Jennings LJ - Search Results

1

Lineage switch from acute myeloid leukemia to B-lymphoblastic lymphoma with an acquired PIK3R1 loss-of-function mutation.

Aldulescu M, Leuer K, Jennings LJ, Yap KL, Gong S. Aldulescu M, et al. Among authors: jennings lj. Am J Hematol. 2023 Jan;98(1):E1-E3. doi: 10.1002/ajh.26770. Epub 2022 Nov 4. Am J Hematol. 2023. PMID: 36288429 Free article. No abstract available.

2

Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study.

Gadd S, Beezhold P, Jennings L, George D, Leuer K, Huang CC, Huff V, Tognon C, Sorensen PH, Triche T, Coffin CM, Perlman EJ. Gadd S, et al. J Pathol. 2012 Sep;228(1):119-30. doi: 10.1002/path.4010. Epub 2012 Jul 2. J Pathol. 2012. PMID: 22374738

3

Expanding the Spectrum of Renal Tumors in Children: Primary Renal Myoepithelial Carcinomas With a Novel EWSR1-KLF15 Fusion.

Cajaiba MM, Jennings LJ, Rohan SM, Leuer KM, Anagnost MR, Fahner JB, Fulton BK, Geller JI, Perlman EJ. Cajaiba MM, et al. Among authors: jennings lj. Am J Surg Pathol. 2016 Mar;40(3):386-94. doi: 10.1097/PAS.0000000000000545. Am J Surg Pathol. 2016. PMID: 26523541

4

ALK-rearranged renal cell carcinomas in children.

Cajaiba MM, Jennings LJ, Rohan SM, Perez-Atayde AR, Marino-Enriquez A, Fletcher JA, Geller JI, Leuer KM, Bridge JA, Perlman EJ. Cajaiba MM, et al. Among authors: jennings lj. Genes Chromosomes Cancer. 2016 May;55(5):442-51. doi: 10.1002/gcc.22346. Epub 2016 Feb 23. Genes Chromosomes Cancer. 2016. PMID: 26773439

5

Inv(11)(q21q23); KMT2A-MAML2, a Recurrent Genetic Abnormality in T-Cell Therapy-related Acute Lymphoblastic Leukemia.

Mariani RA, Silva M, Caparelli E, Jennings LJ, Yap KL, Leuer KM, Weinstein J, Gong S. Mariani RA, et al. Among authors: jennings lj. J Pediatr Hematol Oncol. 2020 May;42(4):e258-e261. doi: 10.1097/MPH.0000000000001572. J Pediatr Hematol Oncol. 2020. PMID: 31343482

6

Morphologic and Immunophenotypic Differences in Juvenile Myelomonocytic Leukemias With CBL and Other Canonical RAS-pathway Gene Mutations: A Single Institutional Experience.

Mariani RA, Jennings L, Zhang S, Bhat R, Gong S. Mariani RA, et al. J Pediatr Hematol Oncol. 2021 Aug 1;43(6):e819-e825. doi: 10.1097/MPH.0000000000002149. J Pediatr Hematol Oncol. 2021. PMID: 33769390

7

Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype-phenotype correlation in congenital central hypoventilation syndrome (CCHS).

Zhou A, Rand CM, Hockney SM, Niewijk G, Reineke P, Speare V, Berry-Kravis EM, Zhou L, Jennings LJ, Yu M, Ceccherini I, Bachetti T, Pennock M, Yap KL, Weese-Mayer DE. Zhou A, et al. Among authors: jennings lj. Genet Med. 2021 Sep;23(9):1656-1663. doi: 10.1038/s41436-021-01178-x. Epub 2021 May 6. Genet Med. 2021. PMID: 33958749 Free article.

8

Relapse of large B-cell lymphoma with IRF4 rearrangement associated with SLAM-associated protein deficiency.

Elhodaky M, Gunderman LM, Bachula M, Liu G, Reilly P, Schmidt ML, Frederiksen JK, Lu X, Jennings L, Rossoff J, Khanolkar A, Gong S. Elhodaky M, et al. Pediatr Blood Cancer. 2023 May 30:e30478. doi: 10.1002/pbc.30478. Online ahead of print. Pediatr Blood Cancer. 2023. PMID: 37254476 No abstract available.

9

ROS1 Alterations as a Potential Driver of Gliomas in Infant, Pediatric, and Adult Patients.

Meredith DM, Cooley LD, Dubuc A, Morrissette J, Sussman RT, Nasrallah MP, Rathbun P, Yap KL, Wadhwani N, Bao L, Wolff DJ, Ida C, Sukhanova M, Horbinski C, Jennings LJ, Farooqi M, Gener M, Ginn K, Kam KL, Sasaki K, Kanagal-Shamanna R, Alexandrescu S, Brat D, Lu X. Meredith DM, et al. Among authors: jennings lj. Mod Pathol. 2023 Nov;36(11):100294. doi: 10.1016/j.modpat.2023.100294. Epub 2023 Jul 31. Mod Pathol. 2023. PMID: 37532182

10

Barnea Slonim L, Gao J, Burkart M, Odetola OE, Kocherginsky M, Dinner SN, Lu X, Wehbe F, Jennings L, Altman JK, Mirza KM, Chen YH, Sukhanova M. Barnea Slonim L, et al. Leukemia. 2021 Jul;35(7):2097-2101. doi: 10.1038/s41375-020-01061-9. Epub 2020 Oct 21. Leukemia. 2021. PMID: 33087830 No abstract available.

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