Siga este link para ver outros tipos de publicações sobre o tema: Locusts Genetics.

Livros sobre o tema "Locusts Genetics"

Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos

Selecione um tipo de fonte:

Veja os 40 melhores livros para estudos sobre o assunto "Locusts Genetics".

Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.

Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.

Veja os livros das mais diversas áreas científicas e compile uma bibliografia correta.

1

Edwards, Sara Joanne. Genetic analysis of the Treacher Collins syndrome locus. Manchester: University of Manchester, 1995.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
2

Gladwin, Amanda Jane. The molecular genetic analysis of the Treacher Collins syndrome locus. Manchester: University of Manchester, 1996.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
3

Perveen, Rahat. Genetic and physical mapping around the Treacher Collins syndrome locus. Manchester: University of Manchester, 1994.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
4

Heather, Lisa Jane. Physical and genetic mapping around a candidate locus for orofacial clefting. Manchester: University of Manchester, 1994.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
5

Plätke, Rosemarie. Die Entstehung von Supergenen in unterteilten Populationen: Ein theoretischer Ansatz anhand eines Zwei-Locus-Modells. Krefeld: Marchal und Matzenbacher, 1986.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
6

Miller, Carey S. Molecular genetic studies of the cytochrome f locus in Vicia faba L. Ottawa: National Library of Canada, 1990.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
7

Crosby, Andrew Harry. Genetic and physical mapping of the dentinogenesis imperfecta type II locus: The exclusion of three candidate genes from a causative role in the pathogenesis of this disorder. Manchester: University of Manchester, 1995.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
8

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes (Genetic Maps) (Genetic Maps). 5th ed. Cold Spring Harbor Laboratory Press, 1990.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
9

Walsh, Bruce, and Michael Lynch. The Population Genetics of Selection. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198830870.003.0005.

Texto completo da fonte
Resumo:
This chapter examines models of one- and two-locus selection in the absence of drift and mutation. Expressions for the per-generation rate of allele-frequency change and the expected time for a specified amount of change are developed for single-locus models, and their equilibrium structure is examined for those settings where selection retains more than one allele. The presence of selection-generated linkage disequilibrium greatly complicates the extension of single-locus results to two loci, and the chapter examines some of the resulting complications. Finally, it examines the nature of sele
Estilos ABNT, Harvard, Vancouver, APA, etc.
10

Iyamabo, Odianosen E. Effects of selection, recombination and plot type on phenotypic and quantitative trait locus analyses in barley (Hordeum vulgare L.). 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
11

Eyre, Steve, and Jane Worthington. Genetics of rheumatoid arthritis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0040.

Texto completo da fonte
Resumo:
A range of epidemiological studies have clearly established that susceptibility to rheumatoid arthritis (RA) is determined by both genetic and environmental factors. Studies over the last five decades have used a variety of approaches to identify the genetic variants associated with disease. HLA DRB1 was the first RA susceptibility locus to be discovered and has the largest effect size. We describe current understanding of the complexities of HLA association for RA. Linkage and small-scale association studies prior to 2007 provided convincing evidence for only one more RA susceptibility locus,
Estilos ABNT, Harvard, Vancouver, APA, etc.
12

Eyre, Steve, Jane Worthington, and Sebastien Viatte. Genetics of rheumatoid arthritis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0040_update_003.

Texto completo da fonte
Resumo:
A range of epidemiological studies have clearly established that susceptibility to rheumatoid arthritis (RA) is determined by both genetic and environmental factors. Studies over the last five decades have used a variety of approaches to identify the genetic variants associated with disease. HLA DRB1 was the first RA susceptibility locus to be discovered and has the largest effect size. We describe current understanding of the complexities of HLA association for RA. Linkage and small-scale association studies prior to 2007 provided convincing evidence for only one more RA susceptibility locus,
Estilos ABNT, Harvard, Vancouver, APA, etc.
13

J, O'Brien Stephen, ed. Genetic maps: Locus maps of complex genomes. 5th ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory, 1990.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
14

Genetic maps: Locus maps of complex genomes. 6th ed. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory, 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
15

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes. 6th ed. Cold Spring Harbor Laboratory Press, 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
16

J, O'Brien Stephen, and Cold Spring Harbor Laboratory, eds. Genetic maps: Locus maps of complex genomes. 5th ed. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory, 1990.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
17

