Similar articles for PMID: 18503583

Year	Number of Results
1960	1
1964	2
1966	1
1967	1
1972	1
1977	1
1981	2
1982	1
1989	1
1991	1
2001	1
2002	1
2005	2
2006	3
2007	22
2008	26
2009	25
2010	9
2011	15
2012	10
2013	7
2014	3
2015	3
2016	7
2017	7
2018	13
2019	5
2020	6
2021	5
2022	4
2023	3
2024	0

1

Mutations in exon 12 of JAK2 are mainly found in JAK2 V617F-negative polycythaemia vera patients.

Kouroupi E, Zoi K, Parquet N, Zoi C, Kiladjian JJ, Grigoraki V, Vainchenker W, Lellouche F, Marzac C, Schlageter MH, Dosquet C, Scott LM, Fenaux P, Loukopoulos D, Chomienne C, Cassinat B. Kouroupi E, et al. Br J Haematol. 2008 Aug;142(4):676-9. doi: 10.1111/j.1365-2141.2008.07223.x. Epub 2008 May 22. Br J Haematol. 2008. PMID: 18503583 Free article. No abstract available.

2

Isolated erythrocytosis in V617F negative patients with JAK2 exon 12 mutations: report of a new mutation.

Bernardi M, Ruggeri M, Albiero E, Madeo D, Rodeghiero F. Bernardi M, et al. Am J Hematol. 2009 Apr;84(4):258-60. doi: 10.1002/ajh.21357. Am J Hematol. 2009. PMID: 19229983 Free article. No abstract available.

3

A novel JAK2 exon 12 mutation identified in the retrospective analysis of paraffin-embedded tissues of polycythemia vera patients.

Burjanivova T, Marcinek J, Lasabova Z, Minarik G, Szepe P, Balharek T, Vanochova A, Polacek H, Plank L. Burjanivova T, et al. Diagn Mol Pathol. 2009 Jun;18(2):108-11. doi: 10.1097/PDM.0b013e318190eed0. Diagn Mol Pathol. 2009. PMID: 19430293

4

Fast and reliable mutation detection of the complete exon 11-15 JAK2 coding region using non-isotopic RNase cleavage assay (NIRCA).

Kambas K, Mitroulis I, Kourtzelis I, Chrysanthopoulou A, Speletas M, Ritis K. Kambas K, et al. Eur J Haematol. 2009 Sep;83(3):215-9. doi: 10.1111/j.1600-0609.2009.01279.x. Epub 2009 Jun 2. Eur J Haematol. 2009. PMID: 19500139

5

Bone marrow morphologic features in polycythemia vera with JAK2 exon 12 mutations.

Lakey MA, Pardanani A, Hoyer JD, Nguyen PL, Lasho TL, Tefferi A, Hanson CA. Lakey MA, et al. Am J Clin Pathol. 2010 Jun;133(6):942-8. doi: 10.1309/AJCP3Z2AKUWRGTNM. Am J Clin Pathol. 2010. PMID: 20472853

6

Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia vera.

Scott LM, Beer PA, Bench AJ, Erber WN, Green AR. Scott LM, et al. Br J Haematol. 2007 Nov;139(3):511-2. doi: 10.1111/j.1365-2141.2007.06806.x. Br J Haematol. 2007. PMID: 17910642 Free article. No abstract available.

7

JAK2 exon 12 mutations in polycythemia vera or idiopathic erythrocytosis.

Martínez-Avilés L, Besses C, Alvarez-Larrán A, Cervantes F, Hernández-Boluda JC, Bellosillo B. Martínez-Avilés L, et al. Haematologica. 2007 Dec;92(12):1717-8. doi: 10.3324/haematol.12011. Haematologica. 2007. PMID: 18056003 Free article.

8

High frequency of JAK2 exon 12 mutations in Korean patients with polycythaemia vera: novel mutations and clinical significance.

Park CH, Lee KO, Jang JH, Jung CW, Kim JW, Kim SH, Kim HJ. Park CH, et al. J Clin Pathol. 2016 Aug;69(8):737-41. doi: 10.1136/jclinpath-2016-203649. Epub 2016 May 19. J Clin Pathol. 2016. PMID: 27198504

9

Detection of JAK2 Exon 12 Mutations in JAK2 V617F-Negative Polycythemia Vera Patients by Cloning Technique.

Leszczynska A, Grzenkowicz-Wydra J, Chmielewska-Gorycka L, Bieniaszewska M, Hellmann A. Leszczynska A, et al. Acta Haematol. 2016;136(2):123-8. doi: 10.1159/000446798. Epub 2016 Jul 14. Acta Haematol. 2016. PMID: 27410038

10

No evidence for JAK2(V617F) mutation in monoclonal B cells in 2 patients with polycythaemia vera and concurrent monoclonal B cell disorder.

Stijnis C, Kroes WG, Balkassmi S, Marijt EW, van Rossum AP, Bakker E, Vlasveld LT. Stijnis C, et al. Acta Haematol. 2012;128(3):183-6. doi: 10.1159/000338831. Epub 2012 Aug 10. Acta Haematol. 2012. PMID: 22890406

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