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  • 1
    Online Resource
    Online Resource
    Oxford :Oxford University Press,
    Keywords: Evolution (Biology). ; Phylogeny. ; Electronic books.
    Description / Table of Contents: This is a comprehensive reference source on the evolution of life, especially the family tree of organisms and when they originated in time. More than 100 experts on different organisms have distilled the latest research on the evolution of life, primarily from analyses of gene sequences but also from the fossil record. - ;The evolutionary history of life includes two primary components: phylogeny and timescale. Phylogeny refers to the branching order (relationships) of species or other taxa within a group and is crucial for understanding the inheritance of traits and for erecting classifications. However, a timescale is equally important because it provides a way to compare phylogeny directly with the evolution of other organisms and with planetary history such as geology, climate, extraterrestrial. impacts, and other features. The Timetree of Life is the first reference book to synthesize the wealth of information relating to the temporal component of phylogenetic trees. In the past, biologists have relied exclusively upon the fossil record to infer an evolutionary timescale. However, recent revolutionary advances in molecular biology have made it possible to not only estimate the relationships of many groups of organisms, but also to estimate their times of divergence with molecular clocks. The routine. estimation and utilization of these so-called 'time-trees' could add exciting new dimensions to biology including enhanced opportunities to integrate large molecular data sets with fossil and biogeographic evidence (and thereby foster greater communication between molecular and traditional systematists). They. could help estimate not only ancestral character states but also evolutionary rates in numerous categories of organismal phenotype; establish more reliable associations between causal historical processes and biological outcomes; develop
    Type of Medium: Online Resource
    Pages: 1 online resource (1268 pages)
    Edition: 1st ed.
    ISBN: 9780191560156
    DDC: 576.8
    Language: English
