SERPINE1 c.506-407A>G

Variant ID: 7-100774749-A-G

NM_000602.4(SERPINE1):c.506-407A>G

This variant was identified in 14 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs2227667
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
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Serpin Family E Member 1 Tag Single-Nucleotide Polymorphisms in Patients with Diabetic Nephropathy: An Association Study and Meta-Analysis Using a Genetic Model-Free Approach.

Genes
Tziastoudi, Maria M; Dardiotis, Efthimios E; Pissas, Georgios G; Filippidis, Georgios G; Golfinopoulos, Spyridon S; Siokas, Vasileios V; Tachmitzi, Sophia V SV; Eleftheriadis, Theodoros T; Hadjigeorgiou, Georgios M GM; Tsironi, Evangelia E; Stefanidis, Ioannis I
Publication Date: 2021-11-25

Variant appearance in text: rs2227667
PubMed Link: 34946835
Variant Present in the following documents:
  • Main text
  • genes-12-01887.pdf
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Serpin Family E Member 1 Tag Single-Nucleotide Polymorphisms in Patients with Diabetic Nephropathy: An Association Study and Meta-Analysis Using a Genetic Model-Free Approach.

Genes
Tziastoudi, Maria M; Dardiotis, Efthimios E; Pissas, Georgios G; Filippidis, Georgios G; Golfinopoulos, Spyridon S; Siokas, Vasileios V; Tachmitzi, Sophia V SV; Eleftheriadis, Theodoros T; Hadjigeorgiou, Georgios M GM; Tsironi, Evangelia E; Stefanidis, Ioannis I
Publication Date: 2021-11-25

Variant appearance in text: rs2227667
PubMed Link: 34946835
Variant Present in the following documents:
  • Main text
  • genes-12-01887.pdf
View BVdb publication page



PAI-1 Polymorphisms Have Significant Associations With Cancer Risk, Especially Feminine Cancer.

Technology In Cancer Research & Treatment
Wang, Jiaxi J; Peng, Yuanyuan Y; Guo, Hejia H; Li, Cuiping C
Publication Date: 2021

Variant appearance in text: rs2227667
PubMed Link: 34521295
Variant Present in the following documents:
  • Main text
  • 10.1177_15330338211037813.pdf
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Association of plasminogen activator inhibitor-1 4G5G Polymorphism with risk of diabetic nephropathy and retinopathy: a systematic review and meta-analysis.

Journal Of Diabetes And Metabolic Disorders
Dastgheib, Seyed Alireza SA; Najafi, Farzaneh F; Shajari, Ahmad A; Bahrami, Reza R; Asadian, Fatemeh F; Sadeghizadeh-Yazdi, Jalal J; Akbarian, Elahe E; Emarati, Seyed Alireza SA; Neamatzadeh, Hossein H
Publication Date: 2020-12

Variant appearance in text: rs2227667
PubMed Link: 33520873
Variant Present in the following documents:
  • Main text
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Interacting hepatic PAI-1/tPA gene regulatory pathways influence impaired fibrinolysis severity in obesity.

The Journal Of Clinical Investigation
Zheng, Ze Z; Nakamura, Keiko K; Gershbaum, Shana S; Wang, Xiaobo X; Thomas, Sherry S; Bessler, Marc M; Schrope, Beth B; Krikhely, Abraham A; Liu, Rui-Ming RM; Ozcan, Lale L; López, José A JA; Tabas, Ira I
Publication Date: 2020-08-03

Variant appearance in text: rs2227667
PubMed Link: 32657780
Variant Present in the following documents:
  • Main text
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Association between Five Common Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms and Colorectal Cancer Susceptibility.

International Journal Of Molecular Sciences
Oh, Jisu J; An, Hui Jeong HJ; Kim, Jung Oh JO; Jun, Hak Hoon HH; Kim, Woo Ram WR; Kim, Eo Jin EJ; Oh, Doyeun D; Kim, Jong Woo JW; Kim, Nam Keun NK
Publication Date: 2020-06-18

Variant appearance in text: rs2227667
PubMed Link: 32570732
Variant Present in the following documents:
  • Main text
  • ijms-21-04334.pdf
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Genetic variants in the plasminogen activator inhibitor-1 gene are associated with an increased risk of radiation pneumonitis in lung cancer patients.

Cancer Medicine
Liu, Bo B; Tang, Yang Y; Yi, Minxiao M; Liu, Qingxu Q; Xiong, Huihua H; Hu, Guangyuan G; Yuan, Xianglin X
Publication Date: 2017-03

Variant appearance in text: rs2227667
PubMed Link: 28211612
Variant Present in the following documents:
  • Main text
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Association of Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms with Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women.

