185 related articles for article (PubMed ID: 30982978)
1. The lncRNA CCAT2 rs6983267 G allele is associated with decreased susceptibility to recurrent miscarriage.
Che D; Huang W; Fang Z; Li L; Wu H; Pi L; Zhou H; Xu Y; Fu L; Tan Y; Lu Z; Li Q; Gu X
J Cell Physiol; 2019 Nov; 234(11):20577-20583. PubMed ID: 30982978
[TBL] [Abstract][Full Text] [Related]
2. The
Wu Z; Liang Y; Zuo Y; Xu Y; Mai H; Pi L; Che D; Gu X
Infect Drug Resist; 2021; 14():2969-2976. PubMed ID: 34377001
[TBL] [Abstract][Full Text] [Related]
3. The lncRNA MALAT1 rs619586 G Variant Confers Decreased Susceptibility to Recurrent Miscarriage.
Che D; Yang Y; Xu Y; Fang Z; Pi L; Fu L; Zhou H; Tan Y; Lu Z; Li L; Liang Q; Xuan Q; Gu X
Front Physiol; 2019; 10():385. PubMed ID: 31024342
[TBL] [Abstract][Full Text] [Related]
4. Association between the rs2288947 polymorphism of the lncRNA TINCR gene and the risk of recurrent miscarriage in a Southern Chinese population.
Huang W; Zhou H; Pi L; Xu Y; Fu L; Yang Y; Che D; Gu X
J Clin Lab Anal; 2019 Jul; 33(6):e22919. PubMed ID: 31124188
[TBL] [Abstract][Full Text] [Related]
5. The lncRNA
Che D; Fang Z; Mai H; Xu Y; Fu L; Zhou H; Zhang L; Pi L; Gu X
J Inflamm Res; 2021; 14():2865-2872. PubMed ID: 34234511
[TBL] [Abstract][Full Text] [Related]
6. Association between the rs3802201 polymorphism of the lncRNA MIR2052HG gene and the risk of recurrent miscarriage in a Southern Chinese population.
Mai H; Cai C; Lin K; Zhang L; Wang Y; He M; Qu Y; Xu Y; Fu L; Pi L; Zhou H; Zeng D; Che D; Zuo L
J Clin Lab Anal; 2022 Jan; 36(1):e24167. PubMed ID: 34910326
[TBL] [Abstract][Full Text] [Related]
7. The
Che D; Fang Z; Pi L; Xu Y; Fu L; Zhou H; Gu X
Int J Womens Health; 2021; 13():111-117. PubMed ID: 33500667
[TBL] [Abstract][Full Text] [Related]
8. The lncRNA SOX2OT rs9839776 C>T Polymorphism Indicates Recurrent Miscarriage Susceptibility in a Southern Chinese Population.
Fang Z; Che D; Qing S; Li Q; Men H; Yuan L; Li L; Gu X
Mediators Inflamm; 2019; 2019():9684703. PubMed ID: 31827385
[TBL] [Abstract][Full Text] [Related]
9. Association of well-characterized lung cancer lncRNA polymorphisms with lung cancer susceptibility and platinum-based chemotherapy response.
Gong WJ; Yin JY; Li XP; Fang C; Xiao D; Zhang W; Zhou HH; Li X; Liu ZQ
Tumour Biol; 2016 Jun; 37(6):8349-58. PubMed ID: 26729200
[TBL] [Abstract][Full Text] [Related]
10. Association between TNF, IL1B, IL6, IL10 and IFNG polymorphisms and recurrent miscarriage: a case control study.
Ma J; Zhang X; He G; Yang C
Reprod Biol Endocrinol; 2017 Oct; 15(1):83. PubMed ID: 29017513
[TBL] [Abstract][Full Text] [Related]
11. Association of lncRNA
Wu ER; Hsieh MJ; Chiang WL; Hsueh KC; Yang SF; Su SC
Int J Environ Res Public Health; 2019 Aug; 16(16):. PubMed ID: 31398859
[TBL] [Abstract][Full Text] [Related]
12. LncRNA PRNCR1 rs1456315 and CCAT2 rs6983267 Polymorphisms on 8q24 Associated with Lung Cancer.
Yu WL; Yao JJ; Xie ZZ; Huang YJ; Xiao S
Int J Gen Med; 2021; 14():255-266. PubMed ID: 33542645
[TBL] [Abstract][Full Text] [Related]
13. Association of rs6983267 at 8q24, HULC rs7763881 polymorphisms and serum lncRNAs CCAT2 and HULC with colorectal cancer in Egyptian patients.
Shaker OG; Senousy MA; Elbaz EM
Sci Rep; 2017 Nov; 7(1):16246. PubMed ID: 29176650
[TBL] [Abstract][Full Text] [Related]
14. Prolactin receptor gene polymorphism and the risk of recurrent pregnancy loss: a case-control study.
Kim JJ; Choi YM; Lee SK; Yang KM; Paik EC; Jeong HJ; Jun JK; Han AR; Hwang KR; Hong MA
J Obstet Gynaecol; 2018 Feb; 38(2):261-264. PubMed ID: 28980840
[TBL] [Abstract][Full Text] [Related]
15. The Expression of CCAT2, a Novel Long Noncoding RNA Transcript, and rs6983267 Single-Nucleotide Polymorphism Genotypes in Colorectal Cancers.
Kasagi Y; Oki E; Ando K; Ito S; Iguchi T; Sugiyama M; Nakashima Y; Ohgaki K; Saeki H; Mimori K; Maehara Y
Oncology; 2017; 92(1):48-54. PubMed ID: 27875818
[TBL] [Abstract][Full Text] [Related]
16. Investigating the association between rs6983267 polymorphism and susceptibility to gastrointestinal cancers in Iranian population.
Karimi F; Amiri-Moghaddam SM; Bagheri Z; Bahrami AR; Goshayeshi L; Allahyari A; Mirsadraee M; Fanipakdel A; Bari A; Emadi-Torghabeh A; Kerachian MA; Rahimi H; Matin MM
Mol Biol Rep; 2021 Mar; 48(3):2273-2284. PubMed ID: 33713253
[TBL] [Abstract][Full Text] [Related]
17. Association of the A/G polymorphism at position 49 in exon 1 of CTLA-4 with the susceptibility to unexplained recurrent spontaneous abortion in the Chinese population.
Wang X; Lin Q; Ma Z; Hong Y; Zhao A; Di W; Lu P
Am J Reprod Immunol; 2005 Feb; 53(2):100-5. PubMed ID: 15790344
[TBL] [Abstract][Full Text] [Related]
18. Lower frequency of the HLA-G UTR-4 haplotype in women with unexplained recurrent miscarriage.
Meuleman T; Drabbels J; van Lith JMM; Dekkers OM; Rozemuller E; Cretu-Stancu M; Claas FHJ; Bloemenkamp KWM; Eikmans M
J Reprod Immunol; 2018 Apr; 126():46-52. PubMed ID: 29481987
[TBL] [Abstract][Full Text] [Related]
19. Interleukin 1 receptor antagonist polymorphism in women with idiopathic recurrent miscarriage.
Unfried G; Tempfer C; Schneeberger C; Widmar B; Nagele F; Huber JC
Fertil Steril; 2001 Apr; 75(4):683-7. PubMed ID: 11287019
[TBL] [Abstract][Full Text] [Related]
20. The obesity-related FTO gene variant associates with the risk of recurrent miscarriage.
Andraweera PH; Dekker GA; Jayasekara RW; Dissanayake VHW; Roberts CT
Acta Obstet Gynecol Scand; 2015 Jul; 94(7):722-726. PubMed ID: 25845303
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
