Advances in molecular characterization of myeloid proliferations associated with Down syndrome
出版年份 2022 全文链接
标题
Advances in molecular characterization of myeloid proliferations associated with Down syndrome
作者
关键词
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出版物
Frontiers in Genetics
Volume 13, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2022-08-10
DOI
10.3389/fgene.2022.891214
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Acquired WT1 mutations contribute to relapse of NPM1-mutated acute myeloid leukemia following allogeneic hematopoietic stem cell transplant
- (2022) Siba El Hussein et al. BONE MARROW TRANSPLANTATION
- DNA methylation: a saga of genome maintenance in hematological perspective
- (2022) Saran Chattopadhyaya et al. Human Cell
- Modeling Down Syndrome Myeloid Leukemia by Sequential Introduction of GATA1 and STAG2 Mutations in Induced Pluripotent Stem Cells with Trisomy 21
- (2022) Sonali P. Barwe et al. Cells
- GATA1 mutation analysis and molecular landscape characterization in acute myeloid leukemia with trisomy 21 in pediatric patients
- (2021) Agnesa Panferova et al. International Journal of Laboratory Hematology
- Smc3 dosage regulates B cell transit through germinal centers and restricts their malignant transformation
- (2021) Martín A. Rivas et al. NATURE IMMUNOLOGY
- son is necessary for proper vertebrate blood development
- (2021) Rebecca L. Belmonte et al. PLoS One
- The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis
- (2021) Ivo S. Muskens et al. Nature Communications
- Molecular Mechanisms of the Genetic Predisposition to Acute Megakaryoblastic Leukemia in Infants With Down Syndrome
- (2021) Juliane Grimm et al. Frontiers in Oncology
- Therapeutic Opportunities of Targeting Canonical and Noncanonical PcG/TrxG Functions in Acute Myeloid Leukemia
- (2021) Bernd B. Zeisig et al. Annual Review of Genomics and Human Genetics
- Targeting RUNX1 in acute myeloid leukemia: preclinical innovations and therapeutic implications
- (2021) Fanny Gonzales et al. EXPERT OPINION ON THERAPEUTIC TARGETS
- Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency
- (2021) Henry Y. Lu et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- SF3B1 as therapeutic target in FLT3/ITD positive acute myeloid leukemia
- (2021) Inge van der Werf et al. LEUKEMIA
- Pluripotent stem cell model of early hematopoiesis in Down syndrome reveals quantitative effects of short-form GATA1 protein on lineage specification
- (2021) Shiori Matsuo et al. PLoS One
- RAS mutations drive proliferative chronic myelomonocytic leukemia via a KMT2A-PLK1 axis
- (2021) Ryan M. Carr et al. Nature Communications
- A cohesin cancer mutation reveals a role for the hinge domain in genome organization and gene expression
- (2021) Zachary M. Carico et al. PLoS Genetics
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- (2021) Eirini Sofia Fasouli et al. Frontiers in Cell and Developmental Biology
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- (2021) Julie A I Thoms et al. BLOOD
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- (2021) Johann-Christoph Jann et al. BLOOD
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- (2021) Stefania Mazzi et al. BLOOD
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- (2021) Shailendra Maurya et al. Epigenetics
- Cohesin Mutations in Cancer: Emerging Therapeutic Targets
- (2021) Jisha Antony et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Dual-Specificity, Tyrosine Phosphorylation-Regulated Kinases (DYRKs) and cdc2-Like Kinases (CLKs) in Human Disease, an Overview
- (2021) Mattias F. Lindberg et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- POLE, POLD1, and NTHL1: the last but not the least hereditary cancer-predisposing genes
- (2021) Luigi Magrin et al. ONCOGENE
- Mapping the cellular origin and early evolution of leukemia in Down syndrome
- (2021) Elvin Wagenblast et al. SCIENCE
- Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome
