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1

Lamm, Wolfgang, and Wolfgang J. Köstler. "Reply to B. Abderrahman and V. C. Jordan." Journal of Clinical Oncology 34, no. 22 (August 1, 2016): 2676–77. http://dx.doi.org/10.1200/jco.2016.67.7542.

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2

Vracko, J., and K. L. Wiechel. "Reply to S. V. Murugesan, C. B. Babbs." Endoscopy 39, no. 04 (April 11, 2007): 379. http://dx.doi.org/10.1055/s-2007-966347.

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3

Chang, Qin, Li-Li Chen, and Shuai Xu. "Study of B c → J/ψV and ${B}_{c}^{* } \rightarrow {\eta }_{c}V$ decays within the QCD factorization." Journal of Physics G: Nuclear and Particle Physics 45, no. 7 (June 12, 2018): 075005. http://dx.doi.org/10.1088/1361-6471/aac732.

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4

Chang, Qin, Xiao-Lin Wang, Jie Zhu, and Xiao-Nan Li. "Study of b⟶c Induced B¯∗⟶Vℓν¯ℓ Decays." Advances in High Energy Physics 2020 (April 29, 2020): 1–12. http://dx.doi.org/10.1155/2020/3079670.

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In this paper, we investigate the tree-dominated B¯u,d,s,c∗⟶Vℓ−ν¯ℓ (V=Du,d∗,Ds∗,J/ψ and ℓ=e,μ,τ) decays in the Standard Model with the relevant form factors obtained in the light-front quark model. These decays involve much more helicity states relative to the corresponding B¯∗⟶Pℓ−ν¯ℓ and B¯⟶Vℓ−ν¯ℓ decays, and moreover, the contribution of longitudinal polarization mode (V meson) is relatively small, ~30%, compared with the corresponding B meson decays. We have also computed the branching fraction, lepton spin asymmetry, forward-backward asymmetry, and ratio RV∗L≡BB¯∗⟶Vτ−ν¯τ/BB¯∗⟶Vℓ′−ν¯ℓ′ℓ′=e,μ. Numerically, the branching fractions of B¯∗⟶Vℓ′−ν¯ℓ′ decays are at the level of O10−7 and are hopeful to be observed by LHC and Belle-II experiments. The ratios RD∗,Ds∗,J/ψ∗L have relatively small theoretical uncertainties and are close to each other, RD∗∗L≃RDs∗∗L≃RJ/ψ∗L≃0.26,0.270.27,0.29, which are a bit different from the predictions in some previous works. The future measurements are expected to make tests on these predictions.
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5

Shuyun, Sheng. "The Extension of the Theorems of C. V. Stanojevic and V. B. Stanojevic." Proceedings of the American Mathematical Society 110, no. 4 (December 1990): 895. http://dx.doi.org/10.2307/2047735.

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6

Kerber, M., and U. Schwalke. "Equilibrium controlled static C-V measurement." Solid-State Electronics 34, no. 10 (October 1991): 1141–48. http://dx.doi.org/10.1016/0038-1101(91)90111-b.

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7

Bassett, Mark J. "A New Recessive Allele at the C Locus for Seedcoat Color in Common Bean." Journal of the American Society for Horticultural Science 120, no. 6 (November 1995): 896–99. http://dx.doi.org/10.21273/jashs.120.6.896.

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The inheritance of a new allele, cv, at the C locus for seedcoat color was studied in common bean (Phaseolus vulgaris L.) using plant introduction (PI) accession 527774 as the source of cv. The cross PI 527774 (yellow-brown seed) x v BC25-593 (mineral-brown seed) genetic tester stock was studied in F1 and F2 progeny. An F3 selection from the above cross, designated F3 cv G b v, was crossed to 5-593 (a Florida breeding line with black seeds), and the F1, and F2 progeny were analyzed for color segregation. The second hackcross [S-593 x F1 (F3 cv G b v x 5-593)] was investigated in selfed progenies from 32 random BC2-F1 parents. Two of the BC2-F2 progenies were further tested in BC2,-F3. A third hackcross of cv to 5-593 was made and analyzed, and an allelism test of cv B V BC2-F35-593 with the cartridge huff cu BC3 5-593 genetic tester stock confirmed that cv is an allele at C. The gene symbol, cv, is proposed for the new allele because it is only expressed with V and gives a grayish-brown seedcoat. Genotypes with C/cv do not show heterozygous mottling with G B v or G b v, and there is no difference in seedcoat color between C G B v and cv G B v, or between C G b v and cv G b v.
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8

McGuinness, S. "A, B, AND C LEADS TO D (FOR DELEGATION!): A, B and C v. Ireland * 25579/05 [2010] ECHR 2032." Medical Law Review 19, no. 3 (August 17, 2011): 476–91. http://dx.doi.org/10.1093/medlaw/fwr021.

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9

Lü, Peng, Keping Chen, Qin Yao, Lu Gao, Ye Pan, Yuanqing He, Guoping Huang, and Lin Wang. "Expression and Localization of Bombyx mori V-ATPase 16 kDa Subunit c." Zeitschrift für Naturforschung C 65, no. 1-2 (February 1, 2010): 119–26. http://dx.doi.org/10.1515/znc-2010-1-219.

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V-ATPase plays a central role in lepidopteran midgut ion transport physiology, and lepidopteran midgut turned out to be a model tissue for the study of V-ATPase. In the present study, the 5’-RACE method is used to obtain the 5’-UTR of V-ATPase c subunit gene from Bombyx mori. Sequence analysis of the promoter region and 3’-UTR of V-ATPase c subunit gene revealed that the transcription of the V-ATPase c subunit gene may be regulated by multi-ways. RT-PCR analysis showed that B. mori V-ATPase c subunit mRNA expresses in the whole developmental stages of B. mori. We also constructed a transient vector to determine the subcellular localization of the B. mori V-ATPase c subunit, and the result demonstrated that it is located in the membrane and some specifi c regions of BmN cells. Real-time PCR analysis further indicated that the c subunit mRNA expression was upregulated signifi cantly at 24 and 72 h in the midguts of resistant B. mori larvae after being inoculated with B. mori nucleopolyhedrovirus, suggesting that it may be related to the immune response against virus infection.
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10

Güven, Evrim. "Some results on generalized derivations and (σ,τ)-Lie ideals." Filomat 32, no. 16 (2018): 5527–35. http://dx.doi.org/10.2298/fil1816527g.

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Let R be a prime ring with characteristic not 2 and ?,?,?,?,?,?,? automorphisms of R. Let h : R ? R be a nonzero left(resp.right)-generalized (?,?)-derivation, b ? R and V ? 0 a left (?,?)-Lie ideal of R. The main object in this article is to study the situations. (1) h(I) ? C?,?(V),(2) bh(I) ? C?,?(V) or h(I)b ? C?,?0V), (3) h?(V)=0,(4) h?(V)b=0 or bh?(V)=0.
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11

Inoue, J., L. D. Kerr, L. J. Ransone, E. Bengal, T. Hunter, and I. M. Verma. "c-rel activates but v-rel suppresses transcription from kappa B sites." Proceedings of the National Academy of Sciences 88, no. 9 (May 1, 1991): 3715–19. http://dx.doi.org/10.1073/pnas.88.9.3715.

