MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13

scientific article

MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13 is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2011PNAS..108.1519S
P356DOI10.1073/PNAS.1018384108
P3181OpenCitations bibliographic resource ID1153538
P932PMC publication ID3029749
P698PubMed publication ID21205891
P5875ResearchGate publication ID49728484

P50authorEric LanderQ970550
Harvey LodishQ5677403
Jo-Anne VergilioQ115916181
P2093author name stringStuart H Orkin
Peng Ji
Tobias F Menne
Jinkuk Kim
Prathapan Thiru
Vijay G Sankaran
Danilo Šćepanović
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Most mammalian mRNAs are conserved targets of microRNAsQ24655061
MicroRNAs modulate hematopoietic lineage differentiationQ27860661
The DLEU2/miR-15a/16-1 cluster controls B cell proliferation and its deletion leads to chronic lymphocytic leukemiaQ28269786
Global regulation of erythroid gene expression by transcription factor GATA-1Q28275891
Developmental and species-divergent globin switching are driven by BCL11AQ28506497
A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screenQ29615061
ENCODE whole-genome data in the UCSC Genome BrowserQ33516102
Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signalingQ33695715
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROMEQ34425268
Influence of cell cycle phase-specific agents on simian fetal hemoglobin synthesisQ34630922
Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesisQ36453536
The c-myb proto-oncogene and microRNA-15a comprise an active autoregulatory feedback loop in human hematopoietic cellsQ37066209
Ontogeny of erythropoiesis in the mammalian embryo.Q37087619
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomiesQ37259226
Control of fetal hemoglobin: new insights emerging from genomics and clinical implicationsQ37379477
c-Myb oncoprotein is an essential target of the dleu2 tumor suppressor microRNA cluster.Q37439625
Advances in the understanding of haemoglobin switchingQ37702418
MicroRNAs in erythropoiesisQ37705918
Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A.Q39908659
Progression through key stages of haemopoiesis is dependent on distinct threshold levels of c-Myb.Q39918427
Clinical delineation of proximal and distal partial 13q trisomyQ40109534
Coordination of erythropoiesis by the transcription factor c-Myb.Q42041452
Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.Q42105357
c-myb supports erythropoiesis through the transactivation of KLF1 and LMO2 expression.Q42946150
Haemoglobin switching in human embryos: asynchrony of zeta----alpha and epsilon----gamma-globin switches in primitive and definite erythropoietic lineageQ44788049
Postnatal fetal and adult hemoglobin synthesis in D 1 trisomy syndromeQ48027395
Arabinosylcytosine Induces Fetal Hemoglobin in Baboons by Perturbing Erythroid Cell Differentiation KineticsQ53552519
cMYB is involved in the regulation of fetal hemoglobin production in adults.Q54591078
Trisomy 13 and trisomy 18 in a defined population: epidemiological, genetic and prenatal observationsQ57492877
A transcription-factor-binding surface of coactivator p300 is required for haematopoiesisQ59098583
Sickle Cell Disease at 100 YearsQ59555153
Persistence of Hemoglobin F in D/D Translocation With Trisomy 13-15 (D1)Q72344928
FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROMEQ76890689
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectmicroRNAQ310899
P304page(s)1519-24
P577publication date2011-01-25
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleMicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13
P478volume108

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