Connection

ROBERT CABRERA to Humans

This is a "connection" page, showing publications ROBERT CABRERA has written about Humans.
Connection Strength

0.170
  1. Dolutegravir-induced neural tube defects in mice are folate responsive. AIDS. 2024 03 15; 38(4):439-446.
    View in: PubMed
    Score: 0.024
  2. The teratogenic effects of sertraline in mice. Birth Defects Res. 2020 08; 112(13):1014-1024.
    View in: PubMed
    Score: 0.018
  3. The antagonism of folate receptor by dolutegravir: developmental toxicity reduction by supplemental folic acid. AIDS. 2019 11 01; 33(13):1967-1976.
    View in: PubMed
    Score: 0.018
  4. Impact of selective serotonin reuptake inhibitors on neural crest stem cell formation. Toxicol Lett. 2017 Nov 05; 281:20-25.
    View in: PubMed
    Score: 0.015
  5. Transcriptional analyses of two mouse models of spina bifida. Birth Defects Res A Clin Mol Teratol. 2012 Oct; 94(10):782-9.
    View in: PubMed
    Score: 0.011
  6. Autoantibodies to folate receptor during pregnancy and neural tube defect risk. J Reprod Immunol. 2008 Oct; 79(1):85-92.
    View in: PubMed
    Score: 0.008
  7. Investigations into the etiology of neural tube defects. Birth Defects Res C Embryo Today. 2004 Dec; 72(4):330-44.
    View in: PubMed
    Score: 0.006
  8. CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
    View in: PubMed
    Score: 0.005
  9. Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects. Epigenetics. 2022 Jan-Feb; 17(2):133-146.
    View in: PubMed
    Score: 0.005
  10. FKBP8 variants are risk factors for spina bifida. Hum Mol Genet. 2020 11 04; 29(18):3132-3144.
    View in: PubMed
    Score: 0.005
  11. CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression. J Med Genet. 2021 07; 58(7):484-494.
    View in: PubMed
    Score: 0.005
  12. Approaches to studying the genomic architecture of complex birth defects. Prenat Diagn. 2020 08; 40(9):1047-1055.
    View in: PubMed
    Score: 0.005
  13. Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida. Hum Mutat. 2020 04; 41(4):786-799.
    View in: PubMed
    Score: 0.005
  14. Hepatic Tumor Formation in Adult Mice Developmentally Exposed to Organotin. Environ Health Perspect. 2020 01; 128(1):17010.
    View in: PubMed
    Score: 0.005
  15. Gene variants in the folate pathway are associated with increased levels of folate receptor autoantibodies. Birth Defects Res. 2018 07 17; 110(12):973-981.
    View in: PubMed
    Score: 0.004
  16. Formate rescues neural tube defects caused by mutations in Slc25a32. Proc Natl Acad Sci U S A. 2018 05 01; 115(18):4690-4695.
    View in: PubMed
    Score: 0.004
  17. Levels of folate receptor autoantibodies in maternal and cord blood and risk of neural tube defects in a Chinese population. Birth Defects Res A Clin Mol Teratol. 2016 Aug; 106(8):685-95.
    View in: PubMed
    Score: 0.004
  18. Autoantibodies against homocysteinylated protein in a mouse model of folate deficiency-induced neural tube defects. Birth Defects Res A Clin Mol Teratol. 2016 Mar; 106(3):201-7.
    View in: PubMed
    Score: 0.003
  19. The transcobalamin receptor knockout mouse: a model for vitamin B12 deficiency in the central nervous system. FASEB J. 2013 Jun; 27(6):2468-75.
    View in: PubMed
    Score: 0.003
  20. Glycerol-3-phosphate acyltransferase-1 gene ablation results in altered thymocyte lipid content and reduces thymic T cell production in mice. Lipids. 2013 Jan; 48(1):3-12.
    View in: PubMed
    Score: 0.003
  21. Overexpression of the CHRNA5/A3/B4 genomic cluster in mice increases the sensitivity to nicotine and modifies its reinforcing effects. Amino Acids. 2012 Aug; 43(2):897-909.
    View in: PubMed
    Score: 0.003
  22. Association between inhibited binding of folic acid to folate receptor alpha in maternal serum and folate-related birth defects in Norway. Hum Reprod. 2011 Aug; 26(8):2232-8.
    View in: PubMed
    Score: 0.003
  23. A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency. Blood. 2011 May 05; 117(18):4895-904.
    View in: PubMed
    Score: 0.002
  24. Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in Denmark. Pediatr Res. 2010 Mar; 67(3):274-9.
    View in: PubMed
    Score: 0.002
  25. Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in mice. FASEB J. 2009 Jun; 23(6):1721-7.
    View in: PubMed
    Score: 0.002
  26. Valproic acid-induced skeletal malformations: associated gene expression cascades. Pharmacogenet Genomics. 2005 Nov; 15(11):787-800.
    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.