(Q43958315)

28 November 2017

Genetic and environmental factors influencing the human factor H plasma levels (English)

1 reference

Santiago Rodriguez de Córdoba

28 November 2017

series ordinal

7

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28 November 2017

4

Laura Almasy

1 reference

28 November 2017

Alfonso Buil

3

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John Blangero

series ordinal

5

object named as

John Blangero

1 reference

28 November 2017

2

José Manuel Soria

1 reference

28 November 2017

6

Jordi Fontcuberta

1 reference

28 November 2017

Jorge Esparza-Gordillo

series ordinal

1

1 reference

PubMed ID

15118848

28 November 2017

language of work or name

English

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publication date

30 April 2004

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28 November 2017

1 reference

28 November 2017

56

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28 November 2017

77-82

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28 November 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1007/s00251-004-0660-7

28 November 2017

0 references

cites work

Robust LOD scores for variance component-based linkage analysis

1 reference

12 December 2020

An integrated map of the human regulator of complement activation (RCA) gene cluster on 1q32

1 reference

12 December 2020

Serum Complement Levels in Infancy: Age Related Changes

1 reference

12 December 2020

ISOLATION OF BETA IF-GLOBULIN FROM HUMAN SERUM AND ITS CHARACTERIZATION AS THE FIFTH COMPONENT OF COMPLEMENT.

1 reference

12 December 2020

Control of the amplification convertase of complement by the plasma protein beta1H

1 reference

12 December 2020

Localization of the heparin-binding site on complement factor H

1 reference

12 December 2020

Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families

1 reference

12 December 2020

A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q

1 reference

12 December 2020

Genetic studies into inherited and sporadic hemolytic uremic syndrome

1 reference

12 December 2020

A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32

1 reference

12 December 2020

Requirements for beta1H globulin and C3b inactivator in the control of the alternative complement pathway in human serum

1 reference

12 December 2020

Human complement factor H deficiency associated with hemolytic uremic syndrome.

1 reference

12 December 2020

Genetic determinants of hemostasis phenotypes in Spanish families.

1 reference

12 December 2020

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

Initiation of the alternative pathway of complement: recognition of activators by bound C3b and assembly of the entire pathway from six isolated proteins

1 reference

12 December 2020

Structure-function relationships of the complement components

1 reference

12 December 2020

Modulation of the alternative complement pathways by beta 1 H globulin

1 reference

12 December 2020

A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility.

1 reference

12 December 2020

Isoforms of human C4b-binding protein. I. Molecular basis for the C4BP isoform pattern and its variations in human plasma.

1 reference

12 December 2020

Complement system in healthy term newborns: reference values in umbilical cord blood.

1 reference

12 December 2020

Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure

1 reference

12 December 2020

Regulation by membrane sialic acid of β1H-dependent decay-dissociation of amplification C3 convertase of the alternative complement pathway

1 reference

12 December 2020

Quantitative variations of the C3b/C4b receptor (CR1) in human erythrocytes are controlled by genes within the regulator of complement activation (RCA) gene cluster

1 reference

12 December 2020

Extensions to multivariate normal models for pedigree analysis

1 reference

12 December 2020

Discrimination between activators and nonactivators of the alternative pathway of complement: regulation via a sialic acid/polyanion binding site on factor H

1 reference

12 December 2020

The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

1 reference

12 December 2020

Multipoint quantitative-trait linkage analysis in general pedigrees

1 reference

12 December 2020

Human genes for three complement components that regulate the activation of C3 are tightly linked

1 reference

12 December 2020

Ascertainment and goodness of fit of variance component models for pedigree data

1 reference

12 December 2020

Factor H and the pathogenesis of renal diseases

1 reference

12 December 2020

Heterozygous and homozygous factor H deficiency states in a Dutch family

1 reference

12 December 2020

Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution

1 reference

12 December 2020

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

1 reference

12 December 2020

The complete amino acid sequence of human complement factor H

1 reference

12 December 2020

Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.

1 reference

12 December 2020

Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition

1 reference

12 December 2020

10.1007/S00251-004-0660-7

Identifiers

DOI

1 reference

28 November 2017

1 reference

PubMed ID

15118848