Lista de obras - Peter Newburger - Dominio Público Uruguay

A limited number of genes are involved in the differentiation of germinal center B cells

artículo científico

A molecular classification of congenital neutropenia syndromes

artículo científico publicado en 2007

A myelopoiesis-associated regulatory intergenic noncoding RNA transcript within the human HOXA cluster

artículo científico publicado en 2009

A panorama of lineage-specific transcription in hematopoiesis

artículo científico publicado en 2004

Activation of the leukocyte NADPH oxidase by phorbol ester requires the phosphorylation of p47PHOX on serine 303 or 304.

artículo científico publicado en 1998

Acute lymphocytic leukemia with eosinophilia and unusual karyotype

artículo científico publicado en 2006

Adolescents with cancer: access to clinical trials and age-appropriate care

artículo científico publicado en 2002

Advances in understanding the pathogenesis of HLH.

artículo científico publicado en 2013

Allogeneic bone marrow transplantation for chronic granulomatous disease

article

An in-frame trinucleotide repeat in the coding region of the human cellular glutathione peroxidase (GPX1) gene: in vivo polymorphism and in vitro instability

artículo científico publicado en 1994

An oral HemokineTM, α-methylhydrocinnamate, enhances myeloid and neutrophil recovery following irradiation in vivo

artículo científico publicado en 2016

An unusual intronic mutation in the CYBB gene giving rise to chronic granulomatous disease

artículo científico publicado en 2001

Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections

artículo científico publicado en 2004

BARCODE-ALL: accelerated and cost-effective genetic risk stratification in acute leukemia using spectrally addressable liquid bead microarrays

article published in 2003

BARCODE-ALL: accelerated and cost-effective genetic risk stratification in acute leukemia using spectrally addressable liquid bead microarrays

Changes in superoxide dismutase, catalase, and the glutathione cycle during induced myeloid differentiation

artículo científico publicado en 1986

Characterization of an immune response gene in mice controlling IgE and IgM antibody responses to ragweed pollen extract and its 2,4-dinitrophenylated derivative

artículo científico publicado en 1974

Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics

artículo científico publicado en 2006

Chronic pain: principles of management

artículo científico publicado en 1981

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

artículo científico publicado en 1986

Comment on "Impaired priming and activation of the neutrophil NADPH oxidase in patients with IRAK4 or NEMO deficiency".

artículo científico publicado en 2009

Comment on: Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in the Absence of Molecular Diagnosis

artículo científico publicado en 2017

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

artículo científico publicado en 2015

Correction of infantile agranulocytosis (Kostmann's syndrome) by allogeneic bone marrow transplantation

artículo científico publicado en 1980

Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes

artículo científico publicado en 2010

Cyclic neutropenia in animals

artículo científico publicado en 2009

Dissociation of opsonized particle phagocytosis and respiratory burst activity in an Epstein-Barr virus-infected myeloid cell line.

artículo científico publicado en 1980

Dynamics of alpha-globin locus chromatin structure and gene expression during erythroid differentiation of human CD34(+) cells in culture

artículo científico publicado en 2009

Editorial overview: Hematology and oncology

artículo científico publicado en 2004

Essential role of nuclear factor-kappaB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes

artículo científico publicado en 2008

Evaluation and management of patients with isolated neutropenia

artículo científico publicado en 2013

Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia

artículo científico publicado en 2012

Frontline Science: Splenic progenitors aid in maintaining high neutrophil numbers at sites of sterile chronic inflammation

artículo científico publicado en 2016

Gene expression in chronic granulomatous disease and interferon-γ receptor-deficient cells treated in vitro with interferon-γ

article

Gene expression in human neutrophils during activation and priming by bacterial lipopolysaccharide

artículo científico publicado en 2003

Gene expression in mature neutrophils: early responses to inflammatory stimuli

artículo científico publicado en 2003

Genomic and proteomic analysis of the myeloid differentiation program

artículo científico publicado en 2001

Genomic and proteomic analysis of the myeloid differentiation program: global analysis of gene expression during induced differentiation in the MPRO cell line

artículo científico publicado en 2002

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

artículo científico publicado en 2011

Global analysis of neutrophil gene expression.

