370 results on '"D'Urso, Michele"'
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2. A Compositional Map of Human Chromosome Band Xq28
3. White Paper on Industrial Applications of Computer Vision and Pattern Recognition
4. Glomerular filtration rate assessed by using creatinine and cystatin in patients treated with dabigatran
5. Functional Characterization of Wiskott-Aldrich Syndrome Protein and Scar Homolog (WASH), a Bi-modular Nucleation-promoting Factor Able to Interact with Biogenesis of Lysosome-related Organelle Subunit 2 (BLOS2) and γ-Tubulin
6. Tissue-Specific Levels of Human Glucose-6-phosphate Dehydrogenase Correlate with Methylation of Specific Sites at the 3 ′ End of the Gene
7. Yeast Artificial Chromosomes with 200- to 800-Kilobase Inserts of Human DNA Containing HLA, Vκ, 5S, and Xq24-Xq28 Sequences
8. Stable Integration and Expression in Mouse Cells of Yeast Artificial Chromosomes Harboring Human Genes
9. Yeast Artificial Chromosomes Spanning 8 Megabases and 10-15 Centimorgans of Human Cytogenetic Band Xq26
10. Conserved Sequence-Tagged Sites: A Phylogenetic Approach to Genome Mapping
11. On the effect of support estimation and of a new model in 2-D inverse scattering problems
12. An effective hybrid approach for the optimal synthesis of monopulse antennas
13. Effective solution of 3-D scattering problems via series expansions: applicability and a new hybrid scheme
14. Solving some array synthesis problems by means of an effective hybrid approach
15. White Paper on Industrial Applications of Computer Vision and Pattern Recognition
16. The DNA sequence of the human X chromosome
17. A hybrid approach for the optimal synthesis of pencil beams through array antennas
18. Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females
19. Microdeletion/Duplication at the Xq28 IP Locus Causes a De Novo IKBKG/NEMO/IKKgamma exon4_10 Deletion in Families with Incontinentia Pigmenti
20. Clinical diagnosis of incontinentia pigmenti in a cohort of male patients
21. Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2–q28 associated with ovarian dysfunction
22. Characterization of the human STAT5A and STAT5B promoters: evidence of a positive and negative mechanism of transcriptional regulation
23. A compositional map of human chromosome band Xq28
24. Human Synaptobrevin-like 1 Gene Basal Transcription Is Regulated through the Interaction of Selenocysteine tRNA Gene Transcription Activating Factor-Zinc Finger 143 Factors with Evolutionary Conserved Cis-elements
25. VAMP subfamilies identified by specific R-SNARE motifs
26. Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-κB activation
27. Incontinentia pigmenti with NEMO mutation in a Turkish family
28. Functional mapping of the human genome by cDNA localization versus sequencing
29. Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes
30. High-resolution methylation analysis of the hMLH1 promoter in sporadic endometrial and colorectal carcinomas
31. Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes
32. A recurrent deletion in the ubiquitously expressed NEMO (IKK-γ) gene accounts for the vast majority of incontinentia pigmenti mutations
33. Severe obesity in haemodialysis: the utility of bioimpedance vector analysis
34. Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia
35. Mutation analysis of the DKC1 gene in incontinentia pigmenti
36. Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity
37. Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa
38. Physical and Genetic Characterization Reveals a Pseudogene, an Evolutionary Junction, and Unstable Loci in Distal Xq28
39. DDX11L: a novel transcript family emerging from human subtelomeric regions
40. MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions
41. Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report
42. Longins: a new evolutionary conserved VAMP family sharing a novel SNARE domain
43. Design, analysis, application and experimental assessment of algorithms for the synthesis of maximally sparse, planar, non-superdirective and steerable arrays
44. Some facts and challenges in array antenna synthesis problems
45. A feasibility study of an innovative tool for microwave breast cancer imaging
46. An effective hybrid approach for multiple beams antennas
47. Power pattern synthesis of arbitrary sources exploiting array methods
48. FAST SYNTHESIS OF PLANAR, MAXIMALLY THINNED ARRAYS
49. Maximally Sparse, Steerable, and Nonsuperdirective Array Antennas via Convex Optimizations
50. Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybrids
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