Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage-Reference-Cited by-同舟云学术

Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage

Published:2014-06-24 Issue:8 Volume:35 Page:972-982
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Nagirnaja Liina¹,Palta Priit²³⁴,Kasak Laura¹,Rull Kristiina¹⁵,Christiansen Ole B.⁶⁷,Nielsen Henriette S.⁶,Steffensen Rudi⁸,Esko Tõnu⁹¹⁰¹¹,Remm Maido²¹²,Laan Maris¹

Affiliation:

1. Human Molecular Genetics Research Group Institute of Molecular and Cell Biology, University of Tartu Tartu Estonia

2. Department of Bioinformatics Institute of Molecular and Cell Biology, University of Tartu Tartu Estonia

3. Institute for Molecular Medicine Finland (FIMM) University of Helsinki Helsinki Finland

4. Wellcome Trust Sanger Institute Wellcome Trust Genome Campus Cambridge United Kingdom

5. Department of Obstetrics and Gynaecology University of Tartu Tartu Estonia

6. The Fertility Clinics, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark

7. Department of Obstetrics and Gynaecology Aalborg University Hospital Aalborg Denmark

8. Department of Clinical Immunology Aalborg University Hospital Aalborg Denmark

9. Estonian Genome Center University of Tartu Tartu Estonia

10. Children's Hospital Boston Boston Massachusetts

11. Medical and Population Genetics Broad Institute Cambridge Massachusetts

12. Estonian Biocentre Tartu Estonia

Funder

Wellcome Trust

Estonian Science Foundation

European Commission

Estonian Ministry of Education and Research

European Regional Development Fund

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.22589

Reference84 articles.

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5. mTOR mediates human trophoblast invasion through regulation of matrix-remodeling enzymes and is associated with serine phosphorylation of STAT3

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