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12

Alvarez, Silvina. "A, B y C v. Irlanda : el derecho al aborto en Europa." Discusiones 17, no. 1 (March 8, 2021): 133–63. http://dx.doi.org/10.52292/j.dsc.2016.2486.

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El artículo se centra en la última decisión del Tribunal Europeo de Derechos Humanos en materia de aborto. De acuerdo con el Tribunal, la legislación irlandesa sobre aborto entra dentro del margen de apreciación del Estado, y no hay discriminación ni quebrantamiento de derechos de la Convención. La decisión final estaría indicando que no basta la existencia de consenso europeo sobre la materia para oponerse a la regulación irlandesa sobre aborto y que haría falta ahondar en el alcance de los derechos comprometidos, tarea esta última que el Tribunal prefiere no emprender.
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13

Smrčková, Eva, Michal Bačuvčík, and Ivan Janotka. "Basic Characteristics of Green Cements of CEM V/A and V/B Kind." Advanced Materials Research 897 (February 2014): 196–99. http://dx.doi.org/10.4028/www.scientific.net/amr.897.196.

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The reduction of the clinker to addition ratio is becoming of main technological importance because energy saving potential by process optimization at the cements manufacture is almost exhausted. The main properties of composite cements of CEM V/A and CEM V/B kinds of Austrian (AT) and Slovak (SK) provenance with cement clinker contents between 45.1 % (CEM V/A-AT) – 52.9 % (CEM V/A-SK) and 26.9 % (CEM V/B-AT) – 30.9 % (CEM V/B-SK), and reference Slovak CEM I 32.5 R cement containing 95 % of the clinker were tested. The composite cements consist of cement clinker with following additions: blast furnace slag, fly ash and natural pozzolan - zeolite. Basic cement properties (normal consistency, initial and final set, volume stability) and fresh mortar properties (workability, volume density, air content) and strength parameters using standard mortars with W/C of 0.5 are introduced. Laboratory-made CEM V/A concrete specimens (AT and SK) demonstrated 90-day cube compressive strength between 49.8 – 50.9 MPa in water and 45.2 – 48.2 MPa in 60 % R.H. dry air; and those of CEM V/B concretes between 39.7 – 40.9 MPa in water and 26.9 – 38.7 MPa in 60 % R.H. dry air opposite to 53.6 MPa in water and 48.3 MPa of the CEM I 32.5 R concrete kept 90 days in 60 % R.H. dry air at (20 ± 1) °C. The use of CEM V/ (A, B) cements for structural concrete is strongly restricted by normative limitations in European countries. In order to improve this circumstance in Austria and Slovakia, the common research project was solved between 2010 and 2012 with the aim to show application possibilities of CEM V/A and CEM V/B cements for common usage in the structural concrete and ready-mixed concrete.
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14

Nunes, Carlos Angelo, Belmira Benedita de Lima, Gilberto Carvalho Coelho, and Paulo Atsushi Suzuki. "Isothermal Section of the V-Si-B System at 1600 °C in the V-VSi2-VB Region." Journal of Phase Equilibria and Diffusion 30, no. 4 (May 30, 2009): 345–50. http://dx.doi.org/10.1007/s11669-009-9533-y.

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15

Mahmood, Shakeel, Farida Tahir, and Azeem Mir. "Interference of Nonstandard Interactions with Standard Model in $${B^0} \to {\pi ^0}\bar vv$$ B 0 → π 0 v ¯ v , $$B_c^ - \to {D^ - }\bar vv$$ B c − → D − v ¯ v and $$\bar B_s^0 \to {K^0}\bar vv$$ B ¯ s 0 → K 0 v ¯ v Decays." Physics of Particles and Nuclei Letters 15, no. 3 (May 2018): 240–46. http://dx.doi.org/10.1134/s1547477118030135.

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16

Septyani, Luh Vela. "Pengaruh Waktu dan Suhu Pemanasan terhadap Stabilitas Sediaan Vitamin C Diukur dengan Metode Titrasi Iodometri." Jurnal Dunia Farmasi 5, no. 2 (May 24, 2021): 74–81. http://dx.doi.org/10.33085/jdf.v5i2.4840.

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Pendahuluan: Stabilitas didefinisikan sebagai kemampuan suatu produk mempertahankan sifat dan karakteristiknya.Pengujian stabilitas penting untuk memastikan bahwa obat akan tetap efektif dan aman selama penyimpanan maupun penggunaan.Vitamin C merupakan salah satu vitamin yang mudah teroksidasi dan dipercepat oleh panas, sinar, alkali, enzim, oksidator, serta oleh katalis tembaga dan besi. Tujuan: Untuk mengetahui pengaruh waktu dan suhu pemanasan terhadap kestabilan dari sediaan vitamin C. Metode: Uji stabilitas vitamin C dilakukan dengan metode uji stabilitas (daya tahan) dipercepat dengan cara melakukan pemanasan sampel vitamin C pada suhu 90ºC dengan interval waktu 30 menit, 60 menit, 90 menit, dan 120 menit. Penetapan kadar menggunakan metode titrasi iodometri dimana larutan Na2S2O sebagai standar. Hasil: Berdasarkan hasil perhitungan, kadar vitamin C yang diperoleh berturut-turut dari waktu pemanasan tercepat adalah 0,177%b/v; 0,158%b/v; 0,158%b/v; 0,150%b/v; 0,146%b/v. Kesimpulan: Semakin lama pemanasan vitamin C akan mempercepat terjadinya proses oksidasi sehingga kadar vitamin C pada sampel akan semakin berkurang.
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17

Lee, M. R., M. Quartern, and S. Jaulmes. "New Crystal Data for Seven Molybdates MIIUMo4O16 (MII = Mg,Mn,Cd,Ca,Hg,Sr,Pb)." Powder Diffraction 3, no. 2 (June 1988): 106–9. http://dx.doi.org/10.1017/s0885715600013361.

