Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus

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Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

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2015年論文

@zh-hk

2015年論文

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2015年論文

@zh-tw

2015年论文

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2015年论文

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2015年论文

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name

Molecular characterization of ...... e systemic lupus erythematosus

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Molecular characterization of ...... e systemic lupus erythematosus

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type

Item

label

Molecular characterization of ...... e systemic lupus erythematosus

@ast

Molecular characterization of ...... e systemic lupus erythematosus

@en

prefLabel

Molecular characterization of ...... e systemic lupus erythematosus

@ast

Molecular characterization of ...... e systemic lupus erythematosus

@en

P1476

Molecular characterization of ...... e systemic lupus erythematosus

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P2093

Adriana A Jesus

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Bernadete L Liphaus

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Clovis A Silva

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Magda Carneiro-Sampaio

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Natalia Umetsu

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Silvia Y Bando

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P2860

Molecular basis of hereditary C1q deficiency

Characterization and organization of the genes encoding the A-, B- and C-chains of human complement subcomponent C1q. The complete derived amino acid sequence of human C1q

The crystal structure of the globular head of complement protein C1q provides a basis for its versatile recognition properties

Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretion

Real-time PCR quantification of human complement C4A and C4B genes.

Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4

Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing

The 1982 revised criteria for the classification of systemic lupus erythematosus

Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus

Listening to silence and understanding nonsense: exonic mutations that affect splicing

P304

220-227

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P31

scholarly article

P356

10.6061/CLINICS/2015(03)12

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P433

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P478

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2015-03-01T00:00:00Z

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277410895

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P698

26017655

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P932

4449463

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