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  • Chemistry  (56)
  • Coloanal anastomosis  (2)
  • [abr] PI-PLC; Phosphatidylinositol specific phospholipase C  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 155 (1988), S. 794-800 
    ISSN: 0006-291X
    Keywords: [abr] CEA; carcinoembryonic antigen ; [abr] CRD; cross-reacting determinant ; [abr] G-PI; glyco-phosphatidylinositol ; [abr] NCA; normal cross-reacting antigen ; [abr] PBS; phosphate buffered saline ; [abr] PI-PLC; Phosphatidylinositol specific phospholipase C
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 155 (1988), S. 794-800 
    ISSN: 0006-291X
    Keywords: [abr] CEA; carcinoembryonic antigen ; [abr] CRD; cross-reacting determinant ; [abr] G-PI; glyco-phosphatidylinositol ; [abr] NCA; normal cross-reacting antigen ; [abr] PBS; phosphate buffered saline ; [abr] PI-PLC; Phosphatidylinositol specific phospholipase C
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1530-0358
    Keywords: Low anterior resection ; Colorectal surgery ; Coloanal anastomosis ; Coloanal reservoir ; Anorectal function ; Incontinence ; Rectal cancer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract AIM: This study was designed to analyze the functional and clinical outcomes of straight coloanal anastomosis compared with colonic J-pouch performed after low anterior resection. MATERIALS AND METHODS: Between September 1989 and June 1996, all patients who underwent low anterior resection with anastomosis less than 4 cm from the dentate line were classified into two groups based on the restoration of intestinal continuity: “straight” coloanal anastomosis (n=39) or colonic J-pouch (n=44). Both groups were assessed according to the level of anastomosis, anastomotic complications (stricture, leak, pelvic abscess), age, and gender. For comparison of functional outcome, daily bowel movements, tenesmus, urgency, incontinence score (range, 0–20), and anorectal manometric findings were evaluated preoperatively and at six months, and one and two years after surgery. RESULTS: There were no significant differences between the groups relative to age: (coloanal anastomosis, 66.3±10.1 (range, 46–86),vs. colonic J-pouch, 64.9±13.2 (range, 39–88) years); gender (females): (coloanal anastomosis, 46.2 percentvs. colonic J-pouch; 38.6 percent); diagnosis: (rectal carcinoma: coloanal anastomosis, 84.6 percent,vs. colonic J-pouch, 77.3 percent); preoperative incontinence score (coloanal anastomosis, 1.5±4.6,vs. colonic J-pouch, 1.1±4); bowel movements: (coloanal anastomosis, 2.1±2.3,vs. colonic J-pouch, 2.1±1.9/day); level of anastomosis: (coloanal anastomosis, 1.8±1.3,vs. colonic J-pouch, 1.5±1.3 cm from the dentate line); history of perioperative radiation therapy: (coloanal anastomosis, 15.4 percent,vs. colonic J-pouch, 20.5 percent); or manometric findings. There was also no significant difference in postoperative mortality: (coloanal anastomosis, 5.1 percent,vs. colonic J-pouch, 2.3 percent); or anastomotic complications: (coloanal anastomosis, 7/39 (17.9 percent),vs. colonic J-pouch, 2/44 (4.5 percent)P=0.08); strictures: (10.3vs. 0 percent); leaks: (5.1vs. 2.3 percent); bleeding: (2.6vs. 0 percent); rectovaginal fistula: (0vs. 2.3 percent). Also, in the colonic J-pouch group, two patients developed pouchitis, and one patient experienced difficult evacuation one year after surgery. There was a statistically significant better function judged by less frequent bowel movements (4±2vs. 2.4±1.3/day;P〈0.005) and urgency (36.7vs. 7.7 percent;P〈0.05), incontinence score (2.2±3.7vs. 0.8±1.6;P〈0.05) up to one year after surgery. At two years, the coloanal anastomosis