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Terminal deoxynucleotidyl transferase promotes acute myeloid leukemia by priming FLT3-ITD replication slippage

Blood, 2019-12, Vol.134 (25), p.2281-2290

2019

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Molecular roulette: nucleophosmin mutations in AML are orchestrated through N-nucleotide addition by TdT

Blood, 2019-12, Vol.134 (25), p.2291-2303

2019

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Pediatric Ependymoma: Biological Perspectives

Molecular cancer research, 2009-06, Vol.7 (6), p.765-786

2009

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NUP98-NSD1 fusion in association with FLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR

Genes chromosomes & cancer, 2013-11, Vol.52 (11), p.1053-1064

2013

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PB1809: COMPARISON OF OPTICAL GENOME MAPPING WITH STANDARD OF CARE TESTING TO INVESTIGATE GENOMIC ABNORMALITIES IN HAEMATOLOGICAL MALIGNANCIES: THE EXPERIENCE OF CENTRAL AND SOUTH GENOMIC LABORATORY HUB, UK

HemaSphere, 2023-08, Vol.7 (S3), p.e89431d8-n/a

2023

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Genomic Imbalances in Pediatric Intracranial Ependymomas Define Clinically Relevant Groups

The American journal of pathology, 2002-12, Vol.161 (6), p.2133-2141

2002

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First case of near haploid philadelphia negative B-Cell acute lymphoblastic leukaemia relapsing as acute myeloid leukemia following allogeneic hematopoietic stem cell transplantation

Leukemia research reports, 2020-01, Vol.14, p.100213-100213, Article 100213

2020

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How to Lose Your Voice

Annals of emergency medicine, 2008-07, Vol.52 (1), p.80-81

Flora, Sara Dyer, MD

2008

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Noncoding mutations drive persistence of a founder preleukemic clone which initiates late relapse in T-ALL

Blood, 2024-03, Vol.143 (10), p.933-937

2024

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Clonal evolution in adult TCF3::HLF-positive acute lymphoblastic leukemia undergoing stem cell transplantation

Annals of hematology, 2022-11, Vol.101 (11), p.2553-2554

2022

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Monoclonal Antibodies Reveal Receptor Specificity among G-Protein-Coupled Receptor Kinases

Proceedings of the National Academy of Sciences - PNAS, 1996-07, Vol.93 (15), p.7649-7654

1996

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1H MRS identifies specific metabolite profiles associated with MYCN-amplified and non-amplified tumour subtypes of neuroblastoma cell lines

NMR in biomedicine, 2007-11, Vol.20 (7), p.692-700

2007

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Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma

Neuro-oncology (Charlottesville, Va.), 2011-08, Vol.13 (8), p.866-879

2011

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Fluorescent in situ hybridization

Methods in molecular biology (Clifton, N.J.), 2002, Vol.187, p.73

2002

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Tips for Returning to In-Person Learning

Credit Union Management, 2021-08, Vol.44 (8), p.11-11

Dyer, Sara

2021

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Five Ways to Get The Most Out of an Online Learning Event

Credit Union Management, 2020-12, Vol.43 (12), p.38-38

Dyer, Sara

2020

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Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma

Genes chromosomes & cancer, 2006-01, Vol.45 (1), p.47-60

2006

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Potentiation of beta-adrenergic signaling by adenoviral-mediated gene transfer in adult rabbit ventricular myocytes

The Journal of clinical investigation, 1997-01, Vol.99 (2), p.288-296

1997

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Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom

Genomic medicine, 2007-09, Vol.1 (1-2), p.35-45

2007

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Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma

European journal of cancer (1990), 2006-08, Vol.42 (12), p.1826-1834

2006

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Hemorrhagic gastritis from topical isopropanol exposure

The Annals of pharmacotherapy, 2002-11, Vol.36 (11), p.1733-1735

2002

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1 H MRS identifies specific metabolite profiles associated with MYCN‐amplified and non‐amplified tumour subtypes of neuroblastoma cell lines

NMR in biomedicine, 2007-11, Vol.20 (7), p.692-700

2007

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del5p/dup5q in a 'cri du chat' patient without parental chromosomal rearrangement

American journal of medical genetics. Part A, 2006-05, Vol.140A (9), p.1016-1020

2006

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Cusped-gaussian wave functions: Spin densities in Li and LiH

Molecular physics, 1986-12, Vol.59 (5), p.1027-1034

1986

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Terminal deoxynucleotidyl transferase promotes acute myeloid leukemia by priming FLT3-ITD replication slippage

Molecular roulette: nucleophosmin mutations in AML are orchestrated through N-nucleotide addition by TdT

Pediatric Ependymoma: Biological Perspectives

NUP98-NSD1 fusion in association with FLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR

PB1809: COMPARISON OF OPTICAL GENOME MAPPING WITH STANDARD OF CARE TESTING TO INVESTIGATE GENOMIC ABNORMALITIES IN HAEMATOLOGICAL MALIGNANCIES: THE EXPERIENCE OF CENTRAL AND SOUTH GENOMIC LABORATORY HUB, UK

Genomic Imbalances in Pediatric Intracranial Ependymomas Define Clinically Relevant Groups

First case of near haploid philadelphia negative B-Cell acute lymphoblastic leukaemia relapsing as acute myeloid leukemia following allogeneic hematopoietic stem cell transplantation

How to Lose Your Voice

Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia

Noncoding mutations drive persistence of a founder preleukemic clone which initiates late relapse in T-ALL

Clonal evolution in adult TCF3::HLF-positive acute lymphoblastic leukemia undergoing stem cell transplantation

Monoclonal Antibodies Reveal Receptor Specificity among G-Protein-Coupled Receptor Kinases

1H MRS identifies specific metabolite profiles associated with MYCN-amplified and non-amplified tumour subtypes of neuroblastoma cell lines

Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma

Fluorescent in situ hybridization

Tips for Returning to In-Person Learning

Five Ways to Get The Most Out of an Online Learning Event

Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma

Potentiation of beta-adrenergic signaling by adenoviral-mediated gene transfer in adult rabbit ventricular myocytes

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom

Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma

Hemorrhagic gastritis from topical isopropanol exposure

1 H MRS identifies specific metabolite profiles associated with MYCN‐amplified and non‐amplified tumour subtypes of neuroblastoma cell lines

del5p/dup5q in a 'cri du chat' patient without parental chromosomal rearrangement

Cusped-gaussian wave functions: Spin densities in Li and LiH

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