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Статті в журналах з теми "Incompatibility system"

Автор: Grafiati

Опубліковано: 25 травня 2024

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1

Rashid, Abdul, and Peter A. Peterson. "The RSS system of unidirectional cross-incompatibility in maize. 2. Cytology." Genome 35, no. 4 (1992): 560–64. http://dx.doi.org/10.1139/g92-083.

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In 1975, a number of genetic lines discovered in our maize genetics nursery in Ames, Iowa, showed unidirectional cross-incompatibility. Later, it was found that this unidirectional cross-incompatibility is controlled by three recessive genes. One locus (cif) controls the incompatibility reaction in the female tissue and the other two (cim1 and cim2) control the incompatibility reaction in the pollen grain. The cross is incompatible only when the female parent is homozygous recessive for the cif and the male parent is homozygously recessive for the cim1 as well as the cim2 locus. Cytological st

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2

Paoletti, M., and C. Clavé. "The Fungus-Specific HET Domain Mediates Programmed Cell Death in Podospora anserina." Eukaryotic Cell 6, no. 11 (2007): 2001–8. http://dx.doi.org/10.1128/ec.00129-07.

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ABSTRACT Vegetative incompatibility is a programmed cell death reaction that occurs when fungal cells of unlike genotypes fuse. Genes defining vegetative incompatibility (het genes) are highly polymorphic, and most if not all incompatibility systems include a protein partner bearing the fungus-specific domain termed the HET domain. The nonallelic het-C/het-E incompatibility system is the best-characterized incompatibility system in Podospora anserina. Cell death is triggered by interaction of specific alleles of het-C, encoding a glycolipid transfer protein, and het-E, encoding a HET domain an

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3

Uyenoyama, M. K. "On the evolution of genetic incompatibility systems. VI. A three-locus modifier model for the origin of gametophytic self-incompatibility." Genetics 128, no. 2 (1991): 453–69. http://dx.doi.org/10.1093/genetics/128.2.453.

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Abstract Recent genetic analyses have demonstrated that self-incompatibility in flowering plants derives from the coordinated expression of a system of loci. To address the selective mechanisms through which a genetic system of this kind evolves, I present a three-locus model for the origin of gametophytic self-incompatibility. Conventional models assume that a single locus encodes all physiological effects associated with self-incompatibility and that the viability of offspring depends only on whether they were derived by selfing or outcrossing. My model explicitly represents the genetic dete

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4

Gabrielov, A., V. Keilis-Borok, and D. D. Jackson. "Geometric incompatibility in a fault system." Proceedings of the National Academy of Sciences 93, no. 9 (1996): 3838–42. http://dx.doi.org/10.1073/pnas.93.9.3838.

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5

Saupe, Sven J. "Molecular Genetics of Heterokaryon Incompatibility in Filamentous Ascomycetes." Microbiology and Molecular Biology Reviews 64, no. 3 (2000): 489–502. http://dx.doi.org/10.1128/mmbr.64.3.489-502.2000.

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SUMMARY Filamentous fungi spontaneously undergo vegetative cell fusion events within but also between individuals. These cell fusions (anastomoses) lead to cytoplasmic mixing and to the formation of vegetative heterokaryons (i.e., cells containing different nuclear types). The viability of these heterokaryons is genetically controlled by specific loci termed het loci (for heterokaryon incompatibility). Heterokaryotic cells formed between individuals of unlike het genotypes undergo a characteristic cell death reaction or else are severely inhibited in their growth. The biological significance o

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6

Kemp, R. F. O. "Incompatibility in basidiomycetes: The heterogenic Pentax." Edinburgh Journal of Botany 52, no. 1 (1995): 71–89. http://dx.doi.org/10.1017/s0960428600001931.

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A heterogenic system of incompatibility is described in Coprinus bisporus which involves two alleles at two loci, in addition to the unifactorial homogenic incompatibility locus already described for this two-spored species. The patterns of non-allelic heterogenic incompatibility found in C. bisporus are used to predict those expected in species with bifactorial homogenic incompatibility. This type of heterogenic incompatibility could lead to speciation.

