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Caroline Scott

Showing results (31-40 of 39) with videos related to

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British Journal of Haematology|April 13, 2022
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor levelCaroline Scott, Kerol Bartolovic, Sally-Ann Clark, et al.
Nature Communications|June 17, 2022
The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatinJulia Truch, Damien J Downes, Caroline Scott, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
EMBO Reports|May 11, 2017
The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeatsDiu Tt Nguyen, Hsiao Phin J Voon, Barbara Xella, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Claudia Fiorini, et al.
Developmental Cell|August 16, 2023
RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Alexis Caulier, et al.
Haematologica|October 30, 2020
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalitiesCaroline Scott, Damien J Downes, Jill M Brown, et al.
Journal of Medical Genetics|June 11, 2020
Genetic and functional insights into CDA-I prevalence and pathogenesisAude-Anais Olijnik, Noémi B A Roy, Caroline Scott, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
British Journal of Haematology|April 13, 2022
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor levelCaroline Scott, Kerol Bartolovic, Sally-Ann Clark, et al.
Nature Communications|June 17, 2022
The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatinJulia Truch, Damien J Downes, Caroline Scott, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
EMBO Reports|May 11, 2017
The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeatsDiu Tt Nguyen, Hsiao Phin J Voon, Barbara Xella, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Claudia Fiorini, et al.
Developmental Cell|August 16, 2023
RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiationDanya J Martell, Hope E Merens, Alexis Caulier, et al.
Haematologica|October 30, 2020
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalitiesCaroline Scott, Damien J Downes, Jill M Brown, et al.
Journal of Medical Genetics|June 11, 2020
Genetic and functional insights into CDA-I prevalence and pathogenesisAude-Anais Olijnik, Noémi B A Roy, Caroline Scott, et al.
Genome Medicine|November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseasesAlistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
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