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Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families.

Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families.

http://www.wikidata.org/entity/Q35026701

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Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects.

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Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families.

http://www.wikidata.org/entity/Q35026701

description

2010 nî lūn-bûn

@nan

2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@ast

Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@en

type

label

Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@ast

Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@en

prefLabel

Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@ast

Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@en

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International Journal of Nephrology and Renovascular Disease

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Atypical hemolytic uremic synd ...... gene in two Tunisian families.

@en

P2093

Abdelkrim Ayadi

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Houda Aouadi

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Imen Habibi

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Imen Sfar

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Jacques Blouin

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Jihen Methlouthi

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Khaled Ayed

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Mouna Makhlouf

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Mounira Brahim

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Raoudha Dhagbouj

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P2860

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome.

Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations

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

Complement factor H: sequence analysis of 221 kb of human genomic DNA containing the entire fH, fHR-1 and fHR-3 genes

Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

Disease-associated sequence variations congregate in a polyanion recognition patch on human factor H revealed in three-dimensional structure

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

Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site.

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2010-07-01T00:00:00Z

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