Results
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41.
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[A mutation IVS2+1G>A in EXT2 gene causes hereditary multiple exostoses]. [electronic resource] by
- Hu, Zheng-mao
- Zheng, Duo
- Pan, Qian
- Yang, Yi-feng
- Zhao, Tian-li
- Liu, Xiao-ping
- Wu, Ling-qian
- Jiang, Dong-gui
- Xia, Kun
- Xia, Jia-hui
Producer: 20040615
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 21
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44.
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Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas. [electronic resource] by
- Ishimaru, Daichi
- Gotoh, Masanori
- Takayama, Shinichiro
- Kosaki, Rika
- Matsumoto, Yoshihiro
- Narimatsu, Hisashi
- Sato, Takashi
- Kimata, Koji
- Akiyama, Haruhiko
- Shimizu, Katsuji
- Matsumoto, Kazu
Producer: 20161019
In:
BMC genetics vol. 17
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Heparan Sulfate Biosynthetic System Is Inhibited in Human Glioma Due to EXT1/2 and HS6ST1/2 Down-Regulation. [electronic resource] by
- Ushakov, Victor S
- Tsidulko, Alexandra Y
- de La Bourdonnaye, Gabin
- Kazanskaya, Galina M
- Volkov, Alexander M
- Kiselev, Roman S
- Kobozev, Vyacheslav V
- Kostromskaya, Diana V
- Gaytan, Alexey S
- Krivoshapkin, Alexei L
- Aidagulova, Svetlana V
- Grigorieva, Elvira V
Producer: 20180702
In:
International journal of molecular sciences vol. 18
Availability: No items available.
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53.
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Ext1 heterozygosity causes a modest effect on postprandial lipid clearance in humans. [electronic resource] by
- Mooij, Hans L
- Bernelot Moens, Sophie J
- Gordts, PhilipL S M
- Stanford, KristinI
- Foley, ErinM
- van den Boogert, MarjoleinA W
- Witjes, JuliaJ
- Hassing, H Carlijne
- Tanck, MichaelW
- van de Sande, MichielA J
- Levels, J Han
- Kastelein, JohnJ P
- Stroes, ErikS G
- Dallinga-Thie, GeesjeM
- Esko, JeffD
- Nieuwdorp, Max
Producer: 20151116
In:
Journal of lipid research vol. 56
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54.
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55.
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Association between variants of EXT2 and type 2 diabetes: a replication and meta-analysis. [electronic resource] by
- Liu, Lei
- Yang, Xu
- Wang, Haoran
- Cui, Guanglin
- Xu, Yujun
- Wang, Peihua
- Yuan, Gang
- Wang, Xiaojing
- Ding, Hu
- Wang, Dao Wen
Producer: 20130311
In:
Human genetics vol. 132
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56.
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57.
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A combined analytical approach reveals novel EXT1/2 gene mutations in a large cohort of Italian multiple osteochondromas patients. [electronic resource] by
- Signori, Emanuela
- Massi, Emanuela
- Matera, Maria Giovanna
- Poscente, Monica
- Gravina, Carolina
- Falcone, Gianluca
- Rosa, Michele Attilio
- Rinaldi, Monica
- Wuyts, Wim
- Seripa, Davide
- Dallapiccola, Bruno
- Fazio, Vito Michele
Producer: 20071004
In:
Genes, chromosomes & cancer vol. 46
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