PubMed (OMIM) for id: 818

Year	Number of Results
1994	1
1997	2
2000	1
2001	1
2003	1
2005	1
2006	1
2012	1
2018	2
2024	0

1

The intellectual disability-associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain-of-function.

Proietti Onori M, Koopal B, Everman DB, Worthington JD, Jones JR, Ploeg MA, Mientjes E, van Bon BW, Kleefstra T, Schulman H, Kushner SA, Küry S, Elgersma Y, van Woerden GM. Proietti Onori M, et al. Hum Mutat. 2018 Dec;39(12):2008-2024. doi: 10.1002/humu.23647. Epub 2018 Sep 19. Hum Mutat. 2018. PMID: 30184290 Free PMC article.

2

Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy.

Ostrander BEP, Butterfield RJ, Pedersen BS, Farrell AJ, Layer RM, Ward A, Miller C, DiSera T, Filloux FM, Candee MS, Newcomb T, Bonkowsky JL, Marth GT, Quinlan AR. Ostrander BEP, et al. NPJ Genom Med. 2018 Aug 13;3:22. doi: 10.1038/s41525-018-0061-8. eCollection 2018. NPJ Genom Med. 2018. PMID: 30109124 Free PMC article.

3

Diagnostic exome sequencing in persons with severe intellectual disability.

de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, del Rosario M, Hoischen A, Scheffer H, de Vries BB, Brunner HG, Veltman JA, Vissers LE. de Ligt J, et al. N Engl J Med. 2012 Nov 15;367(20):1921-9. doi: 10.1056/NEJMoa1206524. Epub 2012 Oct 3. N Engl J Med. 2012. PMID: 23033978 Free article.

4

Identification of a genetic cluster influencing memory performance and hippocampal activity in humans.

de Quervain DJ, Papassotiropoulos A. de Quervain DJ, et al. Proc Natl Acad Sci U S A. 2006 Mar 14;103(11):4270-4. doi: 10.1073/pnas.0510212103. Epub 2006 Mar 7. Proc Natl Acad Sci U S A. 2006. PMID: 16537520 Free PMC article.

5

Calmodulin kinase II inhibition protects against structural heart disease.

Zhang R, Khoo MS, Wu Y, Yang Y, Grueter CE, Ni G, Price EE Jr, Thiel W, Guatimosim S, Song LS, Madu EC, Shah AN, Vishnivetskaya TA, Atkinson JB, Gurevich VV, Salama G, Lederer WJ, Colbran RJ, Anderson ME. Zhang R, et al. Nat Med. 2005 Apr;11(4):409-17. doi: 10.1038/nm1215. Epub 2005 Mar 27. Nat Med. 2005. PMID: 15793582

6

Linkage of beta1-adrenergic stimulation to apoptotic heart cell death through protein kinase A-independent activation of Ca2+/calmodulin kinase II.

Zhu WZ, Wang SQ, Chakir K, Yang D, Zhang T, Brown JH, Devic E, Kobilka BK, Cheng H, Xiao RP. Zhu WZ, et al. J Clin Invest. 2003 Mar;111(5):617-25. doi: 10.1172/JCI16326. J Clin Invest. 2003. PMID: 12618516 Free PMC article.

7

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, Griffith AJ, Morell RJ, Friedman TB, Riazuddin S, Wilcox ER. Ahmed ZM, et al. Am J Hum Genet. 2001 Jul;69(1):25-34. doi: 10.1086/321277. Epub 2001 Jun 7. Am J Hum Genet. 2001. PMID: 11398101 Free PMC article.

8

A role for CaMKII in T cell memory.

Bui JD, Calbo S, Hayden-Martinez K, Kane LP, Gardner P, Hedrick SM. Bui JD, et al. Cell. 2000 Feb 18;100(4):457-67. doi: 10.1016/s0092-8674(00)80681-9. Cell. 2000. PMID: 10693762 Free article.

9

A truncated isoform of Ca2+/calmodulin-dependent protein kinase II expressed in human islets of Langerhans may result from trans-splicing.

Breen MA, Ashcroft SJ. Breen MA, et al. FEBS Lett. 1997 Jun 16;409(3):375-9. doi: 10.1016/s0014-5793(97)00555-3. FEBS Lett. 1997. PMID: 9224693 Free article.

10

Identification of novel human tumor cell-specific CaMK-II variants.

Tombes RM, Krystal GW. Tombes RM, et al. Biochim Biophys Acta. 1997 Mar 1;1355(3):281-92. doi: 10.1016/s0167-4889(96)00141-3. Biochim Biophys Acta. 1997. PMID: 9060999 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

11 results

Results by year