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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Mammalian Genomearrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Mammalian Genome
Article . 2000 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
Mammalian Genome
Article . 2000
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The mouse adducin gene family: alternative splicing and chromosomal localization

Authors: Suriyapperuma, S P; Lozovatsky, L; Ciciotte, S L; Peters, L L; Gilligan, D M;

The mouse adducin gene family: alternative splicing and chromosomal localization

Abstract

Mouse cDNA sequences encoding alpha, beta, and gamma adducins were cloned from a mouse reticulocyte cDNA library. The purified clones contain alternatively spliced exons from all three adducin genes. In the case of alpha and beta, the inclusion of the alternatively spliced exons results in truncated polypeptide isoforms (called alpha-2 and beta-2). The mouse predicted amino acid sequences are compared with published rat and human sequences. For completion of this comparison, cDNA encoding the rat beta-1 carboxy terminus was cloned by PCR. The carboxy terminal region containing MARCKS homology, calmodulin-binding region-2, and spectrin-actin-binding site, is conserved among alpha-1, beta-1, and gamma-1 isoforms in mouse, rat, and humans. We also report here the localization of the gene encoding gamma adducin (Add3) to murine Chr 19, in a region that shows conserved synteny with human Chr 10.

Related Organizations
Keywords

570, DNA, Complementary, Molecular Sequence Data, 610, Base-Sequence, Sequence-Alignment, Calmodulin-Binding-Proteins, Cytoskeletal-Proteins, Mice, SUPPORT-U-S-GOVT-P-H-S, Animals, Humans, Gene-Library, Amino Acid Sequence, Cloning, Molecular, SUPPORT-NON-U-S-GOVT, DNA Primers, Gene Library, DNA-Primers, Molecular-Sequence-Data, Sequence-Homology-Nucleic-Acid, Base Sequence, Sequence Homology, Amino Acid, Animal, Reverse Transcriptase Polymerase Chain Reaction, Tumor-Cells-Cultured, Chromosome Mapping, Sequence-Homology-Amino-Acid, Exons, Sequence Analysis, DNA, Cloning-Molecular, Rats, Reverse-Transcriptase-Polymerase-Chain-Reaction, Alternative Splicing, Cytoskeletal Proteins, Chromosome-Mapping, Sequence-Analysis-DNA, Amino-Acid-Sequence, Calmodulin-Binding Proteins, DNA-Complementary, Sequence Alignment, Human

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
19
Average
Average
Top 10%
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