    Note: Cover Page -- Title Page -- Copyright Page -- Contents -- Foreword -- Preface -- List of Contributors -- INTRODUCTION -- Discovering the Timetree of Life -- Timetrees: beyond cladograms, phenograms, and phylograms -- The geologic time scale -- Calibrating and constraining molecular clocks -- TIMETREES -- Life -- SUPERKINGDOMS -- Archaebacteria -- Eubacteria -- Eukaryotes (Eukaryota) -- PROTISTS -- Haptophyte algae (Haptophyta) -- Diatoms (Bacillariophyta) -- PLANTS -- Land plants (Embryophyta) -- Mosses (Bryophyta) -- Liverworts (Marchantiophyta) -- Ferns -- Gymnosperms -- Flowering plants (Magnoliophyta) -- Magnoliids -- Eudicots -- Asterids -- Eurosid I -- Eurosid II -- Monocots -- FUNGI -- Fungi -- ANIMALS -- Animals (Metazoa) -- INVERTEBRATES -- Cnidarians (Cnidaria) -- Scaphopod mollusks (Scaphopoda) -- Cephalopod mollusks (Cephalopoda) -- Nematodes (Nematoda) -- Arthropods (Arthropoda) -- Spiders (Araneae) -- Holometabolous insects (Holometabola) -- Bees, ants, and stinging wasps (Aculeata) -- True flies (Diptera) -- Beetles (Coleoptera) -- Lacewings (Neuroptera) -- Crabs, shrimps, and lobsters (Decapoda) -- Stalked and acorn barnacles (Thoracica) -- Sea urchins (Echinoidea) -- VERTEBRATES -- Vertebrates (Vertebrata) -- FISHES -- Jawless fishes (Cyclostomata) -- Cartilaginous fishes (Chondrichthyes) -- Ray-finned fishes (Actinopterygii) -- Sturgeons and paddlefishes (Acipenseriformes) -- Teleost fishes (Teleostei) -- Notothenioid fishes (Notothenioidei) -- Labyrinth fishes (Anabantoidei) -- Lungfishes (Dipnoi) -- AMPHIBIANS -- Amphibians (Lissamphibia) -- Frogs and toads (Anura) -- Salamanders (Caudata) -- Caecilians (Gymnophiona) -- AMNIOTES -- Amniotes (Amniota) -- REPTILES -- Lizards, snakes, and amphisbaenians (Squamata) -- Snakes (Serpentes) -- Turtles (Testudines) -- Crocodylians (Crocodylia) -- BIRDS -- Birds (Aves). , Ratites and tinamous (Paleognathae) -- Waterfowl and gamefowl (Galloanserae) -- Advanced birds (Neoaves) -- Passerine birds (Passeriformes) -- Shorebirds (Charadriiformes) -- Diurnal birds of prey (Falconiformes) -- Cranes, rails, and allies (Gruiformes) -- Woodpeckers, toucans, barbets, and allies (Piciformes) -- Owls (Strigiformes) -- Swifts, treeswifts, and hummingbirds (Apodiformes) -- MAMMALS -- Mammals (Mammalia) -- Monotremes (Prototheria) -- Marsupials (Metatheria) -- Placental mammals (Eutheria) -- Armadillos, anteaters, and sloths (Xenarthra) -- Tenrecs and golden moles (Afrosoricida) -- Primates (Primates) -- Pikas, hares, and rabbits (Lagomorpha) -- Rodents (Rodentia) -- Hedgehogs, shrews, moles, and solenodons (Eulipotyphla) -- Bats (Chiroptera) -- Carnivores (Carnivora) -- Rhinoceroses, tapirs, and horses (Perissodactyla) -- Whales and even-toed ungulates (Cetartiodactyla) -- Index.
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Brain chemistry. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (634 pages)
    Edition: 1st ed.
    ISBN: 9781483153599
    Language: English
