28 results on '"J-P Bourquin"'
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2. S108: PEDIATRIC T- ALL RELAPSE: CONSTITUTIONAL CANCER PREDISPOSITION AND HYPERMUTATATOR PHENOTYPES
3. P319: THE TESTICULAR NICHE OF ACUTE LYMPHOBLASTIC LEUKEMIA – MOLECULAR AND CELLULAR FACTORS FOR THE PREFERENTIAL MIGRATION AND SURVIVAL
4. SOD2 Promotes Acute Leukemia Adaptation to Amino Acid Starvation Through the N-Degron Pathway
5. Complementary activities of DOT1L and Menin inhibitors in MLL-rearranged leukemia
6. Correction: CRISPR/Cas9-edited NSG mice as PDX models of human leukemia to address the role of niche-derived SPARC
7. Genotype-outcome correlations in pediatric AML: the impact of a monosomal karyotype in trial AML-BFM 2004
8. Randomised Introduction of 2-CDA as Intensification during Consolidation for Children with High-risk AML – Results from Study AML-BFM 2004
9. Die another way: necroptosis as alternative route to cell death
10. Illuminating the leukemogenic transformation activity of TCF3-HLF in pediatric ALL
11. Targeting BET proteins improves the therapeutic efficacy of BCL-2 inhibition in T-cell acute lymphoblastic leukemia
12. S128 BCP- AND T-ALL CELLS HIDE IN DISTINCT NICHES OF THE BONE MARROW
13. Additional treatment with 2-Chloro-2-Deoxyadenosine during consolidation in children with high-risk acute myeloid leukemia does not improve survival
14. Monitoring minimal residual disease in children with high-risk relapses of acute lymphoblastic leukemia: prognostic relevance of early and late assessment
15. Pharmacological activity of CB-103: An oral pan-NOTCH inhibitor with a novel mode of action
16. PHARMACOLOGICAL ACTIVITY OF CB-103 IN HAEMATOLOGICAL MALIGNANCIES - AN ORAL PAN-NOTCH INHIBITOR WITH A NOVEL MODE OF ACTION
17. An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome
18. Favorable outcome in infants with AML after intensive first- and second-line treatment: an AML-BFM study group report
19. Biological activity of biotin and its analogues
20. CCDs as low-energy X-ray detectors
21. Zur Kenntnis des Lavendelöls. (2. Mitteilung). Die Konstitution des Lavandulols
22. Versuche zur Synthese des β-Biotins. (Vitamin H.). 1. Mitteilung. Synthese des 2-Methyl-3,4-(2′-oxo-tetrahydro-imidazol)-thiophans
23. Versuche zur Synthese von β-Biotin. (Vitamin H.). 2. Mitteilung. Synthese von d,l-2-(ω-Carboxybutyl)-3,4-(2′-oxo-tetrahydro-imidazol)-thiophanen (d,l-Ψ-β-Biotin, d,l-iso-β-Biotin und d,l-β-Biotin)
24. Versuche zur Synthese des β-Biotins. (Vitamin H.) 3. Mitteilung. Synthese von 4-Methyl-5-(ω-carboxy-n-pentyl)-2-oxo-tetrahydro-imidazol und 4-Methyl-5-(ω-carboxy-n-butyl)-2-oxo-tetrahydro-imidazol (d,l-Desthiobiotin und d,l-nor-Desthiobiotin)
25. Synthese von Estern halogenierter Chinaldine und Chinoline
26. Synthesen auf dem Phenothiazin-Gebiet. 4. Mitteilung. N-substituierte Mercapto-azaphenothiazin-Derivate
27. Versuche zur Synthese von β-Biotin (Vitamin H). 4. Mitteilung. Die stereoisomeren synthetischend,l-Biotine. Nachtrag zur 2. Mitteilung
28. De l'activité biologique de la biotine et de ses analogues
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