159 results on '"Buckle, Veronica J."'
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2. Predicting the three-dimensional folding of cis-regulatory regions in mammalian genomes using bioinformatic data and polymer models
3. A Dynamic Folded Hairpin Conformation Is Associated with α-Globin Activation in Erythroid Cells
4. Cohesin Disrupts Polycomb-Dependent Chromosome Interactions in Embryonic Stem Cells
5. High-resolution targeted 3C interrogation of cis-regulatory element organization at genome-wide scale
6. Coregulated Human Globin Genes Are Frequently in Spatial Proximity when Active
7. Dynamics of the 4D genome during in vivo lineage specification and differentiation
8. Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domains
9. A Regulatory SNP Causes a Human Genetic Disease by Creating a New Transcriptional Promoter
10. A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactions
11. Intragenic Enhancers Act as Alternative Promoters
12. Association between Active Genes Occurs at Nuclear Speckles and Is Modulated by Chromatin Environment
13. Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts
14. Global gene expression analysis of human erythroid progenitors
15. On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation
16. Expanded GAA repeats impair FXN gene expression and reposition the FXN locus to the nuclear lamina in single cells
17. Loss of Both CSF1R (FMS) Alleles in Patients with Myelodysplasia and a Chromosome 5 Deletion
18. De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder
19. Genetic and functional insights into CDA-I prevalence and pathogenesis
20. Genetic and functional insights into CDA-I prevalence and pathogenesis
21. Coregulated human globin genes are frequently in spatial proximity' when active
22. Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects
23. Detection of Nascent RNA Transcripts by Fluorescence In Situ Hybridization
24. Recapitulation of erythropoiesis in congenital dyserythropoietic anemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
25. Genetic and functional insights into CDA-I prevalence and pathogenesis
26. Targeted high-resolution chromosome conformation capture at genome-wide scale
27. Genetic and functional insights into CDA-I prevalence and pathogenesis
28. ATR-16 syndrome: mechanisms linking monosomy to phenotype
29. An integrated platform to systematically identify causal variants and genes for polygenic human traits
30. Dynamics of the 4D genome during lineage specification, differentiation and maturation in vivo
31. Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I)
32. alpha -particle-induced chromosomal instability in human bone marrow cells
33. Relationship between Novel Isoforms, Functionally Important Domains, and Subcellular Distribution of CD164/Endolyn
34. Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors
35. Single-cell chromatin interactions reveal regulatory hubs in dynamic compartmentalized domains
36. A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactions
37. Predicting the three-dimensional folding of cis-regulatory regions in mammalian genomes using bioinformatic data and polymer models
38. Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
39. Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
40. Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
41. Unusual Types of α Thalassemia
42. A biophysical model for transcription factories
43. A biophysical model for transcription factories
44. Does Transcription of Remote α-Globin Regulatory Elements Affect Their Function?.
45. Lawler [née Corben; other married name Bagshawe], Sylvia Dorothy (1922–1996), human geneticist
46. Expression of α- and β-globin genes occurs within different nuclear domains in haemopoietic cells
47. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
48. A Large Duplicated Area in the Polycystic Kidney Disease 1 (PKD1) Region of Chromosome 16 Is Prone to Rearrangement
49. Untwirling dirvish
50. Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders
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