HuGE Literature Finder
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Records 1-48
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Gene Polymorphisms in Cardiovascular Disease and Cancer.
Angiology 2018 Jan 3319718774693. Katsiki Niki, Kolovou Vana, Tsipis Aggelos, Mihas Constantinos, Vartela Vasiliki, Koutelou Maria, Manolopoulou Dionisia, Leondiadis Evangelos, Iakovou Ioannis, Mavrogieni Sophia, Kolovou Genove |
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TP53 polymorphism in plasma cell myeloma.
Folia histochemica et cytobiologica 2018 Jan . Zmorzynski Szymon Andrzej, Korszen-Pilecka Iwona, Wojcierowska-Litwin Magdalena, Kwiatkowska-Drabik Barbara, Luterek Malgorzata, Chocholska Sylwia, Koczkodaj Dorota, Popek Sylwia, Michalak-Wojnowska Malgorzata, Swiderska-Kolacz Grazyna, Januszewska Joanna, Surowiec Iwona, Tomczak Waldemar, Hus Marek, Dmoszynska Anna, Pasiarski Marcin, Poniewierska-Jasak Katarzyna, Cieplinska Katarzyna, Jankowska-Lecka Olga, Filip Agata An |
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Tumor Protein p53 (TP53) Gene and Left Main Coronary Artery Disease.
Angiology 2018 Jan 3319718760075. Kolovou Vana, Tsipis Angelos, Mihas Constantinos, Katsiki Niki, Vartela Vasiliki, Koutelou Maria, Manolopoulou Dionisia, Leondiadis Evaggelos, Iakovou Ioannis, Mavrogieni Sophie, Kolovou Genove |
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TP53 rs1042522 and rs8064946 variants in myocardial infarction.
Bratislavske lekarske listy 2018 119 (12): 747-751. Hakobjanyan A, Stahelova A, Mrazek F, Petrkova J, Navratilova Z, Petrek |
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Comprehensive molecular profiling of 718 Multiple Myelomas reveals significant differences in mutation frequencies between African and European descent cases.
PLoS genetics 2017 Nov 13 (11): e1007087. Manojlovic Zarko, Christofferson Austin, Liang Winnie S, Aldrich Jessica, Washington Megan, Wong Shukmei, Rohrer Daniel, Jewell Scott, Kittles Rick A, Derome Mary, Auclair Daniel, Craig David Wesley, Keats Jonathan, Carpten John |
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TP53 mutation and its prognostic significance in Waldenstrom's Macroglobulinemia.
Clinical cancer research : an official journal of the American Association for Cancer Research 2017 Jul . Poulain Stéphanie, Roumier Christophe, Bertrand Elisabeth, Renneville Aline, Venet-Caillault Aurelie, Doye Emmanuelle, Geffroy Sandrine, Sebda Scheherazade, Nibourel Olivier, Nudel Morgane, Herbaux Charles, Renaud Loic, Tomowiak Cecile, Guidez Stéphanie, Tricot Sabine, Roche-Lestienne Catherine, Quesnel Bruno, Preudhomme Claude, Leleu Xavi |
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TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals.
Scientific reports 2017 Mar 7 (1): 336. Kodal Jakob B, Vedel-Krogh Signe, Kobylecki Camilla J, Nordestgaard Børge G, Bojesen Stig |
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Polymorphism in ANRIL is associated with relapse in patients with multiple myeloma after autologous stem cell transplant.
Molecular carcinogenesis 2017 Feb . Poi Ming J, Li Junan, Sborov Douglas W, VanGundy Zachary, Cho Yu Kyoung, Lamprecht Misty, Pichiorri Flavia, Phelps Mitch A, Hofmeister Craig |
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The varied distribution and impact of RAS codon and other key DNA alterations across the translocation cyclin D subgroups in multiple myeloma.
Oncotarget 2017 Feb . Stein Caleb K, Pawlyn Charlotte, Chavan Shweta, Rasche Leo, Weinhold Niels, Corken Adam, Buros Amy, Sonneveld Pieter, Jackson Graham H, Landgren Ola, Mughal Tariq, He Jie, Barlogie Bart, Leif Bergsagel P, Davies Faith E, Walker Brian A, Morgan Gareth |
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Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53.
BMC nephrology 2016 Nov 17 (1): 183. Duffy David L, McDonald Stephen P, Hayhurst Beverley, Panagiotopoulos Sianna, Smith Trudy J, Wang Xing L, Wilcken David E, Duarte Natalia L, Mathews John, Hoy Wendy |
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Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients.