    Note: Front Cover -- Biochemistry of Brain -- Copyright Page -- Table of Contents -- Preface -- CHAPTER 1. STRUCTURE, FUNCTION AND METABOLISM OF GLYCOSPHINGOLIPIDS -- INTRODUCTION -- STRUCTURE AND NOMENCLATURE OF SPHINGOSINE AND RELATED BASES -- CLASSIFICATION OF SPHINGOLIPIDS -- CHEMICAL STRUCTURES AND OCCURRENCE -- ISOLATION OF GLYCOSPHINGOLIPIDS -- BIOSYNTHESIS OF GLYCOSPHINGOLIPIDS -- CATABOLISM OF GLYCOSPHINGOLIPIDS -- PHYSIOLOGICAL FUNCTIONS OF GLYCOSPHINGOLIPIDS -- ACKNOWLEDGEMENT -- REFERENCES -- CHAPTER 2. METABOLIC DISORDERS IN SPHINGOLIPIDOSES -- INTRODUCTION -- BIOCHEMICAL GENETICS OF SPHINGOLIPID STORAGE DISORDERS -- TAY-SACHS AND SANDHOFF'S DISEASES -- FABRY'S DISEASE -- METACHROMATIC LEUKODYSTROPHY (SULFATIDE LIPIDOSIS) -- NIEMANN-PICK DISEASE -- GAUCHER'S DISEASE -- ACKNOWLEDGEMENT -- REFERENCES -- CHAPTER 3. MYELIN BASIC PROTEIN: WHAT DOES IT DO? -- I. STRUCTURE OF THE BASIC PROTEIN -- II. ORIENTATION OF THE BASIC PROTEIN WITHINTHE MYELIN SHEATH -- III. BASIC PROTEIN-LIPID INTERACTIONS -- IV. METHYLATION OF THE BASIC PROTEIN -- V. PHOSPHORYLATION AND DEPHOSPHORYLATIONOF THE BASIC PROTEIN -- VI. PRESENCE OF TWO DIFFERENT BASIC PROTEINSIN THE CNS MYELIN OF SOME RODENTS -- CONCLUDING REMARKS -- ACKNOWLEDGEMENTS -- REFERENCES -- CHAPTER 4. THE BIOCHEMICAL ANDMORPHOLOGICAL HETEROGENEITY OFMYELIN AND MYELIN-RELATED MEMBRANES -- INTRODUCTION -- SUBFRACTIONATION OF PURIFIED MYELIN -- MYELIN-RELATED MEMBRANES WHICH ARE DISCARDEDDURING THE PURIFICATION OF MYELIN -- POSSIBLE MORPHOLOGICAL SIGNIFICANCEOF MYELIN SUBFRACTIONS -- OLIGODENDROGLIAL DERIVED FRACTIONS ASPOSSIBLE PRECURSORS OF MYELIN -- MYELIN-SUBFRACTIONS IN PATHOLOGICAL STATES -- CURRENT STATUS AND POSSIBLE DIRECTIONSFOR FURTHER RESEARCH -- ACKNOWLEDGEMENTS -- ADDENDUM -- REFERENCES -- CHAPTER 5. FOLATE METABOLISM IN BRAIN -- INTRODUCTION -- 1. GENERAL ASPECTS OF FOLATE BIOCHEMISTRY. , 2. TRANSPORT OF FOLATE INTO THE CENTRALNERVOUS SYSTEM -- 3. FOLATE AND RELATED ENZYMES IN BRAIN -- 4. INBORN ERRORS OF FOLATE METABOLISM -- 5. FOLATE DEFICIENCY -- 6. CONVULSANT EFFECTS OF FOLATE ADMINISTRATION -- ADDENDUM -- REFERENCES -- CHAPTER 6. VITAMIN B12 AND THE NERVOUS SYSTEM -- 1. INTRODUCTION -- 2. CLINICAL SYNDROMES: FETUS, INFANCY AND CHILDHOOD -- 3. CLINICAL SYNDROMES: ADULTS -- 4. PREVALENCE OF NERVOUS SYSTEM INVOLVEMENT -- 5. INTERMEDIARY METABOLISM -- 6. CONGENITAL DISORDERS OF INTERMEDIARY METABOLISM -- 7. CONCLUSIONS -- ADDENDUM -- REFERENCES -- CHAPTER 7. BRAIN BIOGENIC AMINES IN MENTALDYSFUNCTIONS ATTRIBUTABLE TOTHYROID HORMONE ABNORMALITIES -- 1. INTRODUCTION -- 2. HORMONAL IMPACT ON BIOCHEMICAL MATURATIONOF THE CENTRAL