Vaiman D - Search Results

1

Genetic regulation of recurrent spontaneous abortion in humans.

Vaiman D. Vaiman D. Biomed J. 2015 Jan-Feb;38(1):11-24. doi: 10.4103/2319-4170.133777. Biomed J. 2015. PMID: 25179715 Free article. Review.

2

Novel genes and mutations in patients affected by recurrent pregnancy loss.

Quintero-Ronderos P, Mercier E, Fukuda M, González R, Suárez CF, Patarroyo MA, Vaiman D, Gris JC, Laissue P. Quintero-Ronderos P, et al. Among authors: vaiman d. PLoS One. 2017 Oct 10;12(10):e0186149. doi: 10.1371/journal.pone.0186149. eCollection 2017. PLoS One. 2017. PMID: 29016666 Free PMC article.

3

Polymorphisms of human placental alkaline phosphatase are associated with in vitro fertilization success and recurrent pregnancy loss.

Vatin M, Bouvier S, Bellazi L, Montagutelli X, Laissue P, Ziyyat A, Serres C, De Mazancourt P, Dieudonné MN, Mornet E, Vaiman D, Gris JC. Vatin M, et al. Among authors: vaiman d. Am J Pathol. 2014 Feb;184(2):362-8. doi: 10.1016/j.ajpath.2013.10.024. Epub 2013 Dec 2. Am J Pathol. 2014. PMID: 24296104

4

Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans.

Laissue P, Lakhal B, Vatin M, Batista F, Burgio G, Mercier E, Santos ED, Buffat C, Sierra-Diaz DC, Renault G, Montagutelli X, Salmon J, Monget P, Veitia RA, Méhats C, Fellous M, Gris JC, Cocquet J, Vaiman D. Laissue P, et al. Among authors: vaiman d. Open Biol. 2016 Oct;6(10):160109. doi: 10.1098/rsob.160109. Open Biol. 2016. PMID: 27805902 Free PMC article.

5

THBD sequence variants potentially related to recurrent pregnancy loss.

Quintero-Ronderos P, Mercier E, Gris JC, Esteban-Perez C, Moreno-Ortiz H, Fonseca DJ, Lucena E, Vaiman D, Laissue P. Quintero-Ronderos P, et al. Among authors: vaiman d. Reprod Biol Endocrinol. 2017 Dec 1;15(1):92. doi: 10.1186/s12958-017-0311-0. Reprod Biol Endocrinol. 2017. PMID: 29195508 Free PMC article.

6

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia.

Quintero-Ronderos P, Jiménez KM, Esteban-Pérez C, Ojeda DA, Bello S, Fonseca DJ, Coronel MA, Moreno-Ortiz H, Sierra-Díaz DC, Lucena E, Barbaux S, Vaiman D, Laissue P. Quintero-Ronderos P, et al. Among authors: vaiman d. Mol Med. 2019 Aug 8;25(1):37. doi: 10.1186/s10020-019-0104-3. Mol Med. 2019. PMID: 31395028 Free PMC article.

7

Re-evaluation of the role of STOX1 transcription factor in placental development and preeclampsia.

Rigourd V, Chelbi S, Chauvet C, Rebourcet R, Barbaux S, Bessières B, Mondon F, Mignot TM, Danan JL, Vaiman D. Rigourd V, et al. Among authors: vaiman d. J Reprod Immunol. 2009 Nov;82(2):174-81. doi: 10.1016/j.jri.2009.05.001. Epub 2009 Jul 3. J Reprod Immunol. 2009. PMID: 19577309 Review.

8

Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death.

Vatin M, Burgio G, Renault G, Laissue P, Firlej V, Mondon F, Montagutelli X, Vaiman D, Serres C, Ziyyat A. Vatin M, et al. Among authors: vaiman d. PLoS One. 2012;7(8):e43356. doi: 10.1371/journal.pone.0043356. Epub 2012 Aug 16. PLoS One. 2012. PMID: 22916247 Free PMC article.

9

Why preeclampsia still exists?

Chelbi ST, Veitia RA, Vaiman D. Chelbi ST, et al. Among authors: vaiman d. Med Hypotheses. 2013 Aug;81(2):259-63. doi: 10.1016/j.mehy.2013.04.034. Epub 2013 May 10. Med Hypotheses. 2013. PMID: 23669375

10

miR-34a expression, epigenetic regulation, and function in human placental diseases.

Doridot L, Houry D, Gaillard H, Chelbi ST, Barbaux S, Vaiman D. Doridot L, et al. Among authors: vaiman d. Epigenetics. 2014 Jan;9(1):142-51. doi: 10.4161/epi.26196. Epub 2013 Sep 30. Epigenetics. 2014. PMID: 24081307 Free PMC article.

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