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Search results (21)

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Sister chromatid cohesion is mediated by individual cohesin complexes.

Ochs F. et al, (2024), Science, 383, 1122 - 1130

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

Scott C. et al, (2021), Haematologica, 106, 2960 - 2970

Genetic and functional insights into CDA-I prevalence and pathogenesis.

Olijnik A-A. et al, (2021), J Med Genet, 58, 185 - 195

Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors.

Moir-Meyer G. et al, (2018), Methods Protoc, 1

Predicting the three-dimensional folding of cis-regulatory regions in mammalian genomes using bioinformatic data and polymer models.

Brackley CA. et al, (2016), Genome Biol, 17

Expanded GAA repeats impair FXN gene expression and reposition the FXN locus to the nuclear lamina in single cells.

Silva AM. et al, (2015), Hum Mol Genet, 24, 3457 - 3471

Chromatin organisation at the alpha globin locus

Brown JM. et al, (2015), CHROMOSOME RESEARCH, 23, 362 - 363

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.

Babbs C. et al, (2013), Haematologica, 98, 1383 - 1387

Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression

Schödel J. et al, (2012), Nature Genetics, 44, 420 - 425

Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression.

Schödel J. et al, (2012), Nat Genet, 44, 420 - S2

Intragenic enhancers act as alternative promoters.

Kowalczyk MS. et al, (2012), Mol Cell, 45, 447 - 458

Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression

Schödel J. et al, (2012), Nature Genetics, 44, 420 - 425

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.

Renella R. et al, (2011), Blood, 117, 6928 - 6938

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts

Renella R. et al, (2011), Blood, 117, 6928 - 6938

Detection of nascent RNA transcripts by fluorescence in situ hybridization.

Brown JM. and Buckle VJ., (2010), Methods Mol Biol, 659, 33 - 50

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