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AbstractSeven isotopic molybdates MIIUMo4O16 have been synthesized by solid state reaction with MII = Mg, Mn, Cd, Ca, Hg, Sr, Pb. Single crystals of CaUMo4O16 were obtained. Previously reported as triclinic, this compound is monoclinic, space group P2/n. Unit-cell parameters for the seven compounds are:MgUMo4O16: a = 11.393(2), b = 6.505(1), c = 7.918(2) Å, β = 89.81(3)°, V = 586.8(5) Å3, Z = 2, Dx = 5.12 Mg m−3;MnUMo4O16: a = 11.413(2), b = 6.555(1), c = 8.023(1) Å, β = 89.86(2)°, V = 600.2(4)Å3, Z = 2, Dx = 5.18 Mg m−3;CdUMo4O16: a = 11.427(2), b = 6.607(1), c = 8.144(2) Å3, β = 90.40(2)°, V = 614.8(5)Å3, Z = 2, Dx = 5.37 Mg m−3;CaUMo4O16: a = 11.443(3), b = 6.653(2), c = 8.239(2)Å, β = 90.51(3)°, V = 627.2(6)Å3, Z = 2, Dm = 4.83(5), Dx = 4.88 Mg m−3;HgUMo4O16: a = 11.439(3), b = 6.643(1), c = 8.257(2)Å, β = 90.53(3)°, V = 627.4(6)Å3, Z = 2, Dx = 5.73 Mg m−3;SrUMo4O16: 11.465(3), b = 6.768(2), c = 8.492(2) Å, β = 90.86(3)°, V = 658.8(6)Å3, Z = 2, Dx = 4.88 Mg m−3;PbUMo4O16: a = 11.470(4), b = 6.813(2), c = 8.557(2)Å, β = 90.88(4)°, V = 668.7(8)Å3, Dx = 5.41 Mg m−3;Powder diffraction data for each phase are reported.
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18

Balogun, Bola O. "C*-algebras associated with amalgamated products of groups." Glasgow Mathematical Journal 29, no. 2 (July 1987): 143–48. http://dx.doi.org/10.1017/s0017089500006789.

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Let V denote the class of discrete groups G which satisfy the following conditions (a), (b) and (c):(a) G = (A * B; K = φ(H)) is the free product of two groups A and B with the subgroup H amalgamated.(b) H does not contain the verbal subgroup A(X2) of A and K does not contain the verbal subgroup B(X2)of B.
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19

Calvet, T., M. A. Cuevas, E. Tauler, M. Labrador, Y. Haget, and E. Estop. "Crystal data for p-bromochlorobenzene/p-dibromobenzene mixed crystals at 293 K." Journal of Applied Crystallography 19, no. 3 (June 1, 1986): 202. http://dx.doi.org/10.1107/s002188988608963x.

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The powder data for p-bromochlorobenzene/p-dibromobenzene mixed crystals [pBCB] x [pDBB]1 − x at 293 K are reported; their thermal stability at 293 K is given. Vertical diffractometer, graphite monochromator, Cu Kα, λ = 1.54056 Å. They are all isomorphous, monoclinic, P21/a with Z = 2. a = 15.176(6), b = 5.847(3), c = 4.078(2) Å, β = 112.57(3)°, V = 334.2 Å3, Dx = 1.947 Mg m−3 for [pBCB]0.90[pDBB]0.10; JCPDS No. 36-1975. a = 15.222 (7), b = 5.847 (3), c = 4.083(2) Å, β = 112.60(3)°, V = 335.5 Å3, Dx = 1.984 Mg m−3 for [pBCB]0.80[pDBB]0.20; JCPDS No. 36-1974. a = 15.260(5), b = 5.839(2), c = 4.084(2) Å, β = 112.57(1)°, V = 336.1 Å3, Dx = 2.024 Mg m−3 for [pBCB]0.70[pDBB]0.30; JCPDS No. 36-1973. a = 15.298(4), b = 5.845(3), c = 4.091(2) Å, β = 112.60(2), V = 337.7 Å3, Dx = 2.058 Mg m−3 for [pBCB]0.60[pDBB]0.40; JCPDS No. 36-1972. a = 15.340(4), b = 5.844(2), c = 4.092(2) Å, β = 112.60(2)°, V = 338.7 Å3, Dx = 2.096 Mg m−3 for [pBCB]0.50[pDBB]0.50; JCPDS No. 36-1971. a = 15.370(5), b = 5.843(2), c = 4.097(2) Å, β = 112.62(2)°, V = 339.6 Å3, Dx = 2.134 Mg m−3 for [pBCB]0.40[pDBB]0.60; JCPDS No. 36-1970. a = 15.404(6), b = 5.840(2), c = 4.100(2) Å, β = 112.67(2)°, V = 340.4 Å3, Dx = 2.172 Mg m−3 for [pBCB]0.30[pDBB]0.70; JCPDS No. 36-1969. a = 15.437(5), b = 5.842(2), c = 4.103(2) Å, β = 112.66(2)°, V = 341.4 Å3, Dx = 2.209 Mg m−3 for [pBCB]0.20[pDBB]0.80; JCPDS No. 36-1968. a = 15.468(4), b = 5.838(2), c = 4.104(2) Å, β = 112.70(2)°, V = 341.9 Å3, Dx = 2.249 Mg m−3 for [pBCB]0.10[pDBB]0.90; JCPDS No. 36-1967.
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20

Zou, Xiaoming, Feng Cong, Margaret Coutts, Giorgio Cattoretti, Stephen P. Goff, and Kathryn Calame. "p53 Deficiency Increases Transformation by v-Abl and Rescues the Ability of a C-Terminally Truncated v-Abl Mutant To Induce Pre-B Lymphoma In Vivo." Molecular and Cellular Biology 20, no. 2 (January 15, 2000): 628–33. http://dx.doi.org/10.1128/mcb.20.2.628-633.2000.

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ABSTRACT Abelson murine leukemia virus (A-MuLV) is an acute transforming retrovirus that preferentially transforms early B-lineage cells both in vivo and in vitro. Its transforming protein, v-Abl, is a tyrosine kinase related to v-Src but containing an extended C-terminal domain. Many mutations affecting the C-terminal portion of the molecule block the pre-B-transforming activity of v-Abl without affecting the fibroblast-transforming ability. In this study we have determined the abilities of both wild-type and C-terminally truncated (p90) forms of v-Abl to transform cells from p53−/− mice. Lack of p53 increases the susceptibility of bone marrow cells to transformation by v-Abl by a factor of more than 7 but does not alter v-Abl's preference for B220+ IgM− pre-B cells. p53-deficient mice have earlier tumor onset, more rapid tumor progression, and decreased survival time following A-MuLV infection, but all of the tumors are pre-B lymphomas. Thus, p53-dependent pathways inhibit v-Abl transformation but play no role in conferring preferential transformation of pre-B cells. Surprisingly, the C-terminally truncated form of v-Abl (p90) transforms pre-B cells very efficiently in mice lacking p53, thus demonstrating that the C terminus of v-Abl does not determine preB tropism but is necessary to overcome p53-dependent inhibition of transformation.
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21

Yin, Guo-jie. "Crystal structure of 5,5-bis(4-iodophenyl)-5H-cyclopenta[2,1-b:3,4-b′]dipyridine, C23H14I2N2." Zeitschrift für Kristallographie - New Crystal Structures 231, no. 3 (September 1, 2016): 685–86. http://dx.doi.org/10.1515/ncrs-2015-0225.

