85 related articles for article (PubMed ID: 11448109)
1. Alternative splicing of Rh blood group polypeptide mRNA produces a novel transcript containing a short nucleotide insertion on human erythroleukemia K562 cells.
Sakata N; Yamazaki K; Kogure T; Mukai T
Cell Biol Int; 2001; 25(7):697-703. PubMed ID: 11448109
[TBL] [Abstract][Full Text] [Related]
2. Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy.
Yagi M; Takeshima Y; Wada H; Nakamura H; Matsuo M
Hum Genet; 2003 Feb; 112(2):164-70. PubMed ID: 12522557
[TBL] [Abstract][Full Text] [Related]
3. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
4. A novel cryptic exon in intron 2 of the human dystrophin gene evolved from an intron by acquiring consensus sequences for splicing at different stages of anthropoid evolution.
Dwi Pramono ZA; Takeshima Y; Surono A; Ishida T; Matsuo M
Biochem Biophys Res Commun; 2000 Jan; 267(1):321-8. PubMed ID: 10623618
[TBL] [Abstract][Full Text] [Related]
5. A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5.
Suminaga R; Takeshima Y; Adachi K; Yagi M; Nakamura H; Matsuo M
J Hum Genet; 2002; 47(4):196-201. PubMed ID: 12166656
[TBL] [Abstract][Full Text] [Related]
6. A novel insertion variant of the human IL-23 receptor-alpha chain transcript.
Mancini G; Kan SH; Gallagher G
Genes Immun; 2008 Sep; 9(6):566-9. PubMed ID: 18615094
[TBL] [Abstract][Full Text] [Related]
7. Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript.
De Rosa M; Morelli G; Cesaro E; Duraturo F; Turano M; Rossi GB; Delrio P; Izzo P
Gene; 2007 Jun; 395(1-2):8-14. PubMed ID: 17360132
[TBL] [Abstract][Full Text] [Related]
8. claudin-18, a novel downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor, encodes lung- and stomach-specific isoforms through alternative splicing.
Niimi T; Nagashima K; Ward JM; Minoo P; Zimonjic DB; Popescu NC; Kimura S
Mol Cell Biol; 2001 Nov; 21(21):7380-90. PubMed ID: 11585919
[TBL] [Abstract][Full Text] [Related]
9. A splicing mutation of the RHAG gene associated with the Rhnull phenotype.
Kawano M; Iwamoto S; Okuda H; Fukuda S; Hasegawa N; Kajii E
Ann Hum Genet; 1998 Mar; 62(Pt 2):107-13. PubMed ID: 9759472
[TBL] [Abstract][Full Text] [Related]
10. Sequence, "subtle" alternative splicing and expression of the CYYR1 (cysteine/tyrosine-rich 1) mRNA in human neuroendocrine tumors.
Vitale L; Frabetti F; Huntsman SA; Canaider S; Casadei R; Lenzi L; Facchin F; Carinci P; Zannotti M; Coppola D; Strippoli P
BMC Cancer; 2007 Apr; 7():66. PubMed ID: 17442112
[TBL] [Abstract][Full Text] [Related]
11. Novel cryptic exons identified in introns 2 and 3 of the human dystrophin gene with duplication of exons 8-11.
Ishibashi K; Takeshima Y; Yagi M; Nishiyama A; Matsuo M
Kobe J Med Sci; 2006; 52(3-4):61-75. PubMed ID: 16849873
[TBL] [Abstract][Full Text] [Related]
12. Identification of a novel splice variant of human PD-L1 mRNA encoding an isoform-lacking Igv-like domain.
He XH; Xu LH; Liu Y
Acta Pharmacol Sin; 2005 Apr; 26(4):462-8. PubMed ID: 15780196
[TBL] [Abstract][Full Text] [Related]
13. A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro.
Thi Tran HT; Takeshima Y; Surono A; Yagi M; Wada H; Matsuo M
Mol Genet Metab; 2005 Jul; 85(3):213-9. PubMed ID: 15979033
[TBL] [Abstract][Full Text] [Related]
14. Rhnull syndrome: identification of a novel mutation in RHce.
Rosa KA; Reid ME; Lomas-Francis C; Powell VI; Costa FF; Stinghen ST; Watanabe AM; Carboni EK; Baldon JP; Jucksch MM; Castilho L
Transfusion; 2005 Nov; 45(11):1796-8. PubMed ID: 16271106
[TBL] [Abstract][Full Text] [Related]
15. Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene.
Isackson PJ; Bujnicki H; Harding CO; Vladutiu GD
Mol Genet Metab; 2005; 86(1-2):250-6. PubMed ID: 16040263
[TBL] [Abstract][Full Text] [Related]
16. [Research of RhD protein in Rh blood group Del phenotype].
Xiong W; Shao CP; Li XM; Zhou YY
Zhonghua Yi Xue Za Zhi; 2006 Jan; 86(2):128-32. PubMed ID: 16620722
[TBL] [Abstract][Full Text] [Related]
17. Identification of two alphaRYR alleles and characterization of alphaRYR transcript variants in turkey skeletal muscle.
Chiang W; Allison CP; Linz JE; Strasburg GM
Gene; 2004 Apr; 330():177-84. PubMed ID: 15087137
[TBL] [Abstract][Full Text] [Related]
18. An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id).
Denecke J; Kranz C; Kemming D; Koch HG; Marquardt T
Hum Mutat; 2004 May; 23(5):477-86. PubMed ID: 15108280
[TBL] [Abstract][Full Text] [Related]
19. The unique cytoplasmic domain of the human integrin variant beta4E is produced by partial retention of intronic sequences.
van Leusden MR; Kuikman I; Sonnenberg A
Biochem Biophys Res Commun; 1997 Jun; 235(3):826-30. PubMed ID: 9207246
[TBL] [Abstract][Full Text] [Related]
20. Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts.
Seim I; Collet C; Herington AC; Chopin LK
BMC Genomics; 2007 Aug; 8():298. PubMed ID: 17727735
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
