(Q53465857)

14 May 2018

title

TNF-alpha and IL-10 gene polymorphisms versus cardioimmunological responses in sudden infant death. (English)

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14 May 2018

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Nasrin Perskvist

1

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14 May 2018

Karin Skoglund

2

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14 May 2018

Erik Edston

3

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14 May 2018

Gerd Bäckström

4

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14 May 2018

Iréne Lodestad

5

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14 May 2018

Ulla Palm

6

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14 May 2018

publication date

1 January 2008

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14 May 2018

Fetal and Pediatric Pathology

published in

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14 May 2018

volume

27

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14 May 2018

issue

3

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14 May 2018

page(s)

149-165

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14 May 2018

Sudden infant death syndrome (SIDS)--standardised investigations and classification: recommendations

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1 reference

https://api.crossref.org/works/10.1080%2F15513810802077651

A second polymorphic dinucleotide repeat in the 5' flanking region of the human IL10 gene

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Interleukin-10 gene polymorphism influences the prognosis of T-cell non-Hodgkin lymphomas.

21 January 2018

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Tumor necrosis factor gene polymorphisms and clearance or progression of hepatitis B virus infection

21 January 2018

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Interleukin 10 secretion in relation to human IL-10 locus haplotypes

21 January 2018

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Cytokine gene polymorphism in human disease: on-line databases

21 January 2018

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21 January 2018

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Role of virus-induced myocardial affections in sudden infant death syndrome: a prospective postmortem study

21 January 2018

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The complex role of interleukin-10 in autoimmunity

21 January 2018

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https://api.crossref.org/works/10.1080%2F15513810802077651

Tumour necrosis factor-alpha: the role of this multifunctional cytokine in asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15513810802077651

Polymorphism of the interleukin-10 gene is associated with susceptibility to Epstein-Barr virus infection

21 January 2018

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Interleukin-10-1082 promoter polymorphism in association with cytokine production and sepsis susceptibility

21 January 2018

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Potential role of interleukin-10-secreting regulatory T cells in allergy and asthma.

21 January 2018

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Prolongation of the QT interval and the sudden infant death syndrome.

21 January 2018

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Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15513810802077651

IL-10 gene polymorphisms are associated with infectious cause of sudden infant death

21 January 2018

1 reference

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Human heat shock protein gene polymorphisms and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15513810802077651

Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15513810802077651

Single base polymorphism in the human tumour necrosis factor alpha (TNF alpha) gene detectable by NcoI restriction of PCR product

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F15513810802077651

Relation of an Interleukin-10 Promoter Polymorphism to Graft-versus-Host Disease and Survival after Hematopoietic-Cell Transplantation

21 January 2018

1 reference

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10.1080/15513810802077651

21 January 2018

Identifiers

DOI

1 reference

14 May 2018

1 reference

14 May 2018