Nonsense-codon-mediated decay in human hereditary complement C3 deficiency (Q44669534)

5 December 2017

Nonsense-codon-mediated decay in human hereditary complement C3 deficiency (English)

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5 December 2017

Edimara S Reis

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5 December 2017

Victor Nudelman

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2

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5 December 2017

Lourdes Isaac

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3

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5 December 2017

language of work or name

English

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publication date

25 November 2003

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55

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10

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667-673

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https://scigraph.springernature.com/pub.10.1007/s00251-003-0624-3

5 December 2017

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Genomic organization of human complement component C3.

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Homozygous hereditary C3 deficiency due to a partial gene deletion

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Molecular basis of hereditary C3 deficiency

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Antibody response to a T-dependent antigen requires B cell expression of complement receptors

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Evidence for an ester linkage between the labile binding site of C3b and receptive surfaces

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A hereditary C3 deficiency due to aberrant splicing of exon 10

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Degradation of mRNA in eukaryotes

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Interleukin 6 stimulates synthesis of complement proteins factor B and C3 in human skin fibroblasts

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Hereditary complement factor I deficiency

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12 December 2020

Identification of a novel mutation (Tyr1081Ter) in sisters with hereditary component C3 deficiency and SLE-like symptoms

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12 December 2020

Homozygous hereditary C3 deficiency due to a premature stop codon

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12 December 2020

Low cytoplasmic mRNA levels of immunoglobulin kappa light chain genes containing nonsense codons correlate with inefficient splicing.

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The third component of complement is transcribed and secreted by cultured human endothelial cells

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When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.

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C3d of complement as a molecular adjuvant: bridging innate and acquired immunity

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Complement deficiency and immune complex disease

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Molecular basis of polymorphisms of human complement component C3.

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Role of complement in induction of antibody production in vivo. Effect of cobra factor and other C3-reactive agents on thymus-dependent and thymus-independent antibody responses

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Biosynthesis and secretion of complement component (C3) by activated human polymorphonuclear leukocytes

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Molecular characterization of homozygous hereditary factor I deficiency

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Evidence for degradation of mRNA encoding alpha-L-iduronidase in Hurler fibroblasts with premature termination alleles.

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Molecular organization and function of the complement system

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On the lability of poly(A) sequences during extraction of messenger RNA from polyribosomes

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Human complement component C3: cDNA coding sequence and derived primary structure

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Chronic myelogenous leukemia-derived basophilic granulocytes express a functional active receptor for the anaphylatoxin C3a.

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Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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Structural requirements for thioester bond formation in human complement component C3. Reassessment of the role of thioester bond integrity on the conformation of C3

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12 December 2020

Hereditary human complement C3 deficiency owing to reduced levels of C3 mRNA

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12 December 2020

10.1007/S00251-003-0624-3

Identifiers

DOI

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5 December 2017

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