HuGE Literature Finder
Records 1-29
|
Clinical significance of the mutational landscape and fragmentation of circulating tumor DNA in renal cell carcinoma.
Cancer science 2019 Feb 110 (2): 617-628. Yamamoto Yoshiyuki, Uemura Motohide, Fujita Masashi, Maejima Kazuhiro, Koh Yoko, Matsushita Makoto, Nakano Kosuke, Hayashi Yujiro, Wang Cong, Ishizuya Yu, Kinouchi Toshiro, Hayashi Takuji, Matsuzaki Kyosuke, Jingushi Kentaro, Kato Taigo, Kawashima Atsunari, Ujike Takeshi, Nagahara Akira, Fujita Kazutoshi, Imamura Ryoichi, Nakagawa Hidewaki, Nonomura Nor |
|
TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups.
Leukemia 2019 Jan . Haase Detlef, Stevenson Kristen E, Neuberg Donna, Maciejewski Jaroslaw P, Nazha Aziz, Sekeres Mikkael A, Ebert Benjamin L, Garcia-Manero Guillermo, Haferlach Claudia, Haferlach Torsten, Kern Wolfgang, Ogawa Seishi, Nagata Yasunobu, Yoshida Kenichi, Graubert Timothy A, Walter Matthew J, List Alan F, Komrokji Rami S, Padron Eric, Sallman David, Papaemmanuil Elli, Campbell Peter J, Savona Michael R, Seegmiller Adam, Adès Lionel, Fenaux Pierre, Shih Lee-Yung, Bowen David, Groves Michael J, Tauro Sudhir, Fontenay Michaela, Kosmider Olivier, Bar-Natan Michal, Steensma David, Stone Richard, Heuser Michael, Thol Felicitas, Cazzola Mario, Malcovati Luca, Karsan Aly, Ganster Christina, Hellström-Lindberg Eva, Boultwood Jacqueline, Pellagatti Andrea, Santini Valeria, Quek Lynn, Vyas Paresh, Tüchler Heinz, Greenberg Peter L, Bejar Rafael, |
|
Correlation Between Single-Nucleotide Polymorphisms Within miR-30a and Related Target Genes and Risk or Prognosis of Nephrotic Syndrome.
DNA and cell biology 2018 Jan . Yang Ruiheng, Hong Hong, Wang Mengjun, Ma Zhongch |
|
Genomically annotated risk model for advanced renal-cell carcinoma: a retrospective cohort study.
The Lancet. Oncology 2018 12 19 (12): 1688-1698. Voss Martin H, Reising Albert, Cheng Yuan, Patel Parul, Marker Mahtab, Kuo Fengshen, Chan Timothy A, Choueiri Toni K, Hsieh James J, Hakimi A Ari, Motzer Robert |
|
A Randomized Phase 2 Study of MK-2206 versus Everolimus in Refractory Renal Cell Carcinoma.
Annals of oncology : official journal of the European Society for Medical Oncology 2017 Jan . Jonasch E, Hasanov E, Corn P, Moss T, Shaw K, Stovall S, Marcott V, Gan B, Bird S, Wang X, Do K, Altamirano P, Zurita A, Doyle L, Lara P, Tannir N |
|
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? |
|
Wide spetcrum mutational analysis of metastatic renal cell cancer: a retrospective next generation sequencing approach.
Oncotarget 2016 Oct . Fiorentino Michelangelo, Gruppioni Elisa, Massari Francesco, Giunchi Francesca, Altimari Annalisa, Ciccarese Chiara, Bimbatti Davide, Scarpa Aldo, Iacovelli Roberto, Porta Camillo, Virinder Sarhadi, Tortora Giampaolo, Artibani Walter, Schiavina Riccardo, Ardizzoni Andrea, Brunelli Matteo, Knuutila Sakari, Martignoni Gui |
|
Analysis of various potential prognostic markers and survival data in clear cell renal cell carcinoma.
International braz j urol : official journal of the Brazilian Society of Urology 2016 Sep . Ebru Tastekin, Fulya Oz Puyan, Hakan Akdere, Vuslat Yurut-Caloglu, Necdet Sut, Nuray Can, Filiz Ozyilm |
|
Anaplastic histology Wilms' tumors registered to the Japan Wilms' Tumor Study Group are less aggressive than that in the National Wilms' Tumor Study 5.