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7

Leppäjärvi, Leevi, and Michal Sedlák. "Incompatibility of quantum instruments." Quantum 8 (February 12, 2024): 1246. http://dx.doi.org/10.22331/q-2024-02-12-1246.

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Quantum instruments describe outcome probability as well as state change induced by measurement of a quantum system. Incompatibility of two instruments, i. e. the impossibility to realize them simultaneously on a given quantum system, generalizes incompatibility of channels and incompatibility of positive operator-valued measures (POVMs). We derive implications of instrument compatibility for the induced POVMs and channels. We also study relation of instrument compatibility to the concept of non-disturbance. Finally, we prove equivalence between instrument compatibility and postprocessing of c

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8

KIM, KYUNGMEE O., and WAY KUO. "TWO-LEVEL BURN-IN FOR RELIABILITY AND ECONOMY IN REPAIRABLE SERIES SYSTEMS HAVING INCOMPATIBILITY." International Journal of Reliability, Quality and Safety Engineering 11, no. 03 (2004): 197–211. http://dx.doi.org/10.1142/s0218539304001464.

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When a system is assembled from components, incompatibility often occurs as a result of the assembly process. The ability to quantify incompatibility is very important for making burn-in decisions because the goal of system burn-in is to minimize the incompatibility factor. In the past, incompatibility has been only partially represented in the system prediction models because it was assumed that assembly had no effect on the components. This paper presents a more accurate model for system prediction by allowing for the possibility that, in some cases, assembly adversely affects the components

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9

Uyenoyama, M. K. "A generalized least-squares estimate for the origin of sporophytic self-incompatibility." Genetics 139, no. 2 (1995): 975–92. http://dx.doi.org/10.1093/genetics/139.2.975.

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Abstract Analysis of nucleotide sequences that regulate the expression of self-incompatibility in flowering plants affords a direct means of examining classical hypotheses for the origin and evolution of this major feature of mating systems. Departing from the classical view of monophyly of all forms of self-incompatibility, the current paradigm for the origin of self-incompatibility postulates multiple episodes of recruitment and modification of preexisting genes. In Brassica, the S locus, which regulates sporophytic self-incompatibility, shows homology to a multigene family present both in s

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10

Franklin-Tong, Vernonica E., and F. C. H. Franklin. "The different mechanisms of gametophytic self–incompatibility." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 358, no. 1434 (2003): 1025–32. http://dx.doi.org/10.1098/rstb.2003.1287.

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Self–incompatibility (SI) involves the recognition and rejection of self or genetically identical pollen. Gametophytic SI is probably the most widespread of the SI systems and, so far, two completely different SI mechanisms, which appear to have evolved separately, have been identified. One mechanism is the RNase system, which is found in the Solanaceae, Rosaceae and Scrophulariaceae. The other is a complex system, so far found only in the Papaveraceae, which involves the triggering of signal transduction cascade(s) that result in rapid pollen tube inhibition and cell death. Here, we present a

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11

Kamei, Almond, and Mamta Anandini Warrior. "Rh incompatibilty: A case study." IP International Journal of Medical Paediatrics and Oncology 8, no. 1 (2022): 36–38. http://dx.doi.org/10.18231/j.ijmpo.2022.008.

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Rh incompatibility occurs during pregnancy. Rh antibodies cross the placenta and attack the baby's red blood cells leading to Hemolytic anemia. With Rh incompatibility, the woman's immune system reacts and creates Rh antibodies. Rh incompatibility happens only when the father of the baby is Rh-positive. Difference in blood type between a pregnant woman and her child causes Rh incompatibility. Nurse plays a vital role to offer psychological support to the mother and also to the members of the family.

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12

Łukaszewski, Marcin. "Zasada incompatibilitas w samorządowym prawie ustrojowym (relacje samorządowiec-parlamentarzysta) i projekt przekształcenia Senatu w Izbę Samorządową." Refleksje. Pismo naukowe studentów i doktorantów WNPiD UAM, no. 4 (October 31, 2018): 147–57. http://dx.doi.org/10.14746/r.2011.4.13.