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22

Euler, H., B. Barbier, A. Meents, and A. Kirfel. "Crystal structure of Tutton’s salts, Cs2[MII(H2O)6](SO4)2, MII = Mg, Mn, Fe, Co, Ni, Zn." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 4 (December 2003): 409–13. http://dx.doi.org/10.1524/ncrs.2003.218.4.409.

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Abstract Cs2H12MgO14S2, monoclinic, P121/a1 (No. 14), a = 9.338(2) Å, b = 12.849(4) Å, c = 6.361(2) Å, β = 107.07(2)°, V = 729.6 Å3, Z = 2, Rgt(F) = 0.017, wRref(F2) = 0.041, T = 293 K. Cs2H12MnO14S2, monoclinic, P121/a1 (No. 14), a = 9.418(3) Å, b = 12.963(2) Å, c = 6.386(3) Å, β = 107.17(4)°, V = 744.9 Å3, Z = 2, Rgt(F) = 0.017, wRref(F2) = 0.030, T = 293 K. Cs2FeO14H12S2, monoclinic, P121/a1 (No. 14), a = 9.357(2) Å, b = 12.886(2) Å, c = 6.381(1) Å, β = 106.94(1)°, V = 736.0 Å3, Z = 2, Rgt(F) = 0.015, wRref(F2) = 0.030, T = 293 K. CoCs2H12O14S2, monoclinic, P121/a1 (No. 14), a = 9.318(1) Å, b = 12.826(3) Å, c = 6.3650(9) Å, β = 107.13(1)°, V = 727.0 Å3, Z = 2, Rgt(F) = 0.021, wRref(F2) = 0.049, T = 293 K. Cs2H12NiO14S2, monoclinic, P121/a1 (No. 14), a = 9.259(2) Å, b = 12.767(2) Å, c = 6.358(1) Å, β = 107.00(2)°, V = 718.7 Å3, Z = 2, Rgt(F) = 0.014, wRref(F2) = 0.027, T = 293 K. Cs2H12O14S2Zn, monoclinic, P121/a1 (No. 14), a = 9.314(2) Å, b = 12.817(2) Å, c = 6.369(2) Å, β = 106.94(2)°, V = 727.3 Å3, Z = 2, Rgt(F) = 0.015, wRref(F2) = 0.033, T = 293 K.
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23

Kubozono, Yoshihiro, Keita Hyodo, Hiroki Mori, Shino Hamao, Hidenori Goto, and Yasushi Nishihara. "Transistor application of new picene-type molecules, 2,9-dialkylated phenanthro[1,2-b:8,7-b′]dithiophenes." Journal of Materials Chemistry C 3, no. 10 (2015): 2413–21. http://dx.doi.org/10.1039/c4tc02413c.

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Field-effect transistors have been fabricated that use thin films of 2,9-dialkylated phenanthro[1,2-b:8,7-b′]dithiophenes (Cn-PDTs), with the transistor based on a thin film of C12-PDT showing aμas high as ∼2 cm2V−1s−1, which is promising for future practical electronics.
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24

Alcobé, X., E. Estop, Y. Haget, M. A. Cuevas, M. Labrador, T. Calvet, and E. Tauler. "Crystal data for p-chloroiodobenzene and p-bromochlorobenzene/p-chloroiodobenzene mixed crystals at 293 K." Journal of Applied Crystallography 20, no. 1 (February 1, 1987): 48. http://dx.doi.org/10.1107/s0021889887087168.

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The powder data for p-chloroiodobenzene and p-bromochlorobenzene/p-chloroiodobenzene mixed crystals [pBCB] x [pCIB]1 − x at 293 K are reported; their stability at 293 K is given. The cell dimensions have been refined by least squares from accurate powder diffractometer data recorded at T = 293 (1) K (quartz as internal standard). Vertical diffractometer, graphite monochromator, Cu Kα 1−Cu Kα 2 correction so that λ = 1.54056 Å. They are all isomorphous, monoclinic, P21/a with Z = 2. a = 15.818(4), b = 5.912(2), c = 4.214(2) Å, β = 113.61(1)°, V = 361.1 Å3, Dx = 2.193 Mg m−3 for pCIB; JCPDS No. 37–2000. a = 15.210(5), b = 5.860(3), c = 4.091(2) Å, β = 112.64(2)°, V = 336.5 Å3, Dx = 1.936 Mg m−3 for [pBCB]0.90[pCIB]0.10; JCPDS No. 37–1989. a = 15.287(6), b = 5.870(3), c = 4.111(2) Å, β = 112.78(2)°, V = 340.1 Å3, Dx = 1.961 Mg m−3 for [pBCB]0.80[pCIB]0.20; JCPDS No. 37–1990. a = 15.360(5), b = 5.880(2), c = 4.126(1) Å, β = 112.87(2)°, V = 343.3 Å3, Dx = 1.988 Mg m−3 for [pBCB]0.70[pCIB]0.30; JCPDS No. 37–1991. a = 15.424(5), b = 5.889(3), c = 4.137(2) Å, β = 112.99(2)°, V = 346.0 Å3, Dx = 2.018 Mg m−3 for [pBCB]0.60[pCIB]0.40; JCPDS No. 37–1992. a = 15.493(4), b = 5.896(2), c = 4.155(2) Å, β = 113.09(2)°, V= 349.1 Å3, Dx = 2.045 Mg m−3 for [pBCB]0.50[pCIB]0.50; JCPDS No. 37–1993. a = 15.566(5), b = 5.901(3), c = 4.168(2) Å, β = 113.20(2)°, V = 351.9 Å3, Dx = 2.073 Mg m−3 for [pBCB]0.40[pCIB]0.60; JCPDS No. 37–1994. a = 15.623(5), b = 5.904(3), c = 4.178(3) Å, β = 113.26(2), V = 354.0 Å3, Dx = 2.105 Mg m−3 for [pBCB]0.30[pCIB]0.70; JCPDS No. 37–1995. a = 15.691(4), b = 5.913(3), c = 4.195(2)Å, β = 113.43(2)°, V = 357.1 Å3, Dx = 2.130 Mg m−3 for [pBCB]0.20[pCIB]0.80; JCPDS No. 37–1996. a = 15.759(4), b = 5.906(2), c = 4.204(2) Å, β = 113.55(2)°, V = 358.7 Å3, Dx = 2.164 Mg m−3 for [pBCB]0.10[pCIB]0.90; JCPDS No. 37–1999.
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25

Robert Wu, C. Y., Hok-Sum Fung, Kuang-Yu Chang, and D. L. Judge. "EUV resonance fluorescence of the c′4→X (0,v″) and b′→X (1,v″) transitions of N2." Planetary and Space Science 56, no. 13 (November 2008): 1725–32. http://dx.doi.org/10.1016/j.pss.2008.07.022.

