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Evidence for a role of RUNX1 as recombinase cofactor for TCRB rearrangements and pathological deletions in ETV6-RUNX1 ALL

NIAID Data Ecosystem2026-03-10 收录

白血病遗传学

淋巴细胞受体重排

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA509233 数据链接链接失效反馈

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资源简介：

Complete and incomplete TCR beta rearrangements in T-ALL patients

应用场景：

创建时间：

2018-12-10

白血病遗传学

基因型-表型关联

Hemophilia A (HA, OMIM#306700) is an X-linked recessive bleeding disorder caused by the defects in the F8 gene, which encodes coagulation factor VIII (FVIII). Intron 22 inversion (Inv22) is found in a

NIAID Data Ecosystem60

Appendix III: Crossover activity

基因重组热点分析

白血病遗传学

PhD thesis: PRDM9 Diversity, Recombination Landscapes and Childhood Leukaemia by Ihthisham Ali Appendix III contains hotspot activity analysis data on DNA3 and AA hotspots in a MHCII sub-region. These

Figshare2020-06-02 更新40

Additional file 7 of NSD2 E1099K drives relapse in pediatric acute lymphoblastic leukemia by disrupting 3D chromatin organization

白血病遗传学

染色质3D结构

Additional file 7. shared_comp_genes_up.csv Expression of increased genes with shared BA compartment switches.

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First case report of a NUP98-PMX1 rearrangement in de novo acute myeloid leukemia

白血病遗传学

基因组测序

This is the first report of a patient with de novo AML carrying the NUP98-PMX1 fusion gene. Next-generation sequencing analysis revealed FMS-like tyrosine kinase-3 (FLT3)-internal tandem duplication (

NIAID Data Ecosystem50

Appendix I: PCR Design

定量PCR实验设计

白血病遗传学

PhD thesis: PRDM9 Diversity, Recombination Landscapes and Childhood Leukaemia by Ihthisham Ali This appendix includes PCR designs for the recombination hotspot crossover assays done in the DNA

DataCite Commons2020-08-25 更新40

Evidence for a role of RUNX1 as recombinase cofactor for TCRB rearrangements and pathological deletions in ETV6-RUNX1 ALL

资源简介：

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