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Eva Dworkin-Rastl

Researcher at Columbia University

Publications -  24
Citations -  1308

Eva Dworkin-Rastl is an academic researcher from Columbia University. The author has contributed to research in topics: Xenopus & Messenger RNA. The author has an hindex of 16, co-authored 24 publications receiving 1287 citations.

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Poly(A) elongation during Xenopus oocyte maturation is required for translational recruitment and is mediated by a short sequence element.

TL;DR: Xenopus oocytes contain several mRNAs that are mobilized into polysomes only at the completion of meiosis (maturation) or at specific times following fertilization, and the dynamic process of polyadenylation, and not the length of the poly(A) tail, is required for translational recruitment during oocyte maturation.
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Expression of a histone H1-like protein is restricted to early Xenopus development.

TL;DR: Northern analysis showed that Xenopus B4 mRNA is expressed in oogenesis and embryogenesis through to the neurula stage and Sequencing of two B4 cDNA clones revealed that the predicted B4 translation product is a 29-kD protein with 29% identity with histone H1, distributed over the entire length of its sequence.
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Multiple ubiquitin mRNAs during xenopus laevis development contain tandem repeats of the 76 amino acid coding sequence

TL;DR: It is shown that genomic DNA fragments exist that contain at least 12 of these units in tandem and proposed that the different mRNA size classes vary in their number of ubiquitin coding sequences.
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Changes in RNA titers and polyadenylation during oogenesis and oocyte maturation in Xenopus laevis.

TL;DR: The titers of over 90 sequences isolated by cDNA cloning of oocyte poly(A)+RNA were examined during oogenesis in Xenopus laevis, finding several sequences whose titers decrease significantly during the growth phase of oogenesis as well as a few sequenceswhose titers increase slightly during this period.
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Mobilization of specific maternal RNA species into polysomes after fertilization in Xenopus laevis.

TL;DR: In this paper, the authors examined the accumulation of non-polysomal maternal RNAs in polysomes after fertilization in Xenopus laevis by measuring the distributions of specific sequences in nonpolysome and polysomal fractions.