Integrative transcriptome analysis reveals dysregulation of canonical cancer molecular pathways in placenta leading to preeclampsia

Preeclampsia: a bioinformatics approach through protein-protein interaction networks analysis

(2012) Eduardo Tejera et al.   BMC Systems Biology

Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta

(2012) Roxana Moslehi et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A High-Throughput Chromatin Immunoprecipitation Approach Reveals Principles of Dynamic Gene Regulation in Mammals

(2012) Manuel Garber et al.   MOLECULAR CELL

Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene

(2012) Matthew P. Johnson et al.   PLoS One

XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase

(2011) Jill O. Fuss et al.   DNA REPAIR

Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease

(2011) Åsa Johansson et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)

(2011) L. T. Roten et al.   MOLECULAR HUMAN REPRODUCTION

High-risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies

(2011) Deborah Tamura et al.   PRENATAL DIAGNOSIS

Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction

(2011) Haruki Nishizawa et al.   Reproductive Biology and Endocrinology

Towards a knowledge-based Human Protein Atlas

(2010) Mathias Uhlen et al.   NATURE BIOTECHNOLOGY

Genetic and Molecular Functional Characterization of Variants within TNFSF13B, a Positional Candidate Preeclampsia Susceptibility Gene on 13q

(2010) Mona H. Fenstad et al.   PLoS One

Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal development

(2009) R Moslehi et al.   CLINICAL GENETICS

Regulation of gene expression via the core promoter and the basal transcriptional machinery

(2009) Tamar Juven-Gershon et al.   DEVELOPMENTAL BIOLOGY

Placental and Embryonic Growth Restriction in Mice With Reduced Function Epidermal Growth Factor Receptor Alleles

(2009) J. Dackor et al.   GENETICS

The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations

(2009) Matthew P. Johnson et al.   HUMAN GENETICS

ATF3 transcription factor and its emerging roles in immunity and cancer

(2009) Matthew R. Thompson et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Differential Placental Gene Expression in Severe Preeclampsia

(2009) V. Sitras et al.   PLACENTA

Acute hypoxia to endothelial cells induces activating transcription factor 3 (ATF3) expression that is mediated via nitric oxide

(2008) Shih-Chung Chen et al.   ATHEROSCLEROSIS

Transcriptional changes in trichothiodystrophy cells

(2008) Judith Offman et al.   DNA REPAIR

Severe Preeclampsia-Related Changes in Gene Expression at the Maternal-Fetal Interface Include Sialic Acid-Binding Immunoglobulin-Like Lectin-6 and Pappalysin-2

(2008) Virginia D. Winn et al.   ENDOCRINOLOGY

Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)

(2008) Linda T Roten et al.   EUROPEAN JOURNAL OF HUMAN GENETICS