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Publication Listing for the MeSH term sequence. Found 75 abstracts

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Goldgar DE, Healey S, Dowty JG, Da Silva L, Chen XQ, Spurdle AB, Terry MB, Daly MJ, Buys SM, Southey MC, Andrulis I, John EM, Khanna KK, Hopper JL, Oefner PJ, Lakhani S, Chenevix-Trench G. Rare variants in the ATM gene and risk of breast cancer. Breast Cancer Research. 2011 Jan;13(4):R73.   PMCID: PMC3236337
Ishak MB, Giri VN. A Systematic Review of Replication Studies of Prostate Cancer Susceptibility Genetic Variants in High-Risk Men Originally Identified from Genome-Wide Association Studies. Cancer Epidemiology Biomarkers & Prevention. 2011 Aug;20(8):1599-610.   PMCID: not NIH funded
Lin PJ, Jongsma CG, Liao S, Johnson AE. Transmembrane segments of nascent polytopic membrane proteins control cytosol/ER targeting during membrane integration. Journal of Cell Biology. 2011 Oct;195(1):41-54.   PMCID: PMC3187712
Azizi AA, Gelpi E, Yang JW, Rupp B, Godwin AK, Slater C, Slavc I, Lubec G. Mass spectrometric identification of serine hydrolase OVCA2 in the medulloblastoma cell line DAOY. CANCER LETTERS. 2006 Sep;241(2):235-49.
Cianfrocca ME, Kimmel KA, Gallo J, Cardoso T, Brown MM, Hudes G, Lewis N, Weiner L, Lam GN, Brown SC, Shaw DE, Mazar AP, Cohen RB. Phase 1 trial of the antiangiogenic peptide ATN-161 (Ac-PHSCN-NH2), a beta integrin antagonist, in patients with solid tumours. BRITISH JOURNAL OF CANCER. 2006 Jun;94(11):1621-6.
Gudima SO, Chang JH, Taylor JM. Restoration in vivo of defective hepatitis delta virus RNA genomes. RNA-A PUBLICATION OF THE RNA SOCIETY. 2006 Jun;12(6):1061-73.
Calin GA, Trapasso F, Shimizu M, Dumitru CD, Yendamuri S, Godwin AK, Ferracin M, Bernardi G, Chatterjee D, Baldassarre G, Rattan S, Alder H, Mabuchi H, Shiraishi T, Hansen LL, Overgaard J, Herlea V, Mauro FR, Dighiero G, Movsas B, Rassenti L, Kipps T, Baffa R, Fusco A, Mori M, Russo G, Liu CG, Neuberg D, Bullrich F, Negrini M, Croce CM. Familial cancer associated with a polymorphism in ARLTS1. New England Journal of Medicine. 2005 Apr 21;352(16):1667-76.
Chang JH, Gudima SO, Tarn C, Nie XC, Taylor JM. Development of a novel system to study hepatitis delta virus genome replication. Journal of Virology. 2005 Jul;79(13):8182-8.
Wang G, Jin YM, Dunbrack RL. Assessment of fold recognition predictions in CASP6. Proteins-Structure Function and Bioinformatics. 2005 Jan;61:46-66.
Guo DL, Hu K, Lei Y, Wang YC, Ma TL, He DC. Identification and characterization of a novel cytoplasm protein ICF45 that is involved in cell cycle regulation. Journal of Biological Chemistry. 2004 Dec 17;279(51):53498-505.
Andrulis IL, Anton-Culver H, Beck J, Bove B, Boyd J, Buys S, Godwin AK, Hopper JL, Li F, Neuhausen SL, Ozcelik H, Peel D, Santella RM, Southey MC, van Orsouw NJ, Venter DJ, Vijg J, Whittemore AS, Cooperative Family Registry Breast. Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations. Human Mutation. 2002 Jan;20(1):65-73.
Graham DE, Bock CL, Schalk-Hihi C, Lu ZC, Markham GD. Identification of a highly diverged class of S- adenosylmethionine synthetases in the archaea. Journal of Biological Chemistry. 2000 Feb 11;275(6):4055-9.
