654 results on '"Marynen, Peter"'
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2. Molecular Characterization of the Human Peroxisomal Branched-Chain Acyl-CoA Oxidase: cDNA Cloning, Chromosomal Assignment, Tissue Distribution, and Evidence for the Absence of the Protein in Zellweger Syndrome
3. Data from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
4. Supplementary Table 2 from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
5. Supplementary Table 1 from Selective Expansion of Marginal Zone B Cells in Eμ-API2-MALT1 Mice Is Linked to Enhanced IκB Kinase γ Polyubiquitination
6. Data from Selective Expansion of Marginal Zone B Cells in Eμ-API2-MALT1 Mice Is Linked to Enhanced IκB Kinase γ Polyubiquitination
7. Supplementary Figure Legend from Selective Expansion of Marginal Zone B Cells in Eμ-API2-MALT1 Mice Is Linked to Enhanced IκB Kinase γ Polyubiquitination
8. Supplementary Figure 1 from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
9. Supplementary Table 1 from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
10. Supplementary Figure Legends 1-2 from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
11. Supplementary Table 3 from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
12. Supplementary Figure 2 from Coactivated Platelet-Derived Growth Factor Receptor α and Epidermal Growth Factor Receptor Are Potential Therapeutic Targets in Intimal Sarcoma
13. Supplementary Figure 1 from Selective Expansion of Marginal Zone B Cells in Eμ-API2-MALT1 Mice Is Linked to Enhanced IκB Kinase γ Polyubiquitination
14. Allele-specific copy number analysis of tumors
15. JAK2 rearrangements, including the novel SEC31A-JAK2 fusion, are recurrent in classical Hodgkin lymphoma
16. Activation of FIP1L1-PDGFRɑ Requires Disruption of the Juxtamembrane Domain of PDGFRɑ and Is FIP1L1-Independent
17. De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation
18. Comparative expressed sequence hybridization studies of t(11;18)(q21;q21)-positive and -negative gastric MALT lymphomas reveal both unique and overlapping gene programs
19. Molecular Cloning of Amphiglycan, a Novel Integral Membrane Heparan Sulfate Proteoglycan Expressed by Epithelial and Fibroblastic Cells
20. Molecular Cloning of a Phosphatidylinositol-Anchored Membrane Heparan Sulfate Proteoglycan from Human Lung Fibroblasts
21. The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability
22. Evidence for increased SOX3 dosage as a risk factor for X-linked hypopituitarism and neural tube defects
23. Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination
24. Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation
25. Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
26. Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males
27. MAPK phosphatase DUSP16/MKP-7, a candidate tumor suppressor for chromosome region 12p12–13, reduces BCR-ABL-induced transformation
28. A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
29. Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background
30. Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
31. Transformation of hematopoietic cell lines to growth‐factor independence and induction of a fatal myelo‐ and lymphoproliferative disease in mice by retrovirally transduced TEL/JAK2 fusion genes
32. Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adults
33. Structural organisation of the gene encoding the α-subunit of the human amiloride-sensitive epithelial sodium channel
34. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
35. Resistance to tyrosine kinase inhibitors: Calling on extra forces
36. Immature teratoma of the pineal gland with isochromosome 12p
37. Detection of Genomic Copy Number Changes in Patients With Idiopathic Mental Retardation by High-Resolution X-Array-CGH: Important Role for Increased Gene Dosage of XLMR Genes†
38. Interaction partners for human ZNF384/CIZ/NMP4—zyxin as a mediator for p130CAS signaling?
39. cIAP2 is a ubiquitin protein ligase for BCL10 and is dysregulated in mucosa-associated lymphoid tissue lymphomas
40. A NEW RECURRENT INVERSION, INV(7) LEADS TO TRANSCRIPTIONAL ACTIVATION OF HOXA10 AND HOXA11 IN A SUBSET OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA: P.S.002
41. Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis
42. Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of protein in Zellweger syndrome
43. Localization of the gene encoding the α2 subunit of the human VLA-2 receptor to chromosome 5q23-31
44. CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior
45. The novel cryptic translocation t(12;17)(p13;p12) involves the ETV6 and the PER1 genes
46. Recombination hotspot in NF1 microdeletion patients
47. PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative disease
48. Characterization of 12p molecular events outside ETV6 in complex karyotypes of acute myeloid malignancies
49. Evidence for position effects as a variantETV6-mediated leukemogenic mechanism in myeloid leukemias with a t(4;12)(q11-q12;p13) or t(5;12)(q31;p13)
50. Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line
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