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The problem of Senate as a self-government chamber and self-government person – parliament deputy relations were shown in the political history of the Polish Third Republic many times. In 2001, when self-government laws were introduced into the political system of self-government, there was an institution of incompatibilitas (incompatibility of self-governmental and parliamentarian seats). It influenced the subsequent public debate about the role of Senate and the emerging plans to transform it into a self-government chamber.

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13

Jacobson, David J. "Control of mating type heterokaryon incompatibility by the tol gene in Neurospora crassa and N. tetrasperma." Genome 35, no. 2 (1992): 347–53. http://dx.doi.org/10.1139/g92-053.

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The mating-type of Neurospora crassa (A and a) have a dual function: A and a individuals are required for sexual reproduction, but only strains of the same mating type will form a stable vegetative heterokaryon. Neurospora tetrasperma, in contrast, is a naturally occurring A + a heterokaryon. It was shown previously that the mating-type genes of both species are functionally the same and are not responsible for this difference in heterokaryon incompatibility. This suggests that a separate genetic system determines the heterokaryon incompatibility function of mating type. The mutant tolerant (t

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14

Ho, W. F., and C. T. Shii. "INCOMPATIBILITY SYSTEM IN PASSION FRUIT (PASSIFLORA EDULIS SIMS)." Acta Horticulturae, no. 194 (December 1986): 31–38. http://dx.doi.org/10.17660/actahortic.1986.194.2.

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15

Haring, V., J. Gray, B. McClure, M. Anderson, and A. Clarke. "Self-incompatibility: a self-recognition system in plants." Science 250, no. 4983 (1990): 937–41. http://dx.doi.org/10.1126/science.2237440.

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16

Lee, Sang-Yong Tom, and W. Wayne Fu. "Software-Platform Integration, Incompatibility, and System-User Switching." Journal of Media Economics 19, no. 3 (2006): 163–92. http://dx.doi.org/10.1207/s15327736me1903_2.

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17

McCollum, Gin. "Dissonance: A nervous system analog to quantum incompatibility." International Journal of Theoretical Physics 33, no. 1 (1994): 41–52. http://dx.doi.org/10.1007/bf00671613.

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18

LUNDQVIST, ARNE. "The self-incompatibility system in Caltha palustris (Ranunculaceae)." Hereditas 117, no. 2 (2008): 145–51. http://dx.doi.org/10.1111/j.1601-5223.1992.tb00168.x.

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19

Lundqvist, Arne. "The Self-Incompatibility System in Lotus Tenuis (Fabaceae)." Hereditas 119, no. 1 (2004): 59–66. http://dx.doi.org/10.1111/j.1601-5223.1993.00059.x.

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20

Lundqvist, Arne. "The Self-Incompatibility System in Ranunculus Repens (Ranunculaceae)." Hereditas 120, no. 2 (2004): 151–57. http://dx.doi.org/10.1111/j.1601-5223.1994.00151.x.

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21

Stephens, Loren C. "Self-incompatibility in Echinacea purpurea." HortScience 43, no. 5 (2008): 1350–54. http://dx.doi.org/10.21273/hortsci.43.5.1350.

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Progenies derived from self-pollination and parent–offspring backcrosses of Echinacea purpurea (L.) Moench accession PI 631307 revealed that a sporophytic self-incompatibility (SI) system was operating in this germplasm. Offspring of progenies from the original accession were self-incompatible, but most self-pollinations resulted in some self-seed set. One seedling from such a self-pollination was reciprocally crosscompatible with its parent, proving that a sporophytic SI system was operational. The F3BC1 progeny could be classified into two offspring groups. The first group of two seedlings w

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22

CHOU, CHUNG-HUI. "WINDOWS OS VERSUS MAC OS: COULD ONE-WAY COMPATIBILITY BE AN EQUILIBRIUM OUTCOME?" Singapore Economic Review 59, no. 05 (2014): 1450042. http://dx.doi.org/10.1142/s0217590814500428.

