HuGE Literature Finder
Records 1-30
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Assessing the general population frequency of rare coding variants in the EXT1 and EXT2 genes previously implicated in hereditary multiple exostoses.
Bone 2016 Sep 92 196-200. Cousminer Diana L, Arkader Alexandre, Voight Benjamin F, Pacifici Maurizio, Grant Struan F |
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Detection of exostosin glycosyltransferase gene mutations in patients with non-hereditary osteochondromas of the mandibular condyle.
Molecular and clinical oncology 2016 Sep 5 (3): 295-299. Zhou Qin, Yang Chi, Chen Min-Jie, Li Ling-Z |
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Identification of Novel Oncogenic Mutations in Thyroid Cancer.
Journal of the American College of Surgeons 2016 Jan . Pitt Susan C, Hernandez Roland A, Nehs Matthew A, Gawande Atul A, Moore Francis D, Ruan Daniel T, Cho Nancy |
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Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas.
BMC genetics 2016 17 (1): 52. Ishimaru Daichi, Gotoh Masanori, Takayama Shinichiro, Kosaki Rika, Matsumoto Yoshihiro, Narimatsu Hisashi, Sato Takashi, Kimata Koji, Akiyama Haruhiko, Shimizu Katsuji, Matsumoto Ka |
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The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis.
Bone 2015 Mar 72 123-7. Sgariglia Federica, Pedrini Elena, Bradfield Jonathan P, Bhatti Tricia R, D'Adamo Pio, Dormans John P, Gunawardena Aruni T, Hakonarson Hakon, Hecht Jacqueline T, Sangiorgi Luca, Pacifici Maurizio, Enomoto-Iwamoto Motomi, Grant Struan F |
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Impact of variants of the EXT2 gene on Type 2 diabetes and its related traits in the Chinese han population.
Endocrine research 2015 40 (2): 79-82. Ren Qian, Xiao Jianzhong, Han Xueyao, Yang Wenying, Ji Lino |
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Loss of function in heparan sulfate elongation genes EXT1 and EXT 2 results in improved nitric oxide bioavailability and endothelial function.
Journal of the American Heart Association 2014 Dec 3 (6): e001274. Mooij H L, Cabrales P, Bernelot Moens S J, Xu D, Udayappan S D, Tsai A G, van der Sande M A J, de Groot E, Intaglietta M, Kastelein J J P, Dallinga-Thie G M, Esko J D, Stroes E S, Nieuwdorp |
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Hereditary multiple exostoses: anatomical distribution and burden of exostoses is dependent upon genotype and gender.
Scottish medical journal 2014 Feb 59 (1): 35-44. Clement N D, Porter D |
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Validation of type 2 diabetes risk variants identified by genome-wide association studies in Han Chinese population: a replication study and meta-analysis.
PloS one 2014 9 (4): e95045. Chang Yi-Cheng, Liu Pi-Hua, Yu Yu-Hsiang, Kuo Shan-Shan, Chang Tien-Jyun, Jiang Yi-Der, Nong Jiun-Yi, Hwang Juey-Jen, Chuang Lee-Mi |
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Lack of replication of common EXT2 gene variants with susceptibility to type 2 diabetes in Lebanese Arabs.
Diabetes & metabolism 2013 Dec 39 (6): 532-6. Nemr R, Al-Busaidi A S, Sater M S, Echtay A, Saldanha F L, Racoubian E, Keleshian S H, Almawi W |
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ACE I/D and MTHFR C677T polymorphisms are significantly associated with type 2 diabetes in Arab ethnicity: a meta-analysis.
Gene 2013 May 520 (2): 166-77. Al-Rubeaan Khalid, Siddiqui Khalid, Saeb Amr T M, Nazir Nyla, Al-Naqeb Dhekra, Al-Qasim Sa |
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Association between variants of EXT2 and type 2 diabetes: a replication and meta-analysis.
Human genetics 2013 Feb 132 (2): 139-45. Liu Lei, Yang Xu, Wang Haoran, Cui Guanglin, Xu Yujun, Wang Peihua, Yuan Gang, Wang Xiaojing, Ding Hu, Wang Dao W |
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20 novel point mutations and one large deletion in EXT1 and EXT2 genes: Report of diagnostic screening in a large Italian cohort of patients affected by hereditary multiple exostosis.
Gene 2012 Dec . Ciavarella M, Coco M, Baorda F, Stanziale P, Chetta M, Bisceglia L, Palumbo P, Bengala M, Raiteri P, Silengo M, Caldarini C, Facchini R, Lala R, Cavaliere ML, De Brasi D, Pasini B, Zelante L, Guarnieri V, D'Agruma L |
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Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography.
Journal of human genetics 2012 May 57 (5): 305-10. Hotta Kikuko, Kitamoto Aya, Kitamoto Takuya, Mizusawa Seiho, Teranishi Hajime, So Rina, Matsuo Tomoaki, Nakata Yoshio, Hyogo Hideyuki, Ochi Hidenori, Nakamura Takahiro, Kamohara Seika, Miyatake Nobuyuki, Kotani Kazuaki, Komatsu Ryoya, Itoh Naoto, Mineo Ikuo, Wada Jun, Yoneda Masato, Nakajima Atsushi, Funahashi Tohru, Miyazaki Shigeru, Tokunaga Katsuto, Masuzaki Hiroaki, Ueno Takato, Chayama Kazuaki, Hamaguchi Kazuyuki, Yamada Kentaro, Hanafusa Toshiaki, Oikawa Shinichi, Yoshimatsu Hironobu, Sakata Toshiie, Tanaka Kiyoji, Matsuzawa Yuji, Nakao Kazuwa, Sekine Akihi |
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Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factors.
