(Q43587195)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11320527%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects (English)

1 reference

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6 November 2019

1 reference

4

1 reference

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6 November 2019

Richard H. Finnell

5

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6 November 2019

author name string

Stegmann K

1

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6 November 2019

Boecker J

2

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6 November 2019

Richter B

3

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6 November 2019

Ngo ET

6

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6 November 2019

Strehl E

7

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6 November 2019

Ermert A

8

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6 November 2019

Koch MC

9

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6 November 2019

publication date

1 May 2001

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6 November 2019

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6 November 2019

volume

63

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6 November 2019

issue

5

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6 November 2019

page(s)

167-175

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Lack of association between mutations in the folate receptor-alpha gene and spina bifida

6 November 2019

cites work

1 reference

Prevention of neural-tube defects with folic acid in China. China-U.S. Collaborative Project for Neural Tube Defect Prevention

21 January 2018

1 reference

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

21 January 2018

1 reference

An alternatively spliced mRNA from the AP-2 gene encodes a negative regulator of transcriptional activation by AP-2

21 January 2018

1 reference

Prevention of neural tube defects: vitamins, enzymes and genes

21 January 2018

1 reference

The embryonic development of mammalian neural tube defects.

21 January 2018

1 reference

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

21 January 2018

1 reference

The function and evolution of Msx genes: pointers and paradoxes

21 January 2018

1 reference

Apparent lability of neural tube closure in laboratory animals and humans

21 January 2018

1 reference

Genetic landmarks for defects in mouse neural tube closure

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

21 January 2018

1 reference

Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins

21 January 2018

1 reference

Mouse models for neural tube closure defects

21 January 2018

1 reference

Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.

21 January 2018

1 reference

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

21 January 2018

1 reference

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

21 January 2018

1 reference

Development of anencephaly and its variants

21 January 2018

1 reference

AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice

21 January 2018

1 reference

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

21 January 2018

1 reference

Transcription factor AP-2 essential for cranial closure and craniofacial development

21 January 2018

1 reference

Chicken transcription factor AP-2: cloning, expression and its role in outgrowth of facial prominences and limb buds.

21 January 2018

1 reference

Single-nucleotide polymorphisms can cause different structural folds of mRNA.

21 January 2018

1 reference

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

21 January 2018

1 reference

Human transcription factor SLUG: mutation analysis in patients with neural tube defects and identification of a missense mutation (D119E) in the Slug subfamily-defining region

21 January 2018

1 reference

Evidence for multi-site closure of the neural tube in humans

21 January 2018

1 reference

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

21 January 2018

1 reference

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

21 January 2018

1 reference

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

21 January 2018

1 reference

Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice.

21 January 2018

1 reference

Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2

21 January 2018

1 reference

The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

21 January 2018

1 reference

Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population

21 January 2018

1 reference

Molecular genetic analysis of human folate receptors in neural tube defects

21 January 2018

1 reference

Sibs of probands with neural tube defects--a study in the Federal Republic of Germany

21 January 2018

1 reference

Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?

21 January 2018

1 reference

Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)

21 January 2018

1 reference

Codon usage tabulated from the GenBank genetic sequence data

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/TERA.1031

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11320527%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

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