These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

79 related articles for article (PubMed ID: 30321787)

  • 1. Importance of polymorphic variants of phosphatidylethanolamine N-methyltransferase (PEMT) gene in the etiology of intrauterine fetal death in the Polish population.
    Seremak-Mrozikiewicz A; Barlik M; Różycka A; Kurzawińska G; Klejewski A; Wolski H; Drews K
    Eur J Obstet Gynecol Reprod Biol; 2018 Dec; 231():43-47. PubMed ID: 30321787
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Polymorphic variants of genes involved in choline pathway and the risk of intrauterine fetal death.
    Drews K; Różycka A; Barlik M; Klejewski A; Kurzawińska G; Wolski H; Majchrzycki M; Gryszczyńska A; Kamiński A; Seremak-Mrozikiewicz A
    Ginekol Pol; 2017; 88(4):205-211. PubMed ID: 28509322
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A study of the PEMT gene in schizophrenia.
    Liu Y; Zhang H; Ju G; Zhang X; Xu Q; Liu S; Yu Y; Shi J; Boyle S; Wang Z; Shen Y; Wei J
    Neurosci Lett; 2007 Sep; 424(3):203-6. PubMed ID: 17720317
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Choline metabolic pathway gene polymorphisms and risk for Down syndrome: An association study in a population with folate-homocysteine metabolic impairment.
    Jaiswal SK; Sukla KK; Chauhan A; Lakhotia AR; Kumar A; Rai AK
    Eur J Clin Nutr; 2017 Jan; 71(1):45-50. PubMed ID: 27677362
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The phosphatidylethanolamine N-methyltransferase gene V175M single nucleotide polymorphism confers the susceptibility to NASH in Japanese population.
    Dong H; Wang J; Li C; Hirose A; Nozaki Y; Takahashi M; Ono M; Akisawa N; Iwasaki S; Saibara T; Onishi S
    J Hepatol; 2007 May; 46(5):915-20. PubMed ID: 17391797
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MTHFR genetic polymorphism and the risk of intrauterine fetal death in Polish women.
    Wolski H; Kurzawinska G; Drews K; Barlik M; Kadziolka P; Malewski Z; Mikolajska-Ptas P; Bylewski M; Seremak-Mrozikiewicz A
    Ginekol Pol; 2019; 90(2):76-81. PubMed ID: 30860273
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Polymorphic variants of folate and choline metabolism genes and the risk of endometriosis-associated infertility.
    Szczepańska M; Mostowska A; Wirstlein P; Lianeri M; Marianowski P; Skrzypczak J; Jagodziński PP
    Eur J Obstet Gynecol Reprod Biol; 2011 Jul; 157(1):67-72. PubMed ID: 21429654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Higher homocysteine and lower betaine increase the risk of microangiopathy in patients with diabetes mellitus carrying the GG genotype of PEMT G774C.
    Chen L; Chen YM; Wang LJ; Wei J; Tan YZ; Zhou JY; Yang Y; Chen YM; Ling WH; Zhu HL
    Diabetes Metab Res Rev; 2013 Nov; 29(8):607-17. PubMed ID: 23794489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.
    Mostowska A; Hozyasz KK; Biedziak B; Misiak J; Jagodzinski PP
    Eur J Oral Sci; 2010 Aug; 118(4):325-32. PubMed ID: 20662904
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PEMT rs12325817 and PCYT1A rs7639752 polymorphisms are associated with betaine but not choline concentrations in pregnant women.
    Chmurzynska A; Seremak-Mrozikiewicz A; Malinowska AM; Różycka A; Radziejewska A; Szwengiel A; Kurzawińska G; Barlik M; Jagodziński PP; Drews K
    Nutr Res; 2018 Aug; 56():61-70. PubMed ID: 30055775
    [TBL] [Abstract][Full Text] [Related]  

  • 11. No association of the rs4646396 SNP in the PEMT locus with schizophrenia in a Chinese case-control sample.
    Li H; Zhang H; Liu L; Ju G; Jin S; Ye L; Zhang X; Wei J
    Psychiatry Res; 2009 Sep; 169(2):176-7. PubMed ID: 19647326
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD).
    Song J; da Costa KA; Fischer LM; Kohlmeier M; Kwock L; Wang S; Zeisel SH
    FASEB J; 2005 Aug; 19(10):1266-71. PubMed ID: 16051693
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phosphatidylethanolamine N-methyltransferase and choline dehydrogenase gene polymorphisms are associated with human sperm concentration.
    Lazaros L; Xita N; Hatzi E; Kaponis A; Makrydimas G; Takenaka A; Sofikitis N; Stefos T; Zikopoulos K; Georgiou I
    Asian J Androl; 2012 Sep; 14(5):778-83. PubMed ID: 22387881
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Aberrant estrogen regulation of PEMT results in choline deficiency-associated liver dysfunction.
    Resseguie ME; da Costa KA; Galanko JA; Patel M; Davis IJ; Zeisel SH
    J Biol Chem; 2011 Jan; 286(2):1649-58. PubMed ID: 21059658
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phosphatidylethanolamine N-methyltransferase (PEMT) gene polymorphisms and risk of spina bifida.
    Zhang J; Zhu H; Yang W; Shaw GM; Lammer EJ; Finnell RH
    Am J Med Genet A; 2006 Apr; 140(7):785-9. PubMed ID: 16523512
    [No Abstract]   [Full Text] [Related]  

  • 16. Dietary Choline Intake during Pregnancy and PEMT rs7946 Polymorphism on Risk of Preterm Birth: A Case-Control Study.
    Zhu J; Liu YH; He XL; Kohlmeier M; Zhou LL; Shen LW; Yi XX; Tang QY; Cai W; Wang B
    Ann Nutr Metab; 2020; 76(6):431-440. PubMed ID: 33503637
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An Angiopoietin-2 gene polymorphism in unexplained intrauterine fetal death: a multi-center study.
    Huber A; Grimm C; Pietrowski D; Zeillinger R; Bettendorf H; Husslein P; Hefler L
    J Reprod Immunol; 2005 Feb; 65(1):47-53. PubMed ID: 15694966
    [TBL] [Abstract][Full Text] [Related]  

  • 18. TLR2 2258 G>A single nucleotide polymorphism and the risk of congenital infection with human cytomegalovirus.
    Wujcicka W; Paradowska E; Studzińska M; Wilczyński J; Nowakowska D
    Virol J; 2017 Jan; 14(1):12. PubMed ID: 28118851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An interleukin-6 gene promoter polymorphism and unexplained late intrauterine fetal death: a multicenter study.
    Huber A; Grimm C; Jirecek S; Zeillinger R; Heim K; Husslein P; Hefler L
    J Soc Gynecol Investig; 2005 Jan; 12(1):33-6. PubMed ID: 15629668
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphisms of microsomal triglyceride transfer protein gene and phosphatidylethanolamine N-methyltransferase gene in alcoholic and nonalcoholic fatty liver disease in Koreans.
    Jun DW; Han JH; Jang EC; Kim SH; Kim SH; Jo YJ; Park YS; Chae JD
    Eur J Gastroenterol Hepatol; 2009 Jun; 21(6):667-72. PubMed ID: 19262398
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.