Pages that link to "Q31828181"
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The following pages link to Breakage and fusion of the TEL (ETV6) gene in immature B lymphocytes induced by apoptogenic signals (Q31828181):
Displaying 34 items.
- Intergenically Spliced Chimeric RNAs in Cancer (Q30274742) (← links)
- The prenatal origins of cancer (Q33697463) (← links)
- Low numbers of pre-leukemic fusion genes are frequently present in umbilical cord blood without affecting DNA damage response (Q33829330) (← links)
- Genomic DNA breakpoints in AML1/RUNX1 and ETO cluster with topoisomerase II DNA cleavage and DNase I hypersensitive sites in t(8;21) leukemia. (Q34016369) (← links)
- MLL leukemia-associated rearrangements in peripheral blood lymphocytes from healthy individuals. (Q34565527) (← links)
- Childhood acute lymphoblastic leukaemia--current status and future perspectives (Q34570023) (← links)
- Lack of Bcl11b tumor suppressor results in vulnerability to DNA replication stress and damages (Q34609906) (← links)
- Lymphoma- and leukemia-associated chromosomal translocations in healthy individuals (Q35056472) (← links)
- Incidence of common preleukemic gene fusions in umbilical cord blood in Slovak population (Q35118597) (← links)
- Clinical applications of molecular genetic testing in hematologic malignancies: Advantages and limitations (Q35122245) (← links)
- Neonatal infection with species C adenoviruses confirmed in viable cord blood lymphocytes (Q35170786) (← links)
- Origins of chromosome translocations in childhood leukaemia (Q35210004) (← links)
- Absence of leukaemic fusion gene transcripts in preterm infants exposed to diagnostic x rays (Q35293385) (← links)
- Causes of oncogenic chromosomal translocation (Q35570942) (← links)
- The prenatal origin of childhood acute lymphoblastic leukemia (Q35733249) (← links)
- Premature transcript termination, trans-splicing and DNA repair: a vicious path to cancer. (Q35824956) (← links)
- Mechanisms of therapy-related carcinogenesis (Q36315585) (← links)
- Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature (Q36730385) (← links)
- Do non-genomically encoded fusion transcripts cause recurrent chromosomal translocations? (Q37017111) (← links)
- Cytogenetic instability in childhood acute lymphoblastic leukemia survivors. (Q37792821) (← links)
- Cytogenetic and molecular aberrations in endometrial stromal tumors (Q37855166) (← links)
- Significance of ETV6 rearrangement in acute promyelocytic leukemia with t(15;17)/promyelocytic leukemia/retinoic acid receptor alpha (Q38851852) (← links)
- Calcium salicylate-mediated apoptosis in human HT-1080 fibrosarcoma cells (Q40250938) (← links)
- Childhood acute lymphoblastic leukemia (Q40637650) (← links)
- In vitro cleavage of the MLL gene by topoisomerase II inhibitor (etoposide) in normal cord and peripheral blood mononuclear cells (Q44077732) (← links)
- Genomic anatomy of the specific reciprocal translocation t(15;17) in acute promyelocytic leukemia (Q44267064) (← links)
- 5% of healthy newborns have an ETV6-RUNX1 fusion as revealed by DNA-based GIPFEL screening (Q50134082) (← links)
- TEL (ETV6)-AML1 (RUNX1) initiates self-renewing fetal pro-B cells in association with a transcriptional program shared with embryonic stem cells in mice. (Q53135188) (← links)
- Somatic mosaicism: on the road to cancer. (Q53209256) (← links)
- Backtracked analysis of preleukemic fusion genes and DNA repair foci in umbilical cord blood of children with acute leukemia. (Q55279802) (← links)
- Anastasis: recovery from the brink of cell death (Q58715274) (← links)
- Conséquences moléculaires et fonctionnelles des anomalies chromosomiques des hémopathies malignes humaines (Q61772134) (← links)
- TEL-AML1 fusion precedes differentiation to pre-B cells in childhood acute lymphoblastic leukemia (Q78790388) (← links)
- Insights into the prenatal origin of childhood acute lymphoblastic leukemia (Q92417685) (← links)