Reference about TassDB:

• Hiller M, Nikolajewa S, Huse K, Szafranski K, Rosenstiel P, Schuster S, Backofen R, and Platzer M. TassDB: a database of alternative tandem splice sites. Nucleic Acids Res database issue, 2007

Other References about tandem splice sites:

• Hiller M, Huse K, Szafranski K, Rosenstiel P, Schreiber S, Backofen R, and Platzer M. Phylogenetically widespread alternative splicing at unusual GYNGYN donors. Genome Biol. 7(7):R65, 2006
• Hiller M, Huse K, Szafranski K, Jahn N, Hampe J, Schreiber S, Backofen R, and Platzer M. Single-Nucleotide Polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing. Am J Hum Genet. 78(2), 291-302, 2006
• Akerman M, Mandel-Gutfreund Y. Alternative splicing regulation at tandem 3' splice sites. Nucleic Acids Res, 34(1):23-31, 2006.
• Chern TM, van Nimwegen E, Kai C, Kawai J, Carninci P, Hayashizaki Y, and Zavolan M. A simple physical model predicts small exon length variations. PLoS Genet, 2(4):e45, 2006.
  
• Tadokoro K, Yamazaki-Inoue M, Tachibana M, Fujishiro M, Nagao K, Toyoda M, Ozaki M, Ono M, Miki N, Miyashita T, and Yamada M. Frequent occurrence of protein isoforms with or without a single amino acid residue by subtle alternative splicing: the case of Gln in DRPLA affects subcellular localization of the products. J Hum Genet, 50(8):382-394, 2005
• Hiller M, Huse K, Szafranski K, Jahn N, Hampe J, Schreiber S, Backofen R, and Platzer M. Widespread occurrence of alternative splicing at NAGNAG acceptors contributes to proteome plasticity. Nat Genet, 36(12), 1255-7, 2004.
• Sugnet CW, Kent WJ, Ares M, Jr., Haussler D. Transcriptome and genome conservation of alternative splicing events in humans and mice. Pac Symp Biocomput,66-77, 2004.
• Zavolan M, Kondo S, Schonbach C, Adachi J, Hume DA, Hayashizaki Y, Gaasterland T. Impact of alternative initiation, splicing, and termination on the diversity of the mRNA transcripts encoded by the mouse transcriptome. Genome Res, 1290-300, 2003.
  

References describing functional differences for the respective protein isoforms:

• Lorkovic ZJ, Lehner R, Forstner C, Barta A. Evolutionary conservation of minor U12-type spliceosome between plants and humans. RNA, 11(7):1095-1107, 2005.
• Tadokoro K, Yamazaki-Inoue M, Tachibana M, Fujishiro M, Nagao K, Toyoda M, Ozaki M, Ono M, Miki N, Miyashita T, and Yamada M. Frequent occurrence of protein isoforms with or without a single amino acid residue by subtle alternative splicing: the case of Gln in DRPLA affects subcellular localization of the products. J Hum Genet, 50(8):382-394, 2005
• Joyce-Brady M, Jean JC, Hughey RP. gamma -glutamyltransferase and its isoform mediate an endoplasmic reticulum stress response. J Biol Chem., 276(12):9468-77, 2001.
• Ray DW, Davis JR, White A, Clark AJ. Glucocorticoid receptor structure and function in glucocorticoid-resistant small cell lung carcinoma cells. Cancer Res, 56(14):3276-3280, 1996.
• Rivers C, Levy A, Hancock J, Lightman S, Norman M. Insertion of an amino acid in the DNA-binding domain of the glucocorticoid receptor as a result of alternative splicing. J Clin Endocrinol Metab, 84(11):4283-4286, 1999.
  
• Vogan KJ, Underhill DA, Gros P. An alternative splicing event in the Pax-3 paired domain identifies the linker region as a key determinant of paired domain DNA-binding activity. Mol Cell Biol, 16(12):6677-6686, 1996.
• Condorelli G, Bueno R, Smith RJ. Two alternatively spliced forms of the human insulin-like growth factor I receptor have distinct biological activities and internalization kinetics. J Biol Chem, 269(11):8510-8516, 1994.