SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects? (Q40718454)

23 September 2017

title

SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects? (English)

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23 September 2017

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Ute Christine Rogner

1

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23 September 2017

Patrick Danoy

2

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23 September 2017

Fumihiko Matsuda

3

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23 September 2017

Gudrun Elizabeth Moore

4

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23 September 2017

Philip Stanier

5

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23 September 2017

Philip Avner

6

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23 September 2017

publication date

1 July 2002

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American Journal of Medical Genetics Part A

23 September 2017

published in

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23 September 2017

volume

110

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23 September 2017

issue

3

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23 September 2017

page(s)

208-214

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Absence of linkage between familial neural tube defects and PAX3 gene

23 September 2017

cites work

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Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition

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Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

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Folate pathway gene alterations in patients with neural tube defects

21 January 2018

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splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

21 January 2018

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Expression of a new mutation (Axd) causing axial defects in mice correlates with maternal phenotype and age.

21 January 2018

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A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome

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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida

21 January 2018

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Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects

21 January 2018

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Mouse models for neural tube closure defects

21 January 2018

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Pbx-1 Hox heterodimers bind DNA on inseparable half-sites that permit intrinsic DNA binding specificity of the Hox partner at nucleotides 3' to a TAAT motif.

21 January 2018

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Susceptibility to spina bifida; an association study of five candidate genes

21 January 2018

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DNA Methylation and Gene Function

21 January 2018

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DNA methylation in health and disease

21 January 2018

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Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly

21 January 2018

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Control of neurulation by the nucleosome assembly protein-1-like 2.

21 January 2018

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Cloning and characterization of a murine brain specific gene Bpx and its human homologue lying within the Xic candidate region

21 January 2018

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Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly

21 January 2018

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Folic acid and the prevention of neural tube defects

21 January 2018

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Couple screening for cystic fibrosis.

21 January 2018

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Neural tube defects as an X-linked condition

21 January 2018

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Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family

21 January 2018

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undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1

21 January 2018

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Lack of mutations in ZIC3 in three families with neural tube defects

21 January 2018

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A genetic risk factor for mouse neural tube defects: defining the embryonic basis

21 January 2018

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Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects

21 January 2018

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Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects

21 January 2018

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Report of a third kindred with X-linked anencephaly/spina bifida

21 January 2018

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Brief communication: possible X-linked anencephaly and spina bifida--report of a kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10453

21 January 2018

Identifiers

DOI

10.1002/AJMG.10453

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23 September 2017

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