The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils (Q36876308)

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scientific article published on 11 July 2008

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English	The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils	scientific article published on 11 July 2008

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scholarly article

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10 January 2020

The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils (English)

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10 January 2020

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Peter F. Johnson

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10 January 2020

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Tatiana V Cohen

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10 January 2020

Kimberly D Klarmann

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Krisada Sakchaisri

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10 January 2020

Douglas Kuhns

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Miriam Anver

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10 January 2020

Simon C Williams

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10 January 2020

Jonathan R Keller

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10 January 2020

Colin L Stewart

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10 January 2020

publication date

11 July 2008

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10 January 2020

Human Molecular Genetics

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10 January 2020

2921-2933

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10 January 2020

Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia

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Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin

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Blurring the boundary: the nuclear envelope extends its reach.

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"Laminopathies": a wide spectrum of human diseases

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Lamin B receptor plays a role in stimulating nuclear envelope production and targeting membrane vesicles to chromatin during nuclear envelope assembly through direct interaction with importin beta

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The granulocyte nucleus and lamin B receptor: avoiding the ovoid

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The laminopathies: the functional architecture of the nucleus and its contribution to disease

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Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene

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Structural basis for DNA recognition by the basic region leucine zipper transcription factor CCAAT/enhancer-binding protein alpha

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Transcriptional activity of CCAAT/enhancer-binding proteins is controlled by a conserved inhibitory domain that is a target for sumoylation

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29 September 2017

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)

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C/EBPepsilon -/- mice: increased rate of myeloid proliferation and apoptosis

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The role of C/EBP(epsilon) in the terminal stages of granulocyte differentiation

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Regulation of human neutrophil granule protein expression

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CCAAT/enhancer binding protein epsilon is critical for effective neutrophil-mediated response to inflammatory challenge

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Impaired granulopoiesis, myelodysplasia, and early lethality in CCAAT/enhancer binding protein epsilon-deficient mice.

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The lamin B receptor (LBR) provides essential chromatin docking sites at the nuclear envelope

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The inner nuclear membrane protein p58 associates in vivo with a p58 kinase and the nuclear lamins

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RNA association or phosphorylation of the RS domain prevents aggregation of RS domain-containing proteins

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HEM dysplasia and ichthyosis are likely laminopathies and not due to 3beta-hydroxysterol Delta14-reductase deficiency.

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4 September 2018

Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes

1 reference

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1 reference

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4 September 2018

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leukocyte function in Pelger-Huët anomaly of dogs

1 reference

https://pubmed.ncbi.nlm.nih.gov/18621876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The lamin B receptor-associated protein p34 shares sequence homology and antigenic determinants with the splicing factor 2-associated protein p32

1 reference

https://pubmed.ncbi.nlm.nih.gov/18621876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitotic phosphorylation of the lamin B receptor by a serine/arginine kinase and p34(cdc2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18621876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDN191

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10 January 2020

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Europe PubMed Central

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10 January 2020

1 reference

Europe PubMed Central

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10 January 2020

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