scholarly article | Q13442814 |
P356 | DOI | 10.1002/(SICI)1098-2264(199703)18:3<232::AID-GCC10>3.0.CO;2-K |
P698 | PubMed publication ID | 9071577 |
P2093 | author name string | Liu J | |
Zucman-Rossi J | |||
Wright JJ | |||
Allegra CJ | |||
Powell JI | |||
Nau MM | |||
P2860 | cites work | Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours | Q24298221 |
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation | Q28259434 | ||
EWS and WT-1 gene fusion in desmoplastic small round cell tumor of the abdomen | Q28270546 | ||
Identification of protein coding regions by database similarity search | Q29617233 | ||
Reverse Transcriptase Encoded by a Human Transposable Element | Q29618213 | ||
Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy | Q33897836 | ||
Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. | Q34553577 | ||
Characterization of the genomic breakpoint and chimeric transcripts in the EWS-WT1 gene fusion of desmoplastic small round cell tumor | Q34676847 | ||
BCL2 oncogene translocation is mediated by a chi-like consensus | Q36231418 | ||
Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element | Q36416853 | ||
Breakpoint Junctions of Chromosome 9p Deletions in Two Human Glioma Cell Lines | Q36670180 | ||
Unit-length line-1 transcripts in human teratocarcinoma cells | Q36785924 | ||
The sequence of a large L1Md element reveals a tandemly repeated 5' end and several features found in retrotransposons | Q36908687 | ||
The (4;11)(q21;q23) chromosome translocations in acute leukemias involve the VDJ recombinase | Q37281612 | ||
LINE-1: a mammalian transposable element | Q38181068 | ||
Genetic exchange between endogenous and exogenous LINE-1 repetitive elements in mouse cells | Q40525621 | ||
The genomic organization and expression of the WT1 gene | Q41120172 | ||
Integration of a vector containing a repetitive LINE-1 element in the human genome | Q41437885 | ||
LINE-1: a human transposable element | Q42611087 | ||
Isolation of an active human transposable element | Q42614185 | ||
A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion | Q42693461 | ||
Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion. | Q48082303 | ||
Insertional mutagenesis of the myc locus by a LINE-1 sequence in a human breast carcinoma | Q48324246 | ||
The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts | Q57756648 | ||
Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints | Q60035789 | ||
A Novel Reciprocal Chromosome Translocation t(11;22)(p13;q12) in an Intraabdominal Desmoplastic Small Round-Cell Tumor | Q67487724 | ||
Intraabdominal desmoplastic small-cell tumors with divergent differentiation. Observations on three cases of childhood | Q68823094 | ||
The last shall be first | Q70732469 | ||
Intracranial desmoplastic small-cell tumor. Report of a case | Q70835047 | ||
Translocation (11;22)(p13;q12): Primary change in intra‐abdominal desmoplastic small round cell tumor | Q72087891 | ||
Desmoplastic small round cell tumor of the pleura | Q72248899 | ||
A recurring translocation, t(11;22)(p13;q11.2), characterizes intra-abdominal desmoplastic small round-cell tumors | Q72929436 | ||
Intra-abdominal desmoplastic small cell tumor: a light microscopic, immunocytochemical, ultrastructural, and flow cytometric study | Q72931317 | ||
P433 | issue | 3 | |
P304 | page(s) | 232-239 | |
P577 | publication date | 1997-03-01 | |
P1433 | published in | Genes, Chromosomes and Cancer | Q5532697 |
P1476 | title | LINE-I element insertion at the t(11;22) translocation breakpoint of a desmoplastic small round cell tumor | |
P478 | volume | 18 |
Q42115543 | A model of oncogenic rearrangements: differences between chromosomal translocation mechanisms and simple double-strand break repair |
Q73247606 | Characteristic sequence motifs located at the genomic breakpoints of the translocation t(X;18) in synovial sarcomas |
Q36620357 | DNA methylation and expression of LINE-1 and HERV-K provirus sequences in urothelial and renal cell carcinomas |
Q37504031 | Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma |
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Q37196896 | LINE-1 family member GCRG123 gene is up-regulated in human gastric signet-ring cell carcinoma |
Q64065920 | LINE-1 hypomethylation in human hepatocellular carcinomas correlates with shorter overall survival and CIMP phenotype |
Q28729045 | LINEs, SINEs and other retroelements: do birds of a feather flock together? |
Q35687336 | Mobile element insertions are frequent in oesophageal adenocarcinomas and can mislead paired-end sequencing analysis |
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Q44500993 | Promoter hypomethylation of the LINE-1 retrotransposable elements activates sense/antisense transcription and marks the progression of chronic myeloid leukemia |
Q35531702 | Retrofitting the genome: L1 extinction follows endogenous retroviral expansion in a group of muroid rodents |
Q42640386 | Retrotransposable L1 elements expressed in rheumatoid arthritis synovial tissue: association with genomic DNA hypomethylation and influence on gene expression |
Q22252317 | Retrotransposons Revisited: The Restraint and Rehabilitation of Parasites |
Q32183705 | The Role of Somatic L1 Retrotransposition in Human Cancers |
Q36362814 | Transposable Elements in Human Cancer: Causes and Consequences of Deregulation |
Q40474504 | Ultraviolet-induced transformation of keratinocytes: possible involvement of long interspersed element-1 reverse transcriptase. |
Q34990678 | Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors. desmoplastic small round-cell tumors |
Q54307155 | Use of inverse PCR to amplify and sequence breakpoints of HPRT deletion and translocation mutations. |
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