NERVOUS SYSTEM -- 3. CRETINISM-PHYSICAL AND BEHAVIOURAL MANIFESTATIONS -- 4. NEONATAL HYPOTHYROIDISM AND CHANGESIN CENTRAL AMINE METABOLISM -- 5. THYROID HORMONES-VULNERABLE PERIODSOF BRAIN DEVELOPMENT -- 6. THYROID DYSFUNCTION AND AFFECTIVE DISORDERS -- 7. THYROID-IMIPRAMINE INTERACTION AND THE USE OFTHYROID HORMONE IN DEPRESSIVE ILLNESS -- 8. THYROTROPIN RELEASING HORMONE:AN ANTIDEPRESSANT AGENT -- 9. HYPERTHYROIDISM VS. MANIA -- 10. HYPERTHYROIDISM-PHYSICAL ANDBEHAVIOURAL MANIFESTATIONS -- 11. NEONATAL HYPERTHYROIDISM-IMPACT ON BRAINBIOGENIC AMINE METABOLISM -- 12. INFLUENCE OF ADULT HYPERTHYROIDISM ONCENTRAL AMINE METABOLISM -- 13. EFFECT OF LITHIUM IN NEONATALLY HYPERTHYROID RATS -- SUMMARY AND PERSPECTIVE -- ACKNOWLEDGEMENTS -- TRIVIAL NAMES OF ENZYMES -- REFERENCES -- CHAPTER 8. BRAIN SPECIFIC PROTEINS -- INTRODUCTION -- S-100 PROTEIN -- NP PROTEIN -- 14-3-2 PROTEIN -- ANTIGEN-a -- ^-GLYCOPROTEIN -- OLFACTORY BULB PROTEIN -- OTHER PROTEINS -- CONCLUDING COMMENTS -- ACKNOWLEDGEMENTS -- REFERENCES -- NOTE ADDED IN THE PROOF -- CHAPTER 9. BRAIN NUCLEIC ACIDS -- THE CONTENT OF NUCLEIC ACIDS IN THE BRAIN. , THE BIOSYNTHESIS OF NUCLEOTIDES IN THE BRAIN -- THE LESCH-NYHAN SYNDROME -- THE BIOSYNTHESIS OF NUCLEIC ACIDS IN THE BRAIN -- DEVELOPMENTAL ASPECTS OF DNA METABOLISM -- DEVELOPMENTAL ASPECTS OF RNA SYNTHESIS -- CHARACTERISTICS OF BRAIN RNAs -- THE RNA OF BRAIN MITOCHONDRIA AND OF SYNAPTOSOMES -- CHARACTERISTICS OF BRAIN POLYSOMES -- THE TRANSLATION OF SPECIFIC MESSENGERS FROM THE BRAIN -- DIVERSITY OF RNAs IN THE BRAIN -- CHANGES IN RNA CONTENT AND COMPOSITION DUE TO CHEMICALINFLUENCES, ENVIRONMENT, AND TRAINING AND/OR MEMORY -- THE CURRENT STATUS OF RNA AS ENGRAM -- REFERENCES -- CHAPTER 10. FREE NUCLEOTIDES AND NUCLEIC ACIDSDURING BRAIN DEVELOPMENT -- INTRODUCTION -- FREE NUCLEOTIDES, PRECURSORS OF NUCLEIC ACIDS -- DNA AND BRAIN DEVELOPMENT -- RNA AND BRAIN DEVELOPMENT -- CONCLUSIONS AND SUGGESTIONS -- REFERENCES -- CHAPTER 11. TRANSFER RNA's IN BRAIN -- INTRODUCTION -- PURIFICATION OF tRNA -- CHARACTERIZATION OF tRNA -- ISOACCEPTOR tRNAS -- PROCESSING OF tRNA -- METHYLATION OF tRNA -- OTHER tRNA MODIFICATIONS -- SPECIAL FUNCTIONAL ASPECTS -- EFFECTS OF HORMONES, DRUGS AND ELICITED STATES -- FINAL REMARKS -- REFERENCES -- CHAPTER 12. MOLECULAR BIOLOGICAL ASPECTS OFDEGENERATION OF THE NERVOUSSYSTEM CAUSED BY AGING ANDSENSORY DEPRIVATION -- 1. INTRODUCTION -- 2. NERVOUS SYSTEM AS A COMPONENT IN THE AGING PROCESS -- 3. AGE RELATED CHANGES AT THE LEVEL OF TRANSCRIPTION -- 4. AGE RELATED CHANGES AT THE LEVEL OF TRANSLATION -- 5. AGE RELATED QUALITATIVE AND QUANTITATIVECHANGES IN PROTEINS -- 6. AGE RELATED CHANGES IN MITOCHONDRIA ANDSYNAPTIC REGIONS -- 7. STRUCTURAL AND FUNCTIONAL CHANGES RELATED TOSENSORY DEPRIVATION -- 8. SENSORY DEPRIVATION AND AGING -- ACKNOWLEDGEMENTS -- REFERENCES -- CHAPTER 13. NUTRITION AND AMINO ACIDIMBALANCE AS FACTORS INFLUENCINGBRAIN DEVELOPMENT -- CELL PROLIFERATION IN THE CEREBRAL CORTEX -- DEVELOPMENT OF THE CEREBELLUM. , NEURONAL CONNECTIVITY -- NEUROTRANSMITTER ENZYMES -- CHARACTERISTIC INFANT AND JUVENILE BRAIN ENZYMES -- UNDERNUTRITION -- UNDERNUTRITION AND METABOLIC COMPARTMENTATION -- EFFECTS OF UNDERNUTRITION AT THE CELLULAR LEVEL -- DIVISION LINKED TO DIFFERENTIATION -- BUdR AND MYELINATION -- REQUIREMENT FOR PROTEIN SYNTHESIS DURING THECELL CYCLE -- SEX HORMONES AND PROTEIN SYNTHESISIN REGIONAL DIFFERENTIATION -- THE MECHANISM OF STEROID ACTION -- RIBOSOMES, mRNA AND PROTEIN SYNTHESIS -- POLYRIBOSOMES, PROTEIN SYNTHESISAND HYPERPHENYLALANINAEMIA -- THE RELATIONSHIP OF THE INHIBITION OF BRAIN PROTEINSYNTHESIS TO THE STATE OF POLYRIBOSOMAL AGGREGATION -- REFERENCES -- CHAPTER 14. BRAIN AMINO ACIDS -- DISTRIBUTION AND CONTENT OF AMINO ACIDS IN THE BRAIN -- TRANSPORT OF AMINO ACIDS INTO THE BRAIN -- PATHWAYS OF AMINO ACID METABOLISM IN BRAIN -- METABOLIC ERRORS OF AMINO ACID METABOLISMWITH NEUROLOGICAL CONSEQUENCES -- AMINES AND OTHER AMINO ACID DERIVATIVES -- REFERENCES -- CHAPTER 15. MOLECULAR NEUROBIOLOGY OF MEMORY -- INTRODUCTION -- EXPERIMENTAL APPROACHES TO THE PROBLEM -- BEHAVIORAL BIOASSAYS -- ISOLATION OF ACTIVE SUBSTANCES -- TOWARDS A MOLECULAR CODE OF MEMORY -- FUTURE DEVELOPMENTS -- BIBLIOGRAPHY -- CHAPTER 16. NEURAL TISSUE CULTURE: A BIOCHEMICAL TOOL -- INTRODUCTION -- I. NEURAL TISSUE CULTURE: ORGAN AND ORGANOTYPIC -- II. DISSOCIATED NEURAL CELL CULTURES -- III. NEOPLASTIC NEURAL CELL LINES -- CONCLUSIONS -- REFERENCES -- CHAPTER 17. NEUROTOXIC EFFECTS OF HEAVYMETALS AND METALLOIDS -- INTRODUCTION -- LEAD -- MERCURY -- ARSENIC -- MANGANESE -- ALUMINUM -- REFERENCES -- CHAPTER 18. AMINOTRANSFERASES AND THE DEVELOPING BRAIN -- II. AMINOTRANSFERASE ACTIVITY AND MATURATION -- III. REGULATION OF ENZYMATIC ACTIVITYIN THE IMMATURE AND ADULT BRAIN -- CONCLUSIONS -- REFERENCES -- CHAPTER 19. ROLE OF CYCLIC AMP INDEVELOPING BRAIN -- INTRODUCTION. , ROLE OF CYCLIC AMP IN NEURAL INDUCTION -- ROLE OF CYCLIC AMP IN REGULATIONOF NEURAL DIFFERENTIATION -- REGULATION OF NEUROTRANSMITTER METABOLIZING ENZYMES -- REGULATION OF ORNITHINE DECARBOXYLASE -- REGULATION OF GLUCOSE METABOLIZING ENZYMES -- REGULATION OF GANGLIOSIDE METABOLIZING ENZYMES -- REGULATION PROTEASE ACTIVITY -- CHANGES IN NUCLEIC ACID AND PROTEIN SYNTHESISDURING DIFFERENTATIQN -- CHANGES IN POLY A-CONTAINING mRNADURING DIFFERENTIATION -- CHANGES IN THE SYNTHESIS AND PHOSPHORYLATIONOF HISTONE AND NONHISTONE PROTEINS DURINGDIFFERENTIATION -- CHANGES IN ADENYLATE CYCLASE ACTIVITYDURING DIFFERENTIATION -- CHANGES IN INTRACELLULAR LEVEL OF CYCLIC AMP -- CHANGES IN INTRACELLULAR LEVEL OF CYCLIC GMP -- CHANGES IN CYCLIC NUCLEOTIDE PHOSPHODIESTERASEACTIVITY DURING DIFFERENTIATION -- CHANGES IN THE CYCLIC NUCLEOTIDE BINDING PROTEINSAND CYCLIC AMP-DEPENDENT PHOSPHORYLATION ACTIVITYDURING DIFFERENTIATION -- HYPOTHESIS OF CANCER OF NERVE CELLS -- NERVE GROWTH FACTOR AND CYCLIC AMP -- MECHANISM OF INDUCTION AND DIFFERENTIATION -- REFERENCES -- CHAPTER 20. PROTEIN PHOSPHORYLATION-INVOLVEMENTIN BRAIN FUNCTION -- I. INTRODUCTION -- II. THE INVOLVEMENT OF PROTEIN PHOSPHORYLATIONIN BRAIN FUNCTION -- III. CONCLUSION -- ACKNOWLEDGEMENT -- REFERENCES -- CHAPTER 21. NERVE GROWTH FACTOR -- I. INTRODUCTION -- II. MOLECULAR PROPERTIES -- III. NGF AND THE PERIPHERAL NERVOUS SYSTEM -- IV. EFFECTS OF NGF IN THE CENTRAL NERVOUS SYSTEM (CNS -- V. SUMMARY AND CONCLUSIONS -- ACKNOWLEDGEMENT -- REFERENCES -- CHAPTER 22. BRAIN LYSOSOMES AND LYSOSOMAL ENZYMES -- INTRODUCTION -- PHYSICOCHEMICAL PROPERTIES OF LYSOSOMAL ISOENZYMES -- PHYSICOCHEMICAL MODIFICATIONS OF LYSOSOMAL HYDROLASES DURING INTRACELLULAR TRANSPORT -- BIOSYNTHESIS, TRANSPORT, GLYCOSYLATION AND PACKAGING OF LYSOSOMAL GLYCOPROTEINS -- SYNTHESIS AND TURNOVER OF LYSOSOMAL GLYCOPROTEINS.RELATION TO pi's. , PHYSICOCHEMICAL PROPERTIES OF BRAIN ACID HYDROLASES IN NERVE ENDING AND LYSOSOMAL FRACTIONS.
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  • 3
    Online Resource
    Online Resource
    Cary :Oxford University Press, Incorporated,
    Keywords: Evolutionary genetics -- Statistical methods. ; Molecular evolution -- Statistical methods. ; Electronic books.
    Description / Table of Contents: Numerical Examples 1. Molecular Basis of Evolution 2. Evolutionary Change of Amino Acid Sequences 3. Evolutionary Change in DNA Sequences 4. Synonymous and Nonsynonymous Nucleotide Substitutions 5. Phylogenetic Trees 6. Phylogenetic Inference: Distance Methods 7. Phylogenetic Inference: Maximum Parsimony Methods 8. Phylogenetic Inference: Maximum Likelihood Methods 9. Accuracies and Statistical Tests of Phylogenetic Trees 10. Molecular Clocks and Linearized Trees 11. Ancestral Nucleotide and Amino Acid Sequences 12. Genetic Polymorphism and Evolution 13. Population Trees from Genetic Markers 14. Perspectives Appendices References Index.
    Type of Medium: Online Resource
    Pages: 1 online resource (348 pages)
    Edition: 1st ed.