Scientific reports 2016 Oct 6 35188. Grzegorzewska Alicja E, Paciorkowski Mateusz, Mostowska Adrianna, Frycz Bartosz, Warcho? Wojciech, Stolarek Ireneusz, Figlerowicz Marek, Jagodzi?ski Pawe? |
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The Arg72 variant of the p53 functional polymorphism (rs1042522) is associated with coronary artery disease in young South Africans of Indian ancestry.
Gene 2016 Jul . Khan Sajidah, Phulukdaree Alisa, Ramkaran Prithiksha, Moodley Devapregasan, Chuturgoon Anil |
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Single Nucleotide Polymorphisms in TP53 but not KRAS or MDM2 are predictive of clinical outcome in multiple myeloma treated with High-Dose Melphalan and Autologous Stem Cell Support.
Leukemia & lymphoma 2015 Sep 1-11. Gebauer Niklas, Biersack Harald, Czerwinska Ann-Cathrin, Schemme Janina, Hardel Tim Tristan, Bernard Veronica, Rades Dirk, Lehnert Hendrik, Luley Kim Barbara, Thorns Christo |
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Apoptosis for prediction of radiotherapy late toxicity: lymphocyte subset sensitivity and potential effect of TP53 Arg72Pro polymorphism.
Apoptosis : an international journal on programmed cell death 2015 Mar 20 (3): 371-82. Fuentes-Raspall María J, Caragol Isabel, Alonso Carmen, Ramón y Cajal Teresa, Fisas David, Seoane Alejandro, Carvajal Nerea, Bonache Sandra, Díez Orland, Gutiérrez-Enríquez Sa |
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Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy.
Cancer cell 2014 Jan 25 (1): 91-101. Lohr Jens G, Stojanov Petar, Carter Scott L, Cruz-Gordillo Peter, Lawrence Michael S, Auclair Daniel, Sougnez Carrie, Knoechel Birgit, Gould Joshua, Saksena Gordon, Cibulskis Kristian, McKenna Aaron, Chapman Michael A, Straussman Ravid, Levy Joan, Perkins Louise M, Keats Jonathan J, Schumacher Steven E, Rosenberg Mara, , Getz Gad, Golub Todd |
Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations.
Pharmacogenomics 2013 Nov 14 (15): 1857-69. Cornejo-García José Antonio, Liou Lieh-Bang, Blanca-López Natalia, Doña Inmaculada, Chen Chien-Hsiun, Chou Yi-Chun, Chuang Hui-Ping, Wu Jer-Yuarn, Chen Yuan-Tsong, Plaza-Serón María Del Carmen, Mayorga Cristobalina, Guéant-Rodríguez Rosa María, Lin Shih-Chang, Torres María José, Campo Paloma, Rondón Carmen, Laguna José Julio, Fernández Javier, Guéant Jean-Louis, Canto Gabriela, Blanca Miguel, Lee Ming Ta Micha |
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Genetic associations with coronary heart disease: Meta-analyses of 12 candidate genetic variants.
Gene 2013 Jul . Ye H, Wang L, Liao Q, Xu L, Huang Y, Xu L, Xu X, Chen C, Wu H, Le Y, Liu Q, Ye M, Dong C, Duan S |
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Polymorphisms of codon 72 of the TP53 gene in endometrial carcinoma of postmenopausal women.
Post?py higieny i medycyny do?wiadczalnej (Online) 2013 67 (0): 1312-8. Zaj?c Agnieszka, Stachowiak Grzegorz, Smolarz Beata, Wilczy?ski Jacek |
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p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP1.
Medical science monitor : international medical journal of experimental and clinical research 2012 Dec 18 (12): 12. Gloria-Bottini F, Banci M, Saccucci P, Neri A, Bottini E, Magrini A |
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Interactions of miR-34b/c and TP53 Polymorphisms on the Risk of Intracranial Aneurysm.
Clinical & developmental immunology 2012 2012 . Li L, Sima X, Bai P, Zhang L, Sun H, Liang W, Liu J, Zhang L, Gao L |
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NAMPT (visfatin) and AKT1 genetic variants associate with myocardial infarction.
Clinica chimica acta; international journal of clinical chemistry 2012 Apr 413 (7-8): 727-32. Leander Karin, Gigante Bruna, Silveira Angela, Vikström Max, Hamsten Anders, Högberg Joh |
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p53 codon 72 polymorphism and coronary artery disease: evidence of association with left ventricular ejection fraction.
