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H-1

Detection of H 1 parvovirus and Kilham rat virus by PCR

Detection of H 1 parvovirus and Kilham rat virus by PCR

... systems, H-1 and KRV may interfere with research in other ways. H-1 virus has been shown to inhibit experimental tumor induction in hamsters (35, 36) and can cause hepatocel- lular necrosis in ...

5

Mapping of the amino terminus of the H-1 parvovirus major capsid protein.

Mapping of the amino terminus of the H-1 parvovirus major capsid protein.

... 52, 1984 AMINO TERMINUS OF THE H-1 PARVOVIRUS CAPSID PROTEIN coded, uninterrupted, from nucleotide 2800 to the terminator codon at nucleotide 4573.. Figure 3 shows the DNA sequence and t[r] ...

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Synthesis of furano[2,3-c] /pyrrolo[2,3-c]coumarins and synthesis of 1(H)-[1]benzopyrano[3,4-b][1]benzopyrano[3’,4’-d] furan-7(H)-ones /1(H)-[1]benzopyrano[3,4-b][1]benzopyrano [3’,4’-d]pyrrole-7(H)-ones

Synthesis of furano[2,3-c] /pyrrolo[2,3-c]coumarins and synthesis of 1(H)-[1]benzopyrano[3,4-b][1]benzopyrano[3’,4’-d] furan-7(H)-ones /1(H)-[1]benzopyrano[3,4-b][1]benzopyrano [3’,4’-d]pyrrole-7(H)-ones

... various 1-aryl-furano[2,3-c] and 1-phenyl-2-methyl-furano [2,3-c]coumarins;1-aryl-pyrrolo[2,3-c]and1-phenyl- 2methylpyrrolo[2,3c]coumarins; 1aryl1H1] benzopyrano[3,4,-b][1]benzpyrano ...

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Replication process of the parvovirus H-1. IX. Physical mapping studies of the H-1 genome.

Replication process of the parvovirus H-1. IX. Physical mapping studies of the H-1 genome.

... Double digestion with HaeIII and EcoRI or HaeII revealed that both EcoRI and HaeII cleaved only the HaeIII-A fragment 1,570 bp, thus establishing that both cleavage sites are adjacent to[r] ...

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Replication process of the parvovirus H-1. VIII. Partial denaturation mapping and localization of the replication origin of H-1 replicative-form DNA with electron microscopy.

Replication process of the parvovirus H-1. VIII. Partial denaturation mapping and localization of the replication origin of H-1 replicative-form DNA with electron microscopy.

... in the DNAIn addition, this terminus of the A fragment spreading solution; 82% was the formamide concento initiate partial denaturation, hereafter termed the right end of the RF mole- tr[r] ...

8

Table H-1. UNO HC 1 Requirements Data (Continued) Proper Shipping Name

Table H-1. UNO HC 1 Requirements Data (Continued) Proper Shipping Name

... FARP ammunition operations include procedures for storage, safety, arming, and training. Generally, these procedures are subject to the same stringent safety requirements as munitions op[r] ...

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Analysis of the protein-protein interactions in the parvovirus H-1 capsid.

Analysis of the protein-protein interactions in the parvovirus H-1 capsid.

... The ability to form these high-molecularweight species by treatment of purified empty capsids with PEG suggested that these proteins were derived from VP1 or VP2' or both after the capsi[r] ...

9

Studies of vacuum magnetic surfaces in H 1 using tomography

Studies of vacuum magnetic surfaces in H 1 using tomography

... in H-l is the positional error of the PFC with respect to the TFC , particularly a planar displacem ent of the PFC centre from the machine centre (See hgure ...

153

Dense H free graphs are almost (Χ(H) 1) partite

Dense H free graphs are almost (Χ(H) 1) partite

... s vertices. Given a graph H, whose chromatic number is χ(H), we examine all the proper χ(H)-colourings of H. We choose one whose smallest colour class is of smallest possible size; then ...

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DNA polymerase requirements for parvovirus H-1 DNA replication in vitro.

DNA polymerase requirements for parvovirus H-1 DNA replication in vitro.

... We have recently demonstrated the ability of purified polymerase -y to carry out the synthesis in vitro of RF from single-stranded viral DNA 1Sa, a reaction quite similar or identical to[r] ...

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Replication process of the parvovirus H-1 V. Isolation and characterization of temperature-sensitive H-1 mutants.

