301 results on '"Blewitt, Marnie E"'
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2. Increasing histone acetylation improves sociability and restores learning and memory in KAT6B-haploinsufficient mice
3. Mary Lyon and the birth of X-inactivation research
4. Epigenetic Silencing of RIPK3 in Hepatocytes Prevents MLKL-mediated Necroptosis From Contributing to Liver Pathologies
5. Serum iron and transferrin saturation variation are circadian regulated and linked to the harmonic circadian oscillations of erythropoiesis and hepatic Tfrc expression in mice.
6. Maternal SMCHD1 regulates Hox gene expression and patterning in the mouse embryo
7. BAF complex-mediated chromatin relaxation is required for establishment of X chromosome inactivation
8. Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
9. Hippocampal neurogenesis mediates sex-specific effects of social isolation and exercise on fear extinction in adolescence
10. Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects
11. The molecular and cellular anatomy of a fetal programming defect – the impact of low protein diet on the developing kidney
12. Chromatin-mediated silencing on the inactive X chromosome
13. Smchd1 Targeting to the Inactive X Is Dependent on the Xist-HnrnpK-PRC1 Pathway
14. MBD4 guards against methylation damage and germ line deficiency predisposes to clonal hematopoiesis and early-onset AML
15. FSHD2- and BAMS-associated mutations confer opposing effects on SMCHD1 function
16. HBO1 is required for the maintenance of leukaemia stem cells
17. An N-Ethyl-N-Nitrosourea Screen for Genes Involved in Variegation in the Mouse
18. Artificial intelligence takes center stage: exploring the capabilities and implications of ChatGPT and other AI‐assisted technologies in scientific research and education
19. Mary Lyon and the birth of X-inactivation research
20. The Epigenetic Regulator SMCHD1 in Development and Disease
21. Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters
22. Serum iron and hepatic transferrin receptor expression are circadian-regulated
23. Data from Epigenetic Regulator Smchd1 Functions as a Tumor Suppressor
24. Polycomb repressive complex 2 component Suz12 is required for hematopoietic stem cell function and lymphopoiesis
25. Jarid2 regulates hematopoietic stem cell function by acting with polycomb repressive complex 2
26. Genome-wide binding and mechanistic analyses of Smchd1-mediated epigenetic regulation
27. A method for stabilising the XX karyotype in female mESC cultures
28. The polycomb repressive complex 2 governs life and death of peripheral T cells
29. Analysis of Histone Modifications in Acute Myeloid Leukaemia Using Chromatin Immunoprecipitation
30. Suv39h-catalyzed H3K9me3 is critical for euchromatic genome organization and the maintenance of gene transcription
31. Genome-wide DNA methylation analysis identifies hypomethylated genes regulated by FOXP3 in human regulatory T cells
32. Polycomb repressive complex 2 (PRC2) suppresses Eμ-myc lymphoma
33. Epigenetic modifier SMCHD1 maintains a normal pool of long-term hematopoietic stem cells
34. Additional file 4 of Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
35. Additional file 5 of Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
36. Additional file 3 of Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
37. Opposing roles of polycomb repressive complexes in hematopoietic stem and progenitor cells
38. ANALYSIS OF THE MECHANISMS UNDERLYING THE DEVELOPMENTAL REGULATION OF EMBRYONIC AND FETAL β-LIKE GLOBIN GENES: O8
39. KEYNOTE SPEAKER 10: SCREENING FOR AND CHARACTERISING MAMMALIAN EPIGENETIC MODIFIERS
40. NanoMethViz: An R/Bioconductor package for visualizing long-read methylation data
41. Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation
42. Maternal SMCHD1 regulates Hox gene expression and patterning in the mouse embryo
43. Reduced dosage of the modifiers of epigenetic reprogramming Dnmt1, Dnmt3L, SmcHD1 and Foxo3a has no detectable effect on mouse telomere length in vivo
44. SMCHD1's ubiquitin-like domain is required for N-terminal dimerization and chromatin localization
45. A functional genetic screen identifies aurora kinase b as an essential regulator of Sox9-positive mouse embryonic lung progenitor cells
46. SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease
47. The long and the short of it: unlocking nanopore long-read RNA sequencing data with short-read differential expression analysis tools
48. ChIP-seq analysis reveals distinct H3K27me3 profiles that correlate with transcriptional activity
49. RNF41 regulates the damage recognition receptor Clec9A and antigen cross-presentation in mouse dendritic cells
50. Author response: RNF41 regulates the damage recognition receptor Clec9A and antigen cross-presentation in mouse dendritic cells
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