Vitamin D Pathway Genetic Variation and Type 1 Diabetes: A Case-Control Association Study.
Adolescent
Adult
Child
Cholestanetriol 26-Monooxygenase
/ genetics
Cytochrome P450 Family 2
/ genetics
Diabetes Mellitus, Type 1
/ genetics
Female
Humans
Male
Oxidoreductases Acting on CH-CH Group Donors
/ genetics
Polymorphism, Single Nucleotide
Vitamin D
/ genetics
Vitamin D-Binding Protein
/ genetics
Vitamin D3 24-Hydroxylase
/ genetics
SNP
Vitamin D
autoimmune
genetics
single nucleotide polymorphism
type 1 diabetes
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
05 08 2020
05 08 2020
Historique:
received:
05
07
2020
revised:
27
07
2020
accepted:
01
08
2020
entrez:
9
8
2020
pubmed:
9
8
2020
medline:
18
3
2021
Statut:
epublish
Résumé
Vitamin D has immunomodulatory effects, and its deficiency has been implicated in the autoimmune process of type 1 diabetes. Serum vitamin D levels are influenced by variants in genes involved in the synthesis, transport, hydroxylation and degradation of vitamin D. The aim of this study was to assess if single nucleotide polymorphisms (SNPs) at the
Identifiants
pubmed: 32764491
pii: genes11080897
doi: 10.3390/genes11080897
pmc: PMC7465037
pii:
doi:
Substances chimiques
GC protein, human
0
Vitamin D-Binding Protein
0
Vitamin D
1406-16-2
Cytochrome P450 Family 2
EC 1.14.14.1
CYP2R1 protein, human
EC 1.14.14.24
Cholestanetriol 26-Monooxygenase
EC 1.14.15.15
CYP24A1 protein, human
EC 1.14.15.16
Vitamin D3 24-Hydroxylase
EC 1.14.15.16
Oxidoreductases Acting on CH-CH Group Donors
EC 1.3.-
7-dehydrocholesterol reductase
EC 1.3.1.21
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Références
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