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1N. Rhind ; Z. Chen ; M. Yassour ; D. A. Thompson ; B. J. Haas ; N. Habib ; I. Wapinski ; S. Roy ; M. F. Lin ; D. I. Heiman ; S. K. Young ; K. Furuya ; Y. Guo ; A. Pidoux ; H. M. Chen ; B. Robbertse ; J. M. Goldberg ; K. Aoki ; E. H. Bayne ; A. M. Berlin ; C. A. Desjardins ; E. Dobbs ; L. Dukaj ; L. Fan ; M. G. FitzGerald ; C. French ; S. Gujja ; K. Hansen ; D. Keifenheim ; J. Z. Levin ; R. A. Mosher ; C. A. Muller ; J. Pfiffner ; M. Priest ; C. Russ ; A. Smialowska ; P. Swoboda ; S. M. Sykes ; M. Vaughn ; S. Vengrova ; R. Yoder ; Q. Zeng ; R. Allshire ; D. Baulcombe ; B. W. Birren ; W. Brown ; K. Ekwall ; M. Kellis ; J. Leatherwood ; H. Levin ; H. Margalit ; R. Martienssen ; C. A. Nieduszynski ; J. W. Spatafora ; N. Friedman ; J. Z. Dalgaard ; P. Baumann ; H. Niki ; A. Regev ; C. Nusbaum
American Association for the Advancement of Science (AAAS)
Published 2011Staff ViewPublication Date: 2011-04-23Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Centromere/genetics/physiology/ultrastructure ; DNA Transposable Elements ; Evolution, Molecular ; Gene Expression Profiling ; Gene Expression Regulation, Fungal ; Genes, Mating Type, Fungal ; *Genome, Fungal ; Genomics ; Glucose/metabolism ; Meiosis ; Molecular Sequence Annotation ; Molecular Sequence Data ; Phylogeny ; RNA, Antisense/genetics ; RNA, Fungal/genetics ; RNA, Small Interfering/genetics ; RNA, Untranslated/genetics ; Regulatory Elements, Transcriptional ; Schizosaccharomyces/*genetics/growth & development/metabolism ; Schizosaccharomyces pombe Proteins/genetics/metabolism ; Sequence Analysis, DNA ; Species Specificity ; Transcription Factors/genetics/metabolism ; Transcription, GeneticPublished by: -
2C. T. Amemiya ; J. Alfoldi ; A. P. Lee ; S. Fan ; H. Philippe ; I. Maccallum ; I. Braasch ; T. Manousaki ; I. Schneider ; N. Rohner ; C. Organ ; D. Chalopin ; J. J. Smith ; M. Robinson ; R. A. Dorrington ; M. Gerdol ; B. Aken ; M. A. Biscotti ; M. Barucca ; D. Baurain ; A. M. Berlin ; G. L. Blatch ; F. Buonocore ; T. Burmester ; M. S. Campbell ; A. Canapa ; J. P. Cannon ; A. Christoffels ; G. De Moro ; A. L. Edkins ; L. Fan ; A. M. Fausto ; N. Feiner ; M. Forconi ; J. Gamieldien ; S. Gnerre ; A. Gnirke ; J. V. Goldstone ; W. Haerty ; M. E. Hahn ; U. Hesse ; S. Hoffmann ; J. Johnson ; S. I. Karchner ; S. Kuraku ; M. Lara ; J. Z. Levin ; G. W. Litman ; E. Mauceli ; T. Miyake ; M. G. Mueller ; D. R. Nelson ; A. Nitsche ; E. Olmo ; T. Ota ; A. Pallavicini ; S. Panji ; B. Picone ; C. P. Ponting ; S. J. Prohaska ; D. Przybylski ; N. R. Saha ; V. Ravi ; F. J. Ribeiro ; T. Sauka-Spengler ; G. Scapigliati ; S. M. Searle ; T. Sharpe ; O. Simakov ; P. F. Stadler ; J. J. Stegeman ; K. Sumiyama ; D. Tabbaa ; H. Tafer ; J. Turner-Maier ; P. van Heusden ; S. White ; L. Williams ; M. Yandell ; H. Brinkmann ; J. N. Volff ; C. J. Tabin ; N. Shubin ; M. Schartl ; D. B. Jaffe ; J. H. Postlethwait ; B. Venkatesh ; F. Di Palma ; E. S. Lander ; A. Meyer ; K. Lindblad-Toh
Nature Publishing Group (NPG)
Published 2013Staff ViewPublication Date: 2013-04-20Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Animals, Genetically Modified ; *Biological Evolution ; Chick Embryo ; Conserved Sequence/genetics ; Enhancer Elements, Genetic/genetics ; Evolution, Molecular ; Extremities/anatomy & histology/growth & development ; Fishes/anatomy & histology/*classification/*genetics/physiology ; Genes, Homeobox/genetics ; Genome/*genetics ; Genomics ; Immunoglobulin M/genetics ; Mice ; Molecular Sequence Annotation ; Molecular Sequence Data ; Phylogeny ; Sequence Alignment ; Sequence Analysis, DNA ; Vertebrates/anatomy & histology/genetics/physiologyPublished by: -
3Staff View
ISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Summary 1. The first members of a previously unknown class of titanium-containing organic compounds were prepared; chloroethoxy-, chloropropoxy-, and butoxychloro-titanium oxides. 2. By the action of chlorine on diproproxy- and diisobutoxy-titanium oxides, compounds of the following compositions were obtained: Cl2TiO · 2n-C3H7OH and Cl2TiO · 2i-C4H9OH. 3. By the reaction of dialkyldichlorosilanes with dialkoxytitanium oxides, doubly bound oxygen is replaced by two chlorine atoms: $$\left( {n - C_3 H_7 O} \right)_2 TIO + Cl_2 SiR_2 \to \left( {n - C_3 H_7 O} \right)_2 TiCl + \left[ {OSiR_2 } \right]_x $$ An analogous reaction occurs when tetrapropoxysilane acts on the compound Cl2TiO · 2n-C3H7OH $$\begin{gathered} Cl_2 TiO \cdot 2n - C_3 H_7 OH + \left( {C_3 H_7 O} \right)_4 Si. \to Cl_2 Ti\left( {OC_3 H_7 } \right)_2 \cdot n - C_3 H_7 OH + \hfill \\ + n - C_3 H_7 OH + \left[ {OSi\left( {OC_3 H_7 - n} \right)_2 } \right]_x \hfill \\ \end{gathered} $$ 4. The addition of dimethyldipropoxysilane to dipropoxytitanium oxide gives substances of structure:Type of Medium: Electronic ResourceURL: -
4Nesmeyanov, A. N. ; Nogina, O. V. ; Berlin, A. M. ; Girshovich, A. S. ; Shatalov, G. V.
Springer
Published 1961Staff ViewISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Summary 1. The following dicyclopentadienyl titanium derivatives containing acyl groups we're synthesized: 2. It was shown to be'possible to prepare monoalkoxy- and mono(aryloxy)-dicyclopentadienyltitanlum derivatives by the action of alcohols and phenols on (C5H5)2TiCl2 in presence of a tertiary amine. 3. By the action of C5H5Na on (CH3)3SiOTiCl3 we obtained (C5H5)2Ti · [OSi(CH3)3]Cl and C5H5Ti[OSi(CH3)3]3. 4. The refraction increment of the titanium-cyclopentadienyl ring group (Including the atomic refraction of titanium) was determined and found to be 35.28.Type of Medium: Electronic ResourceURL: -
5Staff View
ISSN: 1573-8353Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract The reaction of di(4-acetoacetylphenyl) oxide (I) with β-napthylamine, aniline, 4-aminobiphenyl, and 4-aminodiphenylamine has given the corresponding dianils, and the conditions for their cyclization have been studied. It has been shown that the dianil of I and βnapthylamine cyclizes under the action of HF into the linear di(benzoquinoline) compound and in the presence of β-naphthylamine hydrochloride into the angular di(benzoquinoline) compound; the other dianils do not cyclize under these conditions.Type of Medium: Electronic ResourceURL: -
6Staff View
ISSN: 1573-8353Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract A number of previously undescribed bis(1′,8′-naphthoylene-1,2-benzimidazoles) were obtained by reaction of bis(o-phenylenediamines) with various structures with naphthalic anhydride. Under the same conditions, the reaction of o-phenylenediamine with naphthalene-1,4,5,8-tetracarboxylic acid dianhydride leads to a mixture of cis and trans isomers of bisbenzimidazobenzophenanthrolinedione. The spectral and thermal characteristics of the synthesized compounds were studied.Type of Medium: Electronic ResourceURL: -
7Staff View
ISSN: 1573-8353Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract Heating equimolecular amounts of 1, 1, 2, 2, -tetraacetylethane, 1, 1, 3, 3-tetraacetylpropane, 4, 4′-bis(acetoacetyl)diphenyloxide, by and 1, 4-bis(2′, 2′-diacetoethyl)benzene with 4, 4′-dihydrazino-diphenyl gives new thermostable polymers. Some of their characteristics are reported.Type of Medium: Electronic ResourceURL: -
8Staff View
ISSN: 1573-8353Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract The reaction of bis(naphthalic anhydrides) with aniline and o-phenylenediamine under conditions of hightemperature cyclocondensation in m-cresol in the presence of a catalyst (benzoic acid) gives bis(1,8-naphthylimides) and bis(1′,8′-naphthoylene-1,2-benzimidazoles) which model the elementary units of polyimides and polynaphthoylenebenzimidazoles, respectively.Type of Medium: Electronic ResourceURL: -
9Korshak, V. V. ; Kosobutskii, V. A. ; Bolduzev, A. I. ; Rusanov, A. L. ; Belyakov, V. K. ; Dorofeeva, I. B. ; Berlin, A. M. ; Adyrkhaeva, F. I.
