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Journal Abstract Search

72 related items for PubMed ID: 19422363

  • 1. A point mutation in the splice donor site of intron 7 in the alphas2-casein encoding gene of the Mediterranean River buffalo results in an allele-specific exon skipping.
    Cosenza G, Pauciullo A, Feligini M, Coletta A, Colimoro L, Di Berardino D, Ramunno L.
    Anim Genet; 2009 Oct; 40(5):791. PubMed ID: 19422363
    [No Abstract] [Full Text] [Related]

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  • 3. Molecular cloning and characterization of buffalo alpha(s1)-casein gene.
    Sukla S, Bhattacharya TK, Venkatachalapathy RT, Kumar P, Sharma A.
    DNA Seq; 2007 Oct; 18(5):334-40. PubMed ID: 17654008
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  • 5. [Polymorphism of the kappa-casein gene in populations of the subfamily Bovinae].
    Sulimova GE, Badagueva IuN, Udina IG.
    Genetika; 1996 Nov; 32(11):1576-82. PubMed ID: 9119217
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  • 6. A signature protein-based method to distinguish Mediterranean water buffalo and foreign breed milk.
    Caira S, Pinto G, Balteanu VA, Chianese L, Addeo F.
    Food Chem; 2013 Nov 01; 141(1):597-603. PubMed ID: 23768399
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  • 9. Prevalence of a common point mutation in the dihydropyrimidine dehydrogenase (DPD) gene within the 5'-splice donor site of intron 14 in patients with severe 5-fluorouracil (5-FU)- related toxicity compared with controls.
    Raida M, Schwabe W, Häusler P, Van Kuilenburg AB, Van Gennip AH, Behnke D, Höffken K.
    Clin Cancer Res; 2001 Sep 01; 7(9):2832-9. PubMed ID: 11555601
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  • 11. A novel donor splice site mutation in the glycogen debranching enzyme gene is associated with glycogen storage disease type III.
    Okubo M, Aoyama Y, Murase T.
    Biochem Biophys Res Commun; 1996 Jul 16; 224(2):493-9. PubMed ID: 8702417
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  • 12. Genotyping of the k-casein and β-lactoglobulin genes in Chinese Holstein, Jersey and water buffalo by PCR-RFLP.
    Ren DX, Miao SY, Chen YL, Zou CX, Liang XW, Liu JX.
    J Genet; 2011 Apr 19; 90(1):e1-5. PubMed ID: 21677408
    [No Abstract] [Full Text] [Related]

  • 13. Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
    Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W.
    Hum Mutat; 2004 Nov 19; 24(5):370-80. PubMed ID: 15459959
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  • 14. A single point mutation results in A allele-specific exon skipping in the bovine alpha s1-casein mRNA.
    Mohr U, Koczan D, Linder D, Hobom G, Erhardt G.
    Gene; 1994 Jun 10; 143(2):187-92. PubMed ID: 8206372
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  • 15. Short communication: Translational efficiency of casein transcripts in Mediterranean river buffalo.
    Cosenza G, Pauciullo A, Coletta A, Di Francia A, Feligini M, Gallo D, Di Berardino D, Ramunno L.
    J Dairy Sci; 2011 Nov 10; 94(11):5691-4. PubMed ID: 22032393
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  • 16. 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 10; 85(3):213-9. PubMed ID: 15979033
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  • 17. [Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia].
    Lin J, Wang LY, Liu S, Pan XD, Du LP, Shi FR, Qin YW, Zhao Q, Guo HY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb 10; 21(1):14-8. PubMed ID: 14767901
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  • 19. A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.
    Sironi M, Corti S, Locatelli F, Cagliani R, Comi GP.
    Hum Mutat; 2001 Mar 10; 17(3):239. PubMed ID: 11241855
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  • 20. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4).
    Abed AA, Günther K, Kraus C, Hohenberger W, Ballhausen WG.
    Hum Mutat; 2001 Nov 10; 18(5):397-410. PubMed ID: 11668633
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