Pediatric surgery international 2016 Jul . Oue Takaharu, Koshinaga Tsugumichi, Takimoto Tetsuya, Okita Hajime, Tanaka Yukichi, Nozaki Miwako, Haruta Masayuki, Kaneko Yasuhiko, Fukuzawa Masahiro, |
|
Whole-Exome Sequencing in Two Extreme Phenotypes of Response to VEGF-Targeted Therapies in Patients With Metastatic Clear Cell Renal Cell Carcinoma.
Journal of the National Comprehensive Cancer Network : JNCCN 2016 Jul 14 (7): 820-4. Fay Andre P, de Velasco Guillermo, Ho Thai H, Van Allen Eliezer M, Murray Bradley, Albiges Laurence, Signoretti Sabina, Hakimi A Ari, Stanton Melissa L, Bellmunt Joaquim, McDermott David F, Atkins Michael B, Garraway Levi A, Kwiatkowski David J, Choueiri Toni |
|
Collecting duct carcinoma of the kidney is associated with CDKN2A deletion and SLC family gene up-regulation.
Oncotarget 2016 Apr . Wang Jianmin, Papanicolau-Sengos Antonios, Chintala Sreenivasulu, Wei Lei, Liu Biao, Hu Qiang, Miles Kiersten Marie, Conroy Jeffrey M, Glenn Sean T, Costantini Manuela, Magi-Galluzzi Cristina, Signoretti Sabina, Choueiri Toni, Gallucci Michele, Sentinelli Steno, Fazio Vito M, Poeta Maria Luana, Liu Song, Morrison Carl, Pili Rober |
|
Genetic variations frequencies in Wilms' tumor: a meta-analysis and systematic review.
Cancer science 2016 Feb . Deng Changkai, Dai Rong, Li Xuliang, Liu Fe |
|
Genomic characterization of sarcomatoid transformation in clear cell renal cell carcinoma.
Proceedings of the National Academy of Sciences of the United States of America 2016 Feb . Bi Mark, Zhao Siming, Said Jonathan W, Merino Maria J, Adeniran Adebowale J, Xie Zuoquan, Nawaf Cayce B, Choi Jaehyuk, Belldegrun Arie S, Pantuck Allan J, Kluger Harriet M, Bilgüvar Kaya, Lifton Richard P, Shuch Bri |
|
Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes.
Nature genetics 2015 Jan 47 (1): 13-21. Durinck Steffen, Stawiski Eric W, Pavía-Jiménez Andrea, Modrusan Zora, Kapur Payal, Jaiswal Bijay S, Zhang Na, Toffessi-Tcheuyap Vanina, Nguyen Thong T, Pahuja Kanika Bajaj, Chen Ying-Jiun, Saleem Sadia, Chaudhuri Subhra, Heldens Sherry, Jackson Marlena, Peña-Llopis Samuel, Guillory Joseph, Toy Karen, Ha Connie, Harris Corissa J, Holloman Eboni, Hill Haley M, Stinson Jeremy, Rivers Celina Sanchez, Janakiraman Vasantharajan, Wang Weiru, Kinch Lisa N, Grishin Nick V, Haverty Peter M, Chow Bernard, Gehring Julian S, Reeder Jens, Pau Gregoire, Wu Thomas D, Margulis Vitaly, Lotan Yair, Sagalowsky Arthur, Pedrosa Ivan, de Sauvage Frederic J, Brugarolas James, Seshagiri Somasek |
|
Association of TP53 polymorphisms on the risk of Wilms tumor.
Pediatric blood & cancer 2014 Mar 61 (3): 436-41. Andrade R C, Cardoso L C A, Ferman S E, Faria P S, Seuánez H N, Achatz M I, Vargas F |
|
Multiple analytical approaches demonstrate a complex relationship of genetic and nongenetic factors with cisplatin- and carboplatin-induced nephrotoxicity in lung cancer patients.
BioMed research international 2014 2014 937429. Liu H Eugene, Bai Kuan-Jen, Hsieh Yu-Chen, Yu Ming-Chih, Lee Chun-Nin, Chang Jer-Hua, Hsu Han-Lin, Lu Pei-Chih, Chen Hsiang-Y |
|
TP53 mutational status is a potential marker for risk stratification in Wilms tumour with diffuse anaplasia.
PloS one 2014 9 (10): e109924. Maschietto Mariana, Williams Richard D, Chagtai Tasnim, Popov Sergey D, Sebire Neil J, Vujanic Gordan, Perlman Elizabeth, Anderson James R, Grundy Paul, Dome Jeffrey S, Pritchard-Jones Kat |
|
TP53 codon 72 polymorphisms in favorable histology Wilms tumors.
