mTOR signaling in high-risk acute lymphoblastic leukemia in a pre-clinical model (Q35176311) (← links)
- LCK over-expression drives STAT5 oncogenic signaling in PAX5 translocated BCP-ALL patients (Q35176372) (← links)
- Array-based comparative genomic hybridization analysis reveals chromosomal copy number aberrations associated with clinical outcome in canine diffuse large B-cell lymphoma (Q35396525) (← links)
- Acute leukemia subclassification: a marker protein expression perspective (Q35809438) (← links)
- Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options (Q36154689) (← links)
- Expression of carp-cdx1, a caudal homolog, in embryos of the carp, Cyprinus carpio (Q36311934) (← links)
- Isolation of carp cDNA clones, representing developmentally-regulated genes, using a subtractive-hybridization strategy. (Q36311997) (← links)
- An immediate transcriptional signature associated with response to the histone deacetylase inhibitor Givinostat in T acute lymphoblastic leukemia xenografts (Q36751751) (← links)
- What is the relevance of Ikaros gene deletions as a prognostic marker in pediatric Philadelphia-negative B-cell precursor acute lymphoblastic leukemia? (Q37060647) (← links)
- Clinico-biological features of 5202 patients with acute lymphoblastic leukemia enrolled in the Italian AIEOP and GIMEMA protocols and stratified in age cohorts (Q37273171) (← links)
- Deciphering KRAS and NRAS mutated clone dynamics in MLL-AF4 paediatric leukaemia by ultra deep sequencing analysis (Q37306997) (← links)
- CRLF2 over-expression is a poor prognostic marker in children with high risk T-cell acute lymphoblastic leukemia (Q37644852) (← links)
- Sensing protein antigen and microvesicle analytes using high-capacity biopolymer nano-carriers (Q38815925) (← links)
- Clinical significance of recurrent copy number aberrations in B-lineage acute lymphoblastic leukaemia without recurrent fusion genes across age cohorts (Q38821571) (← links)
- ETV6/RUNX1-like acute lymphoblastic leukemia: A novel B-cell precursor leukemia subtype associated with the CD27/CD44 immunophenotype. (Q38844207) (← links)
- Expression Profiling of Circulating Microvesicles Reveals Intercellular Transmission of Oncogenic Pathways (Q38986346) (← links)
- Sample solution constraints on motor-driven diagnostic nanodevices (Q39213277) (← links)
- Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group (Q39766394) (← links)
- Prognostic and therapeutic role of targetable lesions in B-lineage acute lymphoblastic leukemia without recurrent fusion genes (Q39992854) (← links)
- Hepatocyte growth factor receptor c-MET is associated with FAS and when activated enhances drug-induced apoptosis in pediatric B acute lymphoblastic leukemia with TEL-AML1 translocation (Q40098619) (← links)
- Down-regulation of DLX3 expression in MLL-AF4 childhood lymphoblastic leukemias is mediated by promoter region hypermethylation. (Q40111307) (← links)
- Mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia: a report from the Italian AIEOP study group (Q41259945) (← links)
- Clinical utility of microarray-based gene expression profiling in the diagnosis and subclassification of leukemia: report from the International Microarray Innovations in Leukemia Study Group (Q41508288) (← links)
- Mesenchymal stem cells from Shwachman-Diamond syndrome patients display normal functions and do not contribute to hematological defects. (Q41647887) (← links)
- High expression of miR-125b-2 and SNORD116 noncoding RNA clusters characterize ERG-related B cell precursor acute lymphoblastic leukemia. (Q41823245) (← links)
- Impact of IKZF1 deletions on IKZF1 expression and outcome in Philadelphia chromosome negative childhood BCP-ALL. Reply to "incidence and biological significance of IKZF1/Ikaros gene deletions in pediatric Philadelphia chromosome negative and Philade (Q42831329) (← links)
- Fine tuning of surface CRLF2 expression and its associated signaling profile in childhood B-cell precursor acute lymphoblastic leukemia. (Q42847773) (← links)
- DNA methyltransferase 3a hot-spot locus is not mutated in pediatric patients affected by acute myeloid or T-cell acute lymphoblastic leukemia: an Italian study (Q43004456) (← links)
- PTPN11 mutations in childhood acute lymphoblastic leukemia occur as a secondary event associated with high hyperdiploidy. (Q43272242) (← links)
- New MLLT10 gene recombinations in pediatric T-acute lymphoblastic leukemia. (Q43482067) (← links)
- Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia. (Q43809420) (← links)
- Ultrafast molecular motor driven nanoseparation and biosensing. (Q44529632) (← links)
- Suppressors and activators of JAK-STAT signaling at diagnosis and relapse of acute lymphoblastic leukemia in Down syndrome (Q45233800) (← links)
- Two independent gene signatures in pediatric t(4;11) acute lymphoblastic leukemia patients. (Q46494934) (← links)
- Drosophila CAKI/CMG protein, a homolog of human CASK, is essential for regulation of neurotransmitter vesicle release. (Q47072552) (← links)