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Membrane-derived microvesicles: important and underappreciated mediators of cell-to-cell communication

Leukemia, 2006-09, Vol.20 (9), p.1487-1495

2006

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Stem cell plasticity revisited: CXCR4-positive cells expressing mRNA for early muscle, liver and neural cells 'hide out' in the bone marrow

Leukemia, 2004-01, Vol.18 (1), p.29-40

2004

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Innate immunity as orchestrator of stem cell mobilization

Leukemia, 2010-10, Vol.24 (10), p.1667-1675

2010

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Artificial intelligence guided screening for cardiomyopathies in an obstetric population: a pragmatic randomized clinical trial

Nature medicine, 2024-10, Vol.30 (10), p.2897-2906

2024

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Bcr-abl-positive cells secrete angiogenic factors including matrix metalloproteinases and stimulate angiogenesis in vivo in Matrigel implants

Leukemia, 2002-06, Vol.16 (6), p.1160-1166

2002

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DNA methylation pattern is altered in childhood T-cell acute lymphoblastic leukemia patients as compared with normal thymic subsets: insights into CpG island methylator phenotype in T-ALL

Leukemia, 2012-02, Vol.26 (2), p.367-371

2012

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Structure-based rescue of common tumor-derived p53 mutants

Nature medicine, 1996-10, Vol.2 (10), p.1143-1146

1996

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Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

Nature genetics, 1998-02, Vol.18 (2), p.150-154

1998

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Expression of beta 1 integrin mRNAs in human leukemic blasts

Leukemia, 1994-09, Vol.8 (9), p.1544-1550

1994

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Functional characterization of fibroblastic cells in long-term marrow cultures from patients with acute myelogenous leukemia

Leukemia, 1993-10, Vol.7 (10), p.1564-1569

1993

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Production of tumor necrosis factor-α in human long-term marrow cultures from normal subjects and patients with acute myelogenous leukemia : effect of recombinant macrophage colony-stimulating factor

Leukemia, 1992-11, Vol.6 (11), p.1148-1154

1992

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Effect of rhCSF-1 on human hemopoiesis in long-term cultures from patients with acute myelogenous leukemia

Leukemia, 1991, Vol.5 (1), p.8-13

1991

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A framework for the emergence and analysis of language in social learning agents

Nature communications, 2024-08, Vol.15 (1), p.7590-15, Article 7590

2024

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RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA

Nature communications, 2016-05, Vol.7 (1), p.11752-11752, Article 11752

2016

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Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

Nature genetics, 2006-03, Vol.38 (3), p.294-296

2006

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MHC class II complexes sample intermediate states along the peptide exchange pathway

Nature communications, 2016-11, Vol.7 (1), p.13224-13224, Article 13224

2016

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Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects

Nature communications, 2019-07, Vol.10 (1), p.2966-14, Article 2966

2019

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Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Nature genetics, 2011-01, Vol.43 (1), p.20-22

2011

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Contemporary HIV-1 consensus Env with AI-assisted redesigned hypervariable loops promote antibody binding

Nature communications, 2024-05, Vol.15 (1), p.3924-3924, Article 3924

2024

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Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Nature genetics, 2017-02, Vol.49 (2), p.223-237

2017

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Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome

Nature genetics, 2012-04, Vol.44 (4), p.445-449

2012

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De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

Nature genetics, 2011-08, Vol.43 (8), p.729-731

2011

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Lipid peroxidation and glutathione peroxidase activity relationship in breast cancer depends on functional polymorphism of GPX1

BMC cancer, 2015-10, Vol.15 (1), p.657-657, Article 657

2015

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Membrane-derived microvesicles: important and underappreciated mediators of cell-to-cell communication

Stem cell plasticity revisited: CXCR4-positive cells expressing mRNA for early muscle, liver and neural cells 'hide out' in the bone marrow

Innate immunity as orchestrator of stem cell mobilization

Artificial intelligence guided screening for cardiomyopathies in an obstetric population: a pragmatic randomized clinical trial

Bcr-abl-positive cells secrete angiogenic factors including matrix metalloproteinases and stimulate angiogenesis in vivo in Matrigel implants

DNA methylation pattern is altered in childhood T-cell acute lymphoblastic leukemia patients as compared with normal thymic subsets: insights into CpG island methylator phenotype in T-ALL

Structure-based rescue of common tumor-derived p53 mutants

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

Expression of beta 1 integrin mRNAs in human leukemic blasts

Functional characterization of fibroblastic cells in long-term marrow cultures from patients with acute myelogenous leukemia

Production of tumor necrosis factor-α in human long-term marrow cultures from normal subjects and patients with acute myelogenous leukemia : effect of recombinant macrophage colony-stimulating factor

Effect of rhCSF-1 on human hemopoiesis in long-term cultures from patients with acute myelogenous leukemia

A framework for the emergence and analysis of language in social learning agents

RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

MHC class II complexes sample intermediate states along the peptide exchange pathway

Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects

De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Contemporary HIV-1 consensus Env with AI-assisted redesigned hypervariable loops promote antibody binding

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

Lipid peroxidation and glutathione peroxidase activity relationship in breast cancer depends on functional polymorphism of GPX1

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