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Human molecular genetics [Elektronisk resurs] / Edited by Kenneth W. Adolph.

Adolph, Kenneth W. (redaktör/utgivare)
Publicerad: San Diego : Academic Press, 1996
Odefinierat språk online resource (xvii, 500 s., 1 pl.-s.
Serie: Methods in molecular genetics, 1067-2389 ; 8
  • E-bok
Innehållsförteckning Sammanfattning
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  • Section I Mutation detection in human genes -- [1]Chemical mismatch cleavage /James A. Hejna, Markus Grompe, Robb E. Moses -- [2]Detection of point mutations by solid-phase minisequencing /Ann-Christine Syvänen, Leena Peltonen -- [3]Simple and nonisotopic methods to detect unknown gene mutations in nucleic acids /Susanna Bunge, Sigrid Fuchs, Andreas Gal -- [4]Identification and functional analysis of mutations in the human PAX6 gene /Richard Maas, Jonathan A. Epstein, Tom Glaser -- [5]Mutation detection in the cystic fibrosis transmembrane conductance regulator gene /Ann Harris, Sue Shackleton, Jeremy Hull -- [6]Protein truncation test for presymptomatic diagnosis of familial adenomatous polyposis /Rob B. van der Luijt, P. Meera Khan -- [7]Localization of tumor suppressor genes by loss of heterozygosity and homozygous deletion analysis /Margaret A. Knowles -- Section II Gene mapping, cloning, sequencing -- [8]Mapping human disease genes by linkage analysis /E. Chung, R.M. Gardiner [9]Engineering 100- to 300-kb DNA as persisting extrachromosomal elements in human cells using human artificial episomal chromosome system /Tian-Qiang Sun, Jean-Michel H. Vos -- [10]Isolating and mapping coding regions from complex genomes: Direct cDNA selection /Carol A. Wise, Michael Lovett, Ethylin Wang Jabs -- [11]Isolation of candidate genes for inherited diseases: Application to X-linked retinal degenerations /Denise Yan, Ricardo Fujita, Anand Swaroop -- [12]Fluorescent differential display method for high-speed scanning of tissue- or cell-specific transcripts /Takashi Ito, Yoshiyuki Sakaki -- [13]32P- and fluorescence-labeled DNA sequencing using primers selected from nonamer library /Jeffrey H. Bock, Jerry L. Slightom. 
  • Section III Transcription: Promoters, transcription factors, mRNA -- [14]Analysis of promoter mutations causing human genetic disease /Lutz-Peter Berg, Deborah A. Scopes, Vijay V. Kakkar, David N. Cooper -- [15]Identification of transcription factors and their target genes /Heike L. Pahl, Patrick A. Baeuerle -- [16]Identification and characterization of transcription factors from mammalian cells /Guang L. Wang, Gregg L. Semenza -- [17]In vitro assays for characterization of RNA-protein complexes involved in pro-opiomelanocortin mRNA translation /Stephanie D. Flagg, Corinne M. Spencer, James H. Eberwine -- Section IV RNA editing, ribozymes, antisense RNA -- [18]Mammalian RNA Editing /Lawrence Chan, BaBie Teng -- [19]Ribozymes as therapeutic agents and tools for gene analysis /John J. Rossi, Daniela Castanotto, Edovard Bertrand -- [20]In vivo analysis of signaling elements via targeted, inducible antisense RNA /Patricia A. Galvin-Parton, Hsien-yu Wang, Jiang Fan Chen, Craig C. Malbon, Christopher M. Moxham -- Section V Genome recombination, amplification -- [21]Extrachromosomal substrates to study immunoglobulin heavy chain class switch recombination in mammalian B cells /Ming-Jie Li, Nancy Maizels, Helios Leung -- [22]Gene amplification as marker for studying genomic instability /T.D. Tlsty -- Section VI Receptors, signal transduction -- [23]Intracellular receptor characterization and ligand screening by transactivation and hormone-binding assays /Elizabeth A. Allegretto, Richard A. Heyman -- [24]Control of blood cell differentiation and mechanisms of neoplasia /Arthur J. Sytkowski -- Section VII The mouse as a model system for human molecular genetics -- [25]Selected methods related to the mouse as a model system /Evie Melanitou, Marie-Christine Simmler, Edith Heard, Claire Rougeulle, Philip Avner -- [26]Molecular analysis of cardiac muscle diseases based on mouse genetics /Steven W. Kubalak, John J. Hunter, Kenneth R. Chien, Pieter A. Doevendans, Howard A. Rockman, Nobuaki Tanaka, John Ross Jr.
  • Human Molecular Genetics is a practical guide to the applications of molecular biology and genetics techniques to human cells. A wide range of experimental procedures for investigating human genes and genomes are presented. 
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