Jeter, John Mark. Molecular analysis of the nar1 locus in barley. 1987.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
18

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes : Book 6 : Plants (Genetic Maps Book 6) (Genetic Maps Book 6). 6th ed. Cold Spring Harbor Laboratory Pr, 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
19

Blech-Hermoni, Yotam N. Studies on a conserved genetic locus for chronic pain. 2006.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
20

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes : Book 4 Nonhuman Vertebrates (Genetic Maps Book 4) (Genetic Maps Book 4). 6th ed. Cold Spring Harbor Laboratory Pr, 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
21

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes : Book 3 : Lower Eukaryotes (Genetic Maps Book 3) (Genetic Maps Book 3). 6th ed. Cold Spring Harbor Laboratory Pr, 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
22

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes : Book 2 : Bacteria, Algae, and Protozoa (Genetic Maps Book 2) (Genetic Maps Book 2). 6th ed. Cold Spring Harbor Laboratory Pr, 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
23

O'Brien, Stephen J. Genetic Maps: Locus Maps of Complex Genomes : Bacteria, Algae, and Protozoa, Book 2 (Genetic Maps Book 2) (Genetic Maps Book 2). 5th ed. Cold Spring Harbor Laboratory Press, 1990.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
24

Traore, Abdoulaye. Quantitative trait locus mapping of yield and yield components in barley (Hordeum vulgare L.). 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
25

Pavlus, Janice Elaine. Characterization of two lethal mutations induced by chromosomal rearrangements involving the 4f-rnp locus of Drosophila melanogaster. 1996.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
26

Price, Susan. Genetic bone and joint disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0276.

Texto completo da fonte
Resumo:
Genetic conditions affecting the skeleton and supporting structures are individually rare and heterogeneous. This chapter presents an approach to assessing patients with suspected skeletal dysplasia, osteogenesis imperfecta, Marfan syndrome, and Ehlers–Danlos syndrome. Skeletal dysplasias are caused by abnormalities of bone growth and modelling; the commonest non-lethal type is achondroplasia, with an incidence of 1/10 000 to 1/30 000. The typical presentation of osteogenesis imperfecta is with multiple fractures, sometimes prenatally. There may be associated short stature, bone deformity, den
Estilos ABNT, Harvard, Vancouver, APA, etc.
27

Goldman, David, Zhifeng Zhou, and Colin Hodgkinson. The Genetic Basis of Addictive Disorders. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0042.

Texto completo da fonte
Resumo:
Addictive disorders are moderately to highly heritable, indicating that alleles transmitted from parents are protective, or enhance risk by whatever mechanisms. However, the inheritance of addictive disorders is complex, involving hundreds of genes and variants that are both common and rare, and that vary in effect size and context of action. Genes altering risk for addictions have been identified by pathway and candidate gene studies in humans and model organisms, and genomic approaches including genome-wide association, meiotic linkage, and sequencing. Genes responsible for shared liability
Estilos ABNT, Harvard, Vancouver, APA, etc.
28

Walsh, Bruce, and Michael Lynch. Neutral Evolution in One- and Two-Locus Systems. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198830870.003.0002.

Texto completo da fonte
Resumo:
This chapter reviews the population-genetic theory of neutral alleles in finite populations, examining the probabilities and times to loss or fixation, summary statistics for molecular variation, coalescent theory (the distribution of times back to common ancestry for a sample of alleles), and both mutation-drift and mutation-drift-migration equilibrium models.
Estilos ABNT, Harvard, Vancouver, APA, etc.
29

Serres, F. J. De. Utilization of Mammalian Specific Locus Studies in Hazard Evaluation and Estimation of Genetic Risk. Springer, 2011.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
30

Ivakine, Evgueni. Genetic and molecular analysis of the insulin dependent diabetes 4 locus in the NOD mouse. 2004.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
31

Zhang, Yuan-Ming, Zhenyu Jia, and Jim M. Dunwell, eds. The Applications of New Multi-Locus GWAS Methodologies in the Genetic Dissection of Complex Traits. Frontiers Media SA, 2019. http://dx.doi.org/10.3389/978-2-88945-834-9.

Texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
32

Popovic, Maja. Genetic and physical mapping of the Shwachman-Diamond syndrome locus at the pericentromeric region of chromosome 7. 2003.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
33

A Review of the Genetics of Alcoholism and a Confirmatory Study of an Acute Alcohol Withdrawal Quantitative Trait Locus in Mice. Storming Media, 1999.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
34

Poel, Sheryl Ziemin Van der. Identification of a tumor suppressor gene locus by recognition of interferon gene deletions within human chromosome band 9P22 in human leukemias and identification and isolation of sequences which recognize a previously undiscovered gene MLL, whose transcripts span the human chromosome band 11Q23 translocation breakpoint junctions in human leukemia and whose sequences share homology with the Drosophila trithorax regulatory gene. 1993.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
35

Grams, Morgan E., and Josef Coresh. Chronic kidney disease in the developed world. Edited by David J. Goldsmith. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0095.

Texto completo da fonte
Resumo:
Chronic kidney disease is common, increasing in prevalence, and associated with significant morbidity and mortality. A disease of multiple and complex aetiologies, chronic kidney disease is more prevalent among elderly, hypertensive, and diabetic persons—all growing segments of the developed world. This chapter discusses trends in and determinants of chronic kidney disease prevalence, incidence, and prognosis. In addition, advances in chronic kidney disease staging and reporting as well as the discovery of a major genetic locus for hypertensive kidney disease in populations of African ancestry
Estilos ABNT, Harvard, Vancouver, APA, etc.
36

Aikhenvald, Alexandra Y. Polysynthetic Structures of Lowland Amazonia. Edited by Michael Fortescue, Marianne Mithun, and Nicholas Evans. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199683208.013.18.

Texto completo da fonte
Resumo:
Lowland Amazonia is the locus of substantial linguistic diversity in terms of genetic affiliation, language structure, and numbers of languages. This chapter will focus on the distribution of types of polysynthetic patterns within Lowland Amazonia, with special attention to the spread, and the types, of noun incorporation. The highest concentration of polysynthetic languages in Amazonia is the region south of the Amazon River, spanning adjacent regions of Peru, Brazil, and Bolivia. Polysynthetic patterns can be reconstructed for the protolanguages of some families, such as Panoan, Harakmbet, a
Estilos ABNT, Harvard, Vancouver, APA, etc.
37

Cattran, Daniel C., and Heather N. Reich. Membranous glomerulonephritis. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0064_update_001.

Texto completo da fonte
Resumo:
It has been clear for several decades from comparison with the rodent model disease Heymann nephritis that membranous glomerulonephritis (MGN) is an immune condition in which antibodies, usually autoantibodies, bind to targets on the surface of podocytes. However, the antigen in Heymann nephritis, megalin, is not present on human podocytes. The first potential antigen was identified by studying rare examples of maternal alloimmunization, leading to congenital membranous nephropathy in the infant caused by antibodies to neutral endopeptidase. More recently, the target of autoantibody formation
Estilos ABNT, Harvard, Vancouver, APA, etc.
38

Budimirovic, Dejan B., and Megha Subramanian. Neurobiology of Autism and Intellectual Disability. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0052.

Texto completo da fonte
Resumo:
Fragile X syndrome (FXS) is a neurodevelopmental disorder that manifests with a range of cognitive, behavioral, and social impairments. It is a monogenetic disease caused by silencing of the FMR1 gene, in contrast to autism spectrum disorder (ASD) that is a behaviorally-defined set of complex disorders. Because ASD is a major and growing public health concern, current research is focused on identifying common therapeutic targets among patients with different molecular etiologies. Due to the prevalence of ASD in FXS and its shared neurophysiology with ASD, FXS has been extensively studied as a
Estilos ABNT, Harvard, Vancouver, APA, etc.
39

(Editor), T. Kumazawa, L. Kruger (Editor), and K. Mizumura (Editor), eds. The Polymodal Receptor - A Gateway to Pathological Pain (Progress in Brain Research). Elsevier Science, 1996.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
40

Takao, Kumazawa, Kruger Lawrence, and Mizumura Kazue, eds. The polymodal receptor: A gateway to pathological pain. Amsterdam: Elsevier, 1996.

Encontre o texto completo da fonte
Estilos ABNT, Harvard, Vancouver, APA, etc.
Oferecemos descontos em todos os planos premium para autores cujas obras estão incluídas em seleções literárias temáticas. Contate-nos para obter um código promocional único!