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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2004 | 1 |
2005 | 1 |
2013 | 2 |
2017 | 1 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
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Page 1
Gene expression profile in interleukin-4-stimulated human vascular endothelial cells.
Mol Med. 2004 Jan-Jun;10(1-6):19-27. doi: 10.2119/2004-00024.lee.
Mol Med. 2004.
PMID: 15502879
Free PMC article.
Comparative host gene transcription by microarray analysis early after infection of the Huh7 cell line by severe acute respiratory syndrome coronavirus and human coronavirus 229E.
Tang BS, Chan KH, Cheng VC, Woo PC, Lau SK, Lam CC, Chan TL, Wu AK, Hung IF, Leung SY, Yuen KY.
Tang BS, et al.
J Virol. 2005 May;79(10):6180-93. doi: 10.1128/JVI.79.10.6180-6193.2005.
J Virol. 2005.
PMID: 15858003
Free PMC article.
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Scaffolding protein SPIDR/KIAA0146 connects the Bloom syndrome helicase with homologous recombination repair.
Wan L, Han J, Liu T, Dong S, Xie F, Chen H, Huang J.
Wan L, et al.
Proc Natl Acad Sci U S A. 2013 Jun 25;110(26):10646-51. doi: 10.1073/pnas.1220921110. Epub 2013 Mar 18.
Proc Natl Acad Sci U S A. 2013.
PMID: 23509288
Free PMC article.
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FIGNL1-containing protein complex is required for efficient homologous recombination repair.
Yuan J, Chen J.
Yuan J, et al.
Proc Natl Acad Sci U S A. 2013 Jun 25;110(26):10640-5. doi: 10.1073/pnas.1220662110. Epub 2013 Jun 10.
Proc Natl Acad Sci U S A. 2013.
PMID: 23754376
Free PMC article.
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A Biallelic Mutation in the Homologous Recombination Repair Gene SPIDR Is Associated With Human Gonadal Dysgenesis.
Smirin-Yosef P, Zuckerman-Levin N, Tzur S, Granot Y, Cohen L, Sachsenweger J, Borck G, Lagovsky I, Salmon-Divon M, Wiesmüller L, Basel-Vanagaite L.
Smirin-Yosef P, et al.
J Clin Endocrinol Metab. 2017 Feb 1;102(2):681-688. doi: 10.1210/jc.2016-2714.
J Clin Endocrinol Metab. 2017.
PMID: 27967308
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A SPIDR homozygous nonsense pathogenic variant in isolated primary ovarian insufficiency with chromosomal instability.
Heddar A, Guichoux N, Auger N, Misrahi M.
Heddar A, et al.
Clin Genet. 2022 Feb;101(2):242-246. doi: 10.1111/cge.14080. Epub 2021 Nov 9.
Clin Genet. 2022.
PMID: 34697795
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