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26

Havlin, S., M. Araujo, H. Larralde, H. E. Stanley, and P. Trunfio. "Diffusion-controlled reaction, A+B→C, with initially separated reactants." Physica A: Statistical Mechanics and its Applications 191, no. 1-4 (December 1992): 143–52. http://dx.doi.org/10.1016/0378-4371(92)90519-v.

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27

SANTHAKUMARAN, A. P., and P. TITUS. "MONOPHONIC DISTANCE IN GRAPHS." Discrete Mathematics, Algorithms and Applications 03, no. 02 (June 2011): 159–69. http://dx.doi.org/10.1142/s1793830911001176.

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For any two vertices u and v in a connected graph G, a u – v path is a monophonic path if it contains no chords, and the monophonic distance dm(u, v) from u to v is defined as the length of a longest u – v monophonic path in G. A u – v monophonic path of length dm(u, v) is called a u – v monophonic. The monophonic eccentricity em(v) of a vertex v in G is the maximum monophonic distance from v to a vertex of G. The monophonic radius rad m G of G is the minimum monophonic eccentricity among the vertices of G, while the monophonic diameter diam m G of G is the maximum monophonic eccentricity among the vertices of G. It is shown that rad m G ≤ diam m G for every connected graph G and that every pair a, b of positive integers with a ≤ b is realizable as the monophonic radius and monophonic diameter of some connected graph. Also, for any three positive integers a, b and c with 3 ≤ a ≤ b ≤ c, there is a connected graph G such that rad G = a, rad m G = b and rad DG = c; and for any three positive integers a, b and c with 5 ≤ a ≤ b ≤ c, there is a connected graph G such that diam G = a, diam m G = b and diam D G = c, where rad G, diam G, rad DG and diam D G denote the radius, diameter, detour radius and detour diameter, respectively. The monophonic center of G is the subgraph induced by the vertices of G having monophonic eccentricity rad m G and it is shown that every graph is the monophonic center of some connected graph and also that the monophonic center Cm(G) of every connected graph G is a subgraph of some block of G.
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28

Euler, H., B. Barbier, A. Meents, and A. Kirfel. "Crystal structure of Tutton’s salts, Cs2[MII(H2O)6](SeO4)2, MII = Mg, Mn, Co, Ni, Zn." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 4 (December 2003): 405–8. http://dx.doi.org/10.1524/ncrs.2003.218.4.405.

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Abstract Cs2H12MgO14Se2, monoclinic, P121/a1 (No. 14), a = 9.513(1) Å, b = 13.037(1) Å, c = 6.4730(8) Å, β = 106.244(8)°, V = 770.7 Å3, Z = 2, Rgt(F) = 0.020, wRref(F2) = 0.036, T = 293 K. Cs2H12MnO14Se2, monoclinic, P121/a1 (No. 14), a = 9.591(1) Å, b = 13.141(2) Å, c = 6.5040(9) Å, β = 106.38(1)°, V = 786.5 Å3, Z = 2, Rgt(F) = 0.021, wRref(F2) = 0.043, T = 293 K. CoCs2H12O14Se2, monoclinic, P121/a1 (No. 14), a = 9.494(1)Å, b = 13.009(1) Å, c = 6.4833(8) Å, β = 106.239(9)°, V = 768.8 Å3, Z = 2, Rgt(F) = 0.016, wRref(F2) = 0.032, T = 293 K. Cs2H12NiO14Se2, monoclinic, P121/a1 (No. 14), a = 9.426(3)Å, b = 12.961(2) Å, c = 6.473(2) Å, β = 106.17(2)°, V = 759.5 Å3, Z = 2, Rgt(F) = 0.017, wRref(F2) = 0.034, T = 293 K. Cs2H12O14Se2Zn, monoclinic, P121/a1 (No. 14), a = 9.483(1) Å, b = 13.005(2) Å, c = 6.4850(8) Å, β = 106.16(1)°, V = 768.2 Å3, Z = 2, Rgt(F) = 0.019, wRref(F2) = 0.037, T = 293 K.
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29

Dorsett, Yair, Davide F. Robbiani, Mila Jankovic, Bernardo Reina-San-Martin, Thomas R. Eisenreich, and Michel C. Nussenzweig. "A role for AID in chromosome translocations between c-myc and the IgH variable region." Journal of Experimental Medicine 204, no. 9 (August 27, 2007): 2225–32. http://dx.doi.org/10.1084/jem.20070884.

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Chromosome translocations between oncogenes and the region spanning the immunoglobulin (Ig) heavy chain (IgH) variable (V), diversity (D), and joining (J) gene segments (Ig V-JH region) are found in several mature B cell lymphomas in humans and mice. The breakpoints are frequently adjacent to the recombination signal sequences targeted by recombination activating genes 1 and 2 during antigen receptor assembly in pre–B cells, suggesting that these translocations might be the result of aberrant V(D)J recombination. However, in mature B cells undergoing activation-induced cytidine deaminase (AID)-dependent somatic hypermutation (SHM), duplications or deletions that would necessitate a double-strand break make up 6% of all the Ig V-JH region–associated somatic mutations. Furthermore, DNA breaks can be detected at this locus in B cells undergoing SHM. To determine whether SHM might induce c-myc to Ig V-JH translocations, we searched for such events in both interleukin (IL) 6 transgenic (IL-6 tg) and AID−/− IL-6 tg mice. Here, we report that AID is required for c-myc to Ig V-JH translocations induced by IL-6.
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30

Rybakov, Victor, Vladimir Chernyshev, Ksenia Paseshnichenko, and Victor Sheludyakov. "Crystal structure of salts luminol with Li, Na and K." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1021. http://dx.doi.org/10.1107/s2053273314089785.

