Use of mutated self-cleaving 2A peptides as a molecular rheostat to direct simultaneous formation of membrane and secreted anti-HIV immunoglobulins (Q34500307)

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English	Use of mutated self-cleaving 2A peptides as a molecular rheostat to direct simultaneous formation of membrane and secreted anti-HIV immunoglobulins	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 August 2017

Use of mutated self-cleaving 2A peptides as a molecular rheostat to direct simultaneous formation of membrane and secreted anti-HIV immunoglobulins (English)

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Europe PubMed Central

PubMed publication ID

2 August 2017

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Kenneth K Yu

1

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David Baltimore

7

object named as

David Baltimore

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Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Kiefer Aguilar

2

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Europe PubMed Central

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2 August 2017

Jonathan Tsai

3

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Europe PubMed Central

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2 August 2017

Rachel Galimidi

4

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Europe PubMed Central

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2 August 2017

Priyanthi Gnanapragasam

5

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2 August 2017

Lili Yang

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2 August 2017

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publication date

28 November 2012

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Europe PubMed Central

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2 August 2017

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Europe PubMed Central

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2 August 2017

7

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Europe PubMed Central

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2 August 2017

11

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Europe PubMed Central

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2 August 2017

e50438

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Europe PubMed Central

PubMed publication ID

2 August 2017

copyright license

Creative Commons Attribution 4.0 International

28 November 2012

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April 2022 Public Data File from Crossref

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1 reference

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7 July 2018

Inhibition of in vivo HIV infection in humanized mice by gene therapy of human hematopoietic stem cells with a lentiviral vector encoding a broadly neutralizing anti-HIV antibody

1 reference

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Examination of the contributions of size and avidity to the neutralization mechanisms of the anti-HIV antibodies b12 and 4E10.

1 reference

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The constant region of the membrane immunoglobulin mediates B cell-receptor clustering and signaling in response to membrane antigens.

1 reference

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Site-specific release of nascent chains from ribosomes at a sense codon

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Mechanisms controlling production of membrane and secreted immunoglobulin during B cell development

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VH replacement in mice and humans

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Molecular mechanism of serial VH gene replacement

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Levels of polyadenylation factor CstF-64 control IgM heavy chain mRNA accumulation and other events associated with B cell differentiation

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The polyadenylation factor CstF-64 regulates alternative processing of IgM heavy chain pre-mRNA during B cell differentiation

1 reference

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Gene rearrangement and B-cell development

1 reference

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Antibodies generated from human immunoglobulin miniloci in transgenic mice

1 reference

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Foot-and-mouth disease virus 2A oligopeptide mediated cleavage of an artificial polyprotein

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A convenient method for the construction and expression of GPI-anchored proteins.

1 reference

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Influence of immunoglobulin heavy- and light-chain expression on B-cell differentiation

1 reference

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Molecular mechanisms that control expression of the B lymphocyte antigen receptor complex

1 reference

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B-cell development in man.

1 reference

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Two mRNAs can be produced from a single immunoglobulin mu gene by alternative RNA processing pathways

1 reference

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Two mRNAs with different 3' ends encode membrane-bound and secreted forms of immunoglobulin mu chain

1 reference

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Synthesis of secreted and membrane-bound immunoglobulin mu heavy chains is directed by mRNAs that differ at their 3' ends

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Poly(A) site choice rather than splice site choice governs the regulated production of IgM heavy-chain RNAs

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Relative position and strengths of poly(A) sites as well as transcription termination are critical to membrane versus secreted mu-chain expression during B-cell development

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Regulated production of mu m and mu s mRNA requires linkage of the poly(A) addition sites and is dependent on the length of the mu s-mu m intron

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The developmentally regulated shift from membrane to secreted mu mRNA production is accompanied by an increase in cleavage-polyadenylation efficiency but no measurable change in splicing efficiency

1 reference

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1 reference

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1 reference

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12 December 2020

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10.1371/JOURNAL.PONE.0050438

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Europe PubMed Central

PubMed publication ID

2 August 2017

2012PLoSO...750438Y

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PMC publication ID

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Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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