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Gotowe bibliografie tematyczne / X-linkage

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Gotowa bibliografia na temat „X-linkage”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "X-linkage"

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Chevalier, Fabien, G. Richard Geier, and Jonathan S. Lindsey. "Acidolysis of intermediates used in the preparation of core-modified porphyrinic macrocycles." Journal of Porphyrins and Phthalocyanines 06, no. 03 (2002): 186–97. http://dx.doi.org/10.1142/s108842460200021x.

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The stability towards acidolysis of intermediates used in the preparation of core-modified porphyrinic macrocycles was examined. Experiments were performed using analogs of 5-phenyldipyrromethane in which one of the two pyrrole rings was modified (XPM). The XPMs utilized in these studies had X = 2-furyl (OPM), 2-thienyl (SPM), 2-selenyl (SePM), or 3-pyrrolyl (NCPPM). The XPMs possess a potentially labile linkage to a heteroatom-modified ring as well as a potentially labile linkage to a pyrrole ring. The stability of the two types of linkages was examined under acid catalysis conditions commonl

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Crow, T. J. "X-Y linkage and schizophrenia." BMJ 305, no. 6859 (1992): 958. http://dx.doi.org/10.1136/bmj.305.6859.958-a.

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Gal, Andreas. "X-linked retinoschisis and linkage." Clinical Genetics 33, no. 2 (2008): 143. http://dx.doi.org/10.1111/j.1399-0004.1988.tb03427.x.

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Mendlewicz, J., L. A. Sandkuil, A. De Bruyn, and C. Van Broeckhoven. "X-linkage in bipolar illness." Biological Psychiatry 29, no. 7 (1991): 730–31. http://dx.doi.org/10.1016/0006-3223(91)90150-k.

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Clayton, John F., Christine M. Gosden, Nicholas D. Hastie, and H. John Evans. "Linkage heterogeneity and fragile X." Human Genetics 78, no. 4 (1988): 338–42. http://dx.doi.org/10.1007/bf00291731.

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Risch, Neil. "Description of X-linkage pedigrees." Genetic Epidemiology 6, no. 1 (1989): 187–89. http://dx.doi.org/10.1002/gepi.1370060133.

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Van Eerdewegh, Paul. "Linkage analysis with cohort effects: An application to X-linkage." Genetic Epidemiology 6, no. 1 (1989): 271–76. http://dx.doi.org/10.1002/gepi.1370060147.

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Zou, Rongchao. "Discussion on the Implementation Path of Multi-dimensional Linkage of Sports in Colleges and Universities." Archives des Sciences 74, s2 (2024): 81–90. http://dx.doi.org/10.62227/as/74s210.

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Multiple linkage is an important means of youth sports health promotion and plays an important role in the development of college sports. This paper constructs the sports multiple linkage model based on the theory of overlapping effect from 2 aspects of linkage goal and content structure, and establishes the evaluation index system of linkage effect, including 4 first-level indexes and 17 second-level indexes, such as linkage subject, linkage content, linkage implementation and linkage evaluation. Combining the subjective weights based on AHP method and the objective weights of information ent

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Tillmar, Andreas O., Petter Mostad, Thore Egeland, Bertil Lindblom, Gunilla Holmlund, and Kerstin Montelius. "Analysis of linkage and linkage disequilibrium for eight X-STR markers." Forensic Science International: Genetics 3, no. 1 (2008): 37–41. http://dx.doi.org/10.1016/j.fsigen.2008.09.006.

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Inturri, Serena, Silvia Menegon, Antonio Amoroso, Carlo Torre, and Carlo Robino. "Linkage and linkage disequilibrium analysis of X-STRs in Italian families." Forensic Science International: Genetics 5, no. 2 (2011): 152–54. http://dx.doi.org/10.1016/j.fsigen.2010.10.012.

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Rozprawy doktorskie na temat "X-linkage"

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Millwood, Iona Y. "A genetic linkage map of the rat X chromosome." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390530.

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Kirchgessner, Cordula U. "The Human Synapsin I Gene: Linkage Mapping on the X Chromosome: A Dissertation." eScholarship@UMMS, 1991. http://escholarship.umassmed.edu/gsbs_diss/241.