Zhao RB, Gish K, Murphy M, Yin YX, Notterman D, Hoffman WH, Tom E, Mack DH, Levine AJ. Analysis of p53-regulated gene expression patterns using oligonucleotide arrays. Genes & development. 2000 Apr 15;14(8):981-93.
Hirai H, Taguchi T, Godwin AK. Genomic differentiation of 18S ribosomal DNA and beta-satellite DNA in the hominoid and its evolutionary aspects. Chromosome Research. 1999 Jan;7(7):531-40.
Jaiswal AK, Bell DW, Radjendirane V, Testa JR. Localization of human NQO1 gene to chromosome 16q22 and NQO2- 6p25 and associated polymorphisms. Pharmacogenetics. 1999 Jun;9(3):413-8.
Bouck J, Fu XD, Skalka AM, Katz RA. Role of the constitutive splicing factors U2AF(65) and SAP49 in suboptimal RNA splicing of novel retroviral mutants. Journal of Biological Chemistry. 1998 Jun 12;273(24):15169-76.
Dingle K, Moraleda G, Bichko V, Taylor J. Electrophoretic analysis of the ribonucleoproteins of hepatitis delta virus. Journal of Virological Methods. 1998 Nov;75(2):199-204.
El-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, Al-Alami J. Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene. European Journal of Human Genetics. 1998 May;6(3):251-6.
Joseph P, Jaiswal AK. NAD(P)H : Quinone oxidoreductase 1 reduces the mutagenicity of DNA caused by NADPH : P450 reductase-activated metabolites of benzo(a)pyrene quinones. British Journal of Cancer. 1998 Mar;77(5):709-19.
Khazak V, Estojak J, Cho H, Majors J, Sonoda G, Testa JR, Golemis EA. Analysis of the interaction of the novel RNA polymerase II (pol II) subunit hsRPB4 with its partner hsRPB7 and with pol II. Molecular and Cellular Biology. 1998 Apr;18(4):1935-45.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term sequence

sequence expression ovarian-cancer cancer localization hepatitis delta virus identification tumor-suppressor prediction mutations mass-spectrometry transcription antigen locus mutagenicity proteins complex yeast gene dt-diaphorase region activation 8q24 hereditary wild-type p53 cytotoxicity early-onset mechanisms methylation rna two-dimensional gene scanning reductase dioxin salmonella tester strains NQO2 28s endothelial-growth-factor centrosome chromosome medulloblastoma polymerase benzo(a)pyrene-3 saccharomyces-cerevisiae genes analysis linkage disequilibrium jordan family registry 2 forms cultured-cells P450 reductase sau3a family chromosomal location breast-cancer deletions chondrodysplasia growth exit tunnel FISH beta- polypyrimidine tract molecular testing scanning tests sites complexes Biochemistry & Molecular Biology disorder cdna cloning fluorescence adenosyl-l-methionine missense mutations dna-damage enhancer subcellular-localization populations 6-quinone signal peptidase family autoantibody intramolecular RNA recombination tumor-suppressor locus BRCA1 acid susceptibility metabolism messenger-rna p53-regulated genes enzymes ribosomal DNA cost forms Oncology t4 endonuclease-vii down-regulation chronic lymphocytic-leukemia model alpha 5 beta 1 integrin ATN-161-alpha v beta 3 integrin-phase 1 trial-angiogenesis recombination benchmarking prospects 13q14 carcinogenesis SSCP hdv rna variants RNA polymerase II RNA-directed transcription oligonucleotide microarrays er membrane NAD(P)H : quinone oxidoreductase 1 site OVCA2 viral ribonucleoprotein RNA-protein system inhibitor transcriptional activation descent oxidoreductase hnf1-beta multigene families purification NQO1 EB-1 cells human collagen-x exposure metaanalysis y-chromosome pseudorheumatoid dysplasia CASP6 enzymatic mutation detection ataxia-telangiectasia rat-liver 2-dimensional electrophoresis secretory proteins binding angiogenesis therapy fold recognition multisequence antibodies genome accuracy immunohistochemistry brca1 multiple loci sus-scrofa-domestica african-americans spliceosome allelic loss
Last updated on Thursday, August 02, 2018