PubMed (cited) for id: 115440

Year	Number of Results
1989	1
1991	1
1992	2
1994	1
2001	1
2002	2
2004	1
2005	1
2016	1
2017	1
2018	3
2024	0

1

Refining the clinical phenotype of Okur-Chung neurodevelopmental syndrome.

Akahira-Azuma M, Tsurusaki Y, Enomoto Y, Mitsui J, Kurosawa K. Akahira-Azuma M, et al. Hum Genome Var. 2018 Mar 29;5:18011. doi: 10.1038/hgv.2018.11. eCollection 2018. Hum Genome Var. 2018. PMID: 29619237 Free PMC article.

2

Extending the phenotype associated with the CSNK2A1-related Okur-Chung syndrome-A clinical study of 11 individuals.

Owen CI, Bowden R, Parker MJ, Patterson J, Patterson J, Price S, Sarkar A, Castle B, Deshpande C, Splitt M, Ghali N, Dean J, Green AJ, Crosby C; Deciphering Developmental Disorders Study; Tatton-Brown K. Owen CI, et al. Am J Med Genet A. 2018 May;176(5):1108-1114. doi: 10.1002/ajmg.a.38610. Epub 2018 Jan 31. Am J Med Genet A. 2018. PMID: 29383814

3

Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion.

Chiu ATG, Pei SLC, Mak CCY, Leung GKC, Yu MHC, Lee SL, Vreeburg M, Pfundt R, van der Burgt I, Kleefstra T, Frederic TM, Nambot S, Faivre L, Bruel AL, Rossi M, Isidor B, Küry S, Cogne B, Besnard T, Willems M, Reijnders MRF, Chung BHY. Chiu ATG, et al. Clin Genet. 2018 Apr;93(4):880-890. doi: 10.1111/cge.13196. Epub 2018 Feb 13. Clin Genet. 2018. PMID: 29240241

4

A novel de novo mutation in CSNK2A1: reinforcing the link to neurodevelopmental abnormalities and dysmorphic features.

Trinh J, Hüning I, Budler N, Hingst V, Lohmann K, Gillessen-Kaesbach G. Trinh J, et al. J Hum Genet. 2017 Nov;62(11):1005-1006. doi: 10.1038/jhg.2017.73. Epub 2017 Jul 20. J Hum Genet. 2017. PMID: 28725024 No abstract available.

5

De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.

Okur V, Cho MT, Henderson L, Retterer K, Schneider M, Sattler S, Niyazov D, Azage M, Smith S, Picker J, Lincoln S, Tarnopolsky M, Brady L, Bjornsson HT, Applegate C, Dameron A, Willaert R, Baskin B, Juusola J, Chung WK. Okur V, et al. Hum Genet. 2016 Jul;135(7):699-705. doi: 10.1007/s00439-016-1661-y. Epub 2016 Apr 5. Hum Genet. 2016. PMID: 27048600

6

Functional characterization of core promoter elements: DPE-specific transcription requires the protein kinase CK2 and the PC4 coactivator.

Lewis BA, Sims RJ 3rd, Lane WS, Reinberg D. Lewis BA, et al. Mol Cell. 2005 May 13;18(4):471-81. doi: 10.1016/j.molcel.2005.04.005. Mol Cell. 2005. PMID: 15893730 Free article.

7

The protein kinase CK2 facilitates repair of chromosomal DNA single-strand breaks.

Loizou JI, El-Khamisy SF, Zlatanou A, Moore DJ, Chan DW, Qin J, Sarno S, Meggio F, Pinna LA, Caldecott KW. Loizou JI, et al. Cell. 2004 Apr 2;117(1):17-28. doi: 10.1016/s0092-8674(04)00206-5. Cell. 2004. PMID: 15066279 Free article.

8

A role for casein kinase 2alpha in the Drosophila circadian clock.

Lin JM, Kilman VL, Keegan K, Paddock B, Emery-Le M, Rosbash M, Allada R. Lin JM, et al. Nature. 2002 Dec 19-26;420(6917):816-20. doi: 10.1038/nature01235. Nature. 2002. PMID: 12447397

9

Cooperation of GGAs and AP-1 in packaging MPRs at the trans-Golgi network.

Doray B, Ghosh P, Griffith J, Geuze HJ, Kornfeld S. Doray B, et al. Science. 2002 Sep 6;297(5587):1700-3. doi: 10.1126/science.1075327. Science. 2002. PMID: 12215646

10

A DNA damage-induced p53 serine 392 kinase complex contains CK2, hSpt16, and SSRP1.

Keller DM, Zeng X, Wang Y, Zhang QH, Kapoor M, Shu H, Goodman R, Lozano G, Zhao Y, Lu H. Keller DM, et al. Mol Cell. 2001 Feb;7(2):283-92. doi: 10.1016/s1097-2765(01)00176-9. Mol Cell. 2001. PMID: 11239457 Free article.

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