Pediatric blood & cancer 2012 Aug 59 (2): 326-8. Cost Nicholas G, Mitui Midori, Khokhar Shama, Wickiser Jonathan E, Baker Linda A, Rakheja Dine |
|
The polymorphisms of P53 codon 72 and MDM2 SNP309 and renal cell carcinoma risk in a low arsenic exposure area.
Toxicology and applied pharmacology 2011 Dec 257 (3): 349-55. Huang Chao-Yuan, Su Chien-Tien, Chu Jan-Show, Huang Shu-Pin, Pu Yeong-Shiau, Yang Hsiu-Yuan, Chung Chi-Jung, Wu Chia-Chang, Hsueh Yu-M |
|
[Association of gene TP53 polymorphic marker Pro72Arg with clinical characteristics of chronic glomerulonephritis].
Terapevticheski? arkhiv 2011 83 (6): 27-32. Kamyshova E S, Shvetsov M Iu, Shestakov A E, Kutyrina I M, Nosikov V |
|
Single-nucleotide polymorphisms, acute rejection, and severity of tubulitis in kidney transplantation, accounting for center-to-center variation.
Transplantation 2010 Dec 90 (12): 1401-8. Israni Ajay, Leduc Robert, Holmes John, Jacobson Pamala A, Lamba Vishal, Guan Weihua, Schladt David, Chen Jinbo, Matas Arthur J, Oetting William S, |
|
TP53, EGFR, and KRAS mutations in relation to VHL inactivation and lifestyle risk factors in renal-cell carcinoma from central and eastern Europe.
Cancer letters 2010 Jul 293 (1): 92-8. Szyma?ska K, Moore L E, Rothman N, Chow W H, Waldman F, Jaeger E, Waterboer T, Foretova L, Navratilova M, Janout V, Kollarova H, Zaridze D, Matveev V, Mates D, Szeszenia-Dabrowska N, Holcatova I, Bencko V, Le Calvez-Kelm F, Villar S, Pawlita M, Boffetta P, Hainaut P, Brennan |
|
Polymorphisms of the ApoE, HSD3B1, IL-1beta and p53 genes are associated with the development of early uremic complications in diabetic patients: results of a DNA resequencing array study.
International journal of molecular medicine 2009 Feb 23 (2): 217-27. Szoke Dominika, Molnar Bela, Solymosi Norbert, Racz Karoly, Gergics Peter, Blasko Bernadett, Vasarhelyi Barna, Vannay Adam, Mandy Yvette, Klausz Gergely, Gyulai Zsofia, Galamb Orsolya, Spisak Sandor, Hutkai Bernadett, Somogyi Aniko, Berta Klara, Szabo Andras, Tulassay Tivadar, Tulassay Zso |
|
Lack of association of the TP53 Arg72Pro SNP and the MDM2 SNP309 with systemic lupus erythematosus in Caucasian, African American, and Asian children and adults.
Lupus 2009 Jan 18 (1): 61-6. Onel K B, Huo D, Hastings D, Fryer-Biggs J, Crow M K, Onel |
|
MDM2 SNP309 polymorphism as risk factor for susceptibility and poor prognosis in renal cell carcinoma.
Clinical cancer research : an official journal of the American Association for Cancer Research 2007 Jul 13 (14): 4123-9. Hirata Hiroshi, Hinoda Yuji, Kikuno Nobuyuki, Kawamoto Ken, Suehiro Yutaka, Tanaka Yuichiro, Dahiya Rajv |
|
Germline p53 single-base changes associated with Balkan endemic nephropathy.
Biochemical and biophysical research communications 2006 Apr 342 (2): 562-7. Krasteva Maria Emileva, Georgieva Elena Ivano |
|
[Association of polymorphous markers Pro72Arg and C(-594)CC OF TP53 gene with diabetic polyneuropathy in patients with type 1 diabetes mellitus living in Moscow].
Molekuliarnaia biologiia 0 41 (6): 989-93. Spitsina E V, Iakunina N Iu, Chudakova D A, Nikitin A G, Svetlova G N, Soluianova T N, Strokov I A, Nosikov V |
|
Immunohistochemical expression of GLUT1 and its correlation with unfavorable histology and TP53 codon 72 polymorphism in Wilms tumors.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 15 (4): 286-92. Rakheja Dinesh, Khokhar Shama, Mitui Midori, Cost Nicholas |
|
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:Mar 16, 2019
- Page last updated:Sep 18, 2020
- Content source: