(Q37552016)

English

Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria

scientific article published on 13 September 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria (English)

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

0 references

paroxysmal nocturnal hemoglobinuria

1 reference

based on heuristic

inferred from title

Régis Peffault de Latour

3

object named as

Régis Peffault de Latour

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

13

object named as

Gerard Socie

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

14

object named as

Lucio Luzzatto

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Antonio M Risitano

2

object named as

Antonio M Risitano

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

author name string

Tommaso Rondelli

1

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Michela Sica

4

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Benedetta Peruzzi

5

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Patrizia Ricci

6

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Wilma Barcellini

7

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Anna Paola Iori

8

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Carla Boschetti

9

1 reference

Europe PubMed Central

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21 August 2017

Veronica Valle

10

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Veronique Frémeaux-Bacchi

11

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Maria De Angioletti

12

1 reference

Europe PubMed Central

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21 August 2017

Rosario Notaro

15

1 reference

Europe PubMed Central

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21 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

13 September 2013

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

99

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

262-266

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Predictors of hemoglobin response to eculizumab therapy in paroxysmal nocturnal hemoglobinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Safety and efficacy of the terminal complement inhibitor eculizumab in Japanese patients with paroxysmal nocturnal hemoglobinuria: the AEGIS clinical trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Complement in human diseases: Lessons from complement deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Complement Receptor 1: disease associations and therapeutic implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Variation in complement factor 3 is associated with risk of age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Membranoproliferative glomerulonephritis type II (dense deposit disease): an update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Visualization of the transfer reaction: tracking immune complexes from erythrocyte complement receptor 1 to macrophages

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Natural history of paroxysmal nocturnal hemoglobinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Complement receptor is an inhibitor of the complement cascade

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Control of the function of substrate-bound C4b-C3b by the complement receptor Cr1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Generation of three different fragments of bound C3 with purified factor I or serum. I. Requirements for factor H vs CR1 cofactor activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Genetic polymorphism of the third component of human complement (C'3).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Identification of a restriction fragment length polymorphism by a CR1 cDNA that correlates with the number of CR1 on erythrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

23 August 2017

Management of paroxysmal nocturnal haemoglobinuria: a personal view.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

6 September 2017

Easy genotyping of complement C3 'slow' and 'fast' allotypes by tetra-primer amplification refractory mutation system PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

14 September 2017

Eculizumab prevents intravascular hemolysis in patients with paroxysmal nocturnal hemoglobinuria and unmasks low-level extravascular hemolysis occurring through C3 opsonization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

14 September 2017

Genetic polymorphism of C3 and Bf in IgA nephropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

25 June 2018

Interaction between immune complexes and C3b receptors on erythrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

25 June 2018

Molecular basis of polymorphisms of human complement component C3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

25 June 2018

The complement receptor 2/factor H fusion protein TT30 protects paroxysmal nocturnal hemoglobinuria erythrocytes from complement-mediated hemolysis and C3 fragment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

1 September 2018

Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

1 September 2018

Paroxysmal nocturnal hemoglobinuria and eculizumab

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

1 September 2018

Complement fraction 3 binding on erythrocytes as additional mechanism of disease in paroxysmal nocturnal hemoglobinuria patients treated by eculizumab.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

1 September 2018

Erythrocyte CR1 expression level does not correlate with a HindIII restriction fragment length polymorphism in Africans; implications for studies on malaria susceptibility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

1 September 2018

Quantitative alleles of CR1: coding sequence analysis and comparison of haplotypes in two ethnic groups.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

1 September 2018

Disease-associated loss of erythrocyte complement receptors (CR1, C3b receptors) in patients with systemic lupus erythematosus and other diseases involving autoantibodies and/or complement activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3912955

2 October 2018

Mode of inheritance of decreased C3b receptors on erythrocytes of patients with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/24038027

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal function of CR1 on affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/24038027

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of the mechanisms responsible for the reduction in erythrocyte complement receptors when immune complexes form in vivo in primates

1 reference

https://pubmed.ncbi.nlm.nih.gov/24038027

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories

1 reference

https://pubmed.ncbi.nlm.nih.gov/24038027

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3324/HAEMATOL.2013.090001

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

ResearchGate publication ID

0 references

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