Lista de obras -

(p47)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis

artículo científico publicado en 2019

An AAVS1-targeted minigene platform for correction of iPSCs from all five types of chronic granulomatous disease

artículo científico publicado en 2014

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency

artículo científico publicado en 2015

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

artículo científico publicado en 2016

CRISPR-Cas9 gene repair of hematopoietic stem cells from patients with X-linked chronic granulomatous disease.

artículo científico publicado en 2017

CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation

artículo científico publicado en 2013

Characterization of retroviral and lentiviral vectors pseudotyped with xenotropic murine leukemia virus-related virus envelope glycoprotein

artículo científico publicado en 2010

Chronic granulomatous disease as a risk factor for autoimmune disease

artículo científico publicado en 2008

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

artículo científico publicado en 2020

Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection

artículo científico publicado en 2009

Enhancers are major targets for murine leukemia virus vector integration

artículo científico publicado en 2014

False-positive HIV PCR test following ex vivo lentiviral gene transfer treatment of X-linked severe combined immunodeficiency vector

artículo científico publicado en 2014

Gene Editing in Chronic Granulomatous Disease

artículo científico publicado en 2019

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency

artículo científico publicado en 2007

Gene therapy studies in a canine model of X-linked severe combined immunodeficiency

artículo científico publicado en 2015

Gene-edited pseudogene resurrection corrects p47phox-deficient chronic granulomatous disease

artículo científico publicado en 2016

Genetic Risk for Inflammatory Bowel Disease Is a Determinant of Crohn's Disease Development in Chronic Granulomatous Disease.

artículo científico publicado en 2016

Geosmithia argillacea: an emerging cause of invasive mycosis in human chronic granulomatous disease.

artículo científico publicado en 2011

High levels of Crohn's disease-associated anti-microbial antibodies are present and independent of colitis in chronic granulomatous disease

artículo científico publicado en 2011

Humans with chronic granulomatous disease maintain humoral immunologic memory despite low frequencies of circulating memory B cells

artículo científico publicado en 2012

Hypomorphic Rag mutations can cause destructive midline granulomatous disease

artículo científico publicado en 2010

Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome

artículo científico publicado en 2010

Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1

scientific article published on 01 April 2019

Lentiviral gene therapy for X-linked chronic granulomatous disease

artículo científico publicado en 2020

Lentiviral hematopoietic stem cell gene therapy for X-linked severe combined immunodeficiency.

artículo científico publicado en 2016

MAGT1 messenger RNA-corrected autologous T and natural killer cells for potential cell therapy in X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia disease

artículo científico publicado en 2020

Mobilization characteristics and strategies to improve hematopoietic progenitor cell mobilization and collection in patients with chronic granulomatous disease and severe combined immunodeficiency

artículo científico publicado en 2014

NADPH oxidase correction by mRNA transfection of apheresis granulocytes in chronic granulomatous disease

artículo científico publicado en 2020

Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease

artículo científico publicado en 2016

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

scientific article published on 12 March 2019

Paravertebral mushroom: identification of a novel species of Phellinus as a human pathogen in chronic granulomatous disease.

artículo científico publicado en 2014

Partially corrected X-linked severe combined immunodeficiency: long-term problems and treatment options

artículo científico publicado en 2009

Progressive B Cell Loss in Revertant X-SCID

artículo científico publicado en 2020

Quantitative shearing linear amplification polymerase chain reaction: an improved method for quantifying lentiviral vector insertion sites in transplanted hematopoietic cell systems

artículo científico publicado en 2015

Recurrent erythematous plaques on sun-exposed sites in an African American boy with chronic granulomatous disease

artículo científico publicado en 2014

Sarcoidosis in chronic granulomatous disease

artículo científico publicado en 2006

Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis

artículo científico publicado en 2010

Short stature in partially corrected X-linked severe combined immunodeficiency--suboptimal response to growth hormone

artículo científico publicado en 2008

Targeted Repair of CYBB in X-CGD iPSCs Requires Retention of Intronic Sequences for Expression and Functional Correction

artículo científico publicado en 2017

Targeted gene addition in human CD34(+) hematopoietic cells for correction of X-linked chronic granulomatous disease

artículo científico publicado en 2016

Transgene-free iPSCs generated from small volume peripheral blood nonmobilized CD34+ cells.

artículo científico publicado en 2013

Tryptophan/kynurenine metabolism in human leukocytes is independent of superoxide and is fully maintained in chronic granulomatous disease

artículo científico publicado en 2010

Lista de obras de

(p47)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis

An AAVS1-targeted minigene platform for correction of iPSCs from all five types of chronic granulomatous disease

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency

Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency.

CRISPR-Cas9 gene repair of hematopoietic stem cells from patients with X-linked chronic granulomatous disease.

CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation

Characterization of retroviral and lentiviral vectors pseudotyped with xenotropic murine leukemia virus-related virus envelope glycoprotein

Chronic granulomatous disease as a risk factor for autoimmune disease

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection

Enhancers are major targets for murine leukemia virus vector integration

False-positive HIV PCR test following ex vivo lentiviral gene transfer treatment of X-linked severe combined immunodeficiency vector

Gene Editing in Chronic Granulomatous Disease

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency

Gene therapy studies in a canine model of X-linked severe combined immunodeficiency

Gene-edited pseudogene resurrection corrects p47phox-deficient chronic granulomatous disease

Genetic Risk for Inflammatory Bowel Disease Is a Determinant of Crohn's Disease Development in Chronic Granulomatous Disease.

Geosmithia argillacea: an emerging cause of invasive mycosis in human chronic granulomatous disease.

High levels of Crohn's disease-associated anti-microbial antibodies are present and independent of colitis in chronic granulomatous disease

Humans with chronic granulomatous disease maintain humoral immunologic memory despite low frequencies of circulating memory B cells

Hypomorphic Rag mutations can cause destructive midline granulomatous disease

Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome

Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1

Lentiviral gene therapy for X-linked chronic granulomatous disease

Lentiviral hematopoietic stem cell gene therapy for X-linked severe combined immunodeficiency.

MAGT1 messenger RNA-corrected autologous T and natural killer cells for potential cell therapy in X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia disease

Mobilization characteristics and strategies to improve hematopoietic progenitor cell mobilization and collection in patients with chronic granulomatous disease and severe combined immunodeficiency

NADPH oxidase correction by mRNA transfection of apheresis granulocytes in chronic granulomatous disease

Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

Paravertebral mushroom: identification of a novel species of Phellinus as a human pathogen in chronic granulomatous disease.

Partially corrected X-linked severe combined immunodeficiency: long-term problems and treatment options

Progressive B Cell Loss in Revertant X-SCID

Quantitative shearing linear amplification polymerase chain reaction: an improved method for quantifying lentiviral vector insertion sites in transplanted hematopoietic cell systems

Recurrent erythematous plaques on sun-exposed sites in an African American boy with chronic granulomatous disease

Sarcoidosis in chronic granulomatous disease

Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis

Short stature in partially corrected X-linked severe combined immunodeficiency--suboptimal response to growth hormone

Targeted Repair of CYBB in X-CGD iPSCs Requires Retention of Intronic Sequences for Expression and Functional Correction

Targeted gene addition in human CD34(+) hematopoietic cells for correction of X-linked chronic granulomatous disease

Transgene-free iPSCs generated from small volume peripheral blood nonmobilized CD34+ cells.

Tryptophan/kynurenine metabolism in human leukocytes is independent of superoxide and is fully maintained in chronic granulomatous disease