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In this dissertation I describe the isolation and characterization of genomic clones for the human synapsin I gene, the establishment of a linkage map for the human synapsin I gene locus, and studies of the possible involvement of this gene in neurological disease. Synapsin I is a neuron-specific phosphoprotein which is concentrated at the presynaptic terminal. Evidence suggests that it plays a fundamental role in the regulation of neurotransmitter release. Altogether 27,500 bp of the human synapsin I gene have been isolated, and the gene structure has been partially determined. DNA sequence c

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Yu, Sui. "Molecular basis of fragile X syndrome /." Title page, contents and summary only, 1992. http://web4.library.adelaide.edu.au/theses/09PH/09phy937.pdf.

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Suthers, Graeme Kemble. "The human gene map near the fragile X /." Title page, table of contents and summary only, 1990. http://web4.library.adelaide.edu.au/theses/09PH/09phs966.pdf.

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Thesis (Ph. D.)--Dept. of Paediatrics, Faculty of Medicine, University of Adelaide, 1991.<br>Typescript (Photocopy). Includes published papers co-authored by the author at the end of volume 2. Includes bibliographical references (leaves 195-237 of vol. 1).

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Yariz, Kemal Oral. "The Chronicles of X-Linked Spinal Muscular Atrophy: The Linkage, The Gene and The SMN Complex." Scholarly Repository, 2008. http://scholarlyrepository.miami.edu/oa_dissertations/115.

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Spinal Muscular Atrophy (SMA) is an autosomal recessive motor neuron disease. SMA is associated with homozygous mutations in the Survival of Motor Neuron gene I (SMN1). SMN protein does not appear to exist in cells in isolation but associates with several proteins to form a large multi-protein complex. The functions of SMN complex include assembly, metabolism and transport of diverse classes of ribonucleoproteins. X- Linked Spinal Muscular Atrophy is a rare congenital disorder characterized by multiple joint contractures. It is associated with hypotonia, areflexia, chest deformities and cong

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Lenz, Ryan Rae. "A Novel Genetic Linkage Map of Chokecherry (Prunus Virginiana L.) and QTL Mapping for X-Disease (Candidatus Phytoplasma Pruni) Resistance." Thesis, North Dakota State University, 2016. https://hdl.handle.net/10365/28063.

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A novel chokecherry genetic linkage map was constructed using 565 molecular markers and a previously published mapping population (n=101). Chokecherry (Prunus virginiana L.) is a potential model for genetic research of phytoplasmic diseases because of its natural resistance to X-disease (Candidatus Phytoplasma pruni). The novel chokecherry map was developed using JoinMap 4.0 and contains a complete set of 16 linkage groups. In total, the map spans a genetic distance of 2,172 cM with an average marker density of 3.97 cM. Three significant quantitative trait loci (QTL) associated with X-disease

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Adler, David A. "A tale of two x-linked genes : gene expression, localization and the Ohno hypothesis /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/6344.

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Lapsys, Naras Mykolas. "The FRA 16B locus : long range restriction mapping of 16q13-16q22.1 /." Title page, table of contents and summary only, 1993. http://web4.library.adelaide.edu.au/theses/09PH/09phl317.pdf.

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Marondedze, Claudius. "Functional genomic characterization of fruit quality traits in apple (Malus x domestica Borkh)." Thesis, University of the Western Cape, 2009. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_7794_1286309138.

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<p>&nbsp<br></p> <p align="left">The domesticated apple (<i><font face="TimesNewRomanPS-ItalicMT">Malus </font><font face="TimesNewRomanPSMT">x </font><i><font face="TimesNewRomanPS-ItalicMT">domestica </font><font face="TimesNewRomanPSMT">Borkh.), belonging to the </font><i><font face="TimesNewRomanPS-ItalicMT">Malus </font><font face="TimesNewRomanPSMT">genus of the Rosaceae family, is one of the edible pomaceous fruits. Since it is one of the important commercial fruit crops worldwide, the quality of the fruit is crucial to breeders and farmers as it ultimately determines acceptance of a cu

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Casaretto, Nicolas. "Dynamique structurale par photocristallographie stationnaire et résolue en temps : développements instrumentaux et applications aux matériaux moléculaires photoisomérisables." Thesis, Université de Lorraine, 2017. http://www.theses.fr/2017LORR0163/document.

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Ce travail de thèse s’inscrit dans l’étude des matériaux moléculaires photo-commutables. L’objectif est le contrôle réversible et persistant des propriétés physiques de la matière par application d’un stimulus externe, tel qu’une excitation optique. Le travail de thèse est constitué de deux parties principales. La première partie traite de la photo-isomérisation des ligands NO dans les complexes de ruthénium di-nitrosyle. Une démarche expérimentale systématique a été effectuée sur trois complexes. La spectroscopie infrarouge et la diffraction des rayons-X ont été utilisées conjointement à bass

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Książki na temat "X-linkage"

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Lehrke, Robert Gordon. Sex linkage of intelligence: The X-factor. Praeger, 1997.

