CHARACTERIZATION OF A NEW TISSUE-SPECIFIC MUTATION OF THE YELLOW GENE WHICH SUPPORTS TRANSVECTION

Gene Families ◽  
2001 ◽  
pp. 195-202
Author(s):  
JI-LONG CHEN ◽  
JIE LIU ◽  
KATHRYN HUISINGA ◽  
PAMELA GEYER ◽  
JAMES MORRIS ◽  
...  
2017 ◽  
Vol 43 (6) ◽  
pp. 789
Author(s):  
Rui WANG ◽  
Meng-Lin ZHU ◽  
Fang-Yuan GAO ◽  
Juan-Sheng REN ◽  
Xian-Jun LU ◽  
...  

3 Biotech ◽  
2021 ◽  
Vol 11 (6) ◽  
Author(s):  
Sujay Paul ◽  
Paula Reyes-Pérez ◽  
Paola Isabel Angulo-Bejarano ◽  
Aashish Srivastava ◽  
Sathishkumar Ramalingam ◽  
...  

2001 ◽  
Vol 84 (1) ◽  
pp. 173-187 ◽  
Author(s):  
Derek Kennedy ◽  
Juliet French ◽  
Estelle Guitard ◽  
Kelin Ru ◽  
Bruno Tocque ◽  
...  

2007 ◽  
Vol 44 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Maria Oszvald ◽  
Mark Gardonyi ◽  
Cecília Tamas ◽  
Imre Takacs ◽  
Barnabas Jenes ◽  
...  

1979 ◽  
Vol 36 (1) ◽  
pp. 323-342
Author(s):  
R. Rutz ◽  
J. Lilien

We have developed a quantitative assay for tissue-specific adhesive components which is based on the agglutination of glutaraldehyde-fixed cells. At least 2 components are required for fixed-cell agglutination: a cell-surface ligand which is obtained from tissue culture-conditioned medium, and a soluble ‘agglutinin’ which accumulates in conditioned medium from monolayer cultures. Our results suggest that the surface-binding ligand and the agglutinin interact directly, resulting in tissue-specific agglutination of cells. The agglutination reaction exhibits divalent cation, temperature, and pH dependence. Several models of cell adhesion are described; the simplest of these which can account for the data is a multicomponent model in which the 2 adhesive components have structural roles.


1989 ◽  
Vol 9 (8) ◽  
pp. 3308-3313
Author(s):  
P Fraser ◽  
P Cummings ◽  
P Curtis

We report the isolation and characterization of the mouse carbonic anhydrase I (CAI) gene. Direct RNA sequence analysis of the 5' nontranslated regions of CAI mRNA from mouse colon and mouse erythroleukemia cells demonstrated tissue specificity in the lengths and sequences of CAI transcripts. Analysis of several mouse CAI genomic clones showed that the transcripts arose from a single CAI gene with two tissue-specific promoters and eight exons. CAI transcripts in the colon were found to initiate just upstream of the erythroid exon 2 of the CAI gene region sequence. Erythroid transcripts originated from a novel promoter upstream of exon 1, which was located more than 10 but less than 250 kilobases upstream of exon 2. Erythroid exon 1 contained only a nontranslated sequence, which was spliced to exon 2 via a cryptic splice acceptor site located in the region that encoded the colon mRNA 5' nontranslated sequence. The remaining exon-intron junctions were conserved in comparison with those of the CAII and CAIII genes.


1998 ◽  
Vol 95 (2) ◽  
pp. 582-587 ◽  
Author(s):  
M. V. Nachury ◽  
U. W. Ryder ◽  
A. I. Lamond ◽  
K. Weis

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