The Journal of bone and joint surgery. American volume 2011 Dec 93 (24): 2294-302. Pedrini Elena, Jennes Ivy, Tremosini Morena, Milanesi Annamaria, Mordenti Marina, Parra Alessandro, Sgariglia Federica, Zuntini Monia, Campanacci Laura, Fabbri Nicola, Pignotti Elettra, Wuyts Wim, Sangiorgi Lu |
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Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.
Genetic testing and molecular biomarkers 2011 Jun 15 (6): 399-405. Kifagi Chamseddine, Makni Kaouthar, Boudawara Mouhamed, Mnif Fatma, Hamza Naziha, Abid Mouhamed, Granier Claude, Ayadi Hamma |
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Shoulder exostoses in hereditary multiple exostoses: probability of surgery and malignant change.
Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2011 Mar 20 (2): 290-4. Clement Nicholas David, Ng Che E, Porter Daniel |
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Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.
Diabetes 2010 Mar 59 (3): 751-5. Zhao Jianhua, Bradfield Jonathan P, Zhang Haitao, Annaiah Kiran, Wang Kai, Kim Cecilia E, Glessner Joseph T, Frackelton Edward C, Otieno F George, Doran James, Thomas Kelly A, Garris Maria, Hou Cuiping, Chiavacci Rosetta M, Li Mingyao, Berkowitz Robert I, Hakonarson Hakon, Grant Struan F |
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Association analysis of variation in/near FTO, CDKAL1, SLC30A8, HHEX, EXT2, IGF2BP2, LOC387761, and CDKN2B with type 2 diabetes and related quantitative traits in Pima Indians.
Diabetes 2009 Feb 58 (2): 478-88. Rong Rong, Hanson Robert L, Ortiz Daniel, Wiedrich Christopher, Kobes Sayuko, Knowler William C, Bogardus Clifton, Baier Leslie |
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Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
Diabetes 2008 Oct 57 (10): 2834-42. Wu Ying, Li Huaixing, Loos Ruth J F, Yu Zhijie, Ye Xingwang, Chen Lihua, Pan An, Hu Frank B, Lin |
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Variants of the PPARG, IGF2BP2, CDKAL1, HHEX, and TCF7L2 genes confer risk of type 2 diabetes independently of BMI in the German KORA studies.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2008 Oct 40 (10): 722-6. Herder C, Rathmann W, Strassburger K, Finner H, Grallert H, Huth C, Meisinger C, Gieger C, Martin S, Giani G, Scherbaum W A, Wichmann H-E, Illig |
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Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
Diabetes 2008 Aug 57 (8): 2220-5. Lewis Joshua P, Palmer Nicholette D, Hicks Pamela J, Sale Michele M, Langefeld Carl D, Freedman Barry I, Divers Jasmin, Bowden Donald |
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EXTENSION OF TYPE 2 DIABETES GENOME-WIDE ASSOCIATION SCAN RESULTS IN THE DIABETES PREVENTION PROGRAM.
Diabetes 2008 Jun . Moore AF, Jablonski KA, McAteer JB, Saxena R, Pollin TI, Franks PW, Hanson RL, Shuldiner AR, Knowler WC, Altshuler D, Florez JC |
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Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study.
Journal of molecular medicine (Berlin, Germany) 2008 Mar 86 (3): 341-8. Cauchi Stéphane, Proença Christine, Choquet Hélène, Gaget Stefan, De Graeve Franck, Marre Michel, Balkau Beverley, Tichet Jean, Meyre David, Vaxillaire Martine, Froguel Philippe, |
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Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population.
Diabetes 2008 Mar 57 (3): 791-5. Omori Shintaro, Tanaka Yasushi, Takahashi Atsushi, Hirose Hiroshi, Kashiwagi Atsunori, Kaku Kohei, Kawamori Ryuzo, Nakamura Yusuke, Maeda Shi |
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Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population.
Diabetologia 2007 Dec 50 (12): 2461-6. Horikoshi M, Hara K, Ito C, Shojima N, Nagai R, Ueki K, Froguel P, Kadowaki |
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Nature 2007 Feb 445 (7130): 881-5. Sladek Robert, Rocheleau Ghislain, Rung Johan, Dina Christian, Shen Lishuang, Serre David, Boutin Philippe, Vincent Daniel, Belisle Alexandre, Hadjadj Samy, Balkau Beverley, Heude Barbara, Charpentier Guillaume, Hudson Thomas J, Montpetit Alexandre, Pshezhetsky Alexey V, Prentki Marc, Posner Barry I, Balding David J, Meyre David, Polychronakos Constantin, Froguel Philip |
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Polymorphisms within novel risk loci for type 2 diabetes determine beta-cell function.
PloS one 2007 2 (9): e832. Staiger Harald, Machicao Fausto, Stefan Norbert, Tschritter Otto, Thamer Claus, Kantartzis Konstantinos, Schäfer Silke A, Kirchhoff Kerstin, Fritsche Andreas, Häring Hans-Ulri |
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An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas.
Clinical genetics 2005 Dec 68 (6): 542-7. Wuyts W, Radersma R, Storm K, Vits |
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LOC387761 polymorphism is associated with type 2 diabetes in the Mexican population.
Genetic testing and molecular biomarkers 0 15 (1-2): 79-83. Gutiérrez-Vidal Roxana, Rodríguez-Trejo Adriana, Canizales-Quinteros Samuel, Herrera-Cornejo Martín, Granados-Silvestre Maria Angeles, Montúfar-Robles Isela, Ortiz-López María Guadalupe, Menjívar Mar |
- Page last reviewed:Oct 1, 2020
- Page last updated:Apr 15, 2021
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