The American journal of the medical sciences 2012 Feb 343 (2): 127-30. Gloria-Bottini Fulvia, Banci Maria, Saccucci Patrizia, Nardi Paolo, Scognamiglio Mattia, Papetti Federica, Magrini Andrea, Pellegrino Antonio, Bottini Egidio, Chiariello Lui |
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The clinical impact and molecular biology of del(17p) in multiple myeloma treated with conventional or thalidomide-based therapy.
Genes, chromosomes & cancer 2011 Oct 50 (10): 765-74. Boyd Kevin D, Ross Fiona M, Tapper William J, Chiecchio Laura, Dagrada GianPaolo, Konn Zoe J, Gonzalez David, Walker Brian A, Hockley Sarah L, Wardell Christopher P, Gregory Walter M, Child J Anthony, Jackson Graham H, Davies Faith E, Morgan Gareth J, NCRI Haematology Oncology Studies Grou |
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Genetic polymorphisms of TP53 and FAS promoter modulate the progression of coronary artery disease after coronary artery bypass grafting: a gender-specific view.
Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2011 May 60 (5): 439-45. Beiras-Fernandez A, Angele M K, Koutang C, Lohse P, Reichart B, Lohse P, Eifert |
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Is there a role of p53 codon 72 polymorphism in the susceptibility to type 2 diabetes in overweight subjects? A study in patients with cardiovascular diseases.
Diabetes research and clinical practice 2011 Mar 91 (3): e64-7. Gloria-Bottini F, Banci M, Saccucci P, Magrini A, Bottini |
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The human Tp53 Arg72Pro polymorphism explains different functional prognosis in stroke.
The Journal of experimental medicine 2011 Mar 208 (3): 429-37. Gomez-Sanchez Jose C, Delgado-Esteban Maria, Rodriguez-Hernandez Irene, Sobrino Tomas, Perez de la Ossa Natalia, Reverte Silvia, Bolaños Juan P, Gonzalez-Sarmiento Rogelio, Castillo Jose, Almeida Angel |
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Tumour suppressor gene TP53 mutations in atypical vascular lesions of breast skin following radiotherapy.
Histopathology 2011 Feb 58 (3): 455-66. Santi Raffaella, Cetica Valentina, Franchi Alessandro, Pepi Monica, Cesinaro Anna M, Miracco Clelia, Paglierani Milena, De Giorgi Vincenzo, Delfino Chiara, Difonzo Elisa M, Pimpinelli Nicola, Bianchi Simonetta, Sardi Iacopo, Santucci Marco, Massi Danie |
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Coronary artery disease: evidence of interaction between PTPN22 and p53 genetic polymorphisms.
Cardiology 2011 120 (3): 166-8. Saccucci P, Banci M, Amante A, Bottini E, Gloria-Bottini |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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TP53 codon 72 polymorphism is associated with coronary artery disease in Chilean subjects.
Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2011 20 (2): 171-6. Caamaño José, Saavedra Nicolás, Jaramillo Priscilla C, Lanas Cecilia, Lanas Fernando, Salazar Luis |
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Mutations in TP53 are exclusively associated with del(17p) in multiple myeloma.
Haematologica 2010 Nov 95 (11): 1973-6. Lodé Laurence, Eveillard Marion, Trichet Valérie, Soussi Thierry, Wuillème Soraya, Richebourg Steven, Magrangeas Florence, Ifrah Norbert, Campion Loïc, Traullé Catherine, Guilhot François, Caillot Denis, Marit Gérald, Mathiot Claire, Facon Thierry, Attal Michel, Harousseau Jean-Luc, Moreau Philippe, Minvielle Stéphane, Avet-Loiseau Her |
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[Evaluation of the p53 Arg72Pro polymorphism as a prognostic factor in severe head injury and the inclusion of this indicator in a predictive model].
Revista española de anestesiología y reanimación 2009 Nov 56 (9): 529-35. Martínez Lucas P, Carbayo Herencia J A, Moreno Cuesta J, Jordán J, García Cuesta D C, Escribano Martínez |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Common genetic variants in candidate genes and risk of familial lymphoid malignancies.
British journal of haematology 2009 Aug 146 (4): 418-23. Liang Xueying Sharon, Caporaso Neil, McMaster Mary Lou, Ng David, Landgren Ola, Yeager Meredith, Chanock Stephen, Goldin Lynn |
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P27 and P53 gene polymorphisms and restenosis following coronary implantation of drug-eluting stents.
Cardiology 2009 112 (4): 263-9. Tiroch K, Koch W, Mehilli J, Bottiger C, Schomig A, Kastrati |
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GSTM1 and codon 72 P53 polymorphism in multiple myeloma.
