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Статті в журналах з теми "Human brain cDNA library"
Adams, Mark D., M. Bento Soares, Anthony R. Kerlavage, Chris Fields, and J. Craig Venter. "Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library." Nature Genetics 4, no. 4 (August 1993): 373–80. http://dx.doi.org/10.1038/ng0893-373.
Повний текст джерелаXu, Lei, Jingqi Li, Li Liu, Lixia Lu, Jingxia Gao, and Xueli Li. "Construction of equalized short hairpin RNA library from human brain cDNA." Journal of Biotechnology 128, no. 3 (February 20, 2007): 477–85. http://dx.doi.org/10.1016/j.jbiotec.2006.11.013.
Повний текст джерелаNobis, William, Xiaoning Ren, Steven P. Suchyta, Thomas R. Suchyta, Adroaldo J. Zanella, and Paul M. Coussens. "Development of a porcine brain cDNA library, EST database, and microarray resource." Physiological Genomics 16, no. 1 (December 16, 2003): 153–59. http://dx.doi.org/10.1152/physiolgenomics.00099.2003.
Повний текст джерелаGong, Yuewen, Manna Zhang, Li Cui, and Gerald Y. Minuk. "Sequence and chromosomal assignment of a human novel cDNA: similarity to gamma-aminobutyric acid transporter." Canadian Journal of Physiology and Pharmacology 79, no. 12 (December 1, 2001): 977–84. http://dx.doi.org/10.1139/y01-082.
Повний текст джерелаMICHEL, UWE, BORIS KALLMANN, PETER RIECKMANN, and DIRK ISBRANDT. "UM 9(5)h and UM 9(5)p, human and porcine noncoding transcripts with preferential expression in the cerebellum." RNA 8, no. 12 (December 2002): 1538–47. http://dx.doi.org/10.1017/s1355838202028042.
Повний текст джерелаKIKONYOGO, Alexandra, та Regina PIETRUSZKO. "Aldehyde dehydrogenase from adult human brain that dehydrogenates γ-aminobutyraldehyde: purification, characterization, cloning and distribution". Biochemical Journal 316, № 1 (15 травня 1996): 317–24. http://dx.doi.org/10.1042/bj3160317.
Повний текст джерелаThomson, S. A. M., E. Kennerly, N. Olby, J. R. Mickelson, D. E. Hoffmann, P. J. Dickinson, G. Gibson, and M. Breen. "Microarray Analysis of Differentially Expressed Genes of Primary Tumors in the Canine Central Nervous System." Veterinary Pathology 42, no. 5 (September 2005): 550–58. http://dx.doi.org/10.1354/vp.42-5-550.
Повний текст джерелаMiddlemas, D. S., R. A. Lindberg, and T. Hunter. "trkB, a neural receptor protein-tyrosine kinase: evidence for a full-length and two truncated receptors." Molecular and Cellular Biology 11, no. 1 (January 1991): 143–53. http://dx.doi.org/10.1128/mcb.11.1.143-153.1991.
Повний текст джерелаMiddlemas, D. S., R. A. Lindberg, and T. Hunter. "trkB, a neural receptor protein-tyrosine kinase: evidence for a full-length and two truncated receptors." Molecular and Cellular Biology 11, no. 1 (January 1991): 143–53. http://dx.doi.org/10.1128/mcb.11.1.143.
Повний текст джерелаGérard, C. M., C. Mollereau, G. Vassart, and M. Parmentier. "Molecular cloning of a human cannabinoid receptor which is also expressed in testis." Biochemical Journal 279, no. 1 (October 1, 1991): 129–34. http://dx.doi.org/10.1042/bj2790129.
Повний текст джерелаДисертації з теми "Human brain cDNA library"
Marson, Lorena. "Phage-display epitope library development for biomarkers identification in autoimmune diseases of the Central Nervous System." Doctoral thesis, Università degli studi di Trieste, 2012. http://hdl.handle.net/10077/7405.
Повний текст джерелаThe principal aim of my PhD was the setting of a protocol for the creation of phage libraries to display cDNA fragments encoding real ORF sequences, that could correspond to potential epitopes. A similar phage display library contains all the potential ORF repertoire of a cell or tissue. This tool can be specially used in the study of autoimmune diseases to perform different kind of analysis, such as the identification of epitopes involved in pathological reaction, the comparison between healthy and pathological conditions, or between different pathological conditions. A complex protocol was developed. It provides for: cDNA normalization, cDNA fragmentation to obtain peptides with useful size, and ORF enrichment to obtain really coding fragments. With this system we have created a epitopes library from Human brain mRNA.