artículo científico publicado en 2000

HOX antisense lincRNA HOXA-AS2 is an apoptosis repressor in all trans retinoic acid treated NB4 promyelocytic leukemia cells

artículo científico publicado en 2013

Hematology and oncology

artículo científico publicado en 1999

Hematology and oncology

artículo científico publicado en 2005

Hematology and oncology

artículo científico publicado en 2003

Hematology and oncology

artículo científico publicado en 2000

Hematology and oncology: Editorial overview ⬇️

artículo científico publicado el 1 de febrero de 1998

Hemophagocytic lymphohistiocytosis with MUNC13-4 gene mutation or reduced natural killer cell function prior to onset of childhood leukemia

artículo científico publicado en 2011

IL6 to the rescue

artículo científico publicado en 2008

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

artículo científico publicado en 2007

Identification and molecular cloning of a human selenocysteine insertion sequence-binding protein. A bifunctional role for DNA-binding protein B.

artículo científico publicado en 1998

In memoriam: Robert J. Arceci

artículo científico publicado en 2015

Isolation and chromosomal localization of the human glutathione peroxidase gene.

artículo científico publicado en 1990

Lineage specificity of gene expression patterns

artículo científico publicado en 2004

Local arterial nanoparticle delivery of siRNA for NOX2 knockdown to prevent restenosis in an atherosclerotic rat model

artículo científico publicado en 2010

Long intergenic non-coding RNA HOTAIRM1 regulates cell cycle progression during myeloid maturation in NB4 human promyelocytic leukemia cells

artículo científico publicado en 2014

Measurement of superoxide release in the phagovacuoles of immune complex-stimulated human neutrophils

artículo científico publicado en 1990

Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A).

artículo científico publicado en 2016

Mosaic tetraploidy and transientGFI1mutation in a patient with severe chronic neutropenia

artículo científico publicado en 2008

NADPH oxidase activity and cytochrome b558 content of human Epstein-Barr-virus-transformed B lymphocytes correlate with expression of genes encoding components of the oxidase system

artículo científico publicado en 1998

Neutrophil Responses to Sterile Implant Materials

artículo científico publicado en 2015

Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia

artículo científico publicado en 2007

New perspectives in chronic granulomatous disease

artículo científico publicado en 1988

Novel Transcribed Regions in the Human Genome

article

Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia

artículo científico publicado en 2013

Nuclease sensitive element binding protein 1 associates with the selenocysteine insertion sequence and functions in mammalian selenoprotein translation

scientific journal article

Nuclease sensitive element binding protein 1 gene disruption results in early embryonic lethality

artículo científico publicado en 2006

Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency

artículo científico publicado en 2014

RNA expression patterns change dramatically in human neutrophils exposed to bacteria

artículo científico publicado en 2001

RNA-binding proteins that specifically recognize the selenocysteine insertion sequence of human cellular glutathione peroxidase mRNA.

artículo científico publicado en 1995

RNAi screen identifies UBE2D3 as a mediator of all-trans retinoic acid-induced cell growth arrest in human acute promyelocytic NB4 cells

artículo científico publicado en 2007

Regulation of CYBB Gene Expression in Human Phagocytes by a Distant Upstream NF-κB Binding Site

artículo científico publicado en 2015

Relationships between the cell cycle and the expression of c-myc and transferrin receptor genes during induced myeloid differentiation

artículo científico publicado en 1990

Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia

article

Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients

artículo científico publicado en 2008

Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia

artículo científico publicado en 2010

Selenium regulation of glutathione peroxidase in human hepatoma cell line Hep3B.

artículo científico publicado en 1993

Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation

artículo científico publicado en 2018

Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.

