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May 1, 2024Open Access

Supplemental Table 5 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations

Malathi Kandarpa Dan R. Robinson Yi‐Mi Wu Tingting Qin Kristen Pettit Qing Li Gary D. Luker Maureen A. Sartor Arul M. Chinnaiyan Moshe Talpaz

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Abstract

Supplemental Table 5. Genes mutated in both MF and ET/PV/PrePMF cohorts

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Kandarpa et al. (2024) studied this question.

synapsesocial.com/papers/68e6c4b3b6db64358764351c https://doi.org/10.1158/1078-0432.25728695

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Synapse has enriched 8 closely related papers on similar clinical questions. Consider them for comparative context:

1Supplemental Table 5 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024
2Supplemental Figure 5 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024
3Supplemental Figure 5 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024
4Supplemental Table 4 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024
5Supplemental Table 4 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024
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7Supplemental Figure 4 from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024
8Data from Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations2024