HuGE Literature Finder
Records 1-9
Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.
Journal of endocrinological investigation 2019 Mar . Popovic M, Matana A, Torlak V, Boutin T, Brdar D, Gunjaca I, Kalicanin D, Kolcic I, Boraska Perica V, Punda A, Polašek O, Barbalic M, Hayward C, Zemunik |
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Novel Genetic Variants are Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SCL1A3 and EPHB2.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016 Aug . Nielson Carrie M, Liu Ching-Ti, Smith Albert V, Ackert-Bicknell Cheryl L, Reppe Sjur, Johanna Jakobsdottir, Wassel Christina, Register Thomas C, Oei Ling, Alonso Lopez Nerea, Oei Edwin H, Parimi Neeta, Samelson Elizabeth J, Nalls Mike A, Zmuda Joseph, Lang Thomas, Bouxsein Mary, Latourelle Jeanne, Claussnitzer Melina, Siggeirsdottir Kristin, Srikanth Priya, Lorentzen Erik, Vandenput Liesbeth, Langefeld Carl, Raffield Laura, Terry Greg, Cox Amanda J, Allison Matthew A, Criqui Michael H, Bowden Don, Ikram M Arfan, Mellström Dan, Karlsson Magnus K, Carr John, Budoff Matthew, Phillips Caroline, Cupples L Adrienne, Chou Wen-Chi, Myers Richard H, Ralston Stuart H, Gautvik Kaare M, Cawthon Peggy M, Cummings Steven, Karasik David, Rivadeneira Fernando, Gudnason Vilmundur, Orwoll Eric S, Harris Tamara B, Ohlsson Claes, Kiel Douglas P, Hsu Yi-Hsia |
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A9 region in EPHB2 mutation is frequent in tumors with microsatellite instability. Analysis of prognosis.
Anticancer research 2013 Nov 33 (11): 5159-63. Rafael Sara, Vidaurreta Marta, Veganzones Silvia, De La Orden Virgnia, Mediero Beatriz, Gutierrez Maria Luisa, Maestro Maria Lui |
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EphB2 SNPs and sporadic prostate cancer risk in African American men.
PloS one 2011 6 (5): e19494. Robbins Christiane M, Hooker Stanley, Kittles Rick A, Carpten John |
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Influence of A9 Region Mutation in EphB2 Gene in the Prognosis of Patients with Colorectal Adenocarcinoma.
Annals of surgical oncology 2010 Dec . Vidaurreta M, Rafael S, Veganzones S, de la Orden V, Fernández C, Gómez-Casaseca R, Cerdán J, Maestro M |
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Germline EPHB2 receptor variants in familial colorectal cancer.
PloS one 2008 3 (8): e2885. Zogopoulos George, Jorgensen Claus, Bacani Julinor, Montpetit Alexandre, Lepage Pierre, Ferretti Vincent, Chad Lauren, Selvarajah Subani, Zanke Brent, Hudson Thomas J, Pawson Tony, Gallinger Stev |
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A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.
Journal of medical genetics 2006 Jun 43 (6): 507-11. Kittles R A, Baffoe-Bonnie A B, Moses T Y, Robbins C M, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent J M, Collins F S, Mousses S, Bailey-Wilson J, Furbert-Harris P, Dunston G, Powell I J, Carpten J |
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A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2006 May 43 (3): 310-6. Watanabe Akira, Akita Sadanori, Tin Nguyen Thi Duc, Natsume Nagato, Nakano Yoko, Niikawa Norio, Uchiyama Takeshi, Yoshiura Koh-ichi |
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EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis.
BMC cancer 2006 6 (): 145. Kokko Antti, Laiho Päivi, Lehtonen Rainer, Korja Sanna, Carvajal-Carmona Luis G, Järvinen Heikki, Mecklin Jukka-Pekka, Eng Charis, Schleutker Johanna, Tomlinson Ian P M, Vahteristo Pia, Aaltonen Lauri |
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- Page last updated:Feb 24, 2021
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