Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 35 Records) |
Query Trace: PLG[original query] |
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Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.
European heart journal 2012 Feb 33 (3): 325-34. Qi Qibin, Workalemahu Tsegaselassie, Zhang Cuilin, Hu Frank B, Qi |
Genetic analysis of genes involved in amyloid-ß degradation and clearance in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2012 28 (3): 553-9. Natunen Teemu, Helisalmi Seppo, Vepsäläinen Saila, Sarajärvi Timo, Antikainen Leila, Mäkinen Petra, Herukka Sanna-Kaisa, Koivisto Anne Maria, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
Fibrinolysis alterations in infertile women during controlled ovarian stimulation: influence of BMI and genetic components. Thrombosis research 2012 Jul . Sticchi E, Romagnuolo I, Cellai AP, Lami D, Fedi S, Prisco D, Noci I, Abbate R, Fatini C |
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels.
Blood 2014 Nov 124 (20): 3155-64. Ma Qianyi, Ozel Ayse B, Ramdas Shweta, McGee Beth, Khoriaty Rami, Siemieniak David, Li Hong-Dong, Guan Yuanfang, Brody Lawrence C, Mills James L, Molloy Anne M, Ginsburg David, Li Jun Z, Desch Karl |
Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis. Circulation. Cardiovascular genetics 2015 Feb 8 (1): 159-67. Schaefer Arne S, Bochenek Gregor, Jochens Arne, Ellinghaus David, Dommisch Henrik, Güzeldemir-Akçakanat Esra, Graetz Christian, Harks Inga, Jockel-Schneider Yvonne, Weinspach Knut, Meyle Joerg, Eickholz Peter, Linden Gerry J, Cine Naci, Nohutcu Rahime, Weiss Ervin, Houri-Haddad Yael, Iraqi Fuad, Folwaczny Mathias, Noack Barbara, Strauch Konstantin, Gieger Christian, Waldenberger Melanie, Peters Annette, Wijmenga Cisca, Yilmaz Engin, Lieb Wolfgang, Rosenstiel Philip, Doerfer Christof, Bruckmann Corinna, Erdmann Jeannette, König Inke, Jepsen Søren, Loos Bruno G, Schreiber Stef |
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Sep . Dönmez-Demir Buket, Celkan Tiraje, Sarper Nazan, Deda Gülhis, ?nce Elif, Çal?kan Ümran, Öztürk Gülyüz, Karagün Barbaros, Küpesiz Alphan, Tokgöz Hüseyin, Akar Nejat, Özda? Hil |
Risk Factors for Thrombosis Development in Mexican Patients. Annals of vascular surgery 2015 Aug . Zavala-Hernández César, Hernández-Zamora Edgar, Martínez-Murillo Carlos, Majluf-Cruz Abraham, Vela-Ojeda Jorge, García-Chávez Jaime, Reyes-Maldonado El |
[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Jun 32 (3): 331-4. Wang Yingyu, Ding Hongxiang, Hao Xiuping, Zhu Liqing, Yang Lihong, Jin Yanhui, Wang Mingsh |
No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome. International journal of hematology 2016 Aug 104 (2): 223-7. Miyata Toshiyuki, Uchida Yumiko, Yoshida Yoko, Kato Hideki, Matsumoto Masanori, Kokame Koichi, Fujimura Yoshihiro, Nangaku Masao |
Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations. Clinical and experimental nephrology 2017 9 22 (3): 653-660. Thergaonkar R W, Narang Ankita, Gurjar Bahadur Singh, Tiwari Pradeep, Puraswani Mamta, Saini Himanshi, Sinha Aditi, Varma Binuja, Mukerji Mitali, Hari Pankaj, Bagga Arvi |
Rare coding variants pinpoint genes that control human hematological traits. PLoS genetics 2017 Aug 13 (8): e1006925. Mousas Abdou, Ntritsos Georgios, Chen Ming-Huei, Song Ci, Huffman Jennifer E, Tzoulaki Ioanna, Elliott Paul, Psaty Bruce M, , Auer Paul L, Johnson Andrew D, Evangelou Evangelos, Lettre Guillaume, Reiner Alexander |
A haplotype block downstream of plasminogen is associated with chronic and aggressive periodontitis. Journal of clinical periodontology 2017 May . Munz Matthias, Chen Hong, Jockel-Schneider Yvonne, Adam Knut, Hoffman Per, Berger Klaus, Kocher Thomas, Meyle Jörg, Eickholz Peter, Doerfer Christof, Laudes Matthias, Uitterlinden André, Lieb Wolfgang, Franke Andre, Schreiber Stefan, Offenbacher Steven, Divaris Kimon, Bruckmann Corinna, Loos Bruno G, Jepsen Soeren, Dommisch Henrik, Schaefer Arne |
Validation of single nucleotide polymorphisms in invasive aspergillosis following hematopoietic cell transplantation. Blood 2017 Mar . Fisher Cynthia E, Hohl Tobias M, Fan Wenhong, Storer Barry E, Levine David M, Zhao Lu Ping, Martin Paul J, Warren Edus H, Boeckh Michael, Hansen John |
A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis.
American journal of human genetics 2017 Jan 100 (1): 64-74. Carmona F David, Vaglio Augusto, Mackie Sarah L, Hernández-Rodríguez José, Monach Paul A, Castañeda Santos, Solans Roser, Morado Inmaculada C, Narváez Javier, Ramentol-Sintas Marc, Pease Colin T, Dasgupta Bhaskar, Watts Richard, Khalidi Nader, Langford Carol A, Ytterberg Steven, Boiardi Luigi, Beretta Lorenzo, Govoni Marcello, Emmi Giacomo, Bonatti Francesco, Cimmino Marco A, Witte Torsten, Neumann Thomas, Holle Julia, Schönau Verena, Sailler Laurent, Papo Thomas, Haroche Julien, Mahr Alfred, Mouthon Luc, Molberg Øyvind, Diamantopoulos Andreas P, Voskuyl Alexandre, Brouwer Elisabeth, Daikeler Thomas, Berger Christoph T, Molloy Eamonn S, O'Neill Lorraine, Blockmans Daniel, Lie Benedicte A, Mclaren Paul, Vyse Timothy J, Wijmenga Cisca, Allanore Yannick, Koeleman Bobby P C, , , , Barrett Jennifer H, Cid María C, Salvarani Carlo, Merkel Peter A, Morgan Ann W, González-Gay Miguel A, Martín Javi |
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins. Circulation 2018 Oct 138 (17): 1839-1849. Wei Wei-Qi, Li Xiaohui, Feng Qiping, Kubo Michiaki, Kullo Iftikhar J, Peissig Peggy L, Karlson Elizabeth W, Jarvik Gail P, Lee Ming Ta Michael, Shang Ning, Larson Eric A, Edwards Todd, Shaffer Christian M, Mosley Jonathan D, Maeda Shiro, Horikoshi Momoko, Ritchie Marylyn, Williams Marc S, Larson Eric B, Crosslin David R, Bland Sarah T, Pacheco Jennifer A, Rasmussen-Torvik Laura J, Cronkite David, Hripcsak George, Cox Nancy J, Wilke Russell A, Stein C Michael, Rotter Jerome I, Momozawa Yukihide, Roden Dan M, Krauss Ronald M, Denny Joshua |
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. Journal of immunology (Baltimore, Md. : 1950) 2018 3 200 (7): 2464-2478. Osborne Amy J, Breno Matteo, Borsa Nicolo Ghiringhelli, Bu Fengxiao, Frémeaux-Bacchi Véronique, Gale Daniel P, van den Heuvel Lambertus P, Kavanagh David, Noris Marina, Pinto Sheila, Rallapalli Pavithra M, Remuzzi Giuseppe, Rodríguez de Cordoba Santiago, Ruiz Angela, Smith Richard J H, Vieira-Martins Paula, Volokhina Elena, Wilson Valerie, Goodship Timothy H J, Perkins Stephen |
Genotype-first analysis of a generally healthy population cohort supports genetic testing for diagnosis of hereditary angioedema of unknown cause. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2019 5 15 32. Bodian Dale L, Vilboux Thierry, Hauser Natalie |
Angiotensin-Converting Enzyme Inhibitor-Associated Angioedema: From Bed to Bench. Journal of investigational allergology & clinical immunology 2019 10 30 (4): 272-280. Carucci L, Bova M, Petraroli A, Ferrara A L, Sutic A, de Crescenzo G, Cordisco G, Margaglione M, Gambardella J, Spadaro G, Genovese A, Loffredo |
Multi-omic studies on missense PLG variants in families with otitis media. Scientific reports 2020 Sep 10 (1): 15035. Bootpetch Tori C, Hafrén Lena, Elling Christina L, Baschal Erin E, Manichaikul Ani W, Pine Harold S, Szeremeta Wasyl, Scholes Melissa A, Cass Stephen P, Larson Eric D, Chan Kenny H, Ishaq Rafaqat, Prager Jeremy D, Shaikh Rehan S, Gubbels Samuel P, Yousaf Ayesha, , Wine Todd M, Bamshad Michael J, Yoon Patricia J, Jenkins Herman A, Nickerson Deborah A, Streubel Sven-Olrik, Friedman Norman R, Frank Daniel N, Einarsdottir Elisabet, Kere Juha, Riazuddin Saima, Daly Kathleen A, Leal Suzanne M, Ryan Allen F, Mattila Petri S, Ahmed Zubair M, Sale Michele M, Chonmaitree Tasnee, Santos-Cortez Regie Lyn |
Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population. Disease markers 2020 2020 9738567. Cheema Asma Naseer, Pirim Dilek, Wang Xingbin, Ali Jabar, Bhatti Attya, John Peter, Feingold Eleanor, Demirci F Yesim, Kamboh M Ily |
Study of angiopoietin and plasminogen genes in hereditary angioedema. Revista da Associacao Medica Brasileira (1992) 2020 6 66 (4): 502-506. Kruk Tatielly, Chong-Neto Herberto José, Dias Marina Mendonça, Campos Wagner Narciso, Moreno Adriana Santos, Mikami Liya Regina, Ferrari Lilian Pereira, Arruda Luísa Karla de Paula, Rosário Filho Nels |
Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients. Allergy 2020 3 75 (8): 2099-2102. Parsopoulou Faidra, Charignon Delphine, Tengo Maud, Psarros Fotis, Maas Coen, Gonzalez-Quevedo Teresa, Drouet Christian, Germenis Anastasios E, Ghannam Ari |
Distinct genetic profile with recurrent population-specific missense variants in Korean adult atypical hemolytic uremic syndrome. Thrombosis research 2020 11 194 45-53. Yun Jae Won, Oh Jisu, Lee Ki-O, Lee Seon Ju, Kim Jung Oh, Kim Nam Keun, Kim Jin Seok, Koh Youngil, Yoon Sung-Soo, Yhim Ho-Young, Jo Sang-Kyung, Park Yong, Lee Jung Eun, Park Jinny, Lee Jong Wook, Kim Sun-Hee, Kim Hee-Jin, Oh Doyeun, , |
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor. Journal of clinical medicine 2020 10 9 (11): . Loules Gedeon, Parsopoulou Faidra, Zamanakou Maria, Csuka Dorottya, Bova Maria, González-Quevedo Teresa, Psarros Fotis, Porebski Gregor, Speletas Matthaios, Firinu Davide, Del Giacco Stefano, Suffritti Chiara, Makris Michael, Vatsiou Sofia, Zanichelli Andrea, Farkas Henriette, Germenis Anastasios |
Plasminogen gene polymorphisms [c.924C>T and IVS 8+14 G>A] in periodontitis and familial Mediterranean fever: A case-control study. Journal of periodontal research 2021 12 57 (2): 371-380. Fento?lu Özlem, Tülüceo?lu Eda Evgen, Orhan Hikm |
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. Frontiers in genetics 2022 8 13 914376. Mathey Carina M, Maj Carlo, Scheer Annika B, Fazaal Julia, Wedi Bettina, Wieczorek Dorothea, Amann Philipp M, Löffler Harald, Koch Lukas, Schöffl Clemens, Dickel Heinrich, Ganjuur Nomun, Hornung Thorsten, Forkel Susann, Greve Jens, Wurpts Gerda, Hallberg Pär, Bygum Anette, Von Buchwald Christian, Karawajczyk Malgorzata, Steffens Michael, Stingl Julia, Hoffmann Per, Heilmann-Heimbach Stefanie, Mangold Elisabeth, Ludwig Kerstin U, Rasmussen Eva R, Wadelius Mia, Sachs Bernhardt, Nöthen Markus M, Forstner Andreas |
Severe dysplasminogenemia due to homozygous PLG Ala620Thr variant in a Korean woman without a history of venous thromboembolism: A case report and literature review. Medicine 2022 3 101 (9): e29013. Lee Beomki, Kim Suekyeung, Lee Jae Joon, Heo Seon-Hee, Chung Suryeun, Jang Shin Yi, Kim Sun-Hee, Kim Duk-Kyung, Kim Hee-J |
PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis. Legal medicine (Tokyo, Japan) 2022 2 55 102029. Miura Aya, Funayama Kazuhisa, Nyuzuki Hiromi, Takahashi Naoya, Yamamoto Takuma, Koyama Akihide, Ikeuchi Takeshi, Takatsuka Hisakazu, Nishio Haji |
Plasmin-Mediated Fibrinolysis in Periodontitis Pathogenesis. Journal of dental research 2023 7 220345231171837. L M Silva, K Divaris, T H Bugge, N M Moutsopoul |
Germline genetic variants are associated with development of insulin-dependent diabetes in cancer patients treated with immune checkpoint inhibitors. Journal for immunotherapy of cancer 2023 3 11 (3): . Caulfield Jasmine I, Aizenbud Lilach, Perdigoto Ana Luisa, Meffre Eric, Jilaveanu Lucia, Michalek Dominika A, Rich Stephen S, Aizenbud Yariv, Adeniran Adebowale, Herold Kevan C, Austin Matthew R, Kluger Harri |
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- Page last updated:Apr 22, 2024
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