- (2021) Patricia Garcia et al. Nature Communications
- Efficacy and tolerability of Janus kinase inhibitors in myelofibrosis: a systematic review and network meta-analysis
- (2021) Léa Sureau et al. Blood Cancer Journal
- The Mutational Landscape of Myeloid Leukaemia in Down Syndrome
- (2021) Carini Picardi Morais de Castro et al. Cancers
- The Ups and Downs of STAT Inhibition in Acute Myeloid Leukemia
- (2021) Bernhard Moser et al. Biomedicines
- Germline GATA1s generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotype
- (2021) Henrik Hasle et al. BLOOD
- The megakaryocytic transcription factor ARID3A suppresses leukemia pathogenesis
- (2021) Oriol Alejo-Valle et al. BLOOD
- TP53 in Acute Myeloid Leukemia: Molecular Aspects and Patterns of Mutation
- (2021) Binsah George et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- The IL-3, IL-5, and GM-CSF common receptor beta chain mediates oncogenic activity of FLT3-ITD-positive AML
- (2021) Anne Charlet et al. LEUKEMIA
- A concise review on the molecular genetics of acute myeloid leukemia
- (2021) Devipriya Padmakumar et al. LEUKEMIA RESEARCH
- Functional role and ribosomal position of the unique N-terminal region of DHX29, a factor required for initiation on structured mammalian mRNAs
- (2021) Trevor R Sweeney et al. NUCLEIC ACIDS RESEARCH
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- (2021) Ling Tian et al. PLoS One
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- (2021) Fangxue Yan et al. Cancer Discovery
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- (2021) Jie Zhou et al. Bioengineered
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- (2021) Na Man et al. JCI Insight
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- (2020) Sunil Kumar Joshi et al. BLOOD
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- (2020) Leonidas Benetatos et al. JOURNAL OF MOLECULAR MEDICINE-JMM
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- (2020) Kentaro Yuzawa et al. PEDIATRIC BLOOD & CANCER
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- (2020) Huthayfa Mujahed et al. BLOOD
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- (2020) Alexandra A. Soukup et al. CURRENT OPINION IN HEMATOLOGY
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- (2020) Yoko Nishinaka-Arai et al. HAEMATOLOGICA
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- (2020) Mara Mazzola et al. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
- Gain of chromosome 21 in hematological malignancies: lessons from studying leukemia in children with Down syndrome
- (2020) Anouchka P. Laurent et al. LEUKEMIA
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- (2020) Franco Izzo et al. NATURE GENETICS
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- (2020) Shaima’a Hamarsheh et al. Nature Communications
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- (2020) Lucia Cabal-Hierro et al. Nature Communications
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- (2020) Yotaro Ochi et al. Cancer Discovery
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- (2020) Naveera Zafar et al. Asia-Pacific Journal of Clinical Oncology
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- (2020) Gaëtan Juban et al. HAEMATOLOGICA
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- (2020) Tekin Aksu et al. PEDIATRIC BLOOD & CANCER
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- (2020) Nitza Vara et al. Blood Advances
- SON inhibits megakaryocytic differentiation via repressing RUNX1 and the megakaryocytic gene expression program in acute megakaryoblastic leukemia
- (2020) Lana Vukadin et al. CANCER GENE THERAPY
- Human CREBBP acetyltransferase is impaired by etoposide quinone, an oxidative and leukemogenic metabolite of the anticancer drug etoposide through modification of redox-sensitive zinc-finger cysteine residues
- (2020) Wenchao Zhang et al. FREE RADICAL BIOLOGY AND MEDICINE
- Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms
- (2020) Gabriele Todisco et al. LEUKEMIA
- Impact of Mutational Profile on the Management of Myeloproliferative Neoplasms: A Short Review of the Emerging Data
- (2020) Giuseppe G Loscocco et al. OncoTargets and Therapy
- ETNK1 mutations induce a mutator phenotype that can be reverted with phosphoethanolamine
- (2020) Diletta Fontana et al. Nature Communications
- Modeling Transient Abnormal Myelopoiesis Using Induced Pluripotent Stem Cells and CRISPR/Cas9 Technology
- (2020) Sonali P. Barwe et al. Molecular Therapy-Methods & Clinical Development
- NIPBL: a new player in myeloid cells differentiation
- (2019) Mara Mazzola et al. HAEMATOLOGICA
- Bcor loss perturbs myeloid differentiation and promotes leukaemogenesis
- (2019) Madison J. Kelly et al. Nature Communications
- Human PRPF40B regulates hundreds of alternative splicing targets and represses a hypoxia expression signature
- (2019) Paolo A Lorenzini et al. RNA
- Multifaceted roles of thrombopoietin in hematopoietic stem cell regulation
- (2019) Ayako Nakamura‐Ishizu et al. Annals of the New York Academy of Sciences
- Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome
- (2019) Maurice Labuhn et al. CANCER CELL
- Genetic characterization of ABT-199 sensitivity in human AML
- (2019) Richard Bisaillon et al. LEUKEMIA
- Gene expression dysregulation domains are not a specific feature of Down syndrome
- (2019) Helena Ahlfors et al. Nature Communications
- Loss of EZH2 Reprograms BCAA Metabolism to Drive Leukemic Transformation
- (2019) Zhimin Gu et al. Cancer Discovery
- STAG2 loss-of-function mutation induces PD-L1 expression in U2OS cells
- (2019) Zhirui Nie et al. Annals of Translational Medicine
- Cohesin Members Stag1 and Stag2 Display Distinct Roles in Chromatin Accessibility and Topological Control of HSC Self-Renewal and Differentiation
- (2019) Aaron D. Viny et al. Cell Stem Cell
- DCAF7 is required for maintaining the cellular levels of ERCC1-XPF and nucleotide excision repair
- (2019) Hiroaki Kawara et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Cooperation of Dnmt3a R878H with Nras G12D promotes leukemogenesis in knock-in mice: a pilot study
- (2019) Xiaodong Shi et al. BMC CANCER
- GATA1 and cooperating mutations in myeloid leukaemia of Down syndrome
- (2019) Catherine Garnett et al. IUBMB LIFE
- PTEN in Regulating Hematopoiesis and Leukemogenesis
- (2019) Yilin Wu et al. Cold Spring Harbor Perspectives in Medicine
- NPM1c impedes CTCF functions through cytoplasmic mislocalization in acute myeloid leukemia
- (2019) Atom J. Wang et al. LEUKEMIA
- Expression of mutant Asxl1 perturbs hematopoiesis and promotes susceptibility to leukemic transformation
- (2018) Reina Nagase et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Unique Structural Platforms of Suz12 Dictate Distinct Classes of PRC2 for Chromatin Binding
- (2018) Siming Chen et al. MOLECULAR CELL
- A CHAF1B-Dependent Molecular Switch in Hematopoiesis and Leukemia Pathogenesis
- (2018) Andrew Volk et al. CANCER CELL
- DCAF7/WDR68 is required for normal levels of DYRK1A and DYRK1B
- (2018) Mina Yousefelahiyeh et al. PLoS One
- Smc3 is required for mouse embryonic and adult hematopoiesis
- (2018) Tianjiao Wang et al. EXPERIMENTAL HEMATOLOGY
- Characterization and mechanism of phosphoinositide 3-kinases (PI3Ks) members in insulin-induced changes of protein metabolism in yellow catfish Pelteobagrus fulvidraco
- (2017) Mei-Qin Zhuo et al. GENERAL AND COMPARATIVE ENDOCRINOLOGY
- The role of LNK/SH2B3 genetic alterations in myeloproliferative neoplasms and other hematological disorders
- (2017) N Maslah et al. LEUKEMIA
- Pediatric non–Down syndrome acute megakaryoblastic leukemia is characterized by distinct genomic subsets with varying outcomes
- (2017) Jasmijn D E de Rooij et al. NATURE GENETICS
- An activating mutation of GNB1 is associated with resistance to tyrosine kinase inhibitors in ETV6-ABL1-positive leukemia
