105 related articles for article (PubMed ID: 34012378)
1. Identification of Two Novel Frameshift Mutations in Exostosin 1 in Two Families with Multiple Osteochondromas.
Wang CY; Yu F; Jin JY; He JQ; Fan LL; Tang JY; Xiang R
Mol Syndromol; 2021 Apr; 12(2):96-100. PubMed ID: 34012378
[TBL] [Abstract][Full Text] [Related]
2. Targeted Next-Generation Sequencing Newly Identifies Mutations in Exostosin-1 and Exostosin-2 Genes of Patients with Multiple Osteochondromas.
Guo X; Lin M; Shi T; Yan W; Chen W
Tohoku J Exp Med; 2017 Jul; 242(3):173-181. PubMed ID: 28690282
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel frameshift mutation of the
Xia P; Xu H; Shi Q; Li D
Oncol Lett; 2016 Jan; 11(1):105-110. PubMed ID: 26870176
[TBL] [Abstract][Full Text] [Related]
4. A novel
Chen Z; Bi Q; Kong M; Cao L; Ruan W
Oncol Lett; 2018 Oct; 16(4):5167-5171. PubMed ID: 30250583
[TBL] [Abstract][Full Text] [Related]
5. Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
Jennes I; Pedrini E; Zuntini M; Mordenti M; Balkassmi S; Asteggiano CG; Casey B; Bakker B; Sangiorgi L; Wuyts W
Hum Mutat; 2009 Dec; 30(12):1620-7. PubMed ID: 19810120
[TBL] [Abstract][Full Text] [Related]
6. Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants.
Fusco C; Nardella G; Fischetto R; Copetti M; Petracca A; Annunziata F; Augello B; D'Asdia MC; Petrucci S; Mattina T; Rella A; Cassina M; Bengala M; Biagini T; Causio FA; Caldarini C; Brancati F; De Luca A; Guarnieri V; Micale L; D'Agruma L; Castori M
Hum Mol Genet; 2019 Jul; 28(13):2133-2142. PubMed ID: 30806661
[TBL] [Abstract][Full Text] [Related]
7. Hereditary multiple osteochondromas in Jordanian patients: Mutational and immunohistochemical analysis of
Mohaidat Z; Bodoor K; Almomani R; Alorjani M; Awwad MA; Bany-Khalaf A; Al-Batayneh K
Oncol Lett; 2021 Feb; 21(2):151. PubMed ID: 33552269
[TBL] [Abstract][Full Text] [Related]
8. Somatic loss of an EXT2 gene mutation during malignant progression in a patient with hereditary multiple osteochondromas.
Musso N; Caronia FP; Castorina S; Lo Monte AI; Barresi V; Condorelli DF
Cancer Genet; 2015 Mar; 208(3):62-7. PubMed ID: 25744876
[TBL] [Abstract][Full Text] [Related]
9. Analysis of mutations in EXT1 and EXT2 in Brazilian patients with multiple osteochondromas.
Santos SCL; Rizzo IMPO; Takata RI; Speck-Martins CE; Brum JM; Sollaci C
Mol Genet Genomic Med; 2018 May; 6(3):382-392. PubMed ID: 29529714
[TBL] [Abstract][Full Text] [Related]
10.
Wang Y; Zhong L; Xu Y; Ding L; Ji Y; Schutz S; Férec C; Cooper DN; Xu C; Chen JM; Luo Y
Front Genet; 2020; 11():607838. PubMed ID: 33414810
[TBL] [Abstract][Full Text] [Related]
11. Detection of exostosin glycosyltransferase gene mutations in patients with non-hereditary osteochondromas of the mandibular condyle.
Zhou Q; Yang C; Chen MJ; Li LZ
Mol Clin Oncol; 2016 Sep; 5(3):295-299. PubMed ID: 27588195
[TBL] [Abstract][Full Text] [Related]
12. An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas.
Wuyts W; Radersma R; Storm K; Vits L
Clin Genet; 2005 Dec; 68(6):542-7. PubMed ID: 16283885
[TBL] [Abstract][Full Text] [Related]
13. Novel mutation of EXT2 identified in a large family with multiple osteochondromas.
Chen XJ; Zhang H; Tan ZP; Hu W; Yang YF
Mol Med Rep; 2016 Nov; 14(5):4687-4691. PubMed ID: 27748933
[TBL] [Abstract][Full Text] [Related]
14. Identification and functional characterization of the human EXT1 promoter region.
Jennes I; Zuntini M; Mees K; Palagani A; Pedrini E; De Cock G; Fransen E; Vanden Berghe W; Sangiorgi L; Wuyts W
Gene; 2012 Jan; 492(1):148-59. PubMed ID: 22037484
[TBL] [Abstract][Full Text] [Related]
15. Correlation between mutated genes and forearm deformity in patients with multiple osteochondroma.
Matsumoto K; Ishimaru D; Ogawa H; Komura S; Shimizu K; Akiyama H
J Orthop Sci; 2021 May; 26(3):483-486. PubMed ID: 32636136
[TBL] [Abstract][Full Text] [Related]
16. Three novel EXT1 and EXT2 gene mutations in Taiwanese patients with multiple exostoses.
Chen WC; Chi CH; Chuang CC; Jou IM
J Formos Med Assoc; 2006 May; 105(5):434-7. PubMed ID: 16638657
[TBL] [Abstract][Full Text] [Related]
17. Deletion of exon 8 from the EXT1 gene causes multiple osteochondromas (MO) in a family with three affected members.
Zhuang L; Gerber SD; Kuchen S; Villiger PM; Trueb B
Springerplus; 2016; 5():71. PubMed ID: 26839764
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing.
Hong G; Guo X; Yan W; Li Q; Zhao H; Ma P; Hu X
Mol Med Rep; 2017 Feb; 15(2):657-664. PubMed ID: 28035357
[TBL] [Abstract][Full Text] [Related]
19. Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas.
Güneş N; Uludağ Alkaya D; Toylu A; Özüdoğru P; Çifçi Sunamak E; Şeker A; Demir B; Kuruğoğlu S; Mıhçı E; Tüysüz B
Turk Arch Pediatr; 2023 Jul; 58(4):376-381. PubMed ID: 37317574
[TBL] [Abstract][Full Text] [Related]
20. Identification of mutations in EXT1 and EXT2 genes in six Chinese families with multiple osteochondromas.
Xu Y; Kang Q; Zhang Z
Mol Med Rep; 2017 Oct; 16(4):5599-5605. PubMed ID: 28849184
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
