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| Journal Articles Details
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| Bioinformatics Journals and Computational Biology Journals |
| Zhongguo Shi Yan Xue Ye Xue Za Zhi. 13(4):542-7 |
[Cloning and Bioinformatics Analysis of a Thrombin-like Enzyme Gene from Agkistrodon Acutus.] |
Zhang YY, Ma P, Lu YM, Lü LP, Jiang SY, Zhou XP, Sun SH, Xu JB.
Institute of Transfusion Medicine, Academy of Military Medical Sciences, Beijing 100850, China. |
Publication Date: Tuesday, August 30, 2005
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Click here to view MEDLINE citation |
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More August, 2005 bioinformatics journal articles.- Systems biology: where it's at in 2005.
by Lehner B, Tischler J, Fraser AG.
Journal: Genome Biol. 6(8):338
- PSST-2.0: Protein Data Bank Sequence Search Tool.
by Ananthalakshmi P, Samayamohan K, Chokalingam C, Mayilarasi C, Sekar K.
Journal: Appl Bioinformatics. 4(2):141-5
- [Sequence of Escherichia coli O138 O-antigen gene cluster and gne identification by bioinformatics]
by Kong QK, Cheng JS, Zhao G, Wang L, Guo HJ.
Journal: Wei Sheng Wu Xue Bao. 44(6):756-60
- Functional Diversity in the Gene Network Controlled by the Master Regulator p53 in Humans.
by Resnick MA, Tomso D, Inga A, Menendez D, Bell D.
Journal: Cell Cycle. 4(8):
- In Silico Methods for Evaluating Human Allergenicity to Novel Proteins: International Bioinformatics Workshop Meeting Report February 23-24, 2005.
by Thomas K, Bannon G, Hefle S, Herouet C, Holsapple M, Ladics G, Macintosh S, Privalle L.
Journal: Toxicol Sci. :
- Bioinformatics for whole-genome shotgun sequencing of microbial communities.
by Chen K, Pachter L.
Journal: PLoS Comput Biol. 1(2):e24
- The classification of cancer based on DNA microarray data that uses diverse ensemble genetic programming.
by Hong JH, Cho SB.
Journal: Artif Intell Med. :
- Transfer RNA gene-targeted integration: an adaptation of retrotransposable elements to survive in the compact Dictyostelium discoideum genome.
by Winckler T, Szafranski K, Glöckner G.
Journal: Cytogenet Genome Res. 110(1-4):288-98
- PLoS Computational Biology: A New Community Journal.
by Bourne PE, Brenner SE, Eisen MB.
Journal: PLoS Comput Biol. 1(1):e4
- Mutation of DNAJD2, a human homolog of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.
by Davey KM, Parboosingh JS, McLeod DR, Chan A, Casey R, Ferreira P, Snyder FF, Bridge PJ, Bernier FP.
Journal: J Med Genet. :
- Fuzzy attributes of a DNA complex: Development of a fuzzy inference engine for codon-"junk" codon delineation.
by Arredondo TV, Neelakanta PS, De Groff D.
Journal: Artif Intell Med. :
- Highly accurate and consistent method for prediction of helix and strand content from primary protein sequences.
by Ruan J, Wang K, Yang J, Kurgan LA, Cios K.
Journal: Artif Intell Med. :
- Genome-Wide Identification of Potential Plant E2F Target Genes.
by Vandepoele K, Vlieghe K, Florquin K, Hennig L, Beemster GT, Gruissem W, Van de Peer Y, Inzé D, De Veylder L.
Journal: Plant Physiol. :
- Tools and Strategies for Physiological Genomics - The Rat Genome Database.
by Twigger SN, Pasko D, Nie J, Shimoyama M, Bromberg S, Campbell D, Chen J, Dela Cruz N, Fan C, Foote C, Harris G, Hickmann B, Ji Y, Jin W, Li D, Mathis J, Nenasheva N, Nigam R, Petri V, Reilly D, Ruotti V, Schauberger E, Seiler K, Slyper R, Smith J, Wang W, Wu W, Zhao L, Zuniga-Meyer A, Tonellato PJ, Kwitek AE, Jacob HJ.
Journal: Physiol Genomics. :
- Simpleaffy: a BioConductor package for Affymetrix quality control and data analysis.
by Wilson C, Miller CJ.
Journal: Bioinformatics. :
- Detecting common gene expression patterns in multiple cancer outcome entities.
by Yang X, Bentink S, Spang R.
Journal: Biomed Microdevices. 7(3):247-51
- Comparative genomics on DKK2 and DKK4 orthologs.
by Katoh Y, Katoh M.
Journal: Int J Mol Med. 16(3):477-81
- Discovery 99: accelerate and improve the drug discovery process.
by Young SS.
Journal: IDrugs. 2(7):648-9
- Unsupervised learning of natural languages.
by Solan Z, Horn D, Ruppin E, Edelman S.
Journal: Proc Natl Acad Sci U S A. :
- A bioinformatics framework for genotype-phenotype correlation in humans with Marfan syndrome caused by FBN1 gene mutations.
by Baumgartner C, Mátyás G, Steinmann B, Eberle M, Stein JI, Baumgartner D.
Journal: J Biomed Inform. :
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