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Miller, James R. X-linked traits: A catalog of loci in nonhuman mammals. Cambridge University Press, 1990.

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E, Davies K., ed. The Fragile X syndrome. Oxford University Press, 1989.

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Postel-Vinay, Olivier. La revanche du chromosome X: Enquête sur les origines et le devenir du féminin. JC Lattès, 2007.

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Senior, Jayne Gillian. Linkage analysis of families with the fragile X syndrome, using the DNA probes F9 and ST14. University of Birmingham, 1987.

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Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Universitaẗsbibliothek, 1985.

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Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Universitätsbibliothek, 1985.

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Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Universita tsbibliothek, 1985.

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United Nations Conference on Trade and Development., ed. TNC-SME linkages for development: Issues - experiences - best practices : proceedings of the Special Round Table on TNCs, SMEs and Development, UNCTAD X, 15 February 2000, Bangkok. United Nations, 2000.

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United Nations. Conference on Trade and Development,, ed. TNC-SME linkages for development: Issues - experiences - best practices : proceedings of the Special Round Table on TNCs, SMEs and Development, UNCTAD X, 15 February 2000, Bangkok. United Nations, 2000.

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Części książek na temat "X-linkage"

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Nagylaki, Thomas. "X-Linkage." In Introduction to Theoretical Population Genetics. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76214-7_7.

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Baron, Miron. "X-Linkage Studies in Affective Disorders." In New Directions in Affective Disorders. Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4612-3524-8_42.

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Mendlewicz, Julien. "Recombinant DNA Studies of X Linkage in Affective Disorders." In New Directions in Affective Disorders. Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4612-3524-8_43.

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Ohno, S. "Conservation in toto of the mammalian X-linkage group as a frozen accident." In Chromosomes Today. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-010-9166-4_14.

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Ülker, Özgür, Emin Erkan Korkmaz, and Ender Özcan. "A Grouping Genetic Algorithm Using Linear Linkage Encoding for Bin Packing." In Parallel Problem Solving from Nature – PPSN X. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-87700-4_113.

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Yoo, Eun Sun, and In Mo Yoon. "Development of Fast Synthetic Method and Analytical Technology for Linkage-Isomeric Oligosaccharides." In Key Engineering Materials. Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-958-x.33.

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Reinhold, Klaus. "Preferential Sex Linkage of Sexually Selected Genes: Evidence and a New Explanation." In The Speciation of Modern Homo Sapiens. British Academy, 2004. http://dx.doi.org/10.5871/bacad/9780197263112.003.0014.

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This chapter discusses evidence and theory on sex chromosomal linkage of sexually selected traits that may be the key to a functional separation of sexual and natural selection. It reviews the evidence showing that the X chromosome has a disproportional share concerning the inheritance of sexually selected traits in animals with heterogametic males, and suggests a new explanation that relates this X bias with female choice of heterozygotic males. With numeric simulations, it shows that female choice of heterozygotic males is usually disadvantageous. Because this disadvantage cannot occur when

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"Linkage Between Color-blindness and Hemophilia." In Landmarks in Medical Genetics, edited by Peter S. Harper. Oxford University PressNew York, NY, 2004. http://dx.doi.org/10.1093/oso/9780195159301.003.0020.

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Abstract This truly remarkable paper, by two equally remarkable scientists (Figs. 20–1a, b), not only provided the first human example of genetic linkage, but also laid the foundations for further genetic linkage studies for the next 50 years. It combines clarity with mathematical rigor, the probability estimates being gone through family by family and step by step, as a model for how to study linkage for any genetic character or disorder. The starting point of the study was six hemophilia kindreds also showing color blindness (all with hindsight appear to have been hemophilia A, but the possi

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"Cloning of DNA in an X Chromosome Deletion Patient." In Landmarks in Medical Genetics, edited by Peter S. Harper. Oxford University PressNew York, NY, 2004. http://dx.doi.org/10.1093/oso/9780195159301.003.0025.