- (2017) O Zimmermannova et al. ONCOGENE
- GATA Transcription Factors: Basic Principles and Related Human Disorders
- (2017) Tohru Fujiwara TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
- A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome
- (2017) Daiane Correa de Souza et al. Molecular Cytogenetics
- Protein tyrosine phosphatases receptor type D is a potential tumour suppressor gene inactivated by deoxyribonucleic acid methylation in paediatric acute myeloid leukaemia
- (2016) Lei Song et al. ACTA PAEDIATRICA
- Genomics of chronic neutrophilic leukemia
- (2016) Julia E. Maxson et al. BLOOD
- The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia
- (2016) D. A. Arber et al. BLOOD
- WRN-targeted therapy using inhibitors NSC 19630 and NSC 617145 induce apoptosis in HTLV-1-transformed adult T-cell leukemia cells
- (2016) R. Moles et al. Journal of Hematology & Oncology
- High-Throughput Small Interfering RNA Screening Identifies Phosphatidylinositol 3-Kinase Class II Alpha as Important for Production of Human Cytomegalovirus Virions
- (2016) William S. Polachek et al. JOURNAL OF VIROLOGY
- The cohesin subunit Rad21 is a negative regulator of hematopoietic self-renewal through epigenetic repression of Hoxa7 and Hoxa9
- (2016) J B Fisher et al. LEUKEMIA
- Down syndrome and the complexity of genome dosage imbalance
- (2016) Stylianos E. Antonarakis NATURE REVIEWS GENETICS
- CDKN2B, SLC19A3 and DLEC1 promoter methylation alterations in the bone marrow of patients with acute myeloid leukemia during chemotherapy
- (2016) QINGXIAO HONG et al. Experimental and Therapeutic Medicine
- Upregulation of miR-99a is associated with poor prognosis of acute myeloid leukemia and promotes myeloid leukemia cell expansion
- (2016) Xiaohui Si et al. Oncotarget
- Maintenance of the functional integrity of mouse hematopoiesis by EED and promotion of leukemogenesis by EED haploinsufficiency
- (2016) Kenichiro Ikeda et al. Scientific Reports
- Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities
- (2016) Kimihiko Banno et al. Cell Reports
- Transient Abnormal Myelopoiesis and AML in Down Syndrome: an Update
- (2016) Neha Bhatnagar et al. Current Hematologic Malignancy Reports
- Cytokine‐induced megakaryocytic differentiation is regulated by genome‐wide loss of a uSTAT transcriptional program
- (2015) Hyun Jung Park et al. EMBO JOURNAL
- Expression of the ETS transcription factor GABPα is positively correlated to the BCR-ABL1/ABL1 ratio in CML patients and affects imatinib sensitivity in vitro
- (2015) Georgi Manukjan et al. EXPERIMENTAL HEMATOLOGY
- Global transcriptome and chromatin occupancy analysis reveal the short isoform of GATA1 is deficient for erythroid specification and gene expression
- (2015) T. M. Chlon et al. HAEMATOLOGICA
- Global transcriptome and chromatin occupancy analysis reveal the short isoform of GATA1 is deficient for erythroid specification and gene expression
- (2015) T. M. Chlon et al. HAEMATOLOGICA
- Transient Abnormal Myelopoiesis in Neonates: GATA Get the Diagnosis
- (2014) Melissa Bombery et al. ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
- MicroRNA-486-5p is an erythroid oncomiR of the myeloid leukemias of Down syndrome
- (2014) L. Shaham et al. BLOOD
- C-KIT Signaling in Cancer Treatment
- (2014) Karmen Stankov et al. CURRENT PHARMACEUTICAL DESIGN
- Stem and progenitor cell dysfunction in human trisomies
- (2014) B. Liu et al. EMBO REPORTS
- Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children
- (2014) Rintaro Ono et al. EUROPEAN JOURNAL OF PEDIATRICS
- miR-99a/100 125b tricistrons regulate hematopoietic stem and progenitor cell homeostasis by shifting the balance between TGF and Wnt signaling
- (2014) S. Emmrich et al. GENES & DEVELOPMENT
- Domains of genome-wide gene expression dysregulation in Down’s syndrome
- (2014) Audrey Letourneau et al. NATURE
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- (2014) Christopher J. Kemp et al. Cell Reports
- Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome
- (2013) S. I. Nikolaev et al. BLOOD
- The calcineurin-NFAT pathway negatively regulates megakaryopoiesis
- (2013) A. Zaslavsky et al. BLOOD
- Development of acute megakaryoblastic leukemia in Down syndrome is associated with sequential epigenetic changes
- (2013) S. Malinge et al. BLOOD
- Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome
- (2013) S. Saida et al. BLOOD
- GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia
- (2013) I. Roberts et al. BLOOD
- MiR-99a may serve as a potential oncogene in pediatric myeloid leukemia
- (2013) Lidan Zhang et al. Cancer Cell International
- Loss of PML cooperates with mutant p53 to drive more aggressive cancers in a gender-dependent manner
- (2013) Sue Haupt et al. CELL CYCLE
- AKT collaborates with ERG and Gata1s to dysregulate megakaryopoiesis and promote AMKL
- (2013) M J Stankiewicz et al. LEUKEMIA
- The landscape of somatic mutations in Down syndrome–related myeloid disorders
- (2013) Kenichi Yoshida et al. NATURE GENETICS
- GABP transcription factor is required for development of chronic myelogenous leukemia via its control of PRKD2
- (2013) Z.-F. Yang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells
- (2013) J. Zuin et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Increased dosage of the chromosome 21 ortholog Dyrk1a promotes megakaryoblastic leukemia in a murine model of Down syndrome
- (2012) Sébastien Malinge et al. JOURNAL OF CLINICAL INVESTIGATION
- Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia
- (2012) Panagiotis Ntziachristos et al. NATURE MEDICINE
- Hematopoietic overexpression of the transcription factor Erg induces lymphoid and erythro-megakaryocytic leukemia
- (2012) C. L. Carmichael et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cells
- (2012) S. T. Chou et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- ADP-ribose polymers localized on Ctcf–Parp1–Dnmt1 complex prevent methylation of Ctcf target sites
- (2011) Michele Zampieri et al. BIOCHEMICAL JOURNAL
- Analysis of GATA1 mutations in Down syndrome transient myeloproliferative disorder and myeloid leukemia
- (2011) K. A. Alford et al. BLOOD
- Transient Myeloproliferative Disorder and GATA1 Mutation in Neonates With and Without Down Syndrome
- (2011) Ming-Horng Tsai et al. INDIAN JOURNAL OF PEDIATRICS
- CTCF-promoted RNA polymerase II pausing links DNA methylation to splicing
- (2011) Sanjeev Shukla et al. NATURE
- Trisomy-21 gene dosage over-expression of miRNAs results in the haploinsufficiency of specific target proteins
- (2011) Terry S. Elton et al. RNA Biology
- Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia
- (2010) R. Kanezaki et al. BLOOD
- miR-125b-2 is a potential oncomiR on human chromosome 21 in megakaryoblastic leukemia
- (2010) J.-H. Klusmann et al. GENES & DEVELOPMENT
- ETS2 and ERG promote megakaryopoiesis and synergize with alterations in GATA-1 to immortalize hematopoietic progenitor cells
- (2009) M. J. Stankiewicz et al. BLOOD
- ERG Is a Megakaryocytic Oncogene
- (2009) S. Salek-Ardakani et al. CANCER RESEARCH
- Induction of hyperproliferative fetal megakaryopoiesis by an N-terminally truncated GATA1 mutant
- (2009) Ritsuko Shimizu et al. GENES TO CELLS
- Activating mutations in human acute megakaryoblastic leukemia
- (2008) S. Malinge et al. BLOOD
- Treatment and prognostic impact of transient leukemia in neonates with Down syndrome
- (2008) J.-H. Klusmann et al. BLOOD
- Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome
- (2008) Asahito Hama et al. BRITISH JOURNAL OF HAEMATOLOGY
- Transient Myeloproliferative Disorder in Neonates With and Without Down Syndrome
- (2008) Nataly Apollonsky et al. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
- Polycomb Repressive Complex 2 (PRC2) Restricts Hematopoietic Stem Cell Activity
- (2008) Ian J Majewski et al. PLOS BIOLOGY
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