(Q34775646)

4 August 2017

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title

White blood cell defects: molecular discoveries and clinical management (English)

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4 August 2017

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1

Gulbu Uzel

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4 August 2017

Steven M Holland

2

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4 August 2017

publication date

1 September 2002

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Current Allergy and Asthma Reports

4 August 2017

published in

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4 August 2017

volume

2

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4 August 2017

issue

5

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4 August 2017

page(s)

385-391

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https://scigraph.springernature.com/pub.10.1007/s11882-002-0071-5

4 August 2017

exact match

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cites work

Cyclical neutropenia and other periodic hematological disorders: a review of mechanisms and mathematical models.

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12 December 2020

A family of C/EBP-related proteins capable of forming covalently linked leucine zipper dimers in vitro

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12 December 2020

Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-gamma-receptor (IFNgammaR1) deficiency: mutational analysis and evaluation of therapeutic options

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12 December 2020

Mutations in the neutrophil elastase gene in cyclic and congenital neutropenia

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12 December 2020

Partial interferon-gamma receptor 1 deficiency in a child with tuberculoid bacillus Calmette-Guérin infection and a sibling with clinical tuberculosis

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12 December 2020

Anomalous neutrophil granule distribution in a patient with lactoferrin deficiency: pertinence to the respiratory burst

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12 December 2020

Inherited interleukin 12 deficiency in a child with bacille Calmette-Guérin and Salmonella enteritidis disseminated infection

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12 December 2020

Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guérin infection

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12 December 2020

A marked decrease in defensin mRNA in the only case of congenital neutrophil-specific granule deficiency reported in Japan

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12 December 2020

Microbicidal/cytotoxic proteins of neutrophils are deficient in two disorders: Chediak-Higashi syndrome and "specific" granule deficiency

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12 December 2020

Jak-STAT pathways and transcriptional activation in response to IFNs and other extracellular signaling proteins

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12 December 2020

Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy.

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12 December 2020

A single phosphotyrosine residue of Stat91 required for gene activation by interferon-gamma

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12 December 2020

Absence of the largest platelet-von Willebrand multimers in a patient with lactoferrin deficiency and a bleeding tendency

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12 December 2020

Lactoferrin deficiency associated with altered granulocyte function

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12 December 2020

In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma

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12 December 2020

Interferon-gamma receptor deficiency: An expanding clinical phenotype?

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12 December 2020

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

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12 December 2020

Selective defect in myeloid cell lactoferrin gene expression in neutrophil specific granule deficiency

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12 December 2020

Defective bactericidal activity and absence of specific granules in neutrophils from a patient with recurrent bacterial infections

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12 December 2020

Mendelian susceptibility to mycobacterial infection in man

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12 December 2020

Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria

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12 December 2020

Lactoferrin deficiency as a consequence of a lack of specific granules in neutrophils from a patient with recurrent infections. Detection by immunoperoxidase staining for lactoferrin and cytochemical electron microscopy

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12 December 2020

Early interleukin 12 production by macrophages in response to mycobacterial infection depends on interferon gamma and tumor necrosis factor alpha.

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12 December 2020

Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis.

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12 December 2020

Detection of intracellular phosphorylated STAT-1 by flow cytometry

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12 December 2020

A causative relationship between mutant IFNgR1 alleles and impaired cellular response to IFNgamma in a compound heterozygous child

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12 December 2020

Mutation in the signal-transducing chain of the interferon-gamma receptor and susceptibility to mycobacterial infection

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12 December 2020

Pathophysiology and treatment of severe chronic neutropenia

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12 December 2020

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

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12 December 2020

Ultrastructure of neutrophilic phagosome of autologous platelet in vivo in specific granule deficiency

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12 December 2020

Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds.

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12 December 2020

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

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12 December 2020

Human neutrophil-specific granule deficiency: a model to assess the role of neutrophil-specific granules in the evolution of the inflammatory response

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12 December 2020

Structure of human neutrophil elastase in complex with a peptide chloromethyl ketone inhibitor at 1.84-A resolution

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12 December 2020

Severe mycobacterial and Salmonella infections in interleukin-12 receptor-deficient patients

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12 December 2020

Interferon-gamma receptor deficiency: relationship between genotype, environment, and phenotype (Review)

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12 December 2020

Abnormal regulation of interferon-gamma, interleukin-12, and tumor necrosis factor-alpha in human interferon-gamma receptor 1 deficiency

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12 December 2020

Abnormal neutrophil maturation in a neutrophil defect with morphologic abnormality and impaired function

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12 December 2020

Novel human immunodeficiencies reveal the essential role of type-I cytokines in immunity to intracellular bacteria

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12 December 2020

TNF-alpha response of human monocyte-derived macrophages to Mycobacterium avium, serovar 4, is of brief duration and protein kinase C dependent

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12 December 2020

A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection

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12 December 2020

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

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12 December 2020

Understanding the genetic basis of susceptibility to mycobacterial infection

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12 December 2020

Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia

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12 December 2020

Activation of transcription by IFN-gamma: tyrosine phosphorylation of a 91-kD DNA binding protein

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12 December 2020

Detection of intracellular phosphorylated STAT-4 by flow cytometry

1 reference

12 December 2020

Viral infections in interferon-gamma receptor deficiency

1 reference

12 December 2020

Neutrophil-specific granule deficiency includes eosinophils

1 reference

12 December 2020

Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency

1 reference

12 December 2020

A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection

1 reference

12 December 2020

Impairment of mycobacterial but not viral immunity by a germline human STAT1 mutation

1 reference

12 December 2020

Genetics, phenotype, and natural history of autosomal dominant cyclic hematopoiesis

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12 December 2020

Partial Interferon‐γ Receptor Signaling Chain Deficiency in a Patient with Bacille Calmette‐Guérin andMycobacterium abscessusInfection

1 reference

12 December 2020

Severe chronic neutropenia: pathophysiology and therapy

1 reference

12 December 2020

Neutrophil-specific granule deficiency: homozygous recessive inheritance of a frameshift mutation in the gene encoding transcription factor CCAAT/enhancer binding protein--epsilon

1 reference

12 December 2020

Diagnosis and management of chronic neutropenia during childhood

1 reference

12 December 2020

Neutrophil-specific granule deficiency results from a novel mutation with loss of function of the transcription factor CCAAT/enhancer binding protein epsilon

1 reference

12 December 2020

Mediating immunity to mycobacteria

1 reference

12 December 2020

The molecular biology of selected phagocyte defects.

1 reference

12 December 2020

10.1007/S11882-002-0071-5

Identifiers

DOI

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Dimensions Publication ID

4 August 2017

1036244822

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