group did not show statistical improvement in functional results compared with one year postoperatively. Rectal compliance in manometric findings was significantly increased in the coloanal anastomosis group at one year after surgery (12.4±12.6vs. 4.2±1.5 ml/mmHg;P〈0.05). However, these differences were less profound after two years. CONCLUSION: The functional superiority of the colonic J-pouch was greatest at one year after surgery. By two years, adaptation of the “straight” coloanal anastomosis yielded similar functional results. However, the almost fourfold reduction in anastomotic complications in the colonic J-pouch group reveals a second potential advantage of this technique.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Diseases of the colon & rectum 35 (1992), S. 843-846 
    ISSN: 1530-0358
    Keywords: Rectal cancer ; Colon and rectal surgery ; Coloanal anastomosis ; Colonic reservoir
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Functional results in 33 patients who underwent a coloanal anastomosis with reservoir were prospectively evaluated three months after colostomy closure and later (16.2±5.7 months) and were compared with those of 36 healthy controls. We were unable to demonstrate any significant difference between patients and controls concerning frequency of stools, feeling of the need to defecate, continence of stools and flatus, differentiation between flatus and feces, urgency, and need to wear a protective pad. There was a statistically significant difference concerning the ability to evacuate, which was better in the control group (score=1.03) than in the patients (score=1.63) (P 〈0.001). These results suggest that coloanal anastomosis with reservoir provides nearly normal function except for the ability to evacuate.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 3150-3161 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Temperaturabhängigkeit der NMR-Spektren von C10H12 (Tricyclo-[3.3.2.04.6]decadien-(2.7)) und seinen Derivaten sowie von C10H10 (Bullvalen) wird auf Grund einer schnellen und reversiblen Valenzisomerisierung analysiert. Das entscheidende Strukturelement der beschriebenen Verbindungen ist Bicyclo[5.1.0]octadien-(2.5), auch Homotropiliden genannt.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 98 (1965), S. 3385-3400 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Bromierung von Bullvalen ergibt ein Dibromid, das durch Eliminierung von HBr zu Brombullvalen führt. Aus letzterem entstehen mit Kaliumalkoholaten in Dimethylsulfoxyd in sehr guten Ausbeuten Alkoxybullvalene.  -  Die monosubstituierten Bullvalene unterliegen prinzipiell denselben Valenzisomerisierungen wie das Bullvalen: Keine zwei Kohlenstoffatome bleiben längere Zeit aneinander gebunden. Hier haben aber nicht alle Valenzisomeren (1.2·106) dieselbe Struktur; sie sind in vier Positionsisomere aufgeteilt. Demzufolge gibt es auch sieben Isomerisierungsgeschwindigkeiten.  -  Das Studium der temperaturabhängigen NMR-Spektren der genannten Bullvalenderivate zeigt, daß die Isomeren mit dem Substituenten in olefinischer Position bevorzugt sind. Man kann aus den Spektren Informationen über die relative Größe der Geschwindigkeitskonstanten erhalten.  -  Das unterschiedliche Verhalten der einzelnen Derivate wird durch den Hybridisierungszustand des substituierten C-Atoms und durch die Konjugationsmöglichkeit des Substituenten mit dem Bullvalylsystem erklärt.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 3527-3537 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Brombullvalen (1) bildet in Gegenwart von Kalium-tert.-butylat mit reaktiven Dienen die anellierten Bullvalene 4, 5 und 6.  -  Zum anderen entsteht aus dem Bromid 9 und Kaliumtert.-butylat ein Gemisch der Äther 11 und 13. In Gegenwart von 1.3-Diphenyl-isobenzofuran führt diese Reaktion zu dem Addukt 19 (einem anellierten Homotropiliden-Derivat). - Die Existenz von Kurzfristig auftretendem 3.4-Dehydro-bullvalen (2) und von einem überbrückten Dehydrohomotropiliden-Derivat 12 wird aus diesen experimentellen Befunden hergeleitet.  -  Die Strukturbeweise für die anellierten Bullvalene 4, 5 und 6 gründen sich u. a. auf die temperaturabhängigen NMR-Spektren. Aus diesen Spektren folgt eindeutig, daß den Addukten aus Dehydrobullvalen und Furanen nicht die aus den Diels-Alder-Reaktionen primär zu erwartenden Strukturen 4a und 5a zukommen. Die bei Raumtemperatur im Bullvalen-Skelett leicht ablaufenden Bindungsverschiebungen wandeln die Moleküle in die Strukturen mit der geringsten Energie um, nämlich in 4b sowie 5b und 5c. Für 19 gelten analoge Überlegungen.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 102 (1969), S. 3367-3377 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der UV-Bestrahlung von 9-Fluor-10-chlor-cis-bicyclo[6.2.0]decatetraen-(2.4.6.9) (2) entstehen u. a. zwei Fluor-chlor-bicyclo[4.2.2]decatetraene (3 und 4), die bei erneuter Photolyse Fluor-chlor-bullvalen (21) bilden.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der Bestrahlung von syn-Tricyclo[6.4.0.09.12]dodecatetraen-(2.4.6.10) (1) mit einer Nieder-druck-UV-Lampe bei ca. -30° entstehen cis- und trans-Bicyclo[6.4.0]dodecapentaen-(2.4.6.9.11) (2 bzw. 3). 2 isomerisiert sich bei ca. 20° zum dimeren Benzol 4.  -  Zwischen 2 und 3 scheint ein photochemisches Gleichgewicht zu bestehen. Bei längeren Einstrahlungszeiten bildet sich aus 2 und/oder 3 1-Phenyl-hexatrien-(1.3.5) (5).  -  Die Deutung dieser Befunde fußt auf den Woodward-Hoffmann-Regeln für elektrocyclische und sigmatrope Reaktionen. Der Bildungsmechanismus von 2 und 3 schließt mit größter Wahrscheinlichkeit [12]Annulene ein, deren gemeinsames Merkmal eine ausgeprägte Thermolabilität sein muß.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 1798-1809 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Asteranes, VII. Studies on the Bicyclo[3.1.1]heptane SystemBicyclo[3.1.1]heptan-3-one (10) and other norpinane derivatives are obtained from bicyclo-[3.1.1]heptan-2-one (3). The decomposition of the tosylhydrazone 7 from 3 under varied basic conditions yields different ratios of norbornene (19), tricyclene (20), tricyclo[3.2.0.02.7]-heptane (23) and 2-norpinene (8). The tosylhydrazone 9 from 10 yields 8 exclusively. The photolysis of 3-diazonorpinan-2-one (27) leads only to the ketene dimer 30, which is formed by Wolff rearrangement of the carbene intermediate. The free energy barrier of interconversion in norpinane (1) must be much smaller than that in cyclohexane. The barrier in 3.3-difluoronorpinane (32) is estimated to be of the order of 4 kcal/Mol.
    Notes: Aus Norpinanon-(2) (3) werden Norpinaon-(3) (10) und weitere Norpinanderivate hergestellt. Die alkalische Zersetzung des Tosylhydrazons 7 von 3 liefert unter verschiedenen Bedingungen wechselnde Mengen an Norbornen (19), Tricyclen (20), Tricyclo[3.2.0.02.7]heptan (23) und Norpinen (8); die des Tosylhydrazons 9 von 10 ausschließlich 8. Die Photolyse von 3-Diazo-norpinanon-(2) (27) ergibt als Hauptprodukt das unter Wolff-Umlagerung gebildete Keten-Dimere 30. Die freie Energieschwelle beim Umklappen im Norpinan (1) muß viel tiefer liegen als beim Cyclohexan, die des 3.3-Difluor-norpinans (32) muß ungefähr 4 kcal/Mol sein.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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