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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1957 1
1991 2
1992 1
1993 2
1994 7
1995 5
1996 5
1997 13
1998 16
1999 24
2000 25
2001 13
2002 13
2003 6
2004 6
2005 7
2006 3
2007 1
2008 5
2009 2
2010 2
2011 1
2012 4
2013 12
2014 7
2015 4
2016 3
2017 9
2018 7
2019 7
2020 6
2021 8
2022 3
2023 3
2024 2

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Similar articles for PMID: 10077519

218 results

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Page 1
Establishment of iPSC line from a Chinese infant (XACHi012-A) with Jervell and Lange-Nielsen syndrome carrying combined KCNQ1 frameshift c.431delC(p.I145Sfs*92) and nonsense c.1175G > A (p.W392X) variants and two iPSC lines from the parents (XACHi013-A, XACHi014-A).
Zhou Y, Wang J, Li H, Li A, Wang G, Tan X, Lei M, Zhang Y. Zhou Y, et al. Stem Cell Res. 2021 May;53:102391. doi: 10.1016/j.scr.2021.102391. Epub 2021 May 11. Stem Cell Res. 2021. PMID: 34088017 Free article.
Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression.
González-Garrido A, Domínguez-Pérez M, Jacobo-Albavera L, López-Ramírez O, Guevara-Chávez JG, Zepeda-García O, Iturralde P, Carnevale A, Villarreal-Molina T. González-Garrido A, et al. Front Cardiovasc Med. 2021 Feb 22;8:625449. doi: 10.3389/fcvm.2021.625449. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 33693037 Free PMC article.
218 results