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Abstract This highly original paper could have been placed equally well in Part VII, but seems more appropriate to conclude the present group of papers, as it illustrates the evolution of gene mapping into positional cloning. It also emphasizes that gene location as shown by a chromosomal anomaly may be more valuable than genetic linkage data, by allowing the specific chromosomal defect to be the starting point for the cloning itself. Kunkel et al. took a particularly original approach to isolating the Duchenne muscular dystrophy (DMD) gene, using DNA from a boy with an Xp21 deletion who showe

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Gottlob, Irene. "Genetics and Pharmacological Treatment of Nystagmus: A Review of the Literature and Recent Findings." In Advances in Understanding Mechanisms and Treatment of Infantile Forms of Nystagmus. Oxford University PressNew York, NY, 2008. http://dx.doi.org/10.1093/oso/9780195342185.003.0010.

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Abstract New developments in genetics and pharmacological treatment of nystagmus are reviewed in this chapter. While cases of nystagmus are frequently sporadic, kindreds in which nystagmus segregated as an autosomal dominant, autosomal recessive, or X-linked trait have been reported. Of these, X-linked pedigrees are the most frequent. By linkage analysis, the major X-linked locus for nystagmus, NYS1, was localized to chromosome Xq26-q27. Linkage analysis and DNA-sequence analysis performed in 26 families with idiopathic congenital nystagmus (ICN) led to the detection of a novel gene named FERM

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Streszczenia konferencji na temat "X-linkage"

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Osovsky, Ruth, Sangita Bhowmick, Samuel Castro Lucas, et al. "The influence of Ti doping and post-deposition annealing on the network properties of Ti-doped GeO2 coatings for gravitational-wave detectors." In Optical Interference Coatings. Optica Publishing Group, 2025. https://doi.org/10.1364/oic.2025.fa.5.

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Fourier Transformed Infrared and X-ray Photoelectron spectroscopies of amorphous GeO2 doped with Ti reveal the evolution of the atomic network formed by Ge-O-Ge, Ti-O-Ti and Ti-O-Ge linkages in mixtures with different Ti content and with annealing. It is shown the atomic network configuration affects the onset of crystallization.

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Mayne, Leland C., Gregory P. Harhay, and Bruce Hudson. "Applications of ultraviolet resonance Raman spectroscopy to protein structure." In International Laser Science Conference. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/ils.1986.thl59.

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Resonance Raman spectroscopy of heme proteins and the visual pigments has provided valuable insights into the mechanism of action of these proteins. The performance of Raman experiments with ultraviolet radiation permits resonance with nonchromophoric components of proteins including the peptide bond itself.1,2 Fluorescence from the aromatic residues of proteins does not obscure the Raman signal because the fluorescence occurs at longer wavelengths. The peptide bond gives rise to new Raman active bands with ultraviolet excitation.2 The imino linkage of X-proline sequences results in absorption

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Peng, Baoying, and Weihua Li. "Roundness Error's Coupling Compensation Control in Eccentric Shaft X-C Linkage Grinding." In 2018 3rd International Conference on Mechanical, Control and Computer Engineering (ICMCCE). IEEE, 2018. http://dx.doi.org/10.1109/icmcce.2018.00060.

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Ding, Jianzhong, and Chunjie Wang. "A Geometric Approach for Error Space Estimation of Planar Linkage." In ASME 2021 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/detc2021-66869.

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Abstract This article develops a geometric method to estimate the clearances-induced error space of any planar linkage. The error space discussed here represents the unconstrained mobility of the end-effector when actuators of the mechanism are locked, and is expressed by a connected geometry in 3-dimensional Euclidean frame {x, y, θ}. First, error space of the planar mechanism is modeled and closed-form expressions are derived. Then, levels of joints in error propagation analysis are defined and illustrated with an example of a eight-bar linkage, following which error propagation path among c

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Ura, S., R. Ohyama, T. Suhara, and H. Nishihara. "Electrooptic Waveguide Grating Using New Nonlinear-Optic Polymer p-NAn-PVA." In Nonlinear Guided-Wave Phenomena. Optica Publishing Group, 1991. http://dx.doi.org/10.1364/nlgwp.1991.md3.

