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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

The Lancet (British edition), 2005-03, Vol.365 (9464), p.1054-1061

2005

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KLF2 mutation is the most frequent somatic change in splenic marginal zone lymphoma and identifies a subset with distinct genotype

Leukemia, 2015-05, Vol.29 (5), p.1177-1185

2015

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MARIMO cells harbor a CALR mutation but are not dependent on JAK2/STAT5 signaling

Leukemia, 2015-02, Vol.29 (2), p.494-497

2015

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory

International journal of laboratory hematology, 2012-02, Vol.34 (1), p.21-34

BENCH, A. J.

2012

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Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture

Leukemia, 2013-09, Vol.27 (9), p.1820-1825

2013

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Modeling Fibrillogenesis of Collagen-Mimetic Molecules

Biophysical journal, 2020-11, Vol.119 (9), p.1791-1799

2020

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Analysis of vertebrate SCL loci identifies conserved enhancers

Nature biotechnology, 2000-02, Vol.18 (2), p.181-186

2000

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Chromosome 20 deletions in myeloid malignancies : reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

Oncogene, 2000-08, Vol.19 (34), p.3902-3913

2000

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Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia

Blood, 2000-02, Vol.95 (3), p.738-744

2000

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Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders

Haematologica (Roma), 2008-11, Vol.93 (11), p.1635-1644

2008

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Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia

Blood, 2001-09, Vol.98 (6), p.1732-1738

2001

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Interplay among patient empowerment and clinical and person-centered outcomes in type 2 diabetes. The BENCH-D study

Patient education and counseling, 2015-09, Vol.98 (9), p.1142-1149

2015

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LB1025 Spatiotemporal dynamics of Langerhans cells during skin wound repair in live mice

Journal of investigative dermatology, 2024-08, Vol.144 (8), p.S182-S182

2024

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Long-read sequencing of chicken transcripts and identification of new transcript isoforms

PloS one, 2014-04, Vol.9 (4), p.e94650-e94650

2014

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Spectroscopy and Electronic Structure of Electron Deficient Zinc Phthalocyanines

Journal of the American Chemical Society, 2003-06, Vol.125 (23), p.7067-7085

2003

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Introduction of Bulky Perfluoroalkyl Groups at the Periphery of Zinc Perfluorophthalocyanine: Chemical, Structural, Electronic, and Preliminary Photophysical and Biological Effects

Angewandte Chemie (International ed.), 2002-03, Vol.41 (5), p.747-750

2002

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The complex interplay between clinical and person-centered diabetes outcomes in the two genders

Health and quality of life outcomes, 2017-02, Vol.15 (1), p.41-41, Article 41

2017

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Imprinting of the Human L3MBTL Gene, a Polycomb Family Member Located in a Region of Chromosome 20 Deleted in Human Myeloid Malignancies

Proceedings of the National Academy of Sciences - PNAS, 2004-05, Vol.101 (19), p.7341-7346

2004

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Distinct 5′ SCL Enhancers Direct Transcription to Developing Brain, Spinal Cord, and Endothelium: Neural Expression Is Mediated by GATA Factor Binding Sites

Developmental biology, 1999-05, Vol.209 (1), p.128-142

1999

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Therapy-related acute myeloid leukaemia with t(8;16)(p11;p13);MOZ-CBP and polymorphisms in detoxifying and DNA repair genes

Leukemia, 2009-06, Vol.23 (6), p.1164-1167

2009

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Molecular genetic analysis of haematological malignancies: I. Acute leukaemias and myeloproliferative disorders

Clinical and laboratory haematology, 2005-06, Vol.27 (3), p.148-171

2005

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Molecular genetic analysis of haematological malignancies II: mature lymphoid neoplasms

International journal of laboratory hematology, 2007-08, Vol.29 (4), p.229-260

2007

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Synthesis and Structure of a Biconcave Cobalt Perfluorophthalocyanine and Its Catalysis of Novel Oxidative Carbon-Phosphorus Bonds Formation by Using Air

Angewandte Chemie (International ed.), 2002-03, Vol.41 (5), p.750-754

2002

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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

KLF2 mutation is the most frequent somatic change in splenic marginal zone lymphoma and identifies a subset with distinct genotype

Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study

MARIMO cells harbor a CALR mutation but are not dependent on JAK2/STAT5 signaling

The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory

Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture

Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformation

Modeling Fibrillogenesis of Collagen-Mimetic Molecules

Analysis of vertebrate SCL loci identifies conserved enhancers

Chromosome 20 deletions in myeloid malignancies : reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia

Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders

Deletions of the derivative chromosome 9 occur at the time of the Philadelphia translocation and provide a powerful and independent prognostic indicator in chronic myeloid leukemia

Interplay among patient empowerment and clinical and person-centered outcomes in type 2 diabetes. The BENCH-D study

LB1025 Spatiotemporal dynamics of Langerhans cells during skin wound repair in live mice

Long-read sequencing of chicken transcripts and identification of new transcript isoforms

Spectroscopy and Electronic Structure of Electron Deficient Zinc Phthalocyanines

Introduction of Bulky Perfluoroalkyl Groups at the Periphery of Zinc Perfluorophthalocyanine: Chemical, Structural, Electronic, and Preliminary Photophysical and Biological Effects

The complex interplay between clinical and person-centered diabetes outcomes in the two genders

Imprinting of the Human L3MBTL Gene, a Polycomb Family Member Located in a Region of Chromosome 20 Deleted in Human Myeloid Malignancies

Distinct 5′ SCL Enhancers Direct Transcription to Developing Brain, Spinal Cord, and Endothelium: Neural Expression Is Mediated by GATA Factor Binding Sites

Therapy-related acute myeloid leukaemia with t(8;16)(p11;p13);MOZ-CBP and polymorphisms in detoxifying and DNA repair genes

Molecular genetic analysis of haematological malignancies: I. Acute leukaemias and myeloproliferative disorders

Molecular genetic analysis of haematological malignancies II: mature lymphoid neoplasms

Synthesis and Structure of a Biconcave Cobalt Perfluorophthalocyanine and Its Catalysis of Novel Oxidative Carbon-Phosphorus Bonds Formation by Using Air

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