Connection

IGNATIA VAN DEN VEYVER to Animals

This is a "connection" page, showing publications IGNATIA VAN DEN VEYVER has written about Animals.
Connection Strength

0.435
  1. Maternal loss of mouse Nlrp2 alters the transcriptome and DNA methylome in GV oocytes and impairs zygotic genome activation in embryos. Clin Epigenetics. 2025 Jun 03; 17(1):92.
    View in: PubMed
    Score: 0.053
  2. Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reprod Sci. 2023 09; 30(9):2780-2793.
    View in: PubMed
    Score: 0.046
  3. Take your mother's ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport. J Clin Invest. 2023 01 17; 133(2).
    View in: PubMed
    Score: 0.045
  4. Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect. Reprod Sci. 2021 07; 28(7):1850-1865.
    View in: PubMed
    Score: 0.039
  5. Maternal stress in Shank3ex4-9 mice increases pup-directed care and alters brain white matter in male offspring. PLoS One. 2019; 14(11):e0224876.
    View in: PubMed
    Score: 0.036
  6. Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming. Sci Rep. 2017 03 20; 7:44667.
    View in: PubMed
    Score: 0.030
  7. Chronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring. PLoS One. 2017; 12(1):e0170127.
    View in: PubMed
    Score: 0.030
  8. Deletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome). PLoS One. 2012; 7(3):e32331.
    View in: PubMed
    Score: 0.021
  9. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med Genet. 2006 Jul 21; 7:61.
    View in: PubMed
    Score: 0.014
  10. Tooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus. Calcif Tissue Int. 2005 Jul; 77(1):23-9.
    View in: PubMed
    Score: 0.013
  11. Lethal phenotypes in Mendelian disorders. Genet Med. 2024 Jul; 26(7):101141.
    View in: PubMed
    Score: 0.012
  12. Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome. Hum Mol Genet. 2002 Dec 01; 11(25):3237-48.
    View in: PubMed
    Score: 0.011
  13. Mendelian gene identification through mouse embryo viability screening. Genome Med. 2022 10 13; 14(1):119.
    View in: PubMed
    Score: 0.011
  14. Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders? Cytogenet Genome Res. 2002; 99(1-4):289-96.
    View in: PubMed
    Score: 0.011
  15. Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice. Mamm Genome. 2001 Oct; 12(10):796-8.
    View in: PubMed
    Score: 0.010
  16. The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies. J Soc Gynecol Investig. 2001 Sep-Oct; 8(5):305-13.
    View in: PubMed
    Score: 0.010
  17. Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles. Am J Hum Genet. 2018 11 01; 103(5):740-751.
    View in: PubMed
    Score: 0.008
  18. Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22. Genomics. 1998 Jul 15; 51(2):251-61.
    View in: PubMed
    Score: 0.008
  19. Prostaglandin synthetase inhibitors in pregnancy. Obstet Gynecol Surv. 1993 Jul; 48(7):493-502.
    View in: PubMed
    Score: 0.006
  20. Chronic maternal protein deprivation in mice is associated with overexpression of the cohesin-mediator complex in liver of their offspring. J Nutr. 2011 Dec; 141(12):2106-12.
    View in: PubMed
    Score: 0.005
  21. A NotI-EcoRV promoter library for studies of genetic and epigenetic alterations in mouse models of human malignancies. Genomics. 2004 Oct; 84(4):647-60.
    View in: PubMed
    Score: 0.003
  22. The product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole. Placenta. 2003 Sep-Oct; 24(8-9):835-42.
    View in: PubMed
    Score: 0.003
  23. A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. Mol Cell. 2003 Aug; 12(2):425-35.
    View in: PubMed
    Score: 0.003
  24. Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3. Genomics. 1999 Jul 01; 59(1):77-84.
    View in: PubMed
    Score: 0.002
  25. Iatrogenic gastroschisis decreases pulmonary hypoplasia in an ovine congenital diaphragmatic hernia model. Fetal Diagn Ther. 1995 Mar-Apr; 10(2):119-26.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.