390 results on '"Morel, Frédéric"'
Search Results
2. NUDT6 and NUDT9, two mitochondrial members of the NUDIX family, have distinct hydrolysis activities
3. Development and Characterization of a 3.2 Gb/s Serial Link Transmitter for CMOS Image Sensors in Subatomic Physics Experiments
4. Development of CMOS Pixel Sensors fully adapted to the ILD Vertex Detector Requirements
5. M.i.p. detection performances of a 100 us read-out CMOS pixel sensor with digitised outputs
6. Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters
7. Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry
8. Bypassing Mendel’s First Law: Transmission Ratio Distortion in Mammals
9. Breakpoint heterogeneity in (2;3)(p15–23;q26) translocations involving EVI1 in myeloid hemopathies
10. MLL partner genes in secondary acute lymphoblastic leukemia: Report of a new partner PRRC1 and review of the literature
11. Translocation t(2;7)(p11;q21) associated with the CDK6/IGK rearrangement is a rare but recurrent abnormality in B-cell lymphoproliferative malignancies
12. Genetic aspects of monomorphic teratozoospermia: a review
13. ETV6 fusion genes in hematological malignancies: A review
14. MACS-annexin V cell sorting of semen samples with high TUNEL values decreases the concentration of cells with abnormal chromosomal content: a pilot study
15. Meiotic Segregation of an Isodicentric Derived from Chromosome 15 in Sperm of a Patient with Mosaic Karyotype: Case Report and Review of the Literature
16. Translocations involving 13q14 without associated deletion in chronic lymphoid leukaemia target DLEU2
17. Complex and cryptic chromosomal rearrangements involving the MLL gene in acute leukemia: A study of 7 patients and review of the literature
18. Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders
19. Cytogenetics in pre-B and B-cell acute lymphoblastic leukemia: a study of 208 patients diagnosed between 1981 and 2008
20. Import of Preprocecropin A and Related Precursor Proteins into the Endoplasmic Reticulum
21. Identification of a novel population in high-grade oligodendroglial tumors not deleted on 1p/19q using array CGH
22. Differing mechanisms of meiotic segregation in spermatozoa from three carriers of a pericentric inversion of chromosome 8
23. Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation
24. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions
25. MACS-annexin V cell sorting of semen samples with high TUNEL values decreases the concentration of cells with abnormal chromosomal content: a pilot study.
26. Del(5q) and MLL amplification in homogeneously staining region in acute myeloblastic leukemia: a recurrent cytogenetic association
27. Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions
28. Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations
29. Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemia
30. Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
31. Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16)
32. ABL1 fusion genes in hematological malignancies: a review
33. A complex 1;19;11 translocation involving the MLL gene in a patient with congenital acute monoblastic leukemia identified by molecular and cytogenetic techniques
34. Balanced transmission of a paternal complex chromosomal rearrangement involving chromosomes 2, 3, and 18
35. FLNA, a new partner gene fused to MLL in a patient with acute myelomonoblastic leukaemia
36. Screening by fluorescence in situ hybridization for MLL status at diagnosis in 239 unselected patients with acute myeloblastic leukemia
37. Jumping translocations in multiple myeloma
38. Molecular cytogenetic characterization of an 8p22–8p23.2 duplication derived from a maternal intrachromosomal insertion in a child with congenital heart malformation, delayed puberty, and learning disabilities
39. Familial interstitial deletion of the short arm of chromosome 4 (p15.33–p16.3) characterized by molecular cytogenetic analysis
40. The ILD detector at the ILC
41. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML
42. Meiotic segregation of translocations during male gametogenesis
43. Double minutes containing amplified bcr-abl fusion gene in a case of chronic myeloid leukemia treated by imatinib
44. The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura
45. A fluorescence in situ hybridization study of TEL- AML1 fusion gene in B-cell acute lymphoblastic leukemia (1984–2001)
46. inv(3)(q21q26) RPN1/MECOM
47. Selective mitochondrial DNA degradation following double-strand breaks
48. Maintenance of human mitochondrial DNA following double-strand breaks
49. DNA maintenance following bleomycin-induced strand breaks does not require poly(ADP-ribosyl)ation activation in Drosophila S2 cells
50. Immunoglobulin gene translocations in chronic lymphocytic leukemia: A report of 35 patients and review of the literature
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