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One-way compatibility is a phenomenon often observed in reality and Windows OS versus Mac OS is a good example. A vertical differentiation model is presented herein to analyze system firms' compatibility choices. This paper differs from the existing literature in two aspects: (1) The purebred and hybrid systems are vertically differentiated; (2) Since one-way compatibility is a phenomenon often observed in real life, this paper considers compatibility as being unilateral rather than bilateral and the possibility of one-way compatibility. We find that, depending on the quality of the hybrid sys

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23

Palmer, Christina G. S. "Evidence for Maternal-Fetal Genotype Incompatibility as a Risk Factor for Schizophrenia." Journal of Biomedicine and Biotechnology 2010 (2010): 1–12. http://dx.doi.org/10.1155/2010/576318.

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Prenatal/obstetric complications are implicated in schizophrenia susceptibility. Some complications may arise from maternal-fetal genotype incompatibility, a term used to describe maternal-fetal genotype combinations that produce an adverse prenatal environment. A review of maternal-fetal genotype incompatibility studies suggests that schizophrenia susceptibility is increased by maternal-fetal genotype combinations at theRHDandHLA-Bloci. Maternal-fetal genotype combinations at these loci are hypothesized to have an effect on the maternal immune system during pregnancy which can affect fetal ne

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24

Loehrlein, Marietta, and Sandy Siqueira. "(234) Self-incompatibility in Pink Tickseed, Coreopsis rosea Nutt." HortScience 40, no. 4 (2005): 1001E—1002. http://dx.doi.org/10.21273/hortsci.40.4.1001e.

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Coreopsis rosea is important as a landscape plant and is of some impor-tance for restoration of native species. In both situations it is important to understand the breeding system so that the pollination process may be controlled for optimal seed production. The study of the incompatibility system is important to seed production. In commercial crops, seeds may be products of open pollination or F1 hybrids. In the former, genetic variability exists. In conservation and recovery programs of local flora, seeds with genetic variability are desirable. In development of commercial crops, uniform se

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25

Duarte, Mariana Oliveira, Denise Maria Trombert Oliveira, and Eduardo Leite Borba. "Two Self-Incompatibility Sites Occur Simultaneously in the Same Acianthera Species (Orchidaceae, Pleurothallidinae)." Plants 9, no. 12 (2020): 1758. http://dx.doi.org/10.3390/plants9121758.

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In most species of Pleurothallidinae, the self-incompatibility site occurs in the stylar canal inside the column, which is typical of gametophytic self-incompatibility (GSI). However, in some species of Acianthera, incompatible pollen tubes with anomalous morphology reach the ovary, as those are obstructed in the column. We investigated if a distinct self-incompatibility (SI) system is acting on the ovary of A. johannensis, which is a species with partial self-incompatibility, contrasting with a full SI species, A. fabiobarrosii. We analyzed the morphology and development of pollen tubes in th

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26

VAN GOETHEM, NICOLAS. "DIRECT EXPRESSION OF INCOMPATIBILITY IN CURVILINEAR SYSTEMS." ANZIAM Journal 58, no. 1 (2016): 33–50. http://dx.doi.org/10.1017/s1446181116000158.

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We would like to present a method to compute the incompatibility operator in any system of curvilinear coordinates (components). The procedure is independent of the metric in the sense that the expression can be obtained by means of the basis vectors only, which are first defined as normal or tangential to the domain boundary, and then extended to the whole domain. It is an intrinsic method, to some extent, since the chosen curvilinear system depends solely on the geometry of the domain boundary. As an application, the in-extenso expression of incompatibility in a spherical system is given.

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27

Boshier, D. H. "Incompatibility in Cordia alliodora (Boraginaceae), a neotropical tree." Canadian Journal of Botany 73, no. 3 (1995): 445–56. http://dx.doi.org/10.1139/b95-045.

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Incompatibility and variation in floral morphology in Cordia alliodora (R. & P.) Oken (Boraginaceae) were investigated using a combination of fieldwork and light and ultraviolet microscopy. Results from controlled crosses clearly showed the presence of two groups of trees, where intergroup crosses were compatible but intragroup crosses were incompatible. A sporophytic, diallelic, one-locus incompatibility system was inferred. Limited failure of the incompatibility mechanism was found (approximately 1% of crosses) for both selfs and intragroup crosses. Whereas most authors previously descri

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28

Tammisola, Jussi. "Incompatibility classes and fruit set in natural populations of arctic bramble (Rubus arcticus L.) in Finland." Agricultural and Food Science 60, no. 5 (1988): 327–446. http://dx.doi.org/10.23986/afsci.72299.