International Journal Of Molecular Sciences
Kim, Jung Oh JO; Han, Soo Hong SH; Lee, Yeon Ho YH; Ahn, Tae Keun TK; Lim, Jae Joon JJ; Chung, Young Sun YS; Shin, Dong Eun DE; Lee, Woo Sik WS; Han, In Bo IB; Kim, Nam Keun NK
Publication Date: 2016-12-09

Variant appearance in text: rs2227667
PubMed Link: 27941685
Variant Present in the following documents:
  • Main text
  • ijms-17-02062.pdf
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Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

Arteriosclerosis, Thrombosis, And Vascular Biology
Huang, Jie J; Huffman, Jennifer E JE; Yamakuchi, Munekazu M; Yamkauchi, Munekazu M; Trompet, Stella S; Asselbergs, Folkert W FW; Sabater-Lleal, Maria M; Trégouët, David-Alexandre DA; Chen, Wei-Min WM; Smith, Nicholas L NL; Kleber, Marcus E ME; Shin, So-Youn SY; Becker, Diane M DM; Tang, Weihong W; Dehghan, Abbas A; Johnson, Andrew D AD; Truong, Vinh V; Folkersen, Lasse L; Yang, Qiong Q; Oudot-Mellkah, Tiphaine T; Buckley, Brendan M BM; Moore, Jason H JH; Williams, Frances M K FM; Campbell, Harry H; Silbernagel, Günther G; Vitart, Veronique V; Rudan, Igor I; Tofler, Geoffrey H GH; Navis, Gerjan J GJ; Destefano, Anita A; Wright, Alan F AF; Chen, Ming-Huei MH; de Craen, Anton J M AJ; Worrall, Bradford B BB; Rudnicka, Alicja R AR; Rumley, Ann A; Bookman, Ebony B EB; Psaty, Bruce M BM; Chen, Fang F; Keene, Keith L KL; Franco, Oscar H OH; Böhm, Bernhard O BO; Uitterlinden, Andre G AG; Carter, Angela M AM; Jukema, J Wouter JW; Sattar, Naveed N; Bis, Joshua C JC; Ikram, Mohammad A MA; , ; Sale, Michèle M MM; McKnight, Barbara B; Fornage, Myriam M; Ford, Ian I; Taylor, Kent K; Slagboom, P Eline PE; McArdle, Wendy L WL; Hsu, Fang-Chi FC; Franco-Cereceda, Anders A; Goodall, Alison H AH; Yanek, Lisa R LR; Furie, Karen L KL; Cushman, Mary M; Hofman, Albert A; Witteman, Jacqueline C M JC; Folsom, Aaron R AR; Basu, Saonli S; Matijevic, Nena N; van Gilst, Wiek H WH; Wilson, James F JF; Westendorp, Rudi G J RG; Kathiresan, Sekar S; Reilly, Muredach P MP; , ; Tracy, Russell P RP; Polasek, Ozren O; Winkelmann, Bernhard R BR; Grant, Peter J PJ; Hillege, Hans L HL; Cambien, Francois F; Stott, David J DJ; Lowe, Gordon D GD; Spector, Timothy D TD; Meigs, James B JB; Marz, Winfried W; Eriksson, Per P; Becker, Lewis C LC; Morange, Pierre-Emmanuel PE; Soranzo, Nicole N; Williams, Scott M SM; Hayward, Caroline C; van der Harst, Pim P; Hamsten, Anders A; Lowenstein, Charles J CJ; Strachan, David P DP; O'Donnell, Christopher J CJ; ,
Publication Date: 2014-05

Variant appearance in text: rs2227667
PubMed Link: 24578379
Variant Present in the following documents:
  • Main text
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Familial monoclonal gammopathy of undetermined significance and multiple myeloma: epidemiology, risk factors, and biological characteristics.

Blood
Greenberg, Alexandra J AJ; Rajkumar, S Vincent SV; Vachon, Celine M CM
Publication Date: 2012-06-07

Variant appearance in text: rs2227667
PubMed Link: 22354002
Variant Present in the following documents:
  • Main text
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Variation in innate immunity genes and risk of multiple myeloma.

Hematological Oncology
Purdue, Mark P MP; Lan, Qing Q; Menashe, Idan I; Zheng, Tongzhang T; Zhang, Yawei Y; Yeager, Meredith M; Hosgood, H Dean HD; Zahm, Shelia H SH; Chanock, Stephen J SJ; Rothman, Nathaniel N; Baris, Dalsu D
Publication Date: 2011-03

Variant appearance in text: rs2227667
PubMed Link: 20658475
Variant Present in the following documents:
  • Main text
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SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

Molecular Vision
Kondo, Naoshi N; Bessho, Hiroaki H; Honda, Shigeru S; Negi, Akira A
Publication Date: 2009-09-09

Variant appearance in text: rs2227667
PubMed Link: 19753309
Variant Present in the following documents:
  • Main text
  • mv-v15-1819.pdf
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Replication of findings on the association of genetic variation in 24 hemostasis genes and risk of incident venous thrombosis.

Journal Of Thrombosis And Haemostasis : Jth
Smith, N L NL; Wiggins, K L KL; Reiner, A P AP; Lange, L A LA; Cushman, M M; Heckbert, S R SR; Lumley, T T; Rice, K M KM; Folsom, A R AR; Psaty, B M BM
Publication Date: 2009-10

Variant appearance in text: rs2227667
PubMed Link: 19682239
Variant Present in the following documents:
  • Main text
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Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

Molecular Vision
Bessho, Hiroaki H; Kondo, Naoshi N; Honda, Shigeru S; Kuno, Shin-ichi S; Negi, Akira A
Publication Date: 2009-06-02

Variant appearance in text: rs2227667
PubMed Link: 19503741
Variant Present in the following documents:
  • Main text
View BVdb publication page