Springer
Published 1980Staff ViewISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Conclusions 1. Values of electron affinity appear to be calculational criteria of the reactivities of anhydrides of tetracarboxylic acids in the same homologous series. 2. Differences in the reactivities of phthalic and naphthalic anhydrides are determined by the strength of the anhydride ring. 3. The most electrophilic reaction center is determined by the largest value of positive charge on the carbon atom of the carbonyl group.Type of Medium: Electronic ResourceURL: -
10Berlin, A. M. ; Kofman, N. M. ; Krongauz, E. S. ; Novikov, A. N. ; Gol'ding, I. R.
Springer
Published 1975Staff ViewISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Conclusions The reaction of aromatic diiodides with copper phenylacetylide gave a number of new bis-ethynyl compounds.Type of Medium: Electronic ResourceURL: -
11Staff View
ISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Summary 1. An investigation was made of the polycondensation of N,N,N′,N′-tetraethyl-P-methylphosphonic diamide with the diamines 1,6-hexanediamine, ethylenediamine, and m- and p-phenylenediamines (transamidation). 2. It was shown to be possible in principle to prepare polymers with the aid of the transamidation reaction. 3. The polycondensation of N,N,N′,N′-tetraethyl-P-methylphosphonic diamide with P-phenylphosphonic diamide is accompanied by the side reaction of self-condensation of P-phenylphosphonic diamide.Type of Medium: Electronic ResourceURL: -
12Staff View
ISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Summary 1. By the reaction of cyclopentadienylsodium with (C2H5O)2 TiCl2 and (C3H7O)3 TiCl, C5H5Ti(OC2H5)3 and C5H5Ti(OC3H7)3; were obtained. Some of their properties were studied. 2. Mixed chlorides-alkoxides of π-cyclopentadienyltitanium were prepared: (C5H5)2Ti(OC2H5)Cl, C5H5Ti-(OC3H7(CL2 and C5H5Ti(OC3H7)2Cl.Type of Medium: Electronic ResourceURL: -
13Korshak, V. V. ; Krongauz, E. S. ; Berlin, A. M. ; Gribkova, P. N. ; Sheina, V. E.
Springer
Published 1964Staff ViewISSN: 1573-9171Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Summary 1. The polycyclization reaction was studied for the case of the reaction of bis-β -diketones with dihydrazides of dicarboxylic acids, which leads to polymers with pyrazole rings in the chain. 2. Polycyclization goes in two stages: in the first polyhydrazones are formed, and in the second these are converted into polypyrazoles. 3. Polyhydrazones and polypyrazoles obtained from adipic dihydrazide and the following bis-β-diketones were prepared and investigated: 1,1′-(oxydi-p-phenylene)di-1,3-butanedione,1,1′-(ethylenedi-p-phenylene)di-1,3-butanedione, and 1,14-diphenyl-1,3,12,14-tetradecanetetrone.Type of Medium: Electronic ResourceURL: -
14Korshak, V. V. ; Bulycheva, E. G. ; Shifrina, Z. B. ; Berlin, A. M. ; Shalikiani, M. O. ; Butskhrikidze, B. A. ; Rusanov, A. L. ; Mironov, G. S. ; Moskvichev, Yu. A. ; Timoshenko, G. N. ; Titov, V. I. ; Jedliński, Z. ; Palivoda, A.
Weinheim : Wiley-Blackwell
Published 1988Staff ViewISSN: 0323-7648Keywords: Chemistry ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyPhysicsDescription / Table of Contents: Eine Reihe neuer Bis(naphthalincarbonsäureanhydride) wurden durch Umsatz von Acenaphthen mit Dichloranhydriden von Dicarbonsäuren unter den Bedingungen einer Friedel-Crafts-Reaktion mit Chloral bzw. Bromal und nachfolgender Oxidation der Bis(acenaphthyle) und Anhydridisierung der Tetracarbonsäuren synthetisiert. Aus diesen Anhydriden und Bis(o-phenylendiaminen) erhaltene Poly(naphthoylen-benzoimidazole) vereinen gute thermische Eigenschaften mit Löslichkeit in organischen Lösungsmitteln.Notes: A series of novel bis(naphthalic anhydrides) has been prepared through acenapthene interaction with the dichloroanhydrides of dicarboxylic acids under the conditions of the Friedel-Crafts reaction or with chloral and bromal followed by oxidation of bis-acenaphthyls and anhydrization of the tetracarboxylic acids synthesized. Poly(naphthoylene benzoimidazoles) combining advantageous thermal properties and solubility in organic solvents have been obtained through interaction between the synthesized anhydrides and bis(o-phenylene diamines).Additional Material: 3 Tab.Type of Medium: Electronic ResourceURL: -
15Staff View
ISSN: 0449-2951Keywords: Chemistry ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyPhysicsNotes: By the interaction of linear or branched bis(β-diketones) and dihydrazides of dicarboxylic acids or dihydrazines unknown high molecular compounds with pyrazole rings in the chain have been prepared. Polypyrazoles of the second type (with a free NH-group in the pyrazole ring) were prepared by the interaction of bisdiazoalkanes and diacetylenes. Some features of the polycyclization reaction as well as the structure and properties of polymers obtained are discussed.Additional Material: 6 Tab.Type of Medium: Electronic ResourceURL: