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Interrogation of enhancer function by enhancer-targeting CRISPR epigenetic editing

Nature communications, 2020-01, Vol.11 (1), p.485-485, Article 485

2020

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In Situ Capture of Chromatin Interactions by Biotinylated dCas9

Cell, 2017-08, Vol.170 (5), p.1028-1043.e19

2017

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Loss of EZH2 Reprograms BCAA Metabolism to Drive Leukemic Transformation

Cancer discovery, 2019-09, Vol.9 (9), p.1228-1247

2019

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Regulation of mitochondrial biogenesis in erythropoiesis by mTORC1-mediated protein translation

Nature cell biology, 2017-06, Vol.19 (6), p.626

2017

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Silencing of LINE-1 retrotransposons is a selective dependency of myeloid leukemia

Nature genetics, 2021-05, Vol.53 (5), p.672-682

2021

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Convergence of oncogenic cooperation at single-cell and single-gene levels drives leukemic transformation

Nature communications, 2021-11, Vol.12 (1), p.6323-17, Article 6323

2021

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Therapy Response and Outcome Explained by Leukemia Cell of Origin

Cancer discovery, 2020-10, Vol.10 (10), p.1445-1447

2020

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Pancytopenia and haematopoietic precursor vacuolisation in an infant: Clues to Pearson syndrome

British journal of haematology, 2023-09, Vol.202 (6), p.1079-1080

2023

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Immature Platelet Fraction as a Biomarker for Disease Severity in Pediatric Respiratory Coronavirus Disease 2019

The Journal of pediatrics, 2022-12, Vol.251, p.187-189

2022

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Noncoding Variants Connect Enhancer Dysregulation with Nuclear Receptor Signaling in Hematopoietic Malignancies

Cancer discovery, 2020-05, Vol.10 (5), p.724-745

2020

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Structural variation cooperates with permissive chromatin to control enhancer hijacking–mediated oncogenic transcription

Blood, 2023-07, Vol.142 (4), p.336-351

2023

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Abnormal Uterine Bleeding in Young Women with Blood Disorders

The Pediatric clinics of North America, 2018-06, Vol.65 (3), p.543-560

2018

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T/myeloid mixed phenotype acute leukaemia harbouring TLX3::BCL11B with TLX3 activation

British journal of haematology, 2024-02

2024

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Diagnosis and treatment of pediatric myelodysplastic syndromes: A survey of the North American Pediatric Aplastic Anemia Consortium

Pediatric blood & cancer, 2020-10, Vol.67 (10), p.e28652-n/a

2020

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Disabling Uncompetitive Inhibition of Oncogenic IDH Mutations Drives Acquired Resistance

Cancer discovery, 2023-01, Vol.13 (1), p.170-193

2023

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Central nervous system imprinting of the G protein G(s)alpha and its role in metabolic regulation

Cell metabolism, 2009-06, Vol.9 (6), p.548-555

2009

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Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency

Journal of pediatric hematology/oncology, 2020-07, Vol.42 (5), p.e365

2020

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G(s)alpha deficiency in skeletal muscle leads to reduced muscle mass, fiber-type switching, and glucose intolerance without insulin resistance or deficiency

American Journal of Physiology: Cell Physiology, 2009-04, Vol.296 (4), p.C930-C940

2009

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Successful Use of Granulocyte Transfusion Therapy As a Bridge to Hematopoietic Stem Cell Transplant in a Child with Aplastic Anemia and Refractory Perirectal Abscess

Blood, 2022-11, Vol.140 (Supplement 1), p.11393-11394

2022

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Safety and Feasibility of Treatment with Rivaroxaban in Children for Non-Routine Indications: A Case Series Analysis

Blood, 2016-12, Vol.128 (22), p.5014-5014

2016

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Mavorixafor for Patients with Chronic Neutropenic Disorders: Results from a Phase 1b, Open-Label, Multicenter Study

Blood, 2022-11, Vol.140 (Supplement 1), p.1408-1410

2022

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Structural Variation Cooperates with Permissive Chromatin to Control Enhancer Hijacking-Mediated Oncogenic Transcription

Blood, 2022-11, Vol.140 (Supplement 1), p.1007-1008

2022

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Interrogation of enhancer function by enhancer-targeting CRISPR epigenetic editing

In Situ Capture of Chromatin Interactions by Biotinylated dCas9

Loss of EZH2 Reprograms BCAA Metabolism to Drive Leukemic Transformation

Regulation of mitochondrial biogenesis in erythropoiesis by mTORC1-mediated protein translation

Silencing of LINE-1 retrotransposons is a selective dependency of myeloid leukemia

Convergence of oncogenic cooperation at single-cell and single-gene levels drives leukemic transformation

Therapy Response and Outcome Explained by Leukemia Cell of Origin

Pancytopenia and haematopoietic precursor vacuolisation in an infant: Clues to Pearson syndrome

Immature Platelet Fraction as a Biomarker for Disease Severity in Pediatric Respiratory Coronavirus Disease 2019

Noncoding Variants Connect Enhancer Dysregulation with Nuclear Receptor Signaling in Hematopoietic Malignancies

Structural variation cooperates with permissive chromatin to control enhancer hijacking–mediated oncogenic transcription

Abnormal Uterine Bleeding in Young Women with Blood Disorders

T/myeloid mixed phenotype acute leukaemia harbouring TLX3::BCL11B with TLX3 activation

SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature

Diagnosis and treatment of pediatric myelodysplastic syndromes: A survey of the North American Pediatric Aplastic Anemia Consortium

Disabling Uncompetitive Inhibition of Oncogenic IDH Mutations Drives Acquired Resistance

Central nervous system imprinting of the G protein G(s)alpha and its role in metabolic regulation

Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency

Eradicating acute myeloid leukemia in a Mll(PTD/wt):Flt3(ITD/wt) murine model: a path to novel therapeutic approaches for human disease

G(s)alpha deficiency in skeletal muscle leads to reduced muscle mass, fiber-type switching, and glucose intolerance without insulin resistance or deficiency

Successful Use of Granulocyte Transfusion Therapy As a Bridge to Hematopoietic Stem Cell Transplant in a Child with Aplastic Anemia and Refractory Perirectal Abscess

Safety and Feasibility of Treatment with Rivaroxaban in Children for Non-Routine Indications: A Case Series Analysis

Mavorixafor for Patients with Chronic Neutropenic Disorders: Results from a Phase 1b, Open-Label, Multicenter Study

Structural Variation Cooperates with Permissive Chromatin to Control Enhancer Hijacking-Mediated Oncogenic Transcription

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