Replication process of the parvovirus H-1 V. Isolation and characterization of temperature-sensitive H-1 mutants.

... Synthesis of the viral DNA strand was shown to be diminished for both wild-type virus and these mutants at the restrictive temperature of 39.5 C, but the mutants were more defective than[r] ...

9

Replication Process of the Parvovirus H-1 III. Factors Affecting H-1 RF DNA Synthesis

Replication Process of the Parvovirus H-1 III. Factors Affecting H-1 RF DNA Synthesis

... Inhibition of RF DNA synthesis by cycloheximide, a-amanitin, and actinomycin D added before HA-DNA synthesisa Drug Time Method of RF added h PI extrac- DNA tion Cycloheximide a-Amanitin [r] ...

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Replication Process of the Parvovirus H-1 II. Isolation and Characterization of H-1 Replicative Form DNA

Replication Process of the Parvovirus H-1 II. Isolation and Characterization of H-1 Replicative Form DNA

... If virion populations do contain a minor portion with DNA complementary to the major species, a direct demonstration of this would be possible by separation of the viral strand from its [r] ...

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Replication process of the parvovirus H-1. VI. Characterization of a replication terminus of H-1 replicative-form DNA.

Replication process of the parvovirus H-1. VI. Characterization of a replication terminus of H-1 replicative-form DNA.

... If the covalent linkage of V to C strand in monomer RF DNA was involved in the initiation of replication of RF DNA or progeny DNA synthesis, then rapidly labeled molecules would be enric[r] ...

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Defective interfering particles of parvovirus H-1.

Defective interfering particles of parvovirus H-1.

... The variations in size due to the variable number of additions and deletions in the right half of the molecule caused the HindIII 51/100 fragments of the DI-wt and DI-wt-tsl4 preparation[r] ...

10

Differential impact of prostaglandin H synthase 1 knockdown on platelets and parturition

Differential impact of prostaglandin H synthase 1 knockdown on platelets and parturition

... primer 1 (5′-TCTGGAGATCGT- GACAAGAATCTG-3′), primer 2 (5′-TCTAACTCCACTGTCCAACGTCTG- 3′), and primer 1 in Neo cassette (5′-ATCGCCTTCTTGACGAGTTTC-3′) were used for PCR ...

11

1 (4 Methyl­phenyl­sulfon­yl) 1H 1,2,3 benzotriazole: sheets built from C—H⋯N, C—H⋯O and C—H⋯π(arene) hydrogen bonds

1 (4 Methyl­phenyl­sulfon­yl) 1H 1,2,3 benzotriazole: sheets built from C—H⋯N, C—H⋯O and C—H⋯π(arene) hydrogen bonds

... combination of these two motifs then generates a chain of edge-fused rings running parallel to the [111] direction with the rings built from C—H N hydrogen bonds centred at (n + 0.5, n + 0.5, n + 0.5) (n = zero or ...

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(E) 1 Mercapto 1 (p tolyl­sulfan­yl) N (p tosyl­meth­yl) methanimine: a two dimensional supramolecular network of S—H⋯O and C—H⋯π inter­actions

(E) 1 Mercapto 1 (p tolyl­sulfan­yl) N (p tosyl­meth­yl) methanimine: a two dimensional supramolecular network of S—H⋯O and C—H⋯π inter­actions

... The S—Csp 2 bond lengths agree with the normal S—Csp 2 bond length (1.75 A ˚ ; Allen et al., 1987). Other S—C, S—O and S O bond lengths are comparable to those found in related structures which contain p-toluenesulfonyl ...

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Virtual reconstruction of cranial remains : the H. Heidelbergensis, Kabwe 1 fossil

Virtual reconstruction of cranial remains : the H. Heidelbergensis, Kabwe 1 fossil

... In fact, in a study that examines the impact of different reconstruction 95 approaches and of exclusion of incomplete specimens on morphological analysis, 96 Arbour and Brown 2014 show t[r] ...

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1.LYAPUNOV FUNCTIONS FOR H-DICHOTOMY OF LINEAR DISCRETE-TIME SYSTEMS

1.LYAPUNOV FUNCTIONS FOR H-DICHOTOMY OF LINEAR DISCRETE-TIME SYSTEMS

... for h-dichotomy in terms of Lyapunov functions is Corollary 5.2. Let h be a growth rate which satisfies the hypothesis (H ...is h-dichotomic then there exists a k-Lyapunov function L for (A, P ...

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