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Items: 10

1.
Human DNA polymerase delta requires an iron–sulfur cluster for high-fidelity DNA synthesis
Stanislaw K. Jozwiakowski, Sandra Kummer, Kerstin Gari
Life Sci Alliance. 2019 Aug; 2(4): e201900321. Published online 2019 Jul 5. doi: 10.26508/lsa.201900321
PMCID:
PMC6613617
AbstractArticlePDF–2.3M
2.
Molecular cloning of the cDNA for the catalytic subunit of human DNA polymerase delta.
C L Yang, L S Chang, P Zhang, H Hao, L Zhu, N L Toomey, M Y Lee
Nucleic Acids Res. 1992 Feb 25; 20(4): 735–745. doi: 10.1093/nar/20.4.735
PMCID:
PMC312012
SummaryPage BrowsePDF–2.8M
3.
Primary structure of the catalytic subunit of human DNA polymerase delta and chromosomal location of the gene.
D W Chung, J A Zhang, C K Tan, E W Davie, A G So, K M Downey
Proc Natl Acad Sci U S A. 1991 Dec 15; 88(24): 11197–11201. doi: 10.1073/pnas.88.24.11197
PMCID:
PMC53101
SummaryPage BrowsePDF–1.7M
4.
Current status of the genetic susceptibility in attenuated adenomatous polyposis
Víctor Lorca, Pilar Garre
World J Gastrointest Oncol. 2019 Dec 15; 11(12): 1101–1114. Published online 2019 Dec 15. doi: 10.4251/wjgo.v11.i12.1101
PMCID:
PMC6937445
AbstractArticlePDF–1.0M
5.
Comprehensive mismatch repair gene panel identifies variants in patients with Lynch‐like syndrome
Alexandre Xavier, Maren Fridtjofsen Olsen, Liss A. Lavik, Jostein Johansen, Ashish Kumar Singh, Wenche Sjursen, Rodney J. Scott, Bente A. Talseth‐Palmer
Mol Genet Genomic Med. 2019 Aug; 7(8): e850. Published online 2019 Jul 12. doi: 10.1002/mgg3.850
PMCID:
PMC6687620
AbstractArticlePDF–676K
6.
Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing
Víctor Lorca, Daniel Rueda, Lorena Martín-Morales, María Jesús Fernández-Aceñero, Judith Grolleman, Carmen Poves, Patricia Llovet, Sandra Tapial, Vanesa García-Barberán, Julián Sanz, Pedro Pérez-Segura, Richarda M. de Voer, Eduardo Díaz-Rubio, Miguel de la Hoya, Trinidad Caldés, Pilar Garre
Sci Rep. 2019; 9: 9814. Published online 2019 Jul 8. doi: 10.1038/s41598-019-46403-5
PMCID:
PMC6614360
AbstractArticlePDF–1.3M
7.
Gene screening facilitates diagnosis of complicated symptoms: A case report
Hong Duan, Di Zhang, Jing Cheng, Yu Lu, Huijun Yuan
Mol Med Rep. 2017 Dec; 16(6): 7915–7922. Published online 2017 Sep 22. doi: 10.3892/mmr.2017.7590
PMCID:
PMC5779872
AbstractArticlePDF–1023K
8.
The catalytic subunit of DNA polymerase δ inhibits γTuRC activity and regulates Golgi-derived microtubules
Yuehong Shen, Pengfei Liu, Taolue Jiang, Yu Hu, Franco K. C. Au, Robert Z. Qi
Nat Commun. 2017; 8: 554. Published online 2017 Sep 15. doi: 10.1038/s41467-017-00694-2
PMCID:
PMC5601897
AbstractArticlePDF–3.3M
9.
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment
Valentina S. Vysotskaia, Gregory J. Hogan, Genevieve M. Gould, Xin Wang, Alex D. Robertson, Kevin R. Haas, Mark R. Theilmann, Lindsay Spurka, Peter V. Grauman, Henry H. Lai, Diana Jeon, Genevieve Haliburton, Matt Leggett, Clement S. Chu, Kevin Iori, Jared R. Maguire, Kaylene Ready, Eric A. Evans, Hyunseok P. Kang, Imran S. Haque
PeerJ. 2017; 5: e3046. Published online 2017 Feb 23. doi: 10.7717/peerj.3046
PMCID:
PMC5326550
AbstractArticlePDF–229K
10.
Targeted next‐generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families
Bente A. Talseth‐Palmer, Denis C. Bauer, Wenche Sjursen, Tiffany J. Evans, Mary McPhillips, Anthony Proietto, Geoffrey Otton, Allan D. Spigelman, Rodney J. Scott
Cancer Med. 2016 May; 5(5): 929–941. Published online 2016 Jan 25. doi: 10.1002/cam4.628
PMCID:
PMC4864822
AbstractArticlePDF–336K

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