Biblioscape uses a plain text ASCII file to transfer record data between different Biblioscape databases. You can view the file with any word processor or editor. The Biblioscape tag file uses two-letter codes to represent different data fields. These codes are preceded by two dashes "--", and followed by two dashes plus a space "-- ". The following table lists the data fields and their corresponding two-letter code. An example of a Biblioscape tag file is shown at the end. In a Biblioscape tag file, each record is separated by a line with six dashes “------“. When you need to create bibliographic record in other devices like Plam or PocketPC, you can use Biblioscape Tag File which can be easily imported into Biblioscape database by go to "File | Import". Select the file to be imported after clicking the Browse button, choose import filter "Biblioscape Tag File", click Start button to import.
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Authors |
AU |
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Title |
TI |
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Sec_title |
ST |
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Year_pub |
YP |
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Volume |
VL |
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Number |
NB |
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Page_start |
PS |
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Page_end |
PE |
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Keywords |
KW |
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Ref_mark |
RM |
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Ref_user |
RU |
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Ref_type |
RT |
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Subject |
SB |
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Sec_authors |
SA |
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Notes |
NT |
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Place_pub |
PP |
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Publisher |
PB |
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Tert_authors |
TA |
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Tert_title |
TT |
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Edition |
ED |
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Date_pub |
DP |
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Type_work |
TW |
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Quat_authors |
QA |
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Quat_title |
QT |
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Isbn_issn |
IS |
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Label |
LA |
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Abstract |
AB |
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Date_input |
DI |
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Date_modified |
DM |
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Availability |
AV |
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Priority |
PR |
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Location |
LO |
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Address |
AD |
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Language |
LG |
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Country |
CO |
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Url |
UR |
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Custom_1 |
C1 |
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Custom_2 |
C2 |
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Custom_3 |
C3 |
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Custom_4 |
C4 |
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Ref_doc |
RD |
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Modified_by |
MB |
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Custom_5 |
C5 |
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Custom_6 |
C6 |
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Attachment |
AT |
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File_as |
FA |
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Call_number |
CN |
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Description |
DE |
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Reprint |
RP |
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Date_freeform |
DF |
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Ref_misc |
RS |
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Categories |
CA |
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Web_post_hide |
WP |
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Title_short |
TH |
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Work_reviewed |
WR |
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Extend_work |
EW |
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Section |
SE |
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Accession_number |
AC |
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Last_post |
LP |
The following is an example of a BTF file, each record is seperated by a line with "------".
--AU-- Baklouti, F.; Huang, S. C.; Tang, T. K.; Delaunay, J.; Marchesi, V. T.; Benz, E. J.
--TI-- Asynchronous Regulation OF Splicing Events Within Protein 4.1 Pre-mrna During Erythroid Differentiation
--ST-- Blood
--YP-- 1996
--VL-- 87
--NB-- 9
--PS-- 3934
--PE-- 3941
--KW-- Membrane skeletal protein-4.1; Insertion deletion mutations; Actin binding domain; Molecular analysis; Hereditary elliptocytosis; Expression; Spectrin; Cells; Rna; Isoforms
--RT-- Journal Article
--TW-- Article
--QT-- Clinical medicine.
--IS-- 0006-4971
--AB-- Protein 4.1 is an 80-kD structural component of the red blood cell (RBC) cytoskeleton. It is critical for the formation of the spectrin/actin/protein 4.1 junctional complex, the integrity of which is important for the horizontal strength and elasticity of RBCs. We and others have previously shown that multiple protein 4.1 mRNA isoforms are generated from a single genomic locus by several alternative mRNA splicing events, leading to the insertion or skipping of discrete internal sequence motifs. The physiologic significance of these splicing events has been established for only two of these motifs: (1) an upstream 17-nucleotide sequence located at the 5' end of exon 2 that contains an in-frame ATG initiation codon, the inclusion of which by use of an alternative splice acceptor site in exon 2 allows the production of a 135-kD high-molecular-weight isoform present in nonerythroid cells; (2) exon 16, which encodes a 21-amino acid (21aa) segment located in the 10-kD ''spectrin/actin binding domain'' (SAB), the presence of which is required for junctional complex stability in RBCs. Previous studies by our group and others suggested that, among blood cells, this exon was retained only in mature mRNA in the erythroid lineage. Exon 16 is one of a series of three closely linked alternatively spliced exons, generating eight possible mRNA products with unique configurations of the SAB. In this communication, we report studies of the expression of both the translation initiation region and the SAB region during induced erythroid maturation in mouse erythroleukemia (MEL) cells. We have found that only two of eight possible combinatorial patterns of exon splicing at the SAB region are encountered: the isoform lacking all three exons, present in predifferentiated cells, and the isoform containing only exon 16, which increases in amount during erythroid differentiation. The proteinisoform containing the 21aa segment encoded by exon 16 efficiently and exclusively incorporates into the membrane, whereas the isoform lacking this 21aa segment remains in the cytoplasm, as well as the membrane.
--AD-- Reprint available from: Baklouti F INST PASTEUR LYON CNRS URA 1171 AVE TONY GARNIER F-69365 LYON 07 FRANCE YALE UNIV DEPT INTERNAL MED NEW HAVEN,CT USA YALE UNIV DEPT PATHOL NEW HAVEN, CT USA YALE
--LG-- English
------
--AU-- Sa, M. CM.; Kascheres, A.
--TI-- Electronically Mediated Selectivity IN Ring Opening OF 1-azirines - THE 3-x Mode - Convenient Route To 3-oxazolines
--ST-- Journal of Organic Chemistry
--YP-- 1996
--VL-- 61
--NB-- 11
--PS-- 3749
--PE-- 3752
--RT-- Journal Article
--TW-- Article
--QT-- Chemistry.
--IS-- 0022-3263
--AB-- The mild base-promoted reaction of methyl 2-phenyl-1-azirine-3-acetate (1) with aldehydes and acetone provides a new and simple route to the 3-oxazolines 5, which are formed in good yields by the electrophilic trapping of an imino anion produced by C-N bond cleavage in the 1-azirine enolate intermediate 6. Chloranil oxidation of 5 containing an aromatic substituent at C-2 affords oxazoles 7, while reaction of 5 containing an aliphaticgroup at C-2 produces 5-methylene-3-oxazolines 8 and 5-spiro-2-oxazolines 9 in addition to 7. [References: 11]
--AD-- Reprint available from: Kascheres A UNIV ESTADUAL CAMPINAS INST QUIM CP 6154 BR-13083970 SAO PAULO BRAZIL UNIV ESTADUAL CAMPINAS INST QUIM BR-13083970 SAO PAULO BRAZIL
--LG-- English
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