(Q28259896)

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Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population

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scholarly article

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Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population (English)

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single-nucleotide polymorphism

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based on heuristic

inferred from title

systemic lupus erythematosus

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based on heuristic

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Naoyuki Kamatani

13

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2

object named as

Koichi Matsuda

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8

object named as

Michiaki Kubo

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Yūsuke Nakamura

14

object named as

Yusuke Nakamura

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Toyomasa Katagiri

11

object named as

Toyomasa Katagiri

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Yoichiro Kamatani

1

object named as

Yoichiro Kamatani

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5

object named as

Keiko Yamazaki

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6

object named as

Aritoshi Iida

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7

object named as

Naoya Hosono

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9

object named as

Wako Yumura

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author name string

Tetsuya Ohishi

3

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Shigeru Ohtsubo

4

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Kosaku Nitta

10

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Yasushi Kawaguchi

12

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language of work or name

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publication date

2008

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Journal of Human Genetics

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53

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1

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64-73

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Distinct tissue distribution in pigs of tenascin-X and tenascin-C transcripts

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https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies for genome-wide association studies: optimization of study designs by the stepwise focusing method.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

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A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of susceptibility and severity in systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immune cells and cytokines in systemic lupus erythematosus: an update

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mortality and causes of death in systemic lupus erythematosus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphism analysis of HLA-DR, DQ, DP and C4 alleles in Caucasians with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA antigens in Japanese patients with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of complement C4 and HLA-DR alleles with systemic lupus erythematosus in Koreans

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of statistical power between 2 * 2 allele frequency and allele positivity tables in case-control studies of complex disease genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of human systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of C4A genes in patients with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major histocompatibility complex genes and susceptibility to systemic lupus erythematosus in southern chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high-throughput SNP typing system for genome-wide association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4A gene deletion and HLA associations in black Americans with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement component C4 gene intron 9 as a phylogenetic marker for primates: long terminal repeats of the endogenous retrovirus ERV-K(C4) are a molecular clock of evolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete MHC haplotype sequencing for common disease gene mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The distribution of tenascin-X is distinct and often reciprocal to that of tenascin-C

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of gene deletion for complement C4A deficiency in Japanese patients with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Routine low and high resolution typing of the HLA-DRB gene using the PCR-MPH (microtitre plate hybridization) method

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global variation in copy number in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype analysis revealed no association between the PTPN22 gene and RA in a Japanese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18058064

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-007-0219-1

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