HuGE Literature Finder
|
Records 1-8
Anticancer research 2018 Oct 38 (10): 5983-5990. Kamiza Abram Bunya, Wang Wen-Chang, You Jeng-Fu, Tang Reiping, Wang Yen-Ting, Chien Huei-Tzu, Lai Chih-Hsiung, Chiu Li-Ling, Lo Tsai-Ping, Hung Kuan-Yi, Hsiung Chao Agnes, Yeh Chih-Chi |
Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC).
Carcinogenesis 2016 May . Xicola Rosa M, Bontu Sneha, Doyle Brian J, Rawson Jamie, Garre Pilar, Lee Esther, de la Hoya Miguel, Bessa Xavier, Clofent Joan, Bujanda Luis, Balaguer Francesc, Castellví-Bel Sergi, Alenda Cristina, Jover Rodrigo, Ruiz-Ponte Clara, Syngal Sapna, Andreu Montserrat, Carracedo Angel, Castells Antoni, Newcomb Polly A, Lindor Noralane, Potter John D, Baron John A, Ellis Nathan A, Caldes Trinidad, Llor Xavi |
Analysis of TFGBR1*6A variant in individuals evaluated for Marfan syndrome.
American journal of medical genetics. Part A 2016 Apr . Somers Allyson E, Hinton Robert B, Pilipenko Valentina, Miller Erin, Ware Stephanie |
TGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle.
The Journal of pathology 2012 Oct 228 (2): 251-9. Piva Luisa, Gavassini Bruno F, Bello Luca, Fanin Marina, Soraru Gianni, Barp Andrea, Ermani Mario, Angelini Corrado, Hoffman Eric P, Pegoraro Ele |
Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes.
American journal of medical genetics. Part A 2009 Jul 149A (7): 7. Chung BH, Lam ST, Tong TM, Li SY, Lun KS, Chan DH, Fok SF, Or JS, Smith DK, Yang W, Lau YL |
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders.
Human mutation 2008 Nov 29 (11): E284-95. Stheneur Chantal, Collod-Béroud Gwenaëlle, Faivre Laurence, Gouya Laurent, Sultan Gilles, Le Parc Jean-Marie, Moura Bertrand, Attias David, Muti Christine, Sznajder Marc, Claustres Mireille, Junien Claudine, Baumann Clarisse, Cormier-Daire Valérie, Rio Marlène, Lyonnet Stanislas, Plauchu Henri, Lacombe Didier, Chevallier Bertrand, Jondeau Guillaume, Boileau Catheri |
Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2007 Jun 31 (6): 970-5. Waldmüller Stephan, Müller Melanie, Warnecke Henning, Rees Wolfgang, Schöls Wolfgang, Walterbusch Gerhard, Ennker Jürgen, Scheffold Thom |
Germline mutation analysis of the transforming growth factor beta receptor type II (TGFBR2) and E-cadherin (CDH1) genes in early onset and familial colorectal cancer.
Journal of medical genetics 2001 Feb 38 (2): E7. Verma L, Porter T R, Richards F M, Rajpar M H, Evans D G, Macdonald F, Maher E |
- Page last reviewed:Jul 30, 2019
- Page last updated:Dec 12, 2019
- Content source: