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Human Molecular Genetics

★★★★★
★★★★★

English

By (author): Andrew Read Tom Strachan

Human Molecular Genetics has been carefully crafted over successive editions to provide an authoritative introduction to the molecular aspects of human genetics, genomics and cell biology.

Maintaining the features that have made previous editions so popular, this fifth edition has been completely updated in line with the latest developments in the field. Older technologies such as cloning and hybridization have been merged and summarized, coverage of newer DNA sequencing technologies has been expanded, and powerful new gene editing and single-cell genomics technologies have been added. The coverage of GWAS, functional genomics, stem cells, and disease modeling has been expanded. Greater focus is given to inheritance and variation in the context of populations and on the role of epigenetics in gene regulation.

Key features:

  • Fully integrated approach to the molecular aspects of human genetics, genomics, and cell biology

  • Accessible text is supported and enhanced throughout by superb artwork illustrating the key concepts and mechanisms

  • Summary boxes at the end of each chapter provide clear learning points

  • Annotated further reading helps readers navigate the wealth of additional information in this complex subject and provides direction for further study

  • Reorganized into five sections for improved access to related topics

  • Also new to this edition – brand new chapter on evolution and anthropology from the authors of the highly acclaimed Human Evolutionary Genetics

A proven and popular textbook for upper-level undergraduates and graduate students, the new edition of Human Molecular Genetics remains the ‘go-to’ book for those studying human molecular genetics or genomics courses around the world.

See more
€87.99
A01=Andrew ReadA01=Tom Strachanadeno-associated viral vectoradenoviral vectoraffected sib pairs anaysisAffymetrixAge Group_Uncategorizedalleleallelic exlusionalternative promoteramino acidancestral haplotypeAndrew Readaneuploidyanticodonantiparallelantisenseassociation studiesaugumentationAuthor_Andrew ReadAuthor_Tom Strachanautomatic-updateautoradiographybacterial artificial chromosomebaculovirusbandingBarr bodybase pairbiasbivalentblastocystblood cell disoderbootstrappingcandidate regionCategory1=Non-FictionCategory=PSAKCategory=PSDCategory=PSFcausal variantcell biologycell cyclecell cycle controlcell divisioncell junctionscentimorgancentromerechance effectcharacterchemical modificationchiasmachromatidchromatinchromosomal abnormalityChromosomal DNAchromosomechromosome analysischromosome breakchromosome disorderchromosome engineeringchromosome functionchromosome structureclinical heterogeneityclinical utilityclinical validitycloning systemcodoncoefficient of inbreedingcoefficient of relationshipcoefficient of selectioncomparative genomic hybridizationcomplementarycomplementation groupcomplementation testcomplex diseasecompound heterozygoteconcordancecongenitalconsensus sequenceconstitutive heterochromatinCOP=United Statescopy number variationcounselingCre-loxPcrossovercytogeneticsdegenerationDelivery_Delivery within 10-20 working daysdepersonalized medicinedevelopmentdichotomousdideoxy sequencingdiploiddisease modelingDNADNA CloneDNA ContentDNA fingerprintingDNA FragmentDNA MethylationDNA MoleculeDNA ReplicationDNA rReplicationDNA SequenceDNA sequencing technologiesDNA StrandDNA structureDNase-hypersensitive sitedominantdosagedot-blotdouble helixdrug targetDSBelectrophoresisembryonic stem cellemperic riskendodermenhancerepistasiseq_isMigrated=2eq_non-fictioneq_scienceES CellESCsethicsExome Sequencingexonexon skippingextracellular matrixextrachromosomalFISHfitnessfluorescencefluorophoresforensicfounder effectfragile sitefunctional genomicsgain-of-functiongametegenegene expressiongene superfamilygenetic codegeneticsgenomeGenome EditingGenome Wide Association Studiesgenomic librarygerm layersGerm Line DNAglobal gene expressionGrow DNA StrandhaploidhaploinsufficiencyHaplotype BlocksHapMapHardy-Weinberghemizygousheritabilityheterochromatinheteroduplexhigh copy numberhigh-throughput screeninghomeoboxhuman genetic diseaseHuman molecular geneticshuman-specificidentity by stateIlluminaimmunoblottingimmunoprecipitationimprintinginbreedingindependent assortmentinduced pluripotent stem cellinheritanceinsertional mutagenesisInternational Mouse Knockout Consortiuminterphase chromosomeinterspersed repeatintronISHiterative pyrosequencingJunk DNAkaryotypingknockoutlagging strandLanguage_Englishlarge insert cloninglate onsetleading strandleaky mutationlibrary screeningligaselinear chromosomelipid-mediated gene transferlocus heterogeneityloss of heterozygositylow copy numberlyonizationmAbmale lethalitymapping interactionsmarker genemass spectrometrymassively parallel sequencingmedicinemegabase fragmentsmeiosisMendelianmessenger RNAmethylationMHC Proteinmicrocell-mediated chromosome transfermicroinjectionmisrepairmissensemitochrondrial genomemitosismixoploidymodel organismmodificationmolecular biologymorphogenMorpholinomosaicismmousemultifactorialmutation ratenaked nucleic acidnanoparticlenecrosisnoncoding RNAnondisjunctionnonisotpoicnorthern blotnuclear transfernucleic acidnucleotideodds ratiooligonucleotideone gene-one enzymeoverlapping genePA=Availablepaintingparamutationparental originpattern formationpedigreepedigree patternpersonalized medicinephagemidpharmacodynamicspharmacokineticspharmacongenomicsphase 2 metabolismphase-knownphenotypephenotypic effectphylogenetic treephysical mapPiwi-protein-interaction RNAploidypluripotentPluripotent Stem Cellpolarizationpolymerasepolymorphism information contentpolypeptidepolypillpopulation screeningpositional informationpredicted genePrice_€50 to €100probeprocessingprogrammed cell deathpromoterproofreadingproteinprotein truncation testprotein-protein interactionPS=Activepseudoautosomalpseudogenepurinepyrimidinepyrosequencingquantitative trait lociradioisotopesrecessivereplicationreplication originrestriction endonucleaserestriction fragment length polymorphismretinoblastomaretrotransposonribosomal RNARNARNA genomesRNA structurescreeningsecond messengersegregation ratiosemiconservativesemidiscontinuoussensesequence comparisonsex determinationshort interfering RNAshort tandem repeat polymorphismsib pair analysissingle-strand conformation analysissiRNAsite-specific recombinationSNP ChipsnRNPsoftlaunchsomaticSouthern blotspecializationspindlesplice sitesplicingstainingStem CellstructuresusceptibilitysynapseT-cell Receptortag-SNPTCRstechniquestelomerethree-point crossesthreshold modeltissue stem celltotipotenttranscripttranscript profilingtranscriptiontranscriptometransdifferentiationtransfer RNAtransgenerationaltranslationtransmission disequilibriumtriplet repeat diseasetwin studiestwo-hit paradigmtwo-point mappinguniversaluntranslatedviruswhole exon deletionwhole exon duplicationwhole genomewide association studiesX-inactivationY chromosomeyeast artificial chromosomeyeast two hybrid screeningzinc finger nucleaseszygote
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Product Details
  • Weight: 2330g
  • Dimensions: 210 x 280mm
  • Publication Date: 04 Dec 2018
  • Publisher: Taylor & Francis Inc
  • Publication City/Country: US
  • Language: English
  • ISBN13: 9780815345893

About Andrew ReadTom Strachan

Tom Strachan is Emeritus Professor of Human Molecular Genetics at Newcastle University, Newcastle, UK, and is a Fellow of the Royal Society of Edinburgh and a Fellow of the Academy of Medical Sciences. He was the founding Head of Institute at Newcastle University’s Institute of Human Genetics (now the Institute of Genetic Medicine) and its Scientific Director from 2001 to 2009. Tom’s early research interests were in multigene family evolution and interlocus sequence exchange, notably in the HLA and 21-hydroxylase gene clusters. While pursuing the latter, he became interested in medical genetics. His most recent research has focused on developmental disorders and developmental control genes.


Andrew Read

is Emeritus Professor of Human Genetics at the University of Manchester, UK and a Fellow of the Academy of Medical Sciences. Andrew has been particularly concerned with making the benefits of DNA technology available to people with genetic problems. He established one of the first DNA diagnostic laboratories in the UK over 20 years ago (it is now one of two National Genetics Reference Laboratories), and was founder chairman of the British Society for Human Genetics, the main professional body in this area. His own research is on the molecular pathology of various hereditary syndromes, especially hereditary hearing loss.

Drs. Strachan and Read were recipients of the European Society of Human Genetics Education Award

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