PubMed for id: 186700627

Year	Number of Results
1993	1
1996	1
1997	1
1998	3
2000	1
2013	1
2020	1
2022	1
2023	2
2024	0

1

Diverse Clinical Phenotypes of CASK-Related Disorders and Multiple Functional Domains of CASK Protein.

Mori T, Zhou M, Tabuchi K. Mori T, et al. Genes (Basel). 2023 Aug 20;14(8):1656. doi: 10.3390/genes14081656. Genes (Basel). 2023. PMID: 37628707 Free PMC article. Review.

2

Calcium/calmodulin-dependent serine protein kinase exacerbates mitochondrial calcium uniporter-related mitochondrial calcium overload by phosphorylating α-synuclein in Parkinson's disease.

Zhang Q, Huang Y, Wu A, Duan Q, He P, Huang H, Gao Y, Nie K, Liu Q, Wang L. Zhang Q, et al. Int J Biochem Cell Biol. 2023 Apr;157:106385. doi: 10.1016/j.biocel.2023.106385. Epub 2023 Feb 7. Int J Biochem Cell Biol. 2023. PMID: 36754160

3

Two heterozygous mutations in the calcium/calmodulin-dependent serine protein kinase gene (CASK) in cases with developmental disorders.

Yang K, Lin L, Yuan F, Li X, Liu Z, Lan X, Wang Y, Ren Y, Li J, Chen Y. Yang K, et al. Mol Genet Genomic Med. 2022 Nov;10(11):e2065. doi: 10.1002/mgg3.2065. Epub 2022 Sep 28. Mol Genet Genomic Med. 2022. PMID: 36168867 Free PMC article.

4

CASK Disorders.

Moog U, Kutsche K. Moog U, et al. 2013 Nov 26 [updated 2020 May 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2013 Nov 26 [updated 2020 May 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 24278995 Free Books & Documents. Review.

5

Mapping and expression analysis of the human CASK gene.

Stevenson D, Laverty HG, Wenwieser S, Douglas M, Wilson JB. Stevenson D, et al. Mamm Genome. 2000 Oct;11(10):934-7. doi: 10.1007/s003350010170. Mamm Genome. 2000. PMID: 11003712 No abstract available.

6

The location of human CASK at Xp11.4 identifies this gene as a candidate for X-linked optic atrophy.

Dimitratos SD, Stathakis DG, Nelson CA, Woods DF, Bryant PJ. Dimitratos SD, et al. Genomics. 1998 Jul 15;51(2):308-9. doi: 10.1006/geno.1998.5404. Genomics. 1998. PMID: 9722958 No abstract available.

7

Human CASK/LIN-2 binds syndecan-2 and protein 4.1 and localizes to the basolateral membrane of epithelial cells.

Cohen AR, Woods DF, Marfatia SM, Walther Z, Chishti AH, Anderson JM. Cohen AR, et al. J Cell Biol. 1998 Jul 13;142(1):129-38. doi: 10.1083/jcb.142.1.129. J Cell Biol. 1998. PMID: 9660868 Free PMC article.

8

Crystal structure of the hCASK PDZ domain reveals the structural basis of class II PDZ domain target recognition.

Daniels DL, Cohen AR, Anderson JM, Brünger AT. Daniels DL, et al. Nat Struct Biol. 1998 Apr;5(4):317-25. doi: 10.1038/nsb0498-317. Nat Struct Biol. 1998. PMID: 9546224

9

cDNAs with long CAG trinucleotide repeats from human brain.

Margolis RL, Abraham MR, Gatchell SB, Li SH, Kidwai AS, Breschel TS, Stine OC, Callahan C, McInnis MG, Ross CA. Margolis RL, et al. Hum Genet. 1997 Jul;100(1):114-22. doi: 10.1007/s004390050476. Hum Genet. 1997. PMID: 9225980

10

CASK: a novel dlg/PSD95 homolog with an N-terminal calmodulin-dependent protein kinase domain identified by interaction with neurexins.

Hata Y, Butz S, Südhof TC. Hata Y, et al. J Neurosci. 1996 Apr 15;16(8):2488-94. doi: 10.1523/JNEUROSCI.16-08-02488.1996. J Neurosci. 1996. PMID: 8786425 Free PMC article.

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