artículo científico publicado en 2010

Studies on Low-Dose Hydroxyethyl Starch Leukapheresis: Rate of Elimination of HES in vivo and Function of the Harvested Granulocytes in vitro

scientific article published on 01 January 1984

Temporal evolution of gene expression in rat carotid artery following balloon angioplasty

artículo científico

The American Society of Pediatric Hematology/Oncology distinguished career award goes to Laurence A. Boxer, MD.

artículo científico publicado en 2008

The Role of Toll‐Like Receptors in Herpes Simplex Infection in Neonates

article

The diversity of mutations and clinical outcomes for ELANE-associated neutropenia

artículo científico publicado en 2015

The effect of IFN-gamma and TNF-alpha on the NADPH oxidase system of human colostrum macrophages, blood monocytes, and THP-1 cells

artículo científico publicado en 2005

The effect of IFN-gamma and TNF-alpha on the eosinophilic differentiation and NADPH oxidase activation of human HL-60 clone 15 cells

artículo científico publicado en 2003

The effects of irradiation on blood components

artículo científico publicado en 1981

The human NADPH oxidase: primary and secondary defects impairing the respiratory burst function and the microbicidal ability of phagocytes

artículo científico publicado en 2011

Toll-like receptor-mediated activation of neutrophils by influenza A virus

artículo científico publicado en 2008

Treating Langerhans cell histiocytosis, globally

artículo científico publicado en 2018

Up-regulation of NADPH oxidase components and increased production of interferon-gamma by leukocytes from sickle cell disease patients

article

Use of granulocyte colony-stimulating factor during pregnancy in women with chronic neutropenia

artículo científico publicado en 2015

Use of rituximab for refractory cytopenias associated with autoimmune lymphoproliferative syndrome (ALPS)

artículo científico publicado en 2009

X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils

artículo científico publicado en 2010

X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.

artículo científico publicado en 1998

[16] A modified method for the display of 3′-end restriction fragments of cDNAs: Molecular profiling of gene expression in neutrophils

article

p47(phox) PX domain of NADPH oxidase targets cell membrane via moesin-mediated association with the actin cytoskeleton

artículo científico publicado en 2004

Lista de obras de Peter Newburger

A limited number of genes are involved in the differentiation of germinal center B cells

A molecular classification of congenital neutropenia syndromes

A myelopoiesis-associated regulatory intergenic noncoding RNA transcript within the human HOXA cluster

A panorama of lineage-specific transcription in hematopoiesis

Activation of the leukocyte NADPH oxidase by phorbol ester requires the phosphorylation of p47PHOX on serine 303 or 304.

Acute lymphocytic leukemia with eosinophilia and unusual karyotype

Adolescents with cancer: access to clinical trials and age-appropriate care

Advances in understanding the pathogenesis of HLH.

Allogeneic bone marrow transplantation for chronic granulomatous disease

An in-frame trinucleotide repeat in the coding region of the human cellular glutathione peroxidase (GPX1) gene: in vivo polymorphism and in vitro instability

An oral HemokineTM, α-methylhydrocinnamate, enhances myeloid and neutrophil recovery following irradiation in vivo

An unusual intronic mutation in the CYBB gene giving rise to chronic granulomatous disease

Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections

BARCODE-ALL: accelerated and cost-effective genetic risk stratification in acute leukemia using spectrally addressable liquid bead microarrays

BARCODE-ALL: accelerated and cost-effective genetic risk stratification in acute leukemia using spectrally addressable liquid bead microarrays

Changes in superoxide dismutase, catalase, and the glutathione cycle during induced myeloid differentiation

Characterization of an immune response gene in mice controlling IgE and IgM antibody responses to ragweed pollen extract and its 2,4-dinitrophenylated derivative

Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics

Chronic pain: principles of management

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

Comment on "Impaired priming and activation of the neutrophil NADPH oxidase in patients with IRAK4 or NEMO deficiency".

