301 results on '"Blewitt, Marnie E"'
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52. Author response: Smchd1 is a maternal effect gene required for genomic imprinting
53. Relating SMCHD1 structure to its function in epigenetic silencing
54. The long and the short of it: unlocking nanopore long-read RNA sequencing data with short-read tools
55. Unique properties of a subset of human pluripotent stem cells with high capacity for self-renewal
56. Variable expressivity and epigenetics
57. How the mouse got its spots
58. Smchd1 is a maternal effect gene required for autosomal imprinting
59. HBO1 is required for the maintenance of leukaemia stem cells
60. Xmas ESC: A new female embryonic stem cell system that reveals the BAF complex as a key regulator of the establishment of X chromosome inactivation
61. Development of a KDM6b shRNA conditional knock down mouse model
62. Using long-read sequencing to detect imprinted DNA methylation
63. Metastable epialleles in mammals
64. SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite
65. SMCHD1 is involved inde novomethylation of theDUX4-encoding D4Z4 macrosatellite
66. Crystal structure of the hinge domain of Smchd1 reveals its dimerization mode and nucleic acid–binding residues.
67. Using long-read sequencing to detect imprinted DNA methylation
68. Abstract 1366:MBD4guards against DNA damage from methylcytosine deamination
69. Long-range chromatin interactions on the inactive X and atHoxclusters are regulated by the non-canonical SMC protein Smchd1
70. Studying X chromosome inactivation in the single-cell genomic era
71. FSHD2-and BAMS-associated mutations confer opposing effects on SMCHD1 function
72. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model
73. Germline loss of MBD4 predisposes to leukaemia due to a mutagenic cascade driven by 5mC
74. How do mutations in epigenetic regulators contribute to disease?
75. Comprehensive characterization of distinct states of human naive pluripotency generated by reprogramming
76. Glimma: interactive graphics for gene expression analysis
77. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
78. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
79. High concordance between Illumina HiSeq2500 and NextSeq500 for reduced representation bisulfite sequencing (RRBS)
80. Functional interdependence of BRD4 and DOT1L in MLL leukemia
81. The epigenetic regulator Smchd1 contains a functional GHKL-type ATPase domain
82. Setdb1-mediated H3K9 methylation is enriched on the inactive X and plays a role in its epigenetic silencing
83. The hinge domain of the epigenetic repressor Smchd1 adopts an unconventional homodimeric configuration
84. Transcriptional profiling of the epigenetic regulator Smchd1
85. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model.
86. Ihstone H3 lysine 9 methylation is involved not only in maintaining epigenetic silencing, but is essential for setting up gene silencing
87. Why weight? Modelling sample and observational level variability improves power in RNA-seq analyses
88. Repression of Igf1 expression by Ezh2 prevents basal cell differentiation in the developing lung
89. edgeR: a versatile tool for the analysis of shRNA-seq and CRISPR-Cas9 genetic screens
90. A comparison of control samples for ChIP-seq of histone modifications
91. shRNA-seq data analysis with edgeR
92. Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation
93. An in vivo model for analysis of developmental erythropoiesis and globin gene regulation
94. Transcriptional regulators Myb and BCL11A interplay with DNA methyltransferase 1 in developmental silencing of embryonic and fetal β‐like globin genes
95. Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation
96. Epigenetic Regulator Smchd1 Functions as a Tumor Suppressor
97. The epigenetic regulator Smchd1 contains a functional GHKL-type ATPase domain.
98. An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouse
99. An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse
100. TLR Regulation of SPSB1 Controls Inducible Nitric Oxide Synthase Induction
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