Il principale obiettivo del mio lavoro di ricerca è la messa a punto di un protocollo per la costruzione di librerie fagiche di frammenti di cDNA codificanti per frammenti ORF, e che quindi potrebbero corrispondere a potenziali epitopi. Questo tipo di librerie contengono, potenzialmente, tutto il repertorio ORF di una cellula o di un tessuto e possono quindi essere utilizzate nello studio di malattie autoimmuni al fine di identificare nuovi epitopi coinvolti nella risposta immunitaria, di fare un confronto tra lo stato patologico e quello sano o tra diverse condizioni patologiche. Abbiamo quindi messo a punto un complesso protocollo che prevede: la normalizzazione del cDNA, la sua frammentazione per ottenere peptidi di dimensioni opportune, e l'arricchimento in frammenti realmente codificanti. Con questo sistema abbiamo realizzato una libreria di epitopi a partire da mRNA di cervello umano.
XXIV Ciclo
1984
Chen, Yun-Liang. "Cloning and expression of sperm antigens from a human testis lambda (#lambda#) gt11 cDNA library." Thesis, Queen Mary, University of London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325529.
Повний текст джерелаCollins-De, Peyer Laurence. "Screening of a rat thymus and a human hippocampus cDNA library for a novel fyn-related oncogene." Thesis, Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21253870.
Повний текст джерелаGreen, Melanie Leslie Dawn. "The identification of novel autoantigens by means of serological screening of a cDNA expression library constructed from multiple sclerosis brain tissues." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0018/MQ54892.pdf.
Повний текст джерелаLiang, Binhua. "Molecular cloning and sequence analysis of a human brain cDNA of an Alzheimer amyloid precursor (APP) interacting protein." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0004/MQ45086.pdf.
Повний текст джерелаYamakawa, Tatsuya. "Screening of human cDNA library reveals two differentiation-related genes, HHEX and HLX, as promoters of early phase reprogramming toward pluripotency." Kyoto University, 2016. http://hdl.handle.net/2433/217142.
Повний текст джерелаTseng, Huan-Yi, and 曾煥怡. "Isolation and Characterization of GP-83 encoding cDNA from cDNA library of human epididymis." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/74242961586346401682.
Повний текст джерела國防醫學院
解剖學研究所
83
Mammalian sperm are immature and incapable of fertilization when they just emerge from the testis. During the subsequent passage in epididymis, sperm interact with epididymal secretions, and acquire forward motility and ability to recognize and penetrate zona pellucida of eggs. Several genes of sperm maturation-related proteins, such as PH-30, EAP-1, HE 2 and 3 have been isolated and sequenced. DNA sequence of these molecules reveal proteinase- and disintegrin-encoding domains which are the same as those encoded in the genes of a variety of snake venoms. Our previous studies identified a sperm maturation-related glycoproteins, GP-83, in human epididymis. It was secreted from corpus of epididymis will associated in sperm surface. In order to analyze DNA sequence and predict the biological significance, GP-83 encoding cDNA was isolated from cDNA library of human epididymis by immunoscreening using GP-83 specific antiserum. Three positive clones containing inserts of 1.8 Kb, 1.5 kb and 4.0 kb were isola ted. Partial sequences of these inserts, up to 300-400 bp from 3' end, did not reveal any significant homology to known genes in the GenBank. In cDNA library of snake venomous gland, however, an ancrod-like sequence was identified. In conclusion, GP-83 may be a human epididymis-specific protein containing disintegrin-like domain.
"Identification of human cytosolic malate dehydrogenase by large scale human heart cDNA library sequencing." Chinese University of Hong Kong, 1995. http://library.cuhk.edu.hk/record=b5895590.
Повний текст джерелаThesis (M.Phil.)--Chinese University of Hong Kong, 1995.
Includes bibliographical references (leaves [27-33] (2nd gp.)).
