PubMed for id: 26051260

Year	Number of Results
1993	1
1996	1
1998	3
2010	1
2022	1
2023	5
2024	2

1

Improved classification and pathogenicity assessment by comprehensive functional studies in a large data set of KCNQ2 variants.

Zhang Y, Xue Y, Ma Y, Du X, Lu B, Wang Y, Yan Z. Zhang Y, et al. Life Sci. 2024 Feb 15;339:122378. doi: 10.1016/j.lfs.2023.122378. Epub 2023 Dec 23. Life Sci. 2024. PMID: 38142737

2

Familial KCNQ2 mutation: a psychiatric perspective.

Iftimovici A, Charmet A, Desnous B, Ory A, Delorme R, Coutton C, Devillard F, Milh M, Maruani A. Iftimovici A, et al. Psychiatr Genet. 2024 Feb 1;34(1):24-27. doi: 10.1097/YPG.0000000000000360. Epub 2023 Dec 13. Psychiatr Genet. 2024. PMID: 38108335 Free PMC article.

3

Prognostic Analysis of KCNQ2 Patients via Combining EEG Deep Features and Machine Learning Classifiers.

Zeng Z, Xu Y, Zhou Y, Su R, Tao L, Wang Z, Chen C, Chen W. Zeng Z, et al. Annu Int Conf IEEE Eng Med Biol Soc. 2023 Jul;2023:1-4. doi: 10.1109/EMBC40787.2023.10341098. Annu Int Conf IEEE Eng Med Biol Soc. 2023. PMID: 38083766

4

Ligand activation mechanisms of human KCNQ2 channel.

Ma D, Zheng Y, Li X, Zhou X, Yang Z, Zhang Y, Wang L, Zhang W, Fang J, Zhao G, Hou P, Nan F, Yang W, Su N, Gao Z, Guo J. Ma D, et al. Nat Commun. 2023 Oct 19;14(1):6632. doi: 10.1038/s41467-023-42416-x. Nat Commun. 2023. PMID: 37857637 Free PMC article.

5

Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey.

Cossu A, Lo Barco T, Proietti J, Dalla Bernardina B, Cantalupo G, Ghobert L, Brambilla I, Giarola E, Costa A, De Benito T, Bethge S, Cardot S, Montwill I, Remonato E, Gramaglia S, Darra F. Cossu A, et al. Epilepsy Behav. 2023 May;142:109153. doi: 10.1016/j.yebeh.2023.109153. Epub 2023 Mar 28. Epilepsy Behav. 2023. PMID: 36989566 Free article.

6

KCNQ2-Related Disorders.

Miceli F, Soldovieri MV, Weckhuysen S, Cooper E, Taglialatela M. Miceli F, et al. 2010 Apr 27 [updated 2022 May 19]. 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. 2010 Apr 27 [updated 2022 May 19]. 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: 20437616 Free Books & Documents. Review.

7

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy.

Yang WP, Levesque PC, Little WA, Conder ML, Ramakrishnan P, Neubauer MG, Blanar MA. Yang WP, et al. J Biol Chem. 1998 Jul 31;273(31):19419-23. doi: 10.1074/jbc.273.31.19419. J Biol Chem. 1998. PMID: 9677360 Free article.

8

A potassium channel mutation in neonatal human epilepsy.

Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, Steinlein OK. Biervert C, et al. Science. 1998 Jan 16;279(5349):403-6. doi: 10.1126/science.279.5349.403. Science. 1998. PMID: 9430594

9

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895

10

Identification and cloning of neuroblastoma-specific and nerve tissue-specific genes through compiled expression profiles.

Yokoyama M, Nishi Y, Yoshii J, Okubo K, Matsubara K. Yokoyama M, et al. DNA Res. 1996 Oct 31;3(5):311-20. doi: 10.1093/dnares/3.5.311. DNA Res. 1996. PMID: 9039501 Free article.

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