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The molecular and crystal structures of new drugs Tamerit® (A) and Galavit® (B) which possess high effective immunomodulator, anti-inflammatory and anti-oxidant properties, were studied by single crystal and powder X-ray diffraction methods. As shown, A and B are aminodihydrophtalazindion (luminol) sodium salts, but A - is a dihydrate form and B anhydrous one, moreover it is a mixture two different crystal phases B1 and B2. The phase transition B1 <---> B2 is not registered by DSC method [1]. Crystal data for A: monoclinic system with a = 8.3429(4), b = 22.0562(11), c =5.2825(2) Å, β = 99.893(3)o, V = 957.59(8) Å3, Z = 4, sp.gr. R21/s. Crystal data for B1: monoclinic system with a = 14.7157(18), b = 3.7029(19), c = 16.0233(15) Å, β = 116.682(13)o, V = 780.1(4) Å3, Z = 4, sp.gr. R21/s. Crystal data for B2: orthorhombic system with a = 27.7765(15), b = 3.3980(19), c = 8.1692(19) Å, V = 771.0(5) Å3, Z = 4, sp.gr. Pna21. As a continuation of this work, we studied by the same methods other luminol salts: with Li - monohydrate (C1) and anhydrous (C2) and with K - trihydrate (D1) and anhydrous (D2). Crystal data for C1: monoclinic system with a = 13.0311(15), b = 9.6002(7), c = 7.3227(7) Å, β = 101.320(9)o, V = 898.26(15) Å3, Z = 4, sp.gr. R21/s. Crystal data for C2: monoclinic system with a = 13.0979(14), b = 8.7537(12), c = 14.5358(17) Å, β = 107.061(16)o, V = 1593.3(4) Å3, Z = 8, sp.gr. C2/c. Crystal data for D1: monoclinic system with a = 10.6760(6), b = 14.2905(8), c = 7.4902(5) Å, β = 99.246(5)o, V = 1127.90(12) Å3, Z = 4, sp.gr. R21/s. Crystal data for D2: orthorhombic system with a = 27.3961(19), b = 3.6811(14), c = 8.6672(12) Å, V = 874.1(4) Å3, Z = 4, sp.gr. Pna21 [2]. All X-ray experiments were made at T = 295 K. The features of molecular and crystal structures are discussed.
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31

Meir, A., and J. W. Moon. "On Major and Minor Branches of Rooted Trees." Canadian Journal of Mathematics 39, no. 3 (June 1, 1987): 673–93. http://dx.doi.org/10.4153/cjm-1987-033-3.

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Let denote a rooted tree with n nodes. (For definitions not given here, see, e.g. [4]). For any node v of , let B(v) denote the subtree of determined by v and all nodes u such that v is between u and the root of ; node v serves as the root of B(v). The branches of are the subtrees B(v) such that node v is joined to the root of . A branch B with i nodes is a primary branch of if n/2 ≦ i ≦ n – 1; if has a primary branch B with i nodes, then a branch C with j nodes is a secondary branch if (n – i)/2 ≦ j ≦ n – 1 ≦ i; if has a primary branch B with i nodes and a secondary branch C with j nodes, then a branch D with h nodes is a tertiary branch if
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32

Yang, Bingchuan, Xueyan Lv, Gang Liu, and Rutao Liu. "Crystal structure of catena-poly[(5H-pyrrolo[3,2-b:4,5-b′]dipyridine-κ2 N,N′)-(μ4-hexaoxidodivanadato)dizinc(II)],C10H9N3O6V2Zn." Zeitschrift für Kristallographie - New Crystal Structures 236, no. 2 (January 11, 2021): 447–49. http://dx.doi.org/10.1515/ncrs-2020-0604.

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Abstract C10H9N3O6V2Zn, monoclinic, C2/c (no. 15), a = 8.0106(17) Å, b = 29.957(6) Å, c = 12.050(3) Å, β = 95.025(4) Å, V = 2880.6(10) Å3, Z = 8, R gt (F) = 0.0512, wR ref (F 2) = 0.1975, T = 296(2) K.
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33

Persulessy, Elvinus R. "REGULARISASI SISTEM SINGULAR DENGAN OUTPUT UMPAN BALIK u = Fy + v." BAREKENG: Jurnal Ilmu Matematika dan Terapan 1, no. 1 (March 1, 2007): 32–37. http://dx.doi.org/10.30598/barekengvol1iss1pp32-37.

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(E,A,B,C,D) as a singular system is given. E, A, B and C are real constant matrices if E=I, I is a identify matrix, then (E,A,B,C) is a normal system. A unique solution of a singular system exists if (E,A) is regular. A singular system which is regular and the index is not more than one can be simplified to a normal system.The regularization of a singular system by feedback output u = Fy + v is investigated in this paper. Furthermore a sufficient and necessary condition of the existence of F such that (E, A+BFC) is regular and the index is not more than one is represented.
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34

Gusev, A. I., N. V. Kibko, M. V. Popova, N. A. Kozyrev, and I. V. Osetkovskii. "SURFACING OF DETAILS OF MINING EQUIPMENT BY POWDER WIRES OF C – Si – Mn – Mo – V – B AND C – Si – Mn – Cr – Mo – V SYSTEMS." Izvestiya Visshikh Uchebnykh Zavedenii. Chernaya Metallurgiya = Izvestiya. Ferrous Metallurgy 60, no. 4 (January 1, 2017): 318–23. http://dx.doi.org/10.17073/0368-0797-2017-4-318-323.

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35

Kilminster, Kieryn L., Francis J. Lincoln, Brian W. Skelton, and Allan H. White. "A Barium Vanadium(V) Selenite Hydrate, Ba(VO2)2(SeO3)2·H2O: A Novel 3D Polymer of Cross-Linked Sheets with Embedded ···V–O–V··· 21 Helices." Australian Journal of Chemistry 67, no. 12 (2014): 1878. http://dx.doi.org/10.1071/ch14473.

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The characterisation, by a single-crystal X-ray study at ~150 K, of brown acicular crystals of barium(ii) bis(dioxovanadium(v)) bis(selenite(iv)) monohydrate, BaSe2V2O10·H2O, obtained as a minor product of the synthesis of the previously reported ‘Ba(VO)2(SeO3)2(HSeO3)2’, is recorded. Crystals are monoclinic, P21/c, a = 10.803(2), b = 5.1126(8), c = 17.905(3) Å, β = 92.048(2)°, V = 988.3(3) Å3, 2456 independent diffractometer reflections refining to R1 = 0.032, wR2 = 0.084. A single BaV2Se2O11H2 formula unit, devoid of crystallographic symmetry, comprises the asymmetric unit of the structure, which is a three-dimensional polymer, with component sheets parallel to the crystallographic b axis, containing pentavalent vanadium atoms, one five-, the other six-coordinate, linked by selenite pyramids.
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36

Bassett, Mark J. "A Complex C Region Genotype [? R] that with G B vlae Produces Dark Seal-brown Seedcoat Color in Common Bean." Journal of the American Society for Horticultural Science 121, no. 4 (July 1996): 594–98. http://dx.doi.org/10.21273/jashs.121.4.594.

