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Carlo M. Croce

Researcher at Temple University

Publications -  61
Citations -  4524

Carlo M. Croce is an academic researcher from Temple University. The author has contributed to research in topics: Chromosomal translocation & Gene. The author has an hindex of 36, co-authored 61 publications receiving 4497 citations. Previous affiliations of Carlo M. Croce include New York University.

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Journal Article

Antisense-mediated Inhibition of BCL2 Protooncogene Expression and Leukemic Cell Growth and Survival: Comparisons of Phosphodiester and Phosphorothioate Oligodeoxynucleotides

TL;DR: Data indicate that PO and PS oligodeoxynucleotides targeted against the human BCL2 protooncogene can be sequence-specific inhibitors of leukemic cell growth and survival.
Journal Article

Cloning of the ALL-1 Fusion Partner, the AF-6 Gene, Involved in Acute Myeloid Leukemias with the t(6;11) Chromosome Translocation

TL;DR: The cloning and the characterization of the partner gene from chromosome 6 (AF-6), which is expressed in a variety of cell types and encodes a protein of 1612 amino acids, contains the GLGF motif shared with several proteins of vertebrates and invertebrates thought to be involved in signal transduction at special cell-cell junctions.
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elk, tissue-specific ets-related genes on chromosomes X and 14 near translocation breakpoints

TL;DR: Two new members (elk-1 and elk-2) of the ets oncogene superfamily have now been identified and the possibility that rearrangements of elk loci may be involved in pathogenesis of certain tumors is suggested.
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Differential expression of the normal and of the translocated human c-myc oncogenes in B cells

TL;DR: The ability of the translocated c-myc oncogene to escape the normal transcriptional control occurring in B cells may be important for the expression of B cell neoplasia in mouse and man.
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Cloning of three human tyrosine phosphatases reveals a multigene family of receptor-linked protein-tyrosine-phosphatases expressed in brain

TL;DR: Analysis of sequence comparisons among LCA, the LCA-related protein LAR, and RPTPase alpha, beta, and gamma reveals the existence of a multigene family encoding different RPTPases, each containing a distinct extracellular domain, a single hydrophobic transmembrane region, and two tandemly repeated conserved cytoplasmic domains.