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A new polymer p-NAn-PVA illustrated in Fig. 1 was developed by N. Ogata et al.1) for implementing second-order nonlinear-optic (NLO) devices. p-NA (p-Nitroaniline) is introduced as side-chain to PVA (Polyvinyl Alcohol) main-chain via acetal-linkage, and second-order NLO effects emerge by electric-field induced side-chain alignment (poling). This polymer has some attractive features besides fabrication easiness. Large NLO susceptibility is expected since p-NA has large polarizability and is highly doped (x=0.82), and the relaxation is small in comparison with dispersive type NLO polymers becaus

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Bankole, Ayomipo O., Kamaldeen Olakunle Omosanya, Niyi-Ola Adebisi, et al. "Optimizing Fault Risking Strategies for Subsurface Resource Exploration on the Exmouth Plateau, NW Australia." In SPE Nigeria Annual International Conference and Exhibition. SPE, 2024. http://dx.doi.org/10.2118/221694-ms.

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Abstract The understanding of geological fault growth history is critical in subsurface resource exploration, given the key role faults play in maintaining reservoir integrity. Traditional practices involve assessing fault initiation, propagation, segmentation, linkage, and reactivation to elucidate their growth mechanisms and history. Various traditional methods, complemented by fault growth models, are employed, with the choice of method contingent on the study's scope and objectives. In this study, we use high-quality, high-resolution three-dimensional (3D) seismic reflection data to invest

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Lutze, Margaret, Curtis R. Brandt, Vivianne C. Smith, Joel Pokorny, and Ron G. Gregg. "Genetic studies of normal color vision." In OSA Annual Meeting. Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.fa3.

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We have studied the familial transmissions of Rayleigh match midpoints and photometric matches (667-551 nm) in observers with normal color vision to assess genetic bases for these two color vision traits (Lutze et al., in press). We first employed segregation analysis to evaluate whether each trait was consistent with determination by allelic variation of a single gene, by multiple genes (polygenic), or by environmental factors. We found that each trait was consistent with determination by a single gene. Blood samples were obtained from the majority of family members tested and DNA was isolate

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Chang, Ching Yu, Jorge Angeles, and Max Antonio González-Palacios. "A Semigraphical Method for the Solution of the Burmester Problem." In ASME 1991 Design Technical Conferences. American Society of Mechanical Engineers, 1991. http://dx.doi.org/10.1115/detc1991-0134.

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Abstract The determination of the planar four-bar linkage intended to guide a rigid body through five finitely-separated configurations is known as the Burmester Problem. This is a nonlinear problem that involves finding the roots of a system of four bilinear equations in four unknowns. When solving this problem numerically, for it is evasive to other means, issues such as numerical conditioning, multiplicity of solutions and singularities must be considered. Here we present a semigraphical method of solution that reduces the problem to finding the intersections of two contours in the x-y plan

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Fujimura, K., T. Fujimoto, M. Takemoto, K. Oda, S. Maehama, and A. Kuramoto. "INTERACTION OF MEMBRANE GLYCOPROTEIN GPIIb AND Ilia WITH CYTOSKELETAL PROTEINS DURING PLATELET ACTIVATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643515.

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Experiments were designed and performed to analyse the cytoskeleton assembly and the interaction of glycoprotein (GP)IIb, IIIa and cytoskeletal proteins during platelet activation. A23187 stimulated 125I labeled platelets were solubilised with Triton X-100 solution and centrifuged. The insoluble fraction were analysed by two dimensional electrophoresis and the soluble fraction were fractionated with 5-25% sucrose gradient centrifugation and analysed by SDS PAGE. In Triton X-100 insoluble fraction, high molecular weight protein fraction(MW > 106) was present after stimulation which were cons

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Keller, D. S., C. Feng, J. F. Bloch, and S. Roland du Roscoat. "Local Structural Orientation of Towel and Tissue Grades in Two and Three Dimensions." In Advances in Pulp and Paper Research, Cambridge 2013, edited by S. J. I’Anson. Fundamental Research Committee (FRC), Manchester, 2013. http://dx.doi.org/10.15376/frc.2013.1.3.

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This paper describes the study of new methods for characterizing the orientation of fiber segments in low density paper towel from two- and three-dimensional X-radiographic data sets. The end use properties of the absorbent hygiene grades such as paper towels and tissues stem from an open porous structure where stochastically distributed fibers are contorted by post forming processes to increase bulk, stretch, flexibility and softness, while maintaining adequate strength. The orientation of free fiber segments that form the network are kinked and curved in three dimensions by processes includi

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Raporty organizacyjne na temat "X-linkage"

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Gall, Graham A. E., Gideon Hulata, Eric M. Hallerman, Bernard May, and Umiel Nakdimon. Creating and Characterizing Genetic Variation in Tilapia through the Creation of an Artificial Center of Origin. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7574344.bard.

