(Q30766668)

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Loss of splice consensus signal is responsible for the removal of the entire C(H)1 domain of the functional camel IGG2A heavy-chain antibodies

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

Loss of splice consensus signal is responsible for the removal of the entire C(H)1 domain of the functional camel IGG2A heavy-chain antibodies (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

3

object named as

L Wyns

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Europe PubMed Central

PubMed publication ID

26 June 2017

author name string

V K Nguyen

1

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

R Hamers

2

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

S Muyldermans

4

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

publication date

1 June 1999

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

Molecular Immunology

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Europe PubMed Central

PubMed publication ID

26 June 2017

36

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Europe PubMed Central

PubMed publication ID

26 June 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

515-524

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Europe PubMed Central

PubMed publication ID

26 June 2017

Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system

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Sigma region located between C mu and C delta genes of human immunoglobulin heavy chain: possible involvement of tRNA-like structure in RNA splicing

1 reference

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7 January 2021

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Gene segments encoding membrane domains of the human immunoglobulin gamma 3 and alpha chains

1 reference

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Loss of a consensus splice signal in a mutant immunoglobulin gene eliminates the CH1 domain exon from the mRNA

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Immunoglobulin G: functional sites

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Immunoglobulin gene alterations in human heavy chain diseases.

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A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.

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Crystal structure of a camel single-domain VH antibody fragment in complex with lysozyme

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Localization of the binding site for the human high-affinity Fc receptor on IgG.

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Partial deletion in the heavy chain disease protein ZUC.

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HEAVY CHAIN DISEASE- A NEW DISORDER OF SERUM GAMMA-GLOBULINS : REPORT OF THE FIRST CASE

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Naturally occurring antibodies devoid of light chains

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Organization and reorganization of immunoglobulin heavy-chain genes

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Sequence of a human immunoglobulin gamma 3 heavy chain constant region gene: comparison with the other human C gamma genes

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IgG-Fc-mediated effector functions: molecular definition of interaction sites for effector ligands and the role of glycosylation

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Rearrangement of immunoglobulin gamma 1-chain gene and mechanism for heavy-chain class switch

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Model for the complex between protein G and an antibody Fc fragment in solution.

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Structure of abnormal heavy chains in human heavy-chain-deposition disease.

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The membrane exons of the pseudo-gamma-chain gene of the human immunoglobulin are apparently functional and highly homologous to those of the gamma 1 gene

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The putative transposase of transposable element Ac from Zea mays L. interacts with subterminal sequences of Ac.

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Effector functions of a monoclonal aglycosylated mouse IgG2a: binding and activation of complement component C1 and interaction with human monocyte Fc receptor

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Murine heavy chain disease

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Sequence and structure of VH domain from naturally occurring camel heavy chain immunoglobulins lacking light chains

1 reference

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The specific variable domain of camel heavy-chain antibodies is encoded in the germline

1 reference

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Anatomy of the antibody molecule

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The nucleotide sequence of the maize controlling element Activator.

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1 reference

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Gene segments encoding transmembrane carboxyl termini of immunoglobulin gamma chains.

1 reference

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mRNA for surface immunoglobulin gamma chains encodes a highly conserved transmembrane sequence and a 28-residue intracellular domain

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Identifiers

10.1016/S0161-5890(99)00067-X

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 June 2017

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