Similar articles for PMID: 20186689

Year	Number of Results
1995	1
1999	1
2000	1
2001	1
2002	5
2003	2
2004	4
2005	9
2006	8
2007	8
2008	10
2009	8
2010	6
2011	3
2012	4
2013	5
2014	5
2015	10
2016	2
2018	2
2019	1
2020	2
2024	0

1

Functional PMS2 hybrid alleles containing a pseudogene-specific missense variant trace back to a single ancient intrachromosomal recombination event.

Ganster C, Wernstedt A, Kehrer-Sawatzki H, Messiaen L, Schmidt K, Rahner N, Heinimann K, Fonatsch C, Zschocke J, Wimmer K. Ganster C, et al. Hum Mutat. 2010 May;31(5):552-60. doi: 10.1002/humu.21223. Hum Mutat. 2010. PMID: 20186689 Free PMC article.

2

Improved multiplex ligation-dependent probe amplification analysis identifies a deleterious PMS2 allele generated by recombination with crossover between PMS2 and PMS2CL.

Wernstedt A, Valtorta E, Armelao F, Togni R, Girlando S, Baudis M, Heinimann K, Messiaen L, Staehli N, Zschocke J, Marra G, Wimmer K. Wernstedt A, et al. Genes Chromosomes Cancer. 2012 Sep;51(9):819-31. doi: 10.1002/gcc.21966. Epub 2012 May 14. Genes Chromosomes Cancer. 2012. PMID: 22585707 Free PMC article.

3

PMS2 gene mutational analysis: direct cDNA sequencing to circumvent pseudogene interference.

Wimmer K, Wernstedt A. Wimmer K, et al. Methods Mol Biol. 2014;1167:289-302. doi: 10.1007/978-1-4939-0835-6_20. Methods Mol Biol. 2014. PMID: 24823786

4

Extensive gene conversion at the PMS2 DNA mismatch repair locus.

Hayward BE, De Vos M, Valleley EM, Charlton RS, Taylor GR, Sheridan E, Bonthron DT. Hayward BE, et al. Hum Mutat. 2007 May;28(5):424-30. doi: 10.1002/humu.20457. Hum Mutat. 2007. PMID: 17253626

5

Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients.

van der Klift HM, Tops CM, Bik EC, Boogaard MW, Borgstein AM, Hansson KB, Ausems MG, Gomez Garcia E, Green A, Hes FJ, Izatt L, van Hest LP, Alonso AM, Vriends AH, Wagner A, van Zelst-Stams WA, Vasen HF, Morreau H, Devilee P, Wijnen JT. van der Klift HM, et al. Hum Mutat. 2010 May;31(5):578-87. doi: 10.1002/humu.21229. Hum Mutat. 2010. PMID: 20186688

6

RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference.

Etzler J, Peyrl A, Zatkova A, Schildhaus HU, Ficek A, Merkelbach-Bruse S, Kratz CP, Attarbaschi A, Hainfellner JA, Yao S, Messiaen L, Slavc I, Wimmer K. Etzler J, et al. Hum Mutat. 2008 Feb;29(2):299-305. doi: 10.1002/humu.20657. Hum Mutat. 2008. PMID: 18030674

7

Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene.

Gould GM, Grauman PV, Theilmann MR, Spurka L, Wang IE, Melroy LM, Chin RG, Hite DH, Chu CS, Maguire JR, Hogan GJ, Muzzey D. Gould GM, et al. BMC Med Genet. 2018 Sep 29;19(1):176. doi: 10.1186/s12881-018-0691-9. BMC Med Genet. 2018. PMID: 30268105 Free PMC article.

8

Avoidance of pseudogene interference in the detection of 3' deletions in PMS2.

Vaughn CP, Hart KJ, Samowitz WS, Swensen JJ. Vaughn CP, et al. Hum Mutat. 2011 Sep;32(9):1063-71. doi: 10.1002/humu.21540. Hum Mutat. 2011. PMID: 21618646

9

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes.

Vaughn CP, Robles J, Swensen JJ, Miller CE, Lyon E, Mao R, Bayrak-Toydemir P, Samowitz WS. Vaughn CP, et al. Hum Mutat. 2010 May;31(5):588-93. doi: 10.1002/humu.21230. Hum Mutat. 2010. PMID: 20205264

10

Getting rid of the PMS2 pseudogenes: mission impossible?

Niessen RC, Kleibeuker JH, Jager PO, Sijmons RH, Hofstra RM. Niessen RC, et al. Hum Mutat. 2007 Apr;28(4):414; author reply 415. doi: 10.1002/humu.20447. Hum Mutat. 2007. PMID: 17139668 No abstract available.

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