Meyer JA - Search Results

1

Genomic Characterization of Poorly Differentiated Neuroendocrine Carcinoma in a Pediatric Patient.

Bhatla T, Dandekar S, Lu BY, Wang J, Han E, Bitterman D, Jones CL, Evensen NA, Magid M, Meyer JA, Carroll WL. Bhatla T, et al. Among authors: meyer ja. J Pediatr Hematol Oncol. 2016 Jan;38(1):e21-5. doi: 10.1097/MPH.0000000000000463. J Pediatr Hematol Oncol. 2016. PMID: 26558807 Free PMC article.

2

The biology of relapsed acute lymphoblastic leukemia: opportunities for therapeutic interventions.

Bhatla T, Jones CL, Meyer JA, Vitanza NA, Raetz EA, Carroll WL. Bhatla T, et al. Among authors: meyer ja. J Pediatr Hematol Oncol. 2014 Aug;36(6):413-8. doi: 10.1097/MPH.0000000000000179. J Pediatr Hematol Oncol. 2014. PMID: 24942023 Free PMC article. Review.

3

Ikaros deletions in BCR-ABL-negative childhood acute lymphoblastic leukemia are associated with a distinct gene expression signature but do not result in intrinsic chemoresistance.

Vitanza NA, Zaky W, Blum R, Meyer JA, Wang J, Bhatla T, Morrison DJ, Raetz EA, Carroll WL. Vitanza NA, et al. Among authors: meyer ja. Pediatr Blood Cancer. 2014 Oct;61(10):1779-85. doi: 10.1002/pbc.25119. Epub 2014 Jun 29. Pediatr Blood Cancer. 2014. PMID: 24976218 Free PMC article.

4

State of the art discovery with tumor profiling in pediatric oncology.

Carroll WL, Raetz E, Meyer J. Carroll WL, et al. Am Soc Clin Oncol Educ Book. 2015:e601-7. doi: 10.14694/EdBook_AM.2015.35.e601. Am Soc Clin Oncol Educ Book. 2015. PMID: 25993229 Free article. Review.

5

Splice site mutation in factor X gene manifesting as severe intracranial haemorrhage in neonatal period with a challenging treatment course.

Madhusoodhan PP, Lu BY, Chen J, Jones CL, Meyer JA, Roman EA, Nardi M, Carroll WL, Bhatla T. Madhusoodhan PP, et al. Among authors: meyer ja. Haemophilia. 2017 Mar;23(2):e138-e140. doi: 10.1111/hae.13138. Epub 2016 Dec 19. Haemophilia. 2017. PMID: 27995737 No abstract available.

6

Feasibility of monitoring peripheral blood to detect emerging clones in children with acute lymphoblastic leukemia^†.

Saliba J, Evensen NA, Meyer JA, Newman D, Nersting J, Narang S, Ma X, Schmiegelow K, Carroll WL. Saliba J, et al. Among authors: meyer ja. Pediatr Blood Cancer. 2020 Jul;67(7):e28306. doi: 10.1002/pbc.28306. Epub 2020 May 11. Pediatr Blood Cancer. 2020. PMID: 32391957

7

MSH6 haploinsufficiency at relapse contributes to the development of thiopurine resistance in pediatric B-lymphoblastic leukemia.

Evensen NA, Madhusoodhan PP, Meyer J, Saliba J, Chowdhury A, Araten DJ, Nersting J, Bhatla T, Vincent TL, Teachey D, Hunger SP, Yang J, Schmiegelow K, Carroll WL. Evensen NA, et al. Haematologica. 2018 May;103(5):830-839. doi: 10.3324/haematol.2017.176362. Epub 2018 Feb 15. Haematologica. 2018. PMID: 29449434 Free PMC article.

8

Integrated genomic analysis of relapsed childhood acute lymphoblastic leukemia reveals therapeutic strategies.

Hogan LE, Meyer JA, Yang J, Wang J, Wong N, Yang W, Condos G, Hunger SP, Raetz E, Saffery R, Relling MV, Bhojwani D, Morrison DJ, Carroll WL. Hogan LE, et al. Among authors: meyer ja. Blood. 2011 Nov 10;118(19):5218-26. doi: 10.1182/blood-2011-04-345595. Epub 2011 Sep 14. Blood. 2011. PMID: 21921043 Free PMC article.

9

Relapse-specific mutations in NT5C2 in childhood acute lymphoblastic leukemia.

Meyer JA, Wang J, Hogan LE, Yang JJ, Dandekar S, Patel JP, Tang Z, Zumbo P, Li S, Zavadil J, Levine RL, Cardozo T, Hunger SP, Raetz EA, Evans WE, Morrison DJ, Mason CE, Carroll WL. Meyer JA, et al. Nat Genet. 2013 Mar;45(3):290-4. doi: 10.1038/ng.2558. Epub 2013 Feb 3. Nat Genet. 2013. PMID: 23377183 Free PMC article.

10

Screening for gene mutations: will identification of NT5C2 mutations help predict the chance of relapse in acute lymphoblastic leukemia?

Meyer JA, Carroll WL, Bhatla T. Meyer JA, et al. Expert Rev Hematol. 2013 Jun;6(3):223-4. doi: 10.1586/ehm.13.28. Expert Rev Hematol. 2013. PMID: 23782074 Free PMC article. No abstract available.

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