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In Finnish natural populations, arctic bramble proved uniformly self-incompatible. In vigorous and richly flowering populations, the intensity of fruit set is governed by the number of incompatibility classes present. Most non-fruiting populations contain only one incompatibility class (and most likely only one clone) and therefore totally lack compatible pollen. Richly fruiting populations usually contain at least three incompatibility classes. A clone with an estimated size of 80 metres and age of 160 years was found. This supports the vegetative burst explanation for the “sudden appearance”

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29

Asri, Novena Damar, and Purnomo Yusgiantoro. "Investigating a Hampered NRE Utilization in Kaltim’s Energy System: Is there an Energy Policy with a Syndrome of the Energy-abundant Area?" International Journal of Renewable Energy Development 10, no. 4 (2021): 653–66. http://dx.doi.org/10.14710/ijred.2021.37135.

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Kaltim presumably experiences an energy paradox, where the energy system is unreliable and unsustainable, despite energy-rich. This study presumes that the paradox is caused by the ‘ill-advised energy policy’ shown by ‘energy-area incompatibility’ that is exacerbated by the ‘energy-rich syndrome’ (a mindset of feeling secure due to energy-abundance leading to a wasteful behavior). This study investigates the indication of the syndrome in Kaltim energy policy by first investigating ‘the incompatibility’ and its impacts by examining Kaltim’s geographical characteristics, energy potential, popula

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30

TRAVERS, STEVEN E., JORGE MENA-ALI, and ANDREW G. STEPHENSON. "Plasticity in the self-incompatibility system of Solanum carolinense." Plant Species Biology 19, no. 3 (2004): 127–35. http://dx.doi.org/10.1111/j.1442-1984.2004.00109.x.

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31

McClure, Bruce. "Plant Self-Incompatibility: Ancient System Becomes a New Tool." Current Biology 22, no. 3 (2012): R86—R87. http://dx.doi.org/10.1016/j.cub.2011.12.034.

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32

McClure, Bruce. "Plant Self-Incompatibility: Ancient System Becomes a New Tool." Current Biology 22, no. 5 (2012): 450. http://dx.doi.org/10.1016/j.cub.2012.02.027.

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33

Kawai, Masataka, Mina Yamahara, and Akira Ohta. "Bipolar incompatibility system of an ectomycorrhizal basidiomycete, Rhizopogon rubescens." Mycorrhiza 18, no. 4 (2008): 205–10. http://dx.doi.org/10.1007/s00572-008-0167-4.

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34

Baskorowati, L., M. W. Moncur, S. A. Cunningham, J. C. Doran, and P. J. Kanowski. "Reproductive biology of Melaleuca alternifolia (Myrtaceae) 2. Incompatibility and pollen transfer in relation to the breeding system." Australian Journal of Botany 58, no. 5 (2010): 384. http://dx.doi.org/10.1071/bt10036.

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The onset of stigma receptivity in Melaleuca alternifolia (Maiden & Betche) Cheel was evaluated by observing pollen-tube growth and seed set following controlled pollination. Pollen-tube numbers in the style, following controlled pollinations, increased from Day 1 to Day 6, then declining rapidly. The stigma was most receptive during Days 3–6, and still receptive at low levels as early as shortly after anthesis and as late as 10 days after pollination. The present study found that individuals of M. alternifolia differed in their degree of expression of self-incompatibility. Artificial self

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35

Chen, Wendi, Bin Zhang, Wenjing Ren, et al. "An Identification System Targeting the SRK Gene for Selecting S-Haplotypes and Self-Compatible Lines in Cabbage." Plants 11, no. 10 (2022): 1372. http://dx.doi.org/10.3390/plants11101372.

