Cui TL - Search Results

1

Positional effects of polymorphisms in probe-target sequences on genoplot images of oligonucleotide microarrays.

Cui TL, Nakaoka H, Akiyama K, Kamura H, Hosomichi K, Bae J, Cheong H, Shin H, Yada T, Inoue I. Cui TL, et al. Genet Mol Res. 2010 Mar 23;9(1):524-31. doi: 10.4238/vol9-1gmr737. Genet Mol Res. 2010. PMID: 20391336 Free article.

2

Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution.

Nakaoka H, Takahashi T, Akiyama K, Cui T, Tajima A, Krischek B, Kasuya H, Hata A, Inoue I. Nakaoka H, et al. Stroke. 2010 Aug;41(8):1593-8. doi: 10.1161/STROKEAHA.110.586529. Epub 2010 Jul 1. Stroke. 2010. PMID: 20595659

3

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.

Akiyama K, Narita A, Nakaoka H, Cui T, Takahashi T, Yasuno K, Tajima A, Krischek B, Yamamoto K, Kasuya H, Hata A, Inoue I. Akiyama K, et al. J Hum Genet. 2010 Oct;55(10):656-61. doi: 10.1038/jhg.2010.82. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613766

4

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.

Bae JS, Cheong HS, Park BL, Kim LH, Park TJ, Kim JY, Pasaje CF, Lee JS, Cui T, Inoue I, Shin HD. Bae JS, et al. J Hum Genet. 2010 Nov;55(11):726-30. doi: 10.1038/jhg.2010.97. Epub 2010 Aug 12. J Hum Genet. 2010. PMID: 20703242

5

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population.

Bae JS, Cheong HS, Kim JO, Lee SO, Kim EM, Lee HW, Kim S, Kim JW, Cui T, Inoue I, Shin HD. Bae JS, et al. Biochem Biophys Res Commun. 2008 Sep 5;373(4):593-6. doi: 10.1016/j.bbrc.2008.06.083. Epub 2008 Jul 2. Biochem Biophys Res Commun. 2008. PMID: 18601904

6

Exact break point of a 50 kb deletion 8 kb centromeric of the HLA-A locus with HLA-A*24:02: the same deletion observed in other A*24 alleles and A*23:01 allele.

Mitsunaga S, Okudaira Y, Kunii N, Cui T, Hosomichi K, Oka A, Suzuki Y, Homma Y, Sato S, Inoue I, Inoko H. Mitsunaga S, et al. Immunogenetics. 2011 Aug;63(8):467-74. doi: 10.1007/s00251-011-0521-0. Epub 2011 Apr 26. Immunogenetics. 2011. PMID: 21519861

7

A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis.

Nakaoka H, Cui T, Tajima A, Oka A, Mitsunaga S, Kashiwase K, Homma Y, Sato S, Suzuki Y, Inoko H, Inoue I. Nakaoka H, et al. PLoS One. 2011;6(9):e25389. doi: 10.1371/journal.pone.0025389. Epub 2011 Sep 28. PLoS One. 2011. PMID: 21980439 Free PMC article.

8

A case of surgical treatment combined with interventional therapy for refractory hemodialysis access with catheter-related right atrial thrombosis.

Wang SF, Xu ZJ, Cui TL. Wang SF, et al. Among authors: cui tl. J Vasc Access. 2025 Jan 16:11297298241313005. doi: 10.1177/11297298241313005. Online ahead of print. J Vasc Access. 2025. PMID: 39817462

9

Associative memory neurons of encoding multi-modal signals are recruited by neuroligin-3-mediated new synapse formation.

Xu Y, Cui TL, Li JY, Chen B, Wang JH. Xu Y, et al. Among authors: cui tl. Elife. 2023 Dec 4;12:RP87969. doi: 10.7554/eLife.87969. Elife. 2023. PMID: 38047770 Free PMC article.

10

Risk factors for hypotension in patients with hemodialysis-associated superior vena cava syndrome.

Zhao QY, Li Q, Cui TL. Zhao QY, et al. Among authors: cui tl. J Vasc Surg Venous Lymphat Disord. 2024 Jan;12(1):101682. doi: 10.1016/j.jvsv.2023.08.021. Epub 2023 Sep 12. J Vasc Surg Venous Lymphat Disord. 2024. PMID: 37708936 Free PMC article.

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