Chapter PART 1: --- Human Heart cDNA Library Sequencing
Chapter A) --- Introduction of human heart cDNA library sequencing
Chapter A.1 --- Human genome project
Chapter A.2 --- The aim of human genome project
Chapter A.3 --- Automatic sequencing
Chapter A.4 --- Cycle sequencing reaction
Chapter A.5 --- Human heart cDNA library sequencing project
Chapter B) --- Methods and materials
Chapter (I) --- Preparation of plating bacterial-Y1090
Chapter (II) --- Plating the bacteriophage with blue-white visual selection
Chapter (III) --- Amplification of bacteriophage cDNA clones by PCR
Chapter (IV) --- Purification and quantitation of PCR products
Chapter (V) --- Cycle DNA sequencing of PCR products
Chapter (VI) --- Casting the sequencing gel
Chapter (VII) --- Sequencing by Pharmacia LKB A.L.F. DNA Sequencer
Chapter (VIII) --- Editing and saving the DNA sequence
Chapter (IX) --- Sending the DNA sequence to Genbank by E-mail
Chapter (X) --- Usage of the Genbank database
Chapter C) --- Results
Chapter D) --- Discussions
Chapter D.1 --- Application of human genomic project
Chapter D.2 --- Interpretation of the sequencing results
Chapter D.3 --- Quality of cDNA libraries and representation of mRNA population
Chapter D.4 --- "Gene expression profile in three different organs-heart, brain and liver"
Chapter D.5 --- Population study of the cDNA library
Chapter D.6 --- Isolation of a large number of novel genes by substraction cDNA library
Chapter D.7 --- Screening method to find out the complete coding sequence of interesting genes
Chapter D.8 --- Technical problems encountered and managed
Chapter PART 2: --- Identification of human cytosolic malate dehydrogenase by large scale human heart cDNA library sequencing
Chapter CHAPTER 1: --- Introduction of malate dehydrogenase
Chapter 1.1 --- Malate dehydrogenase--Kreb's cycle enzyme
Chapter 1.2 --- Two stereospecific forms of dehydrogenase
Chapter 1.3 --- NAD-binding domain
Chapter 1.4 --- The active site
Chapter 1.5 --- Comparison of surface properties between cMDH and mMDH
Chapter 1.6 --- N-terminal region and mitochondrial import
Chapter 1.7 --- Subunit-subunit interactions
Chapter 1.8 --- Physiological importance of malate dehydrogenase
Chapter 1.9 --- Secondary structure-total 11 β-strands and 9 α-helixes
Chapter 1.10 --- Objectives of the thesis
Chapter CHAPTER 2: --- Cloning and sequence analysis of human cytosolic malate dehydrogenase (hcMDH)
Chapter 2.1 --- Cloning of human cytosolic malate dehydrogenase (hcMDH)
Chapter 2.1.1 --- Methods and materials
Chapter 2.1.1.1 --- Cloning full length of hcMDH into expression vector pAED4
Chapter 2.1.1.2 --- Preparation of competent cell-JM109 for transformation
Chapter 2.1.1.3 --- Minipreparation of plasmid DNA
Chapter 2.1.1.4 --- Midi-preparation of bacteriophage λDNA by QIAGEN´ёØ
Chapter 2.1.1.5 --- Titration of bacteriophage λ of human adult heart cDNA library
Chapter 2.1.1.6 --- Preparation of soft-agarose lysates
Chapter 2.1.1.7 --- Elution of DNA from agarose gel by GENECLEAN´ёØ
Chapter 2.1.2 --- Results
Chapter 2.1.3 --- Discussions
Chapter 2.2 --- Sequence analysis of human cytosolic malate dehydrogenase (hcMDH)
Chapter 2.2.1 --- Methods and materials: Autoread sequencing
Chapter (I) --- Annealing of primer to double-stranded template
Chapter (II) --- Sequencing
Chapter 2.2.2 --- Results and discussions
Chapter 2.3 --- Amino acids and protein structure analysis of cMDH
Chapter CHAPTER 3 : --- "Protein expression, partial purification and folding experiments of human cytosolic malate dehydrogenase (hcMDH)"
Chapter 3.1 --- Protein expression of hcMDH in E. coli
Chapter 3.1.1 --- Methods and materials
Chapter 3.1.1.1 --- Protein expression induced by IPTG
Chapter 3.1.1.2 --- Isoelectric focusing (IEF)-two dimensional gel electrophoresis
Chapter (I) --- First dimensional electrofocusing
Chapter (II) --- The second dimension SDS-PAGE electrophoresis
Chapter (III) --- Sample preparation
Chapter 3.1.2 --- Results
Chapter 3.1.3 --- Discussions
Chapter 3.1.3.1 --- The properties of expressed protein of hcMDH
Chapter 3.1.3.2 --- T7 expression system
Chapter 3.1.3.3 --- Strong φ 10 promoter
Chapter 3.1.3.4 --- E.coli BL21 host cell
Chapter 3.2 --- Partial purification and folding experiments of hcMDH
Chapter 3.2.1 --- Methods and materials
Chapter 3.2.1.1 --- Partial purification of hcMDH expressed protein
Chapter (I) --- Preparation of supernatant from E.coli crude extract
Chapter (II) --- Ion-exchange column chromatography
Chapter (III) --- Affinity chromatography
Chapter (IV) --- Gel filtration on a Sepharose CL-6B column
Chapter 3.2.1.2 --- Sodium Dodecyl Sulphate Polyacrylamide Gel Electrophoresis (SDS-PAGE)
Chapter 3.2.1.3 --- Staining the protein gel by the Coomassie Blue R-250 method
Chapter 3.2.1.4 --- Staining the protein gel by the Silver staining Method
Chapter 3.2.1.5 --- Quantitation of protein by the Bradford Method
Chapter 3.2.1.6 --- Native gel electrophoresis
Chapter 3.2.1.7 --- Malate dehydrogenase MDH enzyme staining method
Chapter 3.2.1.8 --- Malate dehydrogenase MDH enzyme assay
Chapter 3.2.1.9 --- Fast protein liquid chromatography (FPLC)
Chapter 3.2.1.10 --- Protein folding experiment
Chapter 3.2.1.11 --- Eukaryotic expression of hcMDH
Chapter 3.2.2 --- Results
Chapter 3.2.2.1 --- Partial purification by chromatography
Chapter 3.2.2.2 --- Native gel
Chapter 3.2.2.3 --- FPLC
Chapter 3.2.2.4 --- To aid folding of protein by adding NADH
Chapter 3.2.2.5 --- Eukaryotic expression
Chapter 3.2.3 --- Discussions
Chapter 3.2.3.1 --- Purification of malate dehydrogenase MDH
Chapter 3.2.3.2 --- "Methods for visualizing dehydrogenase enzymes, e.g. malate dehydrogenase"
Chapter 3.2.3.3 --- The presence of unfold hcMDH protein in bacteria
Chapter 3.2.3.4 --- Folding of protein by heat shock protein GroE
Chapter 3.2.3.5 --- Eukaryotic expression
Chapter CHAPTER 4: --- Master screening of single base change by PCR-SSCP (Single Strand Conformational Polymorphism)
Chapter 4.1 --- Theory of SSCP
Chapter 4.2 --- Methods and materials
Chapter 4.3 --- Results
Chapter 4.4 --- Discussions
Chapter 4.4.1 --- The procedure of SSCP
Chapter 4.4.2 --- An alternative quick detection method for polymorphism of hcMDH at position 565--by automatic sequencing
Chapter 4.4.3 --- Other detection methods-- RNA-PCR and ddF
Chapter 4.4.4 --- Parameters affecting sensitivity of SSCP
Chapter 4.4.5 --- Application of SSCP
Chapter CHAPTER 5: --- Southern hybridization and In situ hybridization
Chapter 5.1 --- Southern blot analysis of human cytosolic malate dehydrogenase (hcMDH)
Chapter 5.1.1 --- Methods and materials
Chapter (I) --- Transfer genomic DNA to Nylon membrane
Chapter (II) --- Synthesis of radiolabelling cDNA probe
Chapter (III) --- Pre-hybridization and hybridization reaction
Chapter 5.1.2 --- Results
Chapter 5.1.3 --- Discussions
Chapter 5.2 --- In situ hybridization
Chapter 5.2.1 --- Methods and materials
Chapter (I) --- Preparation of Dig labelling probe by random primed labelling
Chapter (II) --- Estimating the yield of Dig-labelled nucleic acids
Chapter (III) --- Denaturation and hybridization of the hcMDH probe with animal tissues
Chapter (IV) --- Color development of the tissue
Chapter 5.2.2 --- Results
Chapter 5.2.3 --- Discussions
Chapter 5.2.3.1 --- Cellular distribution of hcMDH
Chapter 5.2.3.2 --- The principle of in situ hybridization
Chapter 5.2.3.3 --- Specimen preparation
Chapter 5.2.3.4 --- Hybridization conditions
Chapter 5.2.3.5 --- "Ontogeny of MDH in rabbit fetal brain, heart and lung"
Appendixes:
"Appendix I: 531 random cDNA clones from clone no. J950 to K951 in human heart cDNA library sequencing project. The name of clones, accession number, the length of the partial sequence and percentage of match are listed"
Appendix II: The new accession no. of Novel clones in Genbank
"Appendix III: The enzymatic reaction, molecular weigth, specific activity and Michaelis constants of different sources of malate dehydrogenase"
Appendix IV: The full sequence of nucleic acids and amino acids of human cytosolic malate dehydrogenase hcMDH. Accession no. of hcMDH is U20352 in Genbank
Appendix V: Nucleotide sequences of the mouse cMDH gene
Appendix VI: Nucleotide sequences of the mouse mMDH gene
Appendix VII: Structural organization of the mouse cytosolic malate dehydrogenase and its comparison with that of the mouse mitochondrial malate dehydrogenase gene
"Gene expression of adult human heart as revealed by random sequencing of cDNA library." Chinese University of Hong Kong, 1995. http://library.cuhk.edu.hk/record=b5895472.
Повний текст джерелаThesis (Ph.D.)--Chinese University of Hong Kong, 1995.
Includes bibliographical references (leaves 188-216).
ACKNOWLEDGEMENTS --- p.ii
ABSTRACT --- p.iii
TABLE OF CONTENTS --- p.v
ABBREVIATIONS --- p.ix
Chapter CHAPTER 1 --- INTRODUCTION
Chapter 1.1 --- General introduction --- p.1
Chapter 1.2 --- Human genome project --- p.5
Chapter 1.3 --- Organization of human genome --- p.7
Chapter 1.4 --- Adult human heart cDNA library --- p.9
Chapter 1.5 --- Gene expression in adult human heart --- p.10
Chapter 1.6 --- Polymerase chain reaction --- p.12
Chapter 1.7 --- Purification of PCR products --- p.15
Chapter 1.8 --- Automated DNA sequencing --- p.17
Chapter 1.9 --- Sequence analysis by electronic mail server --- p.21
Chapter 1.10 --- Effects of agar and agarose on Vent´ёØ and Taq DNA polymerases --- p.23
Chapter 1.11 --- Transcription factors and zinc finger proteins --- p.25
Chapter 1.12 --- LIM domain --- p.28
Chapter 1.13 --- Cysteine-rich intestinal protein --- p.30
Chapter CHAPTER 2 --- MATERIALS AND METHODS
Chapter 2.1 --- Plating out the adult human heart cDNA library --- p.32
Chapter 2.2 --- Amplification by polymerase chain reaction --- p.33
Chapter 2.3 --- Purification of the PCR products by Millipore filters --- p.35
Chapter 2.4 --- Elimination of the purification of the PCR products before sequencing --- p.36
Chapter 2.5 --- Cycle sequencing --- p.37
Chapter 2.6 --- Unicycle sequencing --- p.38
Chapter 2.7 --- Sequencing by T7 polymerase --- p.39
Chapter 2.8 --- Gel electrophoresis in the automated A.L.F. sequencer --- p.41
Chapter 2.9 --- Sequence analysis by commercially available softwares --- p.42
Chapter 2.10 --- Sequence analysis through electronic mail server --- p.44
Chapter 2.11 --- Database for storing the result of each clone --- p.46
Chapter 2.12 --- Effects of agar and agarose on Vent´ёØ and Taq DNA polymerase --- p.47
Chapter 2.13 --- Mini-preparation of plasmid DNA --- p.50
Chapter 2.14 --- Large scale preparation of plasmid DNA --- p.51
Chapter 2.15 --- Cloning the human cysteine rich heart protein (hCRHP) into the pAED4 vector --- p.53
Chapter 2.16 --- Expression of hCRHP in E coli --- p.56
Chapter 2.17 --- Northern hybridization --- p.58
Chapter 2.18 --- Partial protein sequencing of hCRHP --- p.59
Chapter CHAPTER 3 --- RESULTS
Chapter 3.1 --- The sequencing results of adult human heart cDNA clones --- p.60
Chapter 3.2 --- Accuracy of sequencing results --- p.63
Chapter 3.3 --- Catalogues of genes expressed in the adult human heart --- p.65
Chapter 3.4 --- Effects of agar and agarose on Vent´ёØ and Taq DNA polymerases --- p.94
Chapter 3.5 --- Elimination of the purification of the PCR products before sequencing --- p.102
Chapter 3.6 --- Sequence analysis of hCRHP --- p.104
Chapter 3.7 --- Northern hybridization of hCRHP --- p.109
Chapter 3.8 --- Expression of hCRHP in E. coli --- p.112
Chapter CHAPTER 4 --- DISCUSSION
Chapter 4.1 --- Random sequencing of adult human heart cDNA clones --- p.118
Chapter 4.2 --- Catalogues of genes expressed in the adult human heart --- p.130
Chapter 4.3 --- Gene expression in the adult human heart --- p.137
Chapter 4.4 --- Importance of nonhuman matches --- p.170
Chapter 4.5 --- Effects of agar and agarose on Vent´ёØ and Taq DNA polymerases --- p.177
Chapter 4.6 --- Elimination of the purification of the PCR products before sequencing --- p.180
Chapter 4.7 --- The possible role of CRIP and hCRHP --- p.184
Chapter 4.8 --- Future prospect --- p.186
REFERENCE --- p.188
LIN, YI-LING, and 林宜玲. "Analysis of ▫ 36A, anintegrated HBV DNA and its cellular flanking sequences clonod from a human hepatocellular carcinoma cell line HCC36, and construction of a cDNA library from HCC 36." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/34740816730930970350.
Повний текст джерелаКниги з теми "Human brain cDNA library"
Cao, Chenglong. Immunological screening of a rat brain cDNA library for genes encoding potential novel glutamate receptors. Ottawa: National Library of Canada, 1993.
Знайти повний текст джерелаThe river that flows uphill: A journey from the Big Bang to the Big Brain. San Francisco: Sierra Club Books, 1986.
Знайти повний текст джерелаThe river that flows uphill: A journey from the Big Bang to the Big Brain. New York: Macmillan, 1986.
Знайти повний текст джерелаKing, Stephen. Mertvai︠a︡ zona. Moskva: AST, 1997.
Знайти повний текст джерелаStephen, King. The dead zone. London: Futura, 1980.
Знайти повний текст джерелаKing, Stephen. La zona muerta. 4th ed. Barcelona, Spain: Plaza & Janés, 1998.
Знайти повний текст джерелаStephen, King. The dead zone. London: Warner Books, 1992.
Знайти повний текст джерелаKing, Stephen. The dead zone. Boston: G.K. Hall, 1993.
Знайти повний текст джерелаKing, Stephen. Nekre zone. Athens: Bell, 2001.
Знайти повний текст джерелаKing, Stephen. The Dead Zone. New York: Penguin USA, Inc., 2009.
Знайти повний текст джерелаЧастини книг з теми "Human brain cDNA library"
Mukherjee, Arkajyoti, Ritik Srivastava, Vansh Bhatia, Utkarsh, and Suneeta Mohanty. "Stimuli Effect of the Human Brain Using EEG SPM Dataset." In Intelligent Systems Reference Library, 213–26. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-37551-5_14.
Повний текст джерелаFukuoka, Shin-Ichi, and Katsumi Shibata. "Characterization and Functional Expression of the Cdna Encoding Human Brain Quinolinate Phosphoribosyltransferase." In Advances in Experimental Medicine and Biology, 611–14. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4709-9_76.
Повний текст джерелаGrübler, Gerd, and Elisabeth Hildt. "On Human–Computer Interaction in Brain–Computer Interfaces." In The International Library of Ethics, Law and Technology, 183–91. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-8996-7_15.
Повний текст джерелаLiew, C. C., D. M. Hwang, R. X. Wang, S. H. Ng, A. Dempsey, D. H. Y. Wen, H. Ma, et al. "Construction of a human heart cDNA library and identification of cardiovascular based genes (CVBest)." In Novel Methods in Molecular and Cellular Biochemistry of Muscle, 81–87. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6353-2_8.
Повний текст джерелаSalehi, Zahra, Susan Ramos, Gary Pearson, Mira Jung, Anatoly Dritschilo, and Francis G. Kern. "Construction of a Unidirectional cDNA Library from a Radioresistant Laryngeal Squamous Cell Carcinoma Cell Line in an Epstein Barr Virus Shuttle Vector." In Neoplastic Transformation in Human Cell Culture, 377–86. Totowa, NJ: Humana Press, 1991. http://dx.doi.org/10.1007/978-1-4612-0411-4_38.
Повний текст джерелаPham, Dung Ngoc. "Profiling General-Purpose Fast Multipole Method (FMM) Using Human Head Topology." In Brain and Human Body Modeling 2020, 347–81. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45623-8_21.
