These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

79 related articles for article (PubMed ID: 7635518)

  • 1. An aberrant splicing using a 3' cryptic splice site within the CH1 exon induces truncated mu-chain production.
    Komori T; Sugiyama H
    Immunology; 1995 May; 85(1):166-70. PubMed ID: 7635518
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of hprt splicing mutations induced by the ultimate carcinogenic metabolite of benzo[a]pyrene in Chinese hamster V-79 cells.
    Hennig EE; Conney AH; Wei SJ
    Cancer Res; 1995 Apr; 55(7):1550-8. PubMed ID: 7882364
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion of the 3' splice site of the leader-variable region intron of immunoglobulin heavy chain genes induces a direct splicing of leader to constant region, resulting in the production of truncated mu-chains.
    Komori T; Sugiyama H
    Eur J Immunogenet; 1995 Jun; 22(3):241-7. PubMed ID: 8547230
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Co-expression of full-length and truncated Ig mu-chains in human B lymphocytes results from alternative splicing of a single primary RNA transcript.
    Caldwell J; McElhone P; Brokaw J; Anker R; Pollok BA
    J Immunol; 1991 Jun; 146(12):4344-51. PubMed ID: 1904080
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alternate splice sites within the human VH gene coding sequences lead to truncated Ig mu-chains.
    Mounir S; Guglielmi P; Preud'homme J; Nau F; Cogné M
    J Immunol; 1990 Jan; 144(1):342-7. PubMed ID: 2104890
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV proband.
    Filie JD; Orrison BM; Wang Q; Lewis MB; Marini JC
    Hum Mutat; 1993; 2(5):380-8. PubMed ID: 8257992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency.
    Fukao T; Sakurai S; Rolland MO; Zabot MT; Schulze A; Yamada K; Kondo N
    Mol Genet Metab; 2006 Nov; 89(3):280-2. PubMed ID: 16765626
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL; Gelbart T; West C; Halloran C; Beutler E
    Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion of a splice donor site ablates expression of the following exon and produces an unphosphorylated RB protein unable to bind SV40 T antigen.
    Shew JY; Chen PL; Bookstein R; Lee EY; Lee WH
    Cell Growth Differ; 1990 Jan; 1(1):17-25. PubMed ID: 1964074
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of three splice variants and genomic organization of the mouse BMAL1 gene.
    Yu W; Ikeda M; Abe H; Honma S; Ebisawa T; Yamauchi T; Honma K; Nomura M
    Biochem Biophys Res Commun; 1999 Jul; 260(3):760-7. PubMed ID: 10403839
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Null allele at Bcd-1 locus in BALB/cByJ mice is due to a deletion in the short-chain acyl-CoA dehydrogenase gene and results in missplicing of mRNA.
    Hinsdale ME; Kelly CL; Wood PA
    Genomics; 1993 Jun; 16(3):605-11. PubMed ID: 8325633
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. BRCA1 IVS16+6T-->C is a deleterious mutation that creates an aberrant transcript by activating a cryptic splice donor site.
    Scholl T; Pyne MT; Russo D; Ward BE
    Am J Med Genet; 1999 Jul; 85(2):113-6. PubMed ID: 10406662
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Normal isotype switching in B cells lacking the I mu exon splice donor site: evidence for multiple I mu-like germline transcripts.
    Kuzin II; Ugine GD; Wu D; Young F; Chen J; Bottaro A
    J Immunol; 2000 Feb; 164(3):1451-7. PubMed ID: 10640761
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of three mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.
    Doyle GA; Rebecca Sheng X; Lin SS; Press DM; Grice DE; Buono RJ; Ferraro TN; Berrettini WH
    Gene; 2007 Feb; 388(1-2):135-47. PubMed ID: 17156941
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays.
    Graham IR; Hill VJ; Manoharan M; Inamati GB; Dickson G
    J Gene Med; 2004 Oct; 6(10):1149-58. PubMed ID: 15386737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Translational efficiency is up-regulated by alternative exon in murine IL-15 mRNA.
    Nishimura H; Washizu J; Nakamura N; Enomoto A; Yoshikai Y
    J Immunol; 1998 Jan; 160(2):936-42. PubMed ID: 9551932
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel single-base substitution (380C>T) that activates a 5-base downstream cryptic splice-acceptor site within exon 5 in almost all transcripts in the human mitochondrial acetoacetyl-CoA thiolase gene.
    Nakamura K; Fukao T; Perez-Cerda C; Luque C; Song XQ; Naiki Y; Kohno Y; Ugarte M; Kondo N
    Mol Genet Metab; 2001 Feb; 72(2):115-21. PubMed ID: 11161837
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A single base mutation in the 5' splice site of intron 7 of the lck gene is responsible for the deletion of exon 7 in lck mRNA of the JCaM1 cell line.
    Rouer E; Brule F; Benarous R
    Oncogene; 1999 Jul; 18(29):4262-8. PubMed ID: 10435639
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diverse splicing pathways of the membrane IgHM pre-mRNA in a Chondrostean, the Siberian sturgeon.
    Lundqvist M; Strömberg S; Bouchenot C; Pilström L; Boudinot P
    Dev Comp Immunol; 2009 Apr; 33(4):507-15. PubMed ID: 19027787
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.