Biochemical and Biophysical Research Communications
Regular ArticleMolecular Cloning and Expression Analysis of a Putative Nuclear Protein, SR-25☆,☆☆
References (32)
Cell
(1986)- et al.
Cell
(1984) - et al.
Cell
(1988) - et al.
Biochem. Biophys. Res. Commun.
(1989) - et al.
J. Biol. Chem.
(1994) - et al.
Cell
(1990) - et al.
Cell
(1994) - et al.
Biochim. Biophys. Acta
(1989) - et al.
Genomics
(1997) - et al.
Diabetologia
(1995)
Proc. Natl. Acad. Sci. USA
Nucleic Acids Res.
Trends Biochem. Sci.
Mol. Cell. Biol.
J. Virol.
Cited by (8)
Characterization of an organic solvent-tolerant polysaccharide lyase from Microbulbifer thermotolerans DAU221
2021, International Journal of Biological MacromoleculesCitation Excerpt :Finally, for Alg7A from Vibrio sp. W13 [30], the Km values were 1.08 mg/mL for polyG, 0.49 mg/mL for sodium alginate, and 1.56 mg/mL [1–61] for polyM. The results of TLC analysis indicated that MtAl138 produces the oligosaccharides, such as di-, tri-, or tetrasaccharides, from polyG and polyM substrates (Fig. 6).
Insights from analyses of low complexity regions with canonical methods for protein sequence comparison
2022, Briefings in BioinformaticsVariations and expression features of CYP2D6 contribute to schizophrenia risk
2021, Molecular PsychiatrySRrp37, a novel splicing regulator located in the nuclear speckles and nucleoli, interacts with SC35 and modulates alternative pre-mRNA splicing in vivo
2009, Journal of Cellular Biochemistry
- ☆
Sequence data from this paper have been submitted to the DDBJ/EMBL/Genbank databases with the Accession Nos. AB035383 and AB035384.
- ☆☆
Abbreviations used: FBS, fetal bovine serum; ORF, open reading frame; RACE, rapid amplification of cDNA ends; RT, reverse transcriptase; snRNP, small nuclear ribonucleoprotein particle; SR repeat, serine-arginine repeat; TdT, terminal deoxynucleotidyl transferase
- 2
To whom correspondence should be addressed at Division of Genetic Information, Institute for Genome Research, University of Tokushima, Tokushima, 770-8503, Japan. Fax: +81-88-631-9476. E-mail: [email protected].