Selenge B - Search Results

1

Impact of L-type amino acid transporter 1 on intrahepatic cholangiocarcinoma.

Selenge B, Yamada S, Morine Y, Ikemoto T, Saito Y, Takasu C, Teraoku H, Okikawa S, Shimada M. Selenge B, et al. J Med Invest. 2023;70(1.2):160-165. doi: 10.2152/jmi.70.160. J Med Invest. 2023. PMID: 37164714 Free article.

2

Impact of L-type amino acid transporter 3 on the prognosis of hepatocellular carcinoma.

Selenge B, Yamada S, Morine Y, Ikemoto T, Saito Y, Takasu C, Teraoku H, Shimada M. Selenge B, et al. Oncol Lett. 2022 Sep 30;24(5):418. doi: 10.3892/ol.2022.13538. eCollection 2022 Nov. Oncol Lett. 2022. PMID: 36245821 Free PMC article.

3

Modifying Effect of Smoking on GSTM1 and NAT2 in Relation to the Risk of Bladder Cancer in Mongolian Population: A Case-Control Study.

Avirmed S, Khuanbai Y, Sanjaajamts A, Selenge B, Dagvadorj BU, Ohashi M. Avirmed S, et al. Among authors: selenge b. Asian Pac J Cancer Prev. 2021 Aug 1;22(8):2479-2485. doi: 10.31557/APJCP.2021.22.8.2479. Asian Pac J Cancer Prev. 2021. PMID: 34452561 Free PMC article.

4

Association between MDM2-SNP309 and p53R72P polymorphisms and the risk of bladder cancer in the Mongolian population.

Avirmed S, Wang BS, Selenge B, Sanjaajamts A, Ganbat B, Erdenebileg U, Purevsuren M, Jigjidsuren S, Batmunkh M, Lee YJ. Avirmed S, et al. Among authors: selenge b. Mol Clin Oncol. 2017 Sep;7(3):412-420. doi: 10.3892/mco.2017.1317. Epub 2017 Jul 13. Mol Clin Oncol. 2017. PMID: 28781817 Free PMC article.

5

Acquired esophagobronchial fistula without Ono's sign and with unusual cause.

Zuunai A, Selenge B, Lee JH, Lee SH. Zuunai A, et al. Among authors: selenge b. BMJ Case Rep. 2013 Sep 10;2013:bcr2013201138. doi: 10.1136/bcr-2013-201138. BMJ Case Rep. 2013. PMID: 24022907 Free PMC article.

6

Novel exon 3B proteolipid protein gene mutation causing late-onset spastic paraplegia type 2 with variable penetrance in female family members.

Sivakumar K, Sambuughin N, Selenge B, Nagle JW, Baasanjav D, Hudson LD, Goldfarb LG. Sivakumar K, et al. Among authors: selenge b. Ann Neurol. 1999 May;45(5):680-3. Ann Neurol. 1999. PMID: 10319897

7

Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15.

Sambuughin N, Sivakumar K, Selenge B, Lee HS, Friedlich D, Baasanjav D, Dalakas MC, Goldfarb LG. Sambuughin N, et al. Among authors: selenge b. J Neurol Sci. 1998 Nov 26;161(1):23-8. doi: 10.1016/s0022-510x(98)00264-0. J Neurol Sci. 1998. PMID: 9879677

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