USF1 c.*187C>T

Variant ID: 1-161009523-G-A

NM_007122.4(USF1):c.*187C>T

This variant was identified in 21 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: rs3737787
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Effects of USF1 SNPs and SNP-Environment Interactions on Serum Lipid Profiles and the Risk of Early-Onset Coronary Artery Disease in the Chinese Population.

Frontiers In Cardiovascular Medicine
Zheng, Peng-Fei PF; Chen, Lu-Zhu LZ; Pan, Hong-Wei HW; Liu, Peng P; Zheng, Zhao-Fen ZF
Publication Date: 2022

Variant appearance in text: rs3737787
PubMed Link: 35783856
Variant Present in the following documents:
  • Main text
  • fcvm-09-882728.pdf
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Homophilic Interaction Between Transmembrane-JAM-A and Soluble JAM-A Regulates Thrombo-Inflammation: Implications for Coronary Artery Disease.

Jacc. Basic To Translational Science
Rath, Dominik D; Rapp, Vera V; Schwartz, Jessica J; Winter, Stefan S; Emschermann, Frederic F; Arnold, Daniel D; Rheinlaender, Johannes J; Büttcher, Manuela M; Strebl, Michael M; Braun, Michael B MB; Altgelt, Konstanze K; Uribe, Álvaro Petersen ÁP; Schories, Christoph C; Canjuga, Denis D; Schaeffeler, Elke E; Borst, Oliver O; Schäffer, Tilman E TE; Langer, Harald H; Stehle, Thilo T; Schwab, Matthias M; Geisler, Tobias T; Gawaz, Meinrad M; Chatterjee, Madhumita M
Publication Date: 2022-05

Variant appearance in text: rs3737787
PubMed Link: 35663628
Variant Present in the following documents:
  • Main text
  • main.pdf
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Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: rs3737787
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Common Variants in 22 Genes Regulate Response to Metformin Intervention in Children with Obesity: A Pharmacogenetic Study of a Randomized Controlled Trial.

Journal Of Clinical Medicine
Anguita-Ruiz, Augusto A; Pastor-Villaescusa, Belén B; Leis, Rosaura R; Bueno, Gloria G; Hoyos, Raúl R; Vázquez-Cobela, Rocío R; Latorre-Millán, Miriam M; Cañete, M Dolores MD; Caballero-Villarraso, Javier J; Gil, Ángel Á; Cañete, Ramón R; Aguilera, Concepción M CM
Publication Date: 2019-09-16

Variant appearance in text: rs3737787
PubMed Link: 31527397
Variant Present in the following documents:
  • Main text
  • jcm-08-01471.pdf
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The rs2516839 Polymorphism of the USF1 Gene May Modulate Serum Triglyceride Levels in Response to Cigarette Smoking.

International Journal Of Molecular Sciences
Niemiec, Pawel P; Nowak, Tomasz T; Iwanicki, Tomasz T; Gorczynska-Kosiorz, Sylwia S; Balcerzyk, Anna A; Krauze, Jolanta J; Grzeszczak, Wladyslaw W; Wiecha, Maria M; Zak, Iwona I
Publication Date: 2015-06-10

Variant appearance in text: rs3737787
PubMed Link: 26068452
Variant Present in the following documents:
  • Main text
  • ijms-16-13203.pdf
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USF-1 genetic polymorphisms confer a high risk of nonalcoholic fatty liver disease in Chinese population.

International Journal Of Clinical And Experimental Medicine
Wang, Ying Y; Wang, Bai-Fang BF; Tong, Jing J; Chang, Bing B; Wang, Bing-Yuan BY
Publication Date: 2015

Variant appearance in text: rs3737787
PubMed Link: 25932200
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of coronary heart disease with reference to ApoAI-CIII-AIV gene region.

World Journal Of Cardiology
Agrawal, Suraksha S; Mastana, Sarabjit S
Publication Date: 2014-08-26

Variant appearance in text: rs3737787
PubMed Link: 25228954
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and environmental determinants of the susceptibility of Amerindian derived populations for having hypertriglyceridemia.

Metabolism: Clinical And Experimental
Aguilar-Salinas, Carlos A CA; Tusie-Luna, Teresa T; Pajukanta, Päivi P
Publication Date: 2014-07

Variant appearance in text: rs3737787
PubMed Link: 24768220
Variant Present in the following documents:
  • Main text
View BVdb publication page



Upstream Transcription Factor 1 (USF1) allelic variants regulate lipoprotein metabolism in women and USF1 expression in atherosclerotic plaque.

Scientific Reports
Fan, Yue-Mei YM; Hernesniemi, Jussi J; Oksala, Niku N; Levula, Mari M; Raitoharju, Emma E; Collings, Auni A; Hutri-Kähönen, Nina N; Juonala, Markus M; Marniemi, Jukka J; Lyytikäinen, Leo-Pekka LP; Seppälä, Ilkka I; Mennander, Ari A; Tarkka, Matti M; Kangas, Antti J AJ; Soininen, Pasi P; Salenius, Juha Pekka JP; Klopp, Norman N; Illig, Thomas T; Laitinen, Tomi T; Ala-Korpela, Mika M; Laaksonen, Reijo R; Viikari, Jorma J; Kähönen, Mika M; Raitakari, Olli T OT; Lehtimäki, Terho T
Publication Date: 2014-04-11

Variant appearance in text: rs3737787
PubMed Link: 24722012
Variant Present in the following documents:
  • Main text
View BVdb publication page



ChIP-seq in steatohepatitis and normal liver tissue identifies candidate disease mechanisms related to progression to cancer.

Bmc Medical Genomics
Bysani, Madhusudhan M; Wallerman, Ola O; Bornelöv, Susanne S; Zatloukal, Kurt K; Komorowski, Jan J; Wadelius, Claes C
Publication Date: 2013-11-08

Variant appearance in text: rs3737787
PubMed Link: 24206787
Variant Present in the following documents:
  • Main text
  • 1755-8794-6-50.pdf
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A Common Polymorphism of Upstream Transcription Factor 1 Gene is associated with Lipid Profile: A Study in Chinese Type 2 Diabetes Families.

International Journal Of Biomedical Science : Ijbs
Song, Yan Y; Li, Na N; He, Liu L; Xun, Tang T; Chen, Dafang D; Hu, Yonghua Y
Publication Date: 2009-09

Variant appearance in text: rs3737787
PubMed Link: 23675152
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic polymorphisms in LDLR, APOB, PCSK9 and other lipid related genes associated with familial hypercholesterolemia in Malaysia.

Plos One
Lye, Say-Hean SH; Chahil, Jagdish Kaur JK; Bagali, Pramod P; Alex, Livy L; Vadivelu, Jamunarani J; Ahmad, Wan Azman Wan WA; Chan, Siew-Pheng SP; Thong, Meow-Keong MK; Zain, Shamsul Mohd SM; Mohamed, Rosmawati R
Publication Date: 2013

Variant appearance in text: rs3737787
PubMed Link: 23593297
Variant Present in the following documents:
  • Main text
View BVdb publication page



Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

Bmc Medical Genetics
Huhn, Stefanie S; Bevier, Melanie M; Rudolph, Anja A; Pardini, Barbara B; Naccarati, Alessio A; Hein, Rebecca R; Hoffmeister, Michael M; Vodickova, Ludmila L; Novotny, Jan J; Brenner, Hermann H; Chang-Claude, Jenny J; Hemminki, Kari K; Vodicka, Pavel P; Försti, Asta A
Publication Date: 2012-10-05

Variant appearance in text: rs3737787
PubMed Link: 23036011
Variant Present in the following documents:
  • 1471-2350-13-94-S1.pdf
View BVdb publication page



Pathway-Targeted Pharmacogenomics of CYP1A2 in Human Liver.

Frontiers In Pharmacology
Klein, Kathrin K; Winter, Stefan S; Turpeinen, Miia M; Schwab, Matthias M; Zanger, Ulrich M UM
Publication Date: 2010

Variant appearance in text: rs3737787
PubMed Link: 21918647
Variant Present in the following documents:
  • Main text
  • fphar-01-00129.pdf
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Profile of participants and genotype distributions of 108 polymorphisms in a cross-sectional study of associations of genotypes with lifestyle and clinical factors: a project in the Japan Multi-Institutional Collaborative Cohort (J-MICC) Study.

Journal Of Epidemiology
Wakai, Kenji K; Hamajima, Nobuyuki N; Okada, Rieko R; Naito, Mariko M; Morita, Emi E; Hishida, Asahi A; Kawai, Sayo S; Nishio, Kazuko K; Yin, Guang G; Asai, Yatami Y; Matsuo, Keitaro K; Hosono, Satoyo S; Ito, Hidemi H; Watanabe, Miki M; Kawase, Takakazu T; Suzuki, Takeshi T; Tajima, Kazuo K; Tanaka, Keitaro K; Higaki, Yasuki Y; Hara, Megumi M; Imaizumi, Takeshi T; Taguchi, Naoto N; Nakamura, Kazuyo K; Nanri, Hinako H; Sakamoto, Tatsuhiko T; Horita, Mikako M; Shinchi, Koichi K; Kita, Yoshikuni Y; Turin, Tanvir Chowdhury TC; Rumana, Nahid N; Matsui, Kenji K; Miura, Katsuyuki K; Ueshima, Hirotsugu H; Takashima, Naoyuki N; Nakamura, Yasuyuki Y; Suzuki, Sadao S; Ando, Ryosuke R; Hosono, Akihiro A; Imaeda, Nahomi N; Shibata, Kiyoshi K; Goto, Chiho C; Hattori, Nami N; Fukatsu, Mitsuru M; Yamada, Tamaki T; Tokudome, Shinkan S; Takezaki, Toshiro T; Niimura, Hideshi H; Hirasada, Kazuyo K; Nakamura, Akihiko A; Tatebo, Masaya M; Ogawa, Shin S; Tsunematsu, Noriko N; Chiba, Shirabe S; Mikami, Haruo H; Kono, Suminori S; Ohnaka, Keizo K; Takayanagi, Ryoichi R; Watanabe, Yoshiyuki Y; Ozaki, Etsuko E; Shigeta, Masako M; Kuriyama, Nagato N; Yoshikawa, Aya A; Matsui, Daisuke D; Watanabe, Isao I; Inoue, Kaoru K; Ozasa, Kotaro K; Mitani, Satoko S; Arisawa, Kokichi K; Uemura, Hirokazu H; Hiyoshi, Mineyoshi M; Takami, Hidenobu H; Yamaguchi, Miwa M; Nakamoto, Mariko M; Takeda, Hideo H; Kubo, Michiaki M; Tanaka, Hideo H; ,
Publication Date: 2011

Variant appearance in text: rs3737787
PubMed Link: 21467728
Variant Present in the following documents:
  • Main text
  • je-21-223.pdf
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Gene-gene interaction between APOA5 and USF1: two candidate genes for the metabolic syndrome.

Obesity Facts
Singmann, Paula P; Baumert, Jens J; Herder, Christian C; Meisinger, Christa C; Holzapfel, Christina C; Klopp, Norman N; Wichmann, H-Erich HE; Klingenspor, Martin M; Rathmann, Wolfgang W; Illig, Thomas T; Grallert, Harald H
Publication Date: 2009

Variant appearance in text: rs3737787
PubMed Link: 20054229
Variant Present in the following documents:
  • Main text
View BVdb publication page



A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.

Plos Genetics
Plaisier, Christopher L CL; Horvath, Steve S; Huertas-Vazquez, Adriana A; Cruz-Bautista, Ivette I; Herrera, Miguel F MF; Tusie-Luna, Teresa T; Aguilar-Salinas, Carlos C; Pajukanta, Päivi P
Publication Date: 2009-09

Variant appearance in text: rs3737787
PubMed Link: 19750004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Body mass index is associated with USF1 haplotype in Korean premenopausal women.

Journal Of Korean Medical Science
Lee, Seong-Kyu SK; Kim, Hyun-Jin HJ; Kim, Byung-Joon BJ; Jo, Young-Suk YS; Park, Kang-Seo KS; Baik, Haing-Woon HW; Hyun, Sung Hee SH; Lee, Je Chul JC; Kim, Soon Ae SA
Publication Date: 2008-02

Variant appearance in text: rs3737787
PubMed Link: 18303204
Variant Present in the following documents:
  • Main text
  • jkms-23-83.pdf
View BVdb publication page



Association analysis of allelic variants of USF1 in coronary atherosclerosis.

Arteriosclerosis, Thrombosis, And Vascular Biology
Kristiansson, Kati K; Ilveskoski, Erkki E; Lehtimäki, Terho T; Peltonen, Leena L; Perola, Markus M; Karhunen, Pekka J PJ
Publication Date: 2008-05

Variant appearance in text: rs3737787
PubMed Link: 18276913
Variant Present in the following documents:
  • Main text
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Association testing in a linked region using large pedigrees.

American Journal Of Human Genetics
Cantor, Rita M RM; Chen, Gary K GK; Pajukanta, Päivi P; Lange, Kenneth K
Publication Date: 2005-03

Variant appearance in text: rs3737787
PubMed Link: 15657872
Variant Present in the following documents:
  • Main text
View BVdb publication page