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Cabbage (Brassica oleracea L. var. capitata) self-incompatibility is important for heterosis. However, the seed production of elite hybrid cannot be facilitated by honey bees due to the cross-incompatibility of the two parents. In this study, the self-compatibility of 58 winter cabbage inbred lines was identified by open-flower self-pollination (OS) and molecular techniques. Based on the NCBI database, a new class I S-haplotype-specific marker, PKC6F/PKC6R, was developed. Verification analyses revealed 9 different S-haplotypes in the 58 cabbage inbred lines; of these lines, 46 and 12 belonged

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36

Dudek, Ewa, and Michał Kozłowski. "Analysis of aeronautical information potential incompatibility – case study." Journal of KONBiN 41, no. 1 (2017): 59–82. http://dx.doi.org/10.1515/jok-2017-0004.

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Abstract This article is a continuation of the authors’ study on the ways to ensure the quality and safety of aeronautical data and information. In its content the Integrated Aeronautical Information Package was presented and its fundamental part AIP Poland was described. In addition, the docking guidance system A-VDGS, being an example of implementation of telematics system in air transport, was discussed as well as its requirements and schematic representation were attached. In the following part of the publication an analysis of AIP Poland in terms of the mentioned aircrafts’ docking system

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37

Gómez, Eva M., Ángela S. Prudencio, and Encarnación Ortega. "Protein Profiling of Pollen–Pistil Interactions in Almond (Prunus dulcis) and Identification of a Transcription Regulator Presumably Involved in Self-Incompatibility." Agronomy 12, no. 2 (2022): 345. http://dx.doi.org/10.3390/agronomy12020345.

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The cultivated almond displays a gametophytic self-incompatibility system, which avoids self-fertilization, and it is controlled by a multi-allelic locus (S-locus) containing two genes specifically expressed in pistil (S-RNase) and pollen (SFB). Studies on almonds with the same S-haplotype but different phenotype pointed to the existence of unknown components in this system to explain its functioning. The increase of knowledge on this reproductive barrier would allow better management of fruit production and germplasm selection. This work proposes candidates to components of the almond gametop

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38

Merçot, H., B. Llorente, M. Jacques, A. Atlan, and C. Montchamp-Moreau. "Variability within the Seychelles cytoplasmic incompatibility system in Drosophila simulans." Genetics 141, no. 3 (1995): 1015–23. http://dx.doi.org/10.1093/genetics/141.3.1015.

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Abstract In Drosophila simulans, we described a cytoplasmic incompatibility (CI) system (Seychelles) restricted to insular populations that harbor the mitochondrial type SiI. Since then, these populations have been shown to be heterogeneous, some being infected by one Wolbachia genetic variant only (wHa), while others are infected simultaneously by wHa and by another variant (wNo) always found in association with wHa. We have experimentally obtained two D. simulans strains only infected by the wNo variant. This variant determines its own cytoplasmic incompatibility type. In particular, the cro

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Xiang, Qijun, and N. Louise Glass. "Identification ofvib-1, a Locus Involved in Vegetative Incompatibility Mediated byhet-cinNeurospora crassa." Genetics 162, no. 1 (2002): 89–101. http://dx.doi.org/10.1093/genetics/162.1.89.

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AbstractA non-self-recognition system called vegetative incompatibility is ubiquitous in filamentous fungi and is genetically regulated by het loci. Different fungal individuals are unable to form viable heterokaryons if they differ in allelic specificity at a het locus. To identify components of vegetative incompatibility mediated by allelic differences at the het-c locus of Neurospora crassa, we isolated mutants that suppressed phenotypic aspects of het-c vegetative incompatibility. Three deletion mutants were identified; the deletions overlapped each other in an ORF named vib-1 (vegetative

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Kawano, Yoshiki, Tsuyoshi Mayama, Ryouji Kondou та Tetsuya Ohashi. "Crystal Plasticity Analysis of Change in Active Slip Systems of α-Phase of Ti-6Al-4V Alloy under Cyclic Loading". Key Engineering Materials 725 (грудень 2016): 183–88. http://dx.doi.org/10.4028/www.scientific.net/kem.725.183.

