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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 2 |
1999 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 9338
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TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.
Am J Hum Genet. 2022 Dec 1;109(12):2270-2282. doi: 10.1016/j.ajhg.2022.10.007. Epub 2022 Nov 10.
Am J Hum Genet. 2022.
PMID: 36368327
Free PMC article.
Genomic structure and chromosomal localization of TCEAL1, a human gene encoding the nuclear phosphoprotein p21/SIIR.
Pillutla RC, Shimamoto A, Furuichi Y, Shatkin AJ.
Pillutla RC, et al.
Genomics. 1999 Mar 1;56(2):217-20. doi: 10.1006/geno.1998.5705.
Genomics. 1999.
PMID: 10051408
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A HeLa-cell-encoded p21 is homologous to transcription elongation factor SII.
Yeh CH, Shatkin AJ.
Yeh CH, et al.
Gene. 1994 Jun 10;143(2):285-7. doi: 10.1016/0378-1119(94)90112-0.
Gene. 1994.
PMID: 8206389
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Down-regulation of Rous sarcoma virus long terminal repeat promoter activity by a HeLa cell basic protein.
Yeh CH, Shatkin AJ.
Yeh CH, et al.
Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):11002-6. doi: 10.1073/pnas.91.23.11002.
Proc Natl Acad Sci U S A. 1994.
PMID: 7971997
Free PMC article.
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