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Five stocks of tilapia [oreochromis niloticus (on), red O. niloticus (ROn), O. aureus (Oa), O. mossambicus (Om), and Sarotherodon galilaeus (Sg)] were used to produce two-way (F1), three-way (3WC) and four-way crosses (4WC). Three 4WC groups, containing equal representation of all four species, formed the base population for a new synthetic stock, called an "artificial center of origin" (ACO). Four genomic maps were created using microsatellite and AFLP markers, two from a 3WC family [Om female and (Oa x ROn) male] and two from a 4WC family [(Om x Oas) females and (Sg x On) male]. Sixty-two lo

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Foulkes, William D. Locating a Prostate Cancer Susceptibility Gene on the X Chromosome by Linkage Disequilibrium Mapping Using Three Founder Populationin Quebec and Switzerland. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada426100.

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Foulkee, William D. Locating a Prostate Cancer Susceptibility Gene on the X Chromosome by Linkage Disequilibrium Mapping Using Three Founder Populations in Quebec and Switzerland. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada443199.

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Foulkes, William D. Locating a Prostate Cancer Susceptibility Gene on the X Chromosome by Linkage Disequilibrium Mapping Using Three Founder Populations in Quebec and Switzerland. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada405914.

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Foulkes, William D. Locating a Prostate Cancer Susceptibility Gene on the X Chromosome by Linkage Disequilibrium Mapping Using Three Founder Populations in Quebec and Switzerland. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada415657.

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Amzeri, Achmad, Kaswan Badami, and Gita Pawana. Inheritance of resistance to downy mildew (Peronosclerospora maydis) in crossing of Madura Maize Plant (Zea mays L.). Innovative Scientific Information & Services Network, 2019. http://dx.doi.org/10.21107/amzeri.2019.1.

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Hybridization of Back cross is one method to get varieties that are resistant to downy mildew. The purpose of this study was to obtain information on inheritance characteristics of downy mildew resistance. This research was conducted at the experiment center of Agro-Technology Study Program of Agriculture Faculty, University of Trunojoyo Madura. Research of Assessment of resistance to Downy Mildew used a randomized block design with 18 treatments (P1, P2, F1, F2, BC1P1 and BC1P2 in three sets of crosses, namely LGL x Mdr-3, T12 x Mdr-1 and E02 x Mdr-2) and three replications so there were 54 e

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Hovav, Ran, Peggy Ozias-Akins, and Scott A. Jackson. The genetics of pod-filling in peanut under water-limiting conditions. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7597923.bard.

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Pod-filling, an important yield-determining stage is strongly influenced by water stress. This is particularly true for peanut (Arachishypogaea), wherein pods are developed underground and are directly affected by the water condition. Pod-filling in peanut has a significant genetic component as well, since genotypes are considerably varied in their pod-fill (PF) and seed-fill (SF) potential. The goals of this research were to: Examine the effects of genotype, irrigation, and genotype X irrigation on PF and SF. Detect global changes in mRNA and metabolites levels that accompany PF and SF. Explo

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Guy, Charles, Gozal Ben-Hayyim, Gloria Moore, Doron Holland, and Yuval Eshdat. Common Mechanisms of Response to the Stresses of High Salinity and Low Temperature and Genetic Mapping of Stress Tolerance Loci in Citrus. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7613013.bard.

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The objectives that were outlined in our original proposal have largely been achieved or will be so by the end of the project in February 1995 with one exception; that of mapping cold tolerance loci based on the segregation of tolerance in the BC1 progeny population. Briefly, our goals were to 1) construct a densely populated linkage map of the citrus genome: 2) map loci important in cold and/or salt stress tolerance; and 3) characterize the expression of genes responsive to cold land salt stress. As can be seen by the preceding listing of accomplishments, our original objectives A and B have

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Sherman, Amir, Rebecca Grumet, Ron Ophir, Nurit Katzir, and Yiqun Weng. Whole genome approach for genetic analysis in cucumber: Fruit size as a test case. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7594399.bard.

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The Cucurbitaceae family includes a broad array of economically and nutritionally important crop species that are consumed as vegetables, staple starches and desserts. Fruit of these species, and types within species, exhibit extensive diversity as evidenced by variation in size, shape, color, flavor, and others. Fruit size and shape are critical quality determinants that delineate uses and market classes and are key traits under selection in breeding programs. However, the underlying genetic bases for variation in fruit size remain to be determined. A few species the Cucurbitaceae family were

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