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Common bean (Phaseolus vulgaris L.) plant introduction 527829 (formerly Lamprecht M0048) has dark seal-brown (DSB) seedcoats and pink flowers. An investigation was conducted to determine the genotype of DSB seedcoat color. M0048 was crossed with Florida breeding line 5-593, which has genotype P [C r] D J G B V Rk. A series of crosses involving M0048, 5-593, and three genetic tester stocks (v BC2 5-593, cu BC2 5-593, and b v BC2 5-593) led to determination of the genotype. Data analysis indicated that M0048 has the genotype P [? R] J G B vlae, where DSB color is produced by the interaction of R with B. Crosses between [? R] and testers with [C r] always produced seedcoat mottling in F1, except where V masks the effect. The cross [? R] B v (DSB) × cu BC2 5-593 (cartridge buff seedcoat) produced marbled seedcoats (black/cartridge buff) with genotype [? R]/[cu?] B V. No way was found to determine whether the mottled or marbled seedcoat patterns were controlled at C or R; hence, the allelic ambiguity is indicated with a question mark. Illustrations are provided showing the difference between seedcoat mottling (a highly variable low-contrast patterning) and seedcoat marbling (a less variable high-contrast patterning, usually with cartridge buff as the background color). The development of a new genetic tester stock, [? R] b v BC3 5-593, was described, where [? R] b v gives unpatterned dominant red seedcoat color.
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37

Balonin, Nikolay, and Dragomir Ðoković. "Conference matrices from Legendre C-pairs." Information and Control Systems, no. 4 (August 24, 2020): 2–10. http://dx.doi.org/10.31799/1684-8853-2020-4-2-10.

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Introduction: There are just a few known methods for the construction of symmetric C-matrices, due to the lack of a universal structure for them. This obstruction is fundamental, in addition, the structure of C-matrices with a double border is incompletely described in literature, which makes its study especially relevant. The purpose: To describe the two-border two-circulant construction in detail with the proposal of the concept of C-pairs Legendre. Results: The paper deals with C-matrices of order n=2v+2 with two borders and extends the so called generalized Legendre pairs, v odd, to a wider class of Legendre C-pairs with even and odd v, defined on a finite abelian group G of order v. Such a pair consists of two functions a, b: G→Z, whose values are +1 or −1 except that a(e)=0, where e is the identity element of G and Z is the ring of integers. To characterize the Legendre C-pairs we use the subsets X={xÎG: a(x)=–1} and Y={xÎG: b(x)=–1} of G. We show that a(x−1)=(−1)v a(x) for all x. For odd v we show that X and Y form a difference family, which is not true for even v. These difference families are precisely the so called Szekeres difference sets, used originally for the construction of skew-Hadamard matrices. We introduce the subclass of the special Legendre C-pairs and prove that they exist whenever 2v+1 is a prime power. In the last two sections of the paper we list examples of special cyclic Legendre C-pairs for lengths v<70. Practical relevance: C-matrices are used extensively in the problems of error-free coding, compression and masking of video information. Programs for search of conference matrices and a library of constructed matrices are used in the mathematical network “mathscinet.ru” together with executable on-line algorithms.
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38

Beninger, C. W., and G. L. Hosfield. "Identification of Flavonoids from the Seedcoats of Phaseolus vulgaris L. Beans of Known Genotype for Seedcoat Color." HortScience 33, no. 3 (June 1998): 528c—528. http://dx.doi.org/10.21273/hortsci.33.3.528c.

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A number of pure flavonoid compounds have been isolated and identified from seedcoats of bean (Phaseolus vulgaris) with known genotypes for seedcoat color. Kaempferol-3-O- -D-glucopyranoside was found to be the major seedcoat flavonol of the “brown” genotypes yellow brown (P C J G b v), mineral brown (P C J G B v), mat mineral brown (PC j G B v), buffy citrine (P C J g B v). This kaempferol glycoside was also found in a yellow bean (`prim' P C j G b v) of the manteca market class, but the diglycoside kaempferol-3-O- -D-glucopyranoside-(2 1)- -D-xylopyranoside was another major flavonol found in manteca. The “brown” genotypes also contained proanthocyanidins that are currently being characterized, but no tannins or proanthocyanidins were found in the manteca bean. Three main anthocyanins have been found in the three “black” genotypes, mat black, 5-593 and dark brown violet. Preliminary identification of the anthocyanins indicates the presence of delphinidin, petunidin and malvidin. Further work on identification of the minor anthocyanins is underway.
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39

Euler, H., B. Barbier, A. Meents, and A. Kirfel. "Crystal structure of Tutton’s salts, Rb2[MII(H2O)6](SeO4)2, MII = Mg, Co, Mn, Zn." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 3 (September 2003): 265–68. http://dx.doi.org/10.1524/ncrs.2003.218.3.265.

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Abstract H12MgO14Rb2Se2, monoclinic, P121/a1 (No. 14), a = 9.401(1) Å, b = 12.658(2) Å, c = 6.339(1) Å, β = 105.25(1)°, V = 727.8 Å3, Z = 2, Rgt(F) = 0.020, wRref(F2) = 0.040, T = 293 K.CoH12O14Rb2Se2, monoclinic, P121/a1 (No. 14), a = 9.363(1) Å, b = 12.618(1) Å, c = 6.3562(7) Å, β = 105.238(9)°, V = 724.5Å3, Z = 2, Rgt(F) = 0.018, wRref(F2) = 0.037, T = 293 K. H12MnO14Rb2Se2, monoclinic, P121/a1 (No. 14), a = 9.4496(8) Å, b = 12.760(1) Å, c = 6.3794(7) Å, β = 105.189(7)°, V = 742.4Å3, Z = 2, Rgt(F) = 0.025, wRref(F2) = 0.056, T = 293 K. H12O14Rb2Se2Zn, monoclinic, P121/a1 (No. 14), a = 9.352(1) Å, b = 12.626(2) Å, c = 6.360(1) Å, β = 105.195(8)°, V = 724.7 Å3, Z = 2, Rgt(F) = 0.024, wRref(F2) = 0.048, T = 293 K.
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40

Rahman, MM, and AC Paul. "(U, M) -derivations in prime ?-rings." Bangladesh Journal of Scientific Research 27, no. 2 (January 4, 2016): 143–53. http://dx.doi.org/10.3329/bjsr.v27i2.26232.

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In this article, we define (U,M)-derivation d of a ? -ring M . For a Lie ideal U of a 2 - torsion free prime ? -ring M satisfying the condition a?b?c = a?b?c for all a,b, c?M and ? ,? ?? , we prove the following results:(i) ifU is an admissible Lie ideal of M, then d(u?v) = d(u)?v + u?d(v) for all u, v?U ,? ??(ii) if u?u?U for all u?U,? ?? , then d(u?m) = d(u)?m + u?d(m) for all m ? M Bangladesh J. Sci. Res. 27(2): 143-153, December-2014
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41

Basmal, Jamal, Yuyun Sekarasih, and Tatit K. Bunasor. "PENGARUH KONSENTRASI BAHAN PEMUCAT DAN JENIS BAHAN PENGENDAP TERHADAP PEMBENTUKAN SODIUM ALGINAT DARI RUMPUT LAUT COKLAT Sargassum filipendula C. AGARTH." Jurnal Penelitian Perikanan Indonesia 7, no. 4 (April 5, 2017): 74. http://dx.doi.org/10.15578/jppi.7.4.2001.74-81.