    ISBN: 9780195350517
    DDC: 572.838
    Language: English
    Note: Intro -- Contents -- Numerical Examples -- 1 Molecular Basis of Evolution -- 1.1. Evolutionary Tree of Life -- 1.2. Mechanism of Evolution -- 1.3. Structure and Function of Genes -- 1.4. Mutational Changes of DNA Sequences -- 1.5. Codon Usage -- 2 Evolutionary Change of Amino Acid Sequences -- 2.1. Amino Acid Differences and Proportion of Different Amino Acids -- 2.2. Poisson Correction (PC) and Gamma Distances -- 2.3. Bootstrap Variances and Covariances -- 2.4. Amino Acid Substitution Matrix -- 2.5. Mutation Rate and Substitution Rate -- 3 Evolutionary Change of DNA Sequences -- 3.1. Nucleotide Differences Between Sequences -- 3.2. Estimation of the Number of Nucleotide Substitutions -- 3.3. Gamma Distances -- 3.4. Numerical Estimation of Evolutionary Distances -- 3.5. Alignment of Nucleotide Sequences -- 3.6. Handling of Sequence Gaps in the Estimation of Evolutionary Distances -- 4 Synonymous and Nonsynonymous Nucleotide Substitutions -- 4.1. Evolutionary Pathway Methods -- 4.2. Methods Based on Kimura's 2-Parameter Model -- 4.3. Nucleotide Substitutions at Different Codon Positions -- 4.4. Likelihood Methods with Codon Substitution Models -- 5 Phylogenetic Trees -- 5.1. Types of Phylogenetic Trees -- 5.2. Topological Differences -- 5.3. Tree-Building Methods -- 6 Phylogenetic Inference: Distance Methods -- 6.1. UPGMA -- 6.2. Least Squares (LS) Methods -- 6.3. Minimum Evolution (ME) Method -- 6.4. Neighbor Joining (NJ) Method -- 6.5. Distance Measures to Be Used for Phylogenetic Reconstruction -- 7 Phylogenetic Inference: Maximum Parsimony Methods -- 7.1. Finding Maximum Parsimony (MP) Trees -- 7.2. Strategies of Searching for MP Trees -- 7.3. Consensus Trees -- 7.4. Estimation of Branch Lengths -- 7.5. Weighted Parsimony -- 7.6. MP Methods for Protein Data -- 7.7. Shared Derived Characters. , 8 Phylogenetic Inference: Maximum Likelihood Methods -- 8.1. Computational Procedure of ML Methods -- 8.2. Models of Nucleotide Substitution -- 8.3. Protein Likelihood Methods -- 8.4. Theoretical Foundation of ML Methods -- 8.5. Parameter Estimation for a Given Topology -- 9 Accuracies and Statistical Tests of Phylogenetic Trees -- 9.1. Optimization Principle and Topological Errors -- 9.2. Interior Branch Tests -- 9.3. Bootstrap Tests -- 9.4. Tests of Topological Differences -- 9.5. Advantages and Disadvantages of Different Tree-Building Methods -- 10 Molecular Clocks and Linearized Trees -- 10.1. Molecular Clock Hypothesis -- 10.2. Relative Rate Tests -- 10.3. Phylogenetic Tests -- 10.4. Linearized Trees -- 11 Ancestral Nucleotide and Amino Acid Sequences -- 11.1. Inference of Ancestral Sequences: Parsimony Approach -- 11.2. Inference of Ancestral Sequences: Bayesian Approach -- 11.3. Synonymous and Nonsynonymous Substitutions in Ancestral Branches -- 11.4. Convergent and Parallel Evolution -- 12 Genetic Polymorphism and Evolution -- 12.1. Evolutionary Significance of Genetic Polymorphism -- 12.2. Analysis of Allele Frequency Data -- 12.3. Genetic Variation in Subdivided Populations -- 12.4. Genetic Variation for Many Loci -- 12.5. DNA Polymorphism -- 12.6. Statistical Tests for Detecting Selection -- 13 Population Trees from Genetic Markers -- 13.1. Genetic Distance for Allele Frequency Data -- 13.2. Analysis of DNA Sequences by Restriction Enzymes -- 13.3. Analysis of RAPD Data -- 14 Perspectives -- 14.1. Statistical Methods -- 14.2. Genome Projects -- 14.3. Molecular Biology and Evolution -- Appendices -- A. Mathematical Symbols and Notations -- B. Geological Timescale -- C. Geological Events in the Cenozoic and Mesozoic Eras -- D. Organismal Evolution Based on the Fossil Record -- References -- Index -- A -- B -- C -- D -- E -- F -- G -- H -- I. , L -- M -- N -- O -- P -- R -- S -- T -- U -- V -- W -- Z.