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In this paper, we investigated changes in active slip systems of α-phase of Ti-6Al-4V alloy under a cyclic plastic loading using a crystal plasticity finite element method. In the analyses, a bicrystal model was employed, and the crystallographic orientations were set so as that prismatic <a> or basal slip system was the primary slip system in each grain. The results showed that there was a mechanism where the basal slip systems could reach the stage of activation under the cyclic plastic loading even though the condition was that the prismatic <a> slips initially operate. The reas

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Reed, Sandra M. "Self-incompatibility in Cornus florida." HortScience 39, no. 2 (2004): 335–38. http://dx.doi.org/10.21273/hortsci.39.2.335.

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Low seed set has been reported following self-pollinations of flowering dogwood (Cornus florida L.). The objective of this study was to verify the presence of self-incompatibility in C. florida. `Cherokee Princess' stigmas and styles were collected 1, 2, 4, 8, 12, 24, 48, and 72 hours after cross- and self-pollinations, stained with aniline blue and observed using a fluorescence microscope. Pollen germinated freely following self-pollinations, but self-pollen tubes grew slower than those resulting from cross-pollinations. By 48 hours after cross-pollination, pollen tubes had reached the bottom

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LUNDQVIST, ARNE. "THE NATURE OF THE TWO-LOCI INCOMPATIBILITY SYSTEM IN GRASSES." Hereditas 48, no. 1-2 (2009): 153–68. http://dx.doi.org/10.1111/j.1601-5223.1962.tb01804.x.

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LUNDQVIST, ARNE. "THE NATURE OF THE TWO-LOCI INCOMPATIBILITY SYSTEM IN GRASSES." Hereditas 48, no. 1-2 (2009): 169–81. http://dx.doi.org/10.1111/j.1601-5223.1962.tb01805.x.

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Knox-Macaulay, Huxley, and Robert McDonald. "DiaMed-ID microtyping system for detection of major ABO incompatibility." Lancet 344, no. 8929 (1994): 1089. http://dx.doi.org/10.1016/s0140-6736(94)91745-0.

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Liao, Jugou, Jinran Dai, Hongmei Kang, et al. "Plasticity in the self-incompatibility system of cultivated Nicotiana alata." Euphytica 208, no. 1 (2015): 129–41. http://dx.doi.org/10.1007/s10681-015-1606-x.

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Varotto, S., L. Pizzoli, M. Lucchin, and P. Parrini. "The incompatibility system in Italian red chicory (Cichorium intybus L.)." Plant Breeding 114, no. 6 (1995): 535–38. http://dx.doi.org/10.1111/j.1439-0523.1995.tb00851.x.

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LUNDQVIST, ARNE. "THE NATURE OF THE TWO-LOCI INCOMPATIBILITY SYSTEM IN GRASSES." Hereditas 52, no. 2 (2009): 189–96. http://dx.doi.org/10.1111/j.1601-5223.1964.tb01951.x.

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LUNDQVIST, ARNE. "THE NATURE OF THE TWO-LOCI INCOMPATIBILITY SYSTEM IN GRASSES." Hereditas 52, no. 2 (2009): 221–34. http://dx.doi.org/10.1111/j.1601-5223.1964.tb01954.x.

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Naaborgh, A. T., and M. T. M. Willemse. "The ovular incompatibility system in Gasteria verrucosa (Mill.) H. Duval." Euphytica 58, no. 3 (1991): 231–40. http://dx.doi.org/10.1007/bf00025254.

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Martin, Audrey A. A., Samir Id-Lahoucine, Dan Tulpan, et al. "31 Gametic Incompatibility: Improving the Success of Mate Allocation in Dairy Cattle." Journal of Animal Science 99, Supplement_3 (2021): 16–17. http://dx.doi.org/10.1093/jas/skab235.026.

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Abstract In the dairy industry, mate allocation is mainly based on the parents’ breeding values and inbreeding coefficients aiming to achieve the producer’s breeding goal. With artificial insemination, the portfolio of sires to choose from is large and the quality of the semen doses is standardized. However, not all sire-dam matings are equally likely to produce a successful pregnancy. Among other reproduction issues, the success of a mating could vary due to the incompatibility of gametes coming from the sire and the dam and could influence the fertilization’s success, additionally to the rep

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