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Penelitian perbaikan kualitas sodium alginat telah dilakukan dengan menggunakan tiga konsentrasi hidrogen peroksida (H2O2) sebagai bahan pemucat yaitu 3%, 6%, dan 9% (v/v) yang kemudian diendapkan menggunakan dura jenis bahan pengendap yaitu sodium karbonat (NarCOr) 5% (b/v) dan sodium hidroksida (NaOH) 5% (b/v).
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42

Dudley, Darryll D., JoAnn Sekiguchi, Chengming Zhu, Moshe J. Sadofsky, Scott Whitlow, Jeffrey DeVido, Robert J. Monroe, Craig H. Bassing, and Frederick W. Alt. "Impaired V(D)J Recombination and Lymphocyte Development in Core RAG1-expressing Mice." Journal of Experimental Medicine 198, no. 9 (October 27, 2003): 1439–50. http://dx.doi.org/10.1084/jem.20030627.

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RAG1 and RAG2 are the lymphocyte-specific components of the V(D)J recombinase. In vitro analyses of RAG function have relied on soluble, highly truncated “core” RAG proteins. To identify potential functions for noncore regions and assess functionality of core RAG1 in vivo, we generated core RAG1 knockin (RAG1c/c) mice. Significant B and T cell numbers are generated in RAG1c/c mice, showing that core RAG1, despite missing ∼40% of the RAG1 sequence, retains significant in vivo function. However, lymphocyte development and the overall level of V(D)J recombination are impaired at the progenitor stage in RAG1c/c mice. Correspondingly, there are reduced numbers of peripheral RAG1c/c B and T lymphocytes. Whereas normal B lymphocytes undergo rearrangement of both JH loci, substantial levels of germline JH loci persist in mature B cells of RAG1c/c mice, demonstrating that DJH rearrangement on both IgH alleles is not required for developmental progression to the stage of VH to DJH recombination. Whereas VH to DJH rearrangements occur, albeit at reduced levels, on the nonselected alleles of RAG1c/c B cells that have undergone D to JH rearrangements, we do not detect VH to DH rearrangements in RAG1c/c B cells that retain germline JH alleles. We discuss the potential implications of these findings for noncore RAG1 functions and for the ordered assembly of VH, DH, and JH segments.
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Staunton, Ciara. "News & Views As Easy as A, B and C: Will A, B and C v. Ireland Be Ireland’s Wake-up Call for Abortion Rights?" European Journal of Health Law 18, no. 2 (2011): 205–19. http://dx.doi.org/10.1163/157180911x564589.

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AbstractThis article examines the development of Ireland’s abortion policy from 1861 to the present day. It explores the reasoning for this policy as well as the inherent problems with this policy. It examines in detail the A, B and C v. Ireland judgement and its impact, (if any) on Irish abortion law. Finally, it discusses the margin of appreciation doctrine used by the European Court of Human Rights in deciding cases of a moral nature.
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44

Shakhatov, V. A., and Yu A. Lebedev. "Kinetics of excitation of N2(A 3Σ u + , v A ), N2(C 3Π u , v c ), and N2(B 3Π g , v B ) in nitrogen discharge plasmas as studied by means of emission spectroscopy and computer simulation." High Energy Chemistry 42, no. 3 (May 2008): 170–204. http://dx.doi.org/10.1134/s0018143908030028.

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45

Thorelli, Elisabeth, Randal J. Kaufman, and Björn Dahlbäck. "The C-terminal Region of the Factor V B-domain Is Crucial for the Anticoagulant Activity of Factor V." Journal of Biological Chemistry 273, no. 26 (June 26, 1998): 16140–45. http://dx.doi.org/10.1074/jbc.273.26.16140.

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46

HARALAMBIDES, J., and S. TRAGOUDAS. "THE PROBLEM OF PARTITIONING WITH DUPLICATIONS AND ITS APPLICATIONS." International Journal on Artificial Intelligence Tools 03, no. 03 (September 1994): 395–405. http://dx.doi.org/10.1142/s0218213094000224.

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The problem of partitioning the elements of a graph G=(V, E) into two equal size sets A and B that share at most d elements such that the total number of edges (u, v), u∈A−B, v∈B−A is minimized, arises in the areas of Hypermedia Organization, Network Integrity, and VLSI Layout. We formulate the problem in terms of element duplication, where each element c∈A∩B is substituted by two copies c′∈A and c″∈B As a result, edges incident to c′ or c″ need not count in the cost of the partition. We show that this partitioning problem is NP-hard in general, and we present a solution which utilizes an optimal polynomial time algorithm for the special case where G is a series-parallel graph. We also discuss special other cases where the partitioning problem or variations are polynomially solvable.
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47

Hirotani, Masao, Chieko Ino, Akiko Hatano, Hiroaki Takayanagi, and Tsutomu Furuya. "Ganomastenols A, B, C and D, cadinene sesquiterpenes, from Ganoderma mastoporum." Phytochemistry 40, no. 1 (September 1995): 161–65. http://dx.doi.org/10.1016/0031-9422(95)00225-v.

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de Preux, J. "Texte de synthèse V-Capture." Revue Internationale de la Croix-Rouge 68, no. 758 (April 1986): 91–101. http://dx.doi.org/10.1017/s0035336100089620.

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— Est hors de combat toute personne:a) qui est au pouvoir d'une Partie adverse,b) qui exprime clairement son intention de se rendre ou,c) qui a perdu connaissance ou est autrement en état d'incapacité et en conséquence incapable de se défendre, à condition qu'elle s'abstienne de tout acte d'hostilité et ne tente pas de s'évader (P. I, art. 41).
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K.C.*, Ebrahim N., Ivvala Anand Shaker, and Abdul Kadhir. "Prevalence of color vision deficiency (CVD) and ABO blood groups in Kannur district of Kerala, India." International Journal of Bioassays 5, no. 01 (January 1, 2016): 4760. http://dx.doi.org/10.21746/ijbio.2016.01.0011.

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Colour’s have profound influence in life. Colour vision deficiency (C. V. D), A. B. O & Rh blood groups are inherited entities with different geographical regions, and from race to race it varies. As the C. V. D once occurred cannot be changed in life time.750 cases of Colour Vision Deficiency individuals were examined and were identified and confirmed by testing colour vision of the person by Ishihara's Chart test for both eyes. Those found to be suffering from congenital colour blindness were then subjected to A, B, O & Rh grouping by slide method. Our results showed statistical significant positive relationship between congenital C. V. D individuals and their A, B, O, R, H blood groups. Our aim was to study relationship between A, B, O blood group, Rh factor, G-6PD and to know if any Colour Vision Deficiency (C. V. D) present in this population.
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Herbst, Leandra, Hendrik G. Visser, and Andreas Roodt. "Crystal structure of (benzoylacetonato-κ2O,O')dichloridodimethoxidotantalum(V), C12H15Cl2O4Ta." Zeitschrift für Kristallographie - New Crystal Structures 228, no. 3 (October 1, 2013): 397–98. http://dx.doi.org/10.1524/ncrs.2013.0200.

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