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 12 (1965), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 17 (1970), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 13 (1966), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Genetics 35 (2001), S. 539-566 
    ISSN: 0066-4197
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Notes: Abstract Early studies of animal mitochondrial DNA (mtDNA) assumed that nucleotide sequence variation was neutral. Recent analyses of sequences from a variety of taxa have brought the validity of this assumption into question. Here we review analytical methods used to test for neutrality and evidence for nonneutral evolution of animal mtDNA. Evaluations of mitochondrial haplotypes in different nuclear backgrounds identified differences in performance, typically favoring coevolved mitochondrial and nuclear genomes. Experimental manipulations also indicated that certain haplotypes have an advantage over others; however, biotic and historical effects and cyto-nuclear interactions make it difficult to assess the relative importance of nonneutral factors. Statistical analyses of sequences have been used to argue for nonneutrality of mtDNA; however, rejection of neutral patterns in the published literature is common but not predominant. Patterns of replacement and synonymous substitutions within and between species identified a trend toward an excess of replacement mutations within species. This pattern has been viewed as support for the existence of mildly deleterious mutations within species; however, other alternative explanations that can produce similar patterns cannot be eliminated.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 41 (1971), S. 18-20 
    ISSN: 1432-2242
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The present experiments revealed a reduction in seedling height and damage at chromosomal level in Pisum treated withEMS and MMS. Further it was observed that GA 3 post-mutagen treatment could reduce this damage considerably by reducing the number of aberrations as well as chromosomal translocations. The GA 3 treatment also increased seedling height as well as pollen fertility.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 51 (2000), S. 544-553 
    ISSN: 1432-1432
    Keywords: Key words: Phylogenetic inference — Neighbor-joining method — Large phylogenies — Zero-length branches — Accuracy — Deep versus shallow branches
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The neighbor-joining (NJ) method is widely used in reconstructing large phylogenies because of its computational speed and the high accuracy in phylogenetic inference as revealed in computer simulation studies. However, most computer simulation studies have quantified the overall performance of the NJ method in terms of the percentage of branches inferred correctly or the percentage of replications in which the correct tree is recovered. We have examined other aspects of its performance, such as the relative efficiency in correctly reconstructing shallow (close to the external branches of the tree) and deep branches in large phylogenies; the contribution of zero-length branches to topological errors in the inferred trees; and the influence of increasing the tree size (number of sequences), evolutionary rate, and sequence length on the efficiency of the NJ method. Results show that the correct reconstruction of deep branches is no more difficult than that of shallower branches. The presence of zero-length branches in realized trees contributes significantly to the overall error observed in the NJ tree, especially in large phylogenies or slowly evolving genes. Furthermore, the tree size does not influence the efficiency of NJ in reconstructing shallow and deep branches in our simulation study, in which the evolutionary process is assumed to be homogeneous in all lineages.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 42 (1996), S. 183-193 
    ISSN: 1432-1432
    Keywords: Key words: Small-subunit ribosomal RNA — Phylogeny — Animals — Fungi — Plants — Alveolates — Heterokonts — Stramenopiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The evolutionary relationships of four eukaryotic kingdoms—Animalia, Plantae, Fungi, and Protista—remain unclear. In particular, statistical support for the closeness of animals to fungi rather than to plants is lacking, and a preferred branching order of these and other eukaryotic lineages is still controversial even though molecular sequences from diverse eukaryotic taxa have been analyzed. We report a statistical analysis of 214 sequences of nuclear small-subunit ribosomal RNA (srRNA) gene undertaken to clarify these evolutionary relationships. We have considered the variability of substitution rates and the nonindependence of nucleotide substitution across sites in the srRNA gene in testing alternative hypotheses regarding the branching patterns of eukaryote phylogeny. We find that the rates of evolution among sites in the srRNA sequences vary substantially and are approximately gamma distributed with size and shape parameter equal to 0.76. Our results suggest that (1) the animals and true fungi are indeed closer to each other than to any other ``crown'' group in the eukaryote tree, (2) red algae are the closest relatives of animals, true fungi, and green plants, and (3) the heterokonts and alveolates probably evolved prior to the divergence of red algae and animal–fungus–green–plant lineages. Furthermore, our analyses indicate that the branching order of the eukaryotic lineages that diverged prior to the evolution of alveolates may be generally difficult to resolve with the srRNA sequence data.
    Type of Medium: Electronic Resource
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