(Q42629757)

English

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas

scientific article published on 18 June 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

1 reference

based on heuristic

inferred from title

object named as

Gerard Pals

13

0 references

Marinus Blankenstein

object named as

Marinus A Blankenstein

15

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author name string

Cees B M Oudejans

1

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Europe PubMed Central

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4 November 2017

Joyce Mulders

2

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Europe PubMed Central

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4 November 2017

Augusta M A Lachmeijer

3

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Europe PubMed Central

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4 November 2017

Marie van Dijk

4

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Europe PubMed Central

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4 November 2017

Andrea A M Könst

5

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Europe PubMed Central

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4 November 2017

Bart A Westerman

6

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Europe PubMed Central

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4 November 2017

Inge J van Wijk

7

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Europe PubMed Central

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4 November 2017

Peter A J Leegwater

8

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Europe PubMed Central

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4 November 2017

Hidenori D Kato

9

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Europe PubMed Central

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4 November 2017

Takao Matsuda

10

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Europe PubMed Central

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4 November 2017

Norio Wake

11

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4 November 2017

Gustaaf A Dekker

12

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Europe PubMed Central

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4 November 2017

Leo P ten Kate

14

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Europe PubMed Central

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4 November 2017

publication date

18 June 2004

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Europe PubMed Central

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4 November 2017

Molecular Human Reproduction

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Europe PubMed Central

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4 November 2017

10

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4 November 2017

8

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4 November 2017

589-598

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4 November 2017

Coupling of c-Src to large conductance voltage- and Ca2+-activated K+ channels as a new mechanism of agonist-induced vasoconstriction

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Pre-eclampsia and peripartum cardiomyopathy in molar pregnancy: clinical implication for maternally imprinted genes

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

The myometrial junctional zone spiral arteries in normal and abnormal pregnancies: a review of the literature

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57KIP2.

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Identification of a human histone acetyltransferase related to monocytic leukemia zinc finger protein

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Altered placental development and intrauterine growth restriction in IGF binding protein-1 transgenic mice

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Roles for genomic imprinting and the zygotic genome in placental development.

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

SHORT INTEGUMENTS1/SUSPENSOR1/CARPEL FACTORY, a Dicer homolog, is a maternal effect gene required for embryo development in Arabidopsis

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Distinct HP1 and Su(var)3-9 complexes bind to sets of developmentally coexpressed genes depending on chromosomal location

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Allegro, a new computer program for multipoint linkage analysis

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

The role of the X chromosome in mammalian extra embryonic development

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

In vitro ischemia-reperfusion injury in term human placenta as a model for oxidative stress in pathological pregnancies

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Translating the Histone Code

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Establishment of functional imprinting of the H19 gene in human developing placentae

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Deficiency in p57Kip2 expression induces preeclampsia-like symptoms in mice

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Antisense transcripts with FANTOM2 clone set and their implications for gene regulation

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A high-resolution recombination map of the human genome

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A genome-wide scan for preeclampsia in the Netherlands

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Characterization of JDP genes, an evolutionarily conserved J domain-only protein family, from human and moths

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A study of placental bed spiral arteries and trophoblast invasion in normal and severe pre-eclamptic pregnancies

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Localisation of the human hSuv3p helicase in the mitochondrial matrix and its preferential unwinding of dsDNA

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Identification of putative noncoding RNAs among the RIKEN mouse full-length cDNA collection

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in development.

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Involvement of the histone deacetylase SIRT1 in chicken ovalbumin upstream promoter transcription factor (COUP-TF)-interacting protein 2-mediated transcriptional repression

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Extravillus endovascular implantation site trophoblast invasion is abnormal in complete versus partial molar pregnancies

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Defective endovascular trophoblast invasion in primary antiphospholipid antibody syndrome-associated early pregnancy failure

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Genetic origin of malignant trophoblastic neoplasms analyzed by sequence tag site polymorphic markers

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Triploid/diploid mosaicism (69XXY/46XX) presenting as severe early onset preeclampsia with a live birth: placental and cytogenetic features

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Oxidative stress reproduces placental abnormalities of preeclampsia

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Computation method to identify differential allelic gene expression and novel imprinted genes

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Preeclampsia is associated with abnormal expression of adhesion molecules by invasive cytotrophoblasts

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH080

21 January 2018

Identifiers

10.1093/MOLEHR/GAH080

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 November 2017

ResearchGate publication ID

0 references

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