X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (20) 20
index medicus (16) 16
mutation (10) 10
female (8) 8
hematology (8) 8
male (8) 8
mice (8) 8
animals (7) 7
research (7) 7
adult (6) 6
biochemistry & molecular biology (6) 6
cell biology (6) 6
in-vivo (6) 6
aged (5) 5
dna methylation (5) 5
expression (5) 5
fetal hemoglobin - genetics (5) 5
fetal hemoglobin - metabolism (5) 5
gene-expression (5) 5
methylation (5) 5
middle aged (5) 5
beta-thalassemia - genetics (4) 4
cells (4) 4
disease (4) 4
erythroid cells - metabolism (4) 4
gene (4) 4
gene expression (4) 4
gene expression regulation, developmental (4) 4
genetic aspects (4) 4
hemic and lymphatic diseases (4) 4
physiological aspects (4) 4
transcription (4) 4
transcription factors (4) 4
transcription, genetic (4) 4
adolescent (3) 3
analysis (3) 3
base sequence (3) 3
binding sites (3) 3
cell line, tumor (3) 3
cells, cultured (3) 3
chromatin (3) 3
erythroid cells - cytology (3) 3
erythroid progenitors (3) 3
erythroid-differentiation (3) 3
gata1 transcription factor - metabolism (3) 3
gene expression profiling (3) 3
gene expression regulation (3) 3
genetic predisposition to disease (3) 3
genetic testing (3) 3
genetic transcription (3) 3
genetics (3) 3
genetics & heredity (3) 3
globins - genetics (3) 3
hydroxyurea (3) 3
inherited disorders (3) 3
k562 cells (3) 3
lymphocytes (3) 3
neutrophil (3) 3
neutrophils - metabolism (3) 3
original (3) 3
promoter regions, genetic (3) 3
proteins (3) 3
transcription factors - metabolism (3) 3
young adult (3) 3
abridged index medicus (2) 2
activation (2) 2
adaptive immunity (2) 2
aged, 80 and over (2) 2
allele specific (2) 2
alternative splicing (2) 2
anopheles (2) 2
articles (2) 2
b-lymphocytes (2) 2
beta-globin locus (2) 2
beta-thalassemia (2) 2
biology (2) 2
biotinylation (2) 2
brain (2) 2
ccctc-binding factor (2) 2
cell line (2) 2
chromatin - metabolism (2) 2
cluster analysis (2) 2
data processing (2) 2
database (2) 2
differentiation (2) 2
dinucleoside phosphates (2) 2
discovery (2) 2
dna binding proteins (2) 2
dna mutational analysis (2) 2
efficient gene delivery (2) 2
enhancers (2) 2
epigenetic inheritance (2) 2
epigenetics (2) 2
epigenome (2) 2
epigenomics (2) 2
erythropoiesis (2) 2
ewas (2) 2
exons (2) 2
fetal globin genes (2) 2
fetal hemoglobin (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Blood, ISSN 0006-4971, 11/2010, Volume 116, Issue 20, pp. 4349 - 4352
textabstractAnestimated 6% to 7% of the earth's population carries a mutation affecting red blood cell function. The β-thalassemias and sickle cell disease are... 
Journal Article
Haematologica, ISSN 0390-6078, 01/2013, Volume 98, Issue 5, pp. 696 - 704
textabstractβ-thalassemia is caused by mutations in the β-globin locus resulting in loss of, or reduced, hemoglobin A (adult hemoglobin, HbA, α2β2) production.... 
Journal Article
Molecular Medicine, ISSN 1076-1551, 04/2015, Volume 21, pp. 346 - 354
textabstractEpidemiological studies indicate that vitamin D exerts a protective effect on the development of various solid cancers. However, concerns have been... 
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 01/2015, Volume 35, Issue 12, pp. 2103 - 2118
textabstractThe ordered assembly of a functional preinitiation complex (PIC), composed of general transcription factors (GTFs), is a prerequisite for the... 
Journal Article
Haematologica, ISSN 0390-6078, 09/2011, Volume 96, Issue 9, pp. 1252 - 1260
textabstractBackground: In erythroblasts, the CoREST repressor complex is recruited to target promoters by the transcription factor Gfi1b, leading to... 
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2014, Volume 124, Issue 4, pp. 1699 - 1710
Journal Article
by Chen, Shu-Huang and Chen, Lu and Ge, Bing and Casale, Francesco Paolo and Vasquez, Louella and Kwan, Tony and Garrido-Martín, Diego and Watt, Stephen and Yan, Ying and Kundu, Kousik and Ecker, Simone and Datta, Avik and Richardson, David and Burden, Frances and Mead, Daniel and Mann, Alice L and Fernandez, Jose Maria and Rowlston, Sophia and Wilder, Steven P and Farrow, Samantha and Shao, Xiaojian and Lambourne, John J and Redensek, Adriana and Albers, Cornelis A and Amstislavskiy, Vyacheslav and Ashford, Sofie and Berentsen, Kim and Bomba, Lorenzo and Bourque, Guillaume and Bujold, David and Busche, Stephan and Caron, Maxime and Cheung, Warren and Delaneau, Oliver and Dermitzakis, Emmanouil T and Elding, Heather and Colgiu, Irina and Bagger, Frederik O and Flicek, Paul and Habibi, Ehsan and Iotchkova, Valentina and Janssen-Megens, Eva and Kim, Bowon and Lehrach, Hans and Lowy, Ernesto and Mandoli, Amit and Matarese, Filomena and Maurano, Matthew T and Morris, John A and Pancaldi, Vera and Pourfarzad, Farzin and Rehnstrom, Karola and Rendon, Augusto and Risch, Thomas and Sharifi, Nilofar and Simon, Marie-Michelle and Sultan, Marc and Valencia, Alfonso and Walter, Klaudia and Wang, Shuang-Yin and Frontini, Mattia and Antonarakis, Stylianos E and Clarke, Laura and Yaspo, Marie-Laure and Beck, Stephan and Guigo, Roderic and Rico, Daniel and Martens, Joost H.A and Ouwehand, Willem H and Kuijpers, Taco W and Paul, Dirk S and Stunnenberg, Hendrik G and Stegle, Oliver and Downes, Kate and Pastinen, Tomi and Soranzo, Nicole
Cell, ISSN 0092-8674, 11/2016, Volume 167, Issue 5, pp. 1398 - 1414.e24
Journal Article
Journal Article
Genome biology, ISSN 1465-6906, 2017, Volume 18, Issue 1, p. 18
Journal Article