Annals of hematology 2007 Nov 86 (11): 815-9. Ortega Manoela M, Honma Helen N, Zambon Lair, Lorand-Metze Irene, Costa Fernando F, De Souza Carmino A, Lima Carmen S |
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TP53 codon 72 polymorphism as a risk factor for cardiovascular disease in a Brazilian population.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2007 Nov 40 (11): 1465-72. Smith M A C, Silva M D A, Cendoroglo M S, Ramos L R, Araujo L M Q, Labio R W, Burbano R R, Chen E S, Payão S L |
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Effects of arsenic exposure and genetic polymorphisms of p53, glutathione S-transferase M1, T1, and P1 on the risk of carotid atherosclerosis in Taiwan.
Atherosclerosis 2007 Jun 192 (2): 305-12. Wang Yuan-Hung, Wu Meei-Maan, Hong Chi-Tzong, Lien Li-Ming, Hsieh Yi-Chen, Tseng Hung-Pin, Chang Shu-Feng, Su Che-Long, Chiou Hung-Yi, Chen Chien-J |
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Polymorphism of p53 gene codon 72 in Kuwaiti with coronary artery disease and diabetes.
International journal of cardiology 2007 Jan 115 (1): 1-6. Alkhalaf Moussa, Al-Bustan Suzanne, Hamoda Hesham, Abdella Nabi |
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TP53 haplotype-based analysis and incidence of post-angioplasty restenosis.
Human genetics 2004 Mar 114 (4): 386-90. Zee Robert Y L, Cook Nancy R, Kim Chung-Ah, Fernandez-Cruz Arturo, Lindpaintner Kla |
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Connection between p53 gene Bam HI RFLP polymorphism with the volume of brain infarction in patients with carotid atherothrombotic ischemic stroke.
Restorative neurology and neuroscience 2004 22 (2): 81-5. Skvortsova V I, Slominsky P A, Gubskii L V, Koltsova E A, Shetova I M, Platonova I A, Tupitsyna T I, Khrunin A V, Limborska S |
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[Association between Bam HI RFLP p53 gene polymorphism and brain infarction volume in patients with atherothrombotic ischemic stroke].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2003 (Suppl 8): 24-9. Skvortsova V I, Limborskaia S A, Slominski? P A, Gubski? L V, Kol'tsova E A, Shetova I M, Shamalov N A, Tupitsina T I, Platonova I |
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Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.
Journal of medical genetics 2002 Apr 39 (4): 225-42. de Jong M M, Nolte I M, te Meerman G J, van der Graaf W T A, Oosterwijk J C, Kleibeuker J H, Schaapveld M, de Vries E G |
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Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease.
The pharmacogenomics journal 2002 2 (3): 197-201. Zee R Y L, Hoh J, Cheng S, Reynolds R, Grow M A, Silbergleit A, Walker K, Steiner L, Zangenberg G, Fernandez-Ortiz A, Macaya C, Pintor E, Fernandez-Cruz A, Ott J, Lindpainter |
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P53 codon 72 polymorphism in coronary artery disease: no evidence for association with increased risk or micronucleus frequency.
Environmental and molecular mutagenesis 2002 40 (2): 110-5. Manfredi Samantha, Masetti Serena, Botto Nicoletta, Colombo Maria Giovanna, Terrazzi Marco, Vassalle Cristina, Biagini Andrea, Andreassi Maria Graz |
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[Investigation of detoxification polymorphisms genes, methylenetetrahydrofolate-reductase (MTHFR) and P53 in the radiosensitive human cells].
Radiatsionnaia biologiia, radioecologiia / Rossi?skaia akademiia nauk 0 50 (2): 128-33. Shagirova Zh M, Ushenkova L N, Mikha?lov V F, Kurbatova L A, Kuz'mina N S, Semiachkina A N, Vasil'eva I M, Mazurik V K, Zasukhina G |
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Genetic influence on cigarette-induced cardiovascular disease.
Progress in cardiovascular diseases 0 45 (5): 361-82. Wang Xing Li, Raveendran Muthuswamy, Wang Ji |
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The p53 G72C and MDM2 T309G single nucleotide polymorphisms in patients with Wegener's granulomatosis.
Clinical and experimental rheumatology 0 26 (3 Suppl 49): S72-5. Assmann G, Wieczorek S, Wibisono D, Roemer K, Arning L, Voswinkel |
- Page last reviewed:Jul 30, 2019
- Page last updated:Aug 22, 2019
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