(Q51474477)

5 April 2018

title

Plasma carnitine ester profiles in Crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypes. (English)

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5 April 2018

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Krisztina Horváth

5

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author name string

Judit Bene

1

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5 April 2018

Katalin Komlósi

2

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Lili Magyari

3

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5 April 2018

Gábor Talián

4

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5 April 2018

Beáta Gasztonyi

6

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Pál Miheller

7

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5 April 2018

Mária Figler

8

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5 April 2018

Gyula Mózsik

9

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Zsolt Tulassay

10

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5 April 2018

Béla Melegh

11

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5 April 2018

publication date

29 March 2007

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5 April 2018

British Journal of Nutrition

published in

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5 April 2018

volume

98

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5 April 2018

issue

2

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5 April 2018

page(s)

345-350

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5 April 2018

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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Dynamic changes of plasma acylcarnitine levels induced by fasting and sunflower oil challenge test in children.

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Plasma carnitine ester profile in adult celiac disease patients maintained on long-term gluten free diet

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

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Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

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Molecular and functional identification of sodium ion-dependent, high affinity human carnitine transporter OCTN2

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CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure

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Pivampicillin-promoted excretion of pivaloylcarnitine in humans.

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Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease

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NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?

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Structural and functional characteristics and tissue distribution pattern of rat OCTN1, an organic cation transporter, cloned from placenta

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Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

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CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

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7 January 2021

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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The molecular classification of the clinical manifestations of Crohn's disease

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7 January 2021

Defining complex contributions of NOD2/CARD15 gene mutations, age at onset, and tobacco use on Crohn's disease phenotypes

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A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

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7 January 2021

The Contribution of OCTN1/2 Variants Within the IBD5 Locus to Disease Susceptibility and Severity in Crohn’s Disease

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7 January 2021

Functional variants of OCTN cation transporter genes are associated with Crohn disease

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7 January 2021

Activation of nuclear factor kappa B inflammatory bowel disease

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7 January 2021

Butyrate inhibits inflammatory responses through NFkappaB inhibition: implications for Crohn's disease

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7 January 2021

Association of Organic Cation Transporter Risk Haplotype With Perianal Penetrating Crohn’s Disease but Not With Susceptibility to IBD

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7 January 2021

NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype-phenotype analysis in Danish and Portuguese patients and controls.

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7 January 2021

cDNA sequence, transport function, and genomic organization of human OCTN2, a new member of the organic cation transporter family

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7 January 2021

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Identifiers

DOI

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5 April 2018

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5 April 2018