Comment on: Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in the Absence of Molecular Diagnosis

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

Correction of infantile agranulocytosis (Kostmann's syndrome) by allogeneic bone marrow transplantation

Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes

Cyclic neutropenia in animals

Dissociation of opsonized particle phagocytosis and respiratory burst activity in an Epstein-Barr virus-infected myeloid cell line.

Dynamics of alpha-globin locus chromatin structure and gene expression during erythroid differentiation of human CD34(+) cells in culture

Editorial overview: Hematology and oncology

Essential role of nuclear factor-kappaB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes

Evaluation and management of patients with isolated neutropenia

Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia

Frontline Science: Splenic progenitors aid in maintaining high neutrophil numbers at sites of sterile chronic inflammation

Gene expression in chronic granulomatous disease and interferon-γ receptor-deficient cells treated in vitro with interferon-γ

Gene expression in human neutrophils during activation and priming by bacterial lipopolysaccharide

Gene expression in mature neutrophils: early responses to inflammatory stimuli

Genomic and proteomic analysis of the myeloid differentiation program

Genomic and proteomic analysis of the myeloid differentiation program: global analysis of gene expression during induced differentiation in the MPRO cell line

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

Global analysis of neutrophil gene expression.

HOX antisense lincRNA HOXA-AS2 is an apoptosis repressor in all trans retinoic acid treated NB4 promyelocytic leukemia cells

Hematology and oncology

Hematology and oncology

Hematology and oncology

Hematology and oncology

Hematology and oncology: Editorial overview ⬇️

Hemophagocytic lymphohistiocytosis with MUNC13-4 gene mutation or reduced natural killer cell function prior to onset of childhood leukemia

IL6 to the rescue

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Identification and molecular cloning of a human selenocysteine insertion sequence-binding protein. A bifunctional role for DNA-binding protein B.

In memoriam: Robert J. Arceci

Isolation and chromosomal localization of the human glutathione peroxidase gene.

Lineage specificity of gene expression patterns

Local arterial nanoparticle delivery of siRNA for NOX2 knockdown to prevent restenosis in an atherosclerotic rat model

Long intergenic non-coding RNA HOTAIRM1 regulates cell cycle progression during myeloid maturation in NB4 human promyelocytic leukemia cells

Measurement of superoxide release in the phagovacuoles of immune complex-stimulated human neutrophils

Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A).

Mosaic tetraploidy and transientGFI1mutation in a patient with severe chronic neutropenia

NADPH oxidase activity and cytochrome b558 content of human Epstein-Barr-virus-transformed B lymphocytes correlate with expression of genes encoding components of the oxidase system

Neutrophil Responses to Sterile Implant Materials

Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia

New perspectives in chronic granulomatous disease

Novel Transcribed Regions in the Human Genome

Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia

Nuclease sensitive element binding protein 1 associates with the selenocysteine insertion sequence and functions in mammalian selenoprotein translation

Nuclease sensitive element binding protein 1 gene disruption results in early embryonic lethality

Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency

RNA expression patterns change dramatically in human neutrophils exposed to bacteria

RNA-binding proteins that specifically recognize the selenocysteine insertion sequence of human cellular glutathione peroxidase mRNA.

RNAi screen identifies UBE2D3 as a mediator of all-trans retinoic acid-induced cell growth arrest in human acute promyelocytic NB4 cells

Regulation of CYBB Gene Expression in Human Phagocytes by a Distant Upstream NF-κB Binding Site

Relationships between the cell cycle and the expression of c-myc and transferrin receptor genes during induced myeloid differentiation

Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia

Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients

Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia

Selenium regulation of glutathione peroxidase in human hepatoma cell line Hep3B.

Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation

Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.

Studies on Low-Dose Hydroxyethyl Starch Leukapheresis: Rate of Elimination of HES in vivo and Function of the Harvested Granulocytes in vitro