191 results on '"Erdel, Martin"'
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2. Mutations in the Δ 7-sterol Reductase Gene in Patients with the Smith--Lemli--Opitz Syndrome
3. Supplementary Figure 1 from E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer
4. Supplementary Figure 2 from E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer
5. Data from E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer
6. Supplementary Figure 3 from E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer
7. Supplementary Tables 1-3, Figure Legends 1-3 from E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer
8. Critical role of scavenger receptor-BI–expressing bone marrow–derived endothelial progenitor cells in the attenuation of allograft vasculopathy after human apo A-I transfer
9. Disruption of the ARID1B and ADAMTS6 Loci due to a t(5;6)(q12.3;q25.3) in a Patient With Developmental Delay
10. Fludarabine/intermediate-dose cytarabine with or without allogeneic hematopoietic stem cell transplantation in poor-risk leukemia: a single center experience
11. Cyclin E dysregulation and chromosomal instability in endometrial cancer
12. High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization
13. Mutation analysis in glycogen storage disease type 1 non-a
14. Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype
15. Successful treatment of MDS with lenalidomide, complicated by transient autoimmune hemolysis
16. Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21)
17. Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman
18. Mutations in the delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome
19. Pre- and Postnatal Findings in Trisomy 17 Mosaicism
20. Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18
21. Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association)
22. Additional file 4: Table S2. of Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3)
23. Additional file 3: Figure S1. of Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3)
24. Additional file 2: Table S1. of Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3)
25. Additional file 1: of Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3)
26. Characterization of a newly identified ETV6-NTRK3 fusion transcript in acute myeloid leukemia
27. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome
28. Molecular genetics and structural genomics of the human protein kinase C gene module
29. Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3)
30. Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism
31. Functional characterization, localization, and inhibitor sensitivity of the TPR-FGFR1 fusion in 8p11 myeloproliferative syndrome
32. Studies on Androgen Receptor Mutations and Amplification in Human Prostate Cancer
33. Disruption of theARID1BandADAMTS6loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay
34. Functional Characterization, Localization, and Inhibitor Sensitivity of the TPR-FGFR1 Fusion in 8p11 Myeloproliferative Syndrome.
35. Isolation and characterization of CD133+CD34+VEGFR-2+CD45− fetal endothelial cells from human term placenta
36. Characterization of a newly identified ETV6-NTRK3 fusion transcript in acute myeloid leukemia
37. Parental origin and mechanism of formation of a 46,X,der(X)(pter→q21.1::p11.4→pter)/45,X karyotype in a woman with mild Turner syndrome
38. E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer
39. “Essentially” pure trisomy 3q27 → qter: Further delineation of the partial trisomy 3q phenotype
40. Successful treatment of MDS with lenalidomide, complicated by transient autoimmune hemolysis
41. Clinical Outcome of B-Cell Chronic Lymphocytic Leukemia Following Alemtuzumab Therapy: Retrospective Study within Various Cytogenetic Risk Categories
42. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant
43. Abstract 3753: Critical Role of Scavenger Receptor-BI Expressing Bone Marrow-Derived Endothelial Progenitor Cells in the Attenuation of Allograft Vasculopathy by Human Apo A-I Transfer
44. Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome
45. Glucocorticoid resistance in two key models of acute lymphoblastic leukemia occurs at the level of the glucocorticoid receptor
46. High rate of molecular alteration in histologically tumour-free bronchial epithelium of NSCLC patients detected by multicolour fluorescence in situ hybridisation
47. Myelodysplastic/myeloproliferative disease with erythropoietic hyperplasia (erythroid preleukemia) and the unique translocation (8;9)(p23;p24): first description of a case
48. Human Endothelial Cells Generated In Vitro from Circulating Progenitors Represent a Safe Tool for Targeting of Myocardial Tissue.
49. Burkitt's Lymphoma of the Stomach: a Case Report with Molecular Cytogenetic Analysis
50. Both Donor and Recipient Origins of Smooth Muscle Cells in Vein Graft Atherosclerotic Lesions
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