Повний текст джерелаWang, Ruoxiang, Eva Cukerman, Baosheng Chen, and Choong-Chin Liew. "Differential Screening and Megasequencing of Human Heart cDNA Library: A Search for Genes Associated with Heart Failure." In Developments in Cardiovascular Medicine, 67–77. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4613-1237-6_6.
Повний текст джерелаPARK, M. S., P. E. PARDINGTON, and D. J. CHEN. "FUNCTIONAL COMPLEMENTATION OF A DNA DOUBLE STRAND REPAIR DEFICIENT CHINESE HAMSTER MUTANT WITH HUMAN cDNA LIBRARY." In Radiation Research: A Twentieth-century Perspective, 329. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-12-168561-4.51102-1.
Повний текст джерелаHorellou, Philippe, Lionel Marlier, Alain Privat, François Darchen, Daniel Scherman, Jean-Pierre Henry, and Jacques Mallet. "Chapter 3 Exogeneous expression of L-dopa and dopamine in various cell lines following transfer of rat and human tyrosine hydroxylase cDNA: grafting in an animal model of Parkinson's disease." In Progress in Brain Research, 23–32. Elsevier, 1990. http://dx.doi.org/10.1016/s0079-6123(08)62586-8.
Повний текст джерелаRuzic, Fjodor. "Information-Communications Systems Convergence Paradigm." In Human Computer Interaction, 2324–40. IGI Global, 2009. http://dx.doi.org/10.4018/978-1-87828-991-9.ch155.
Повний текст джерелаТези доповідей конференцій з теми "Human brain cDNA library"
Edgington, T. S., J. H. Morrissey, and H. Fakhrai. "MOLECULAR CLONING OF HUMAN TISSUE FACTOR cDNA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643740.
Повний текст джерелаMorrissey, J. H., D. S. Fair, and T. S. Edgington. "STRUCTURE AND PROPERTIES OF THE HUMAN TISSUE FACTOR APOPROTEIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643738.
Повний текст джерелаBjorklid, E., T. Johansen, U. R. Pendurthi, L. V. M. Rao, B. Warn-Cramer, and S. T. Rapaport. "HUMAN cDNA CLONES FOR THROMBOPLASTIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643735.
Повний текст джерелаBeeler, D., L. Fritze, G. Soff, R. Jackman, and R. Rosenberg. "HUMAN THROMBOMODULIN cDNA:SEQUENCE AND TRANSLATED STRUCTURE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643967.
Повний текст джерелаDahlbäck, B., and A. LundWall. "ISOLATION AND CHARACTERIZATION OF cDNA CLONES FOR HUMAN FACTOR V." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643886.
Повний текст джерелаSumi, Y., Y. Nakamura, M. Sakai, M. Muramatsu та N. Aoki. "STRUCTURE OF HUMAN α2-PLASMIN INHIBITOR DEDUCED FROM THAT OF cDNA". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644371.
Повний текст джерелаPloos van Amstel, J. K., A. L. van der Zanden, E. Bakker, P. H. Reitsma, and R. M. Bertina. "INDEPENDENT ISOLATION OF HUMAN PROTEIN S cDNA AND THE ASSIGNMENT OF THE GENE TO CHROMOSOME 3." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644638.
Повний текст джерелаKoide, T. "CHARACTERIZATION OF THE GENE FOR HUMAN HISTIDINE-RICH GLYCOPROTEIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643599.
Повний текст джерелаBosma, P. J., E. A. van den Berg, and T. Kooistra. "ISOLATION OF THE GENE CODING FOR HUMAN PLASMINOGEN ACTIVATOR INHIBITOR TYPE 1 (PAI-1)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644440.
Повний текст джерелаvan den Berg, E. A., E. Sprengers, M. Jaye, W. Burgess, and V. W. M. van Hinsbergh. "REGULATION OF PLASMINOGEN ACTIVATOR INHIBITOR-1 mRNA IN HUMAN ENDOTHELIAL CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642856.
Повний текст джерелаЗвіти організацій з теми "Human brain cDNA library"
Sikela, J. M. cDNA expression map of the human genome: Methods development and applications using brain cDNAs. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/5605006.
Повний текст джерелаSikela, J. M. cDNA expression map of the human genome: Methods development and applications using brain cDNAs. Progress report, October 15, 1991--March 14, 1992. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/10112745.
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