16,531 research outputs found
Schulz, C, NX69139
This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/415734Surname: SCHULZ. Given Name(s) or Initials: C. Military Service Number or Last Known Location: NX69139. Missing, Wounded and Prisoner of War Enquiry Card Index Number: 38244.236380
Item: [2016.0049.47995] "Schulz, C, NX69139
Tau protein, A beta 42 and S-100B protein in cerebrospinal fluid of patients with dementia with Lewy bodies
The intra vitam diagnosis of dementia with Lewy bodies (DLB) is still based on clinical grounds. So far no technical investigations have been available to support this diagnosis. As for tau protein and beta-amyloid((1-42)) (Abeta42), promising results for the diagnosis of Alzheimer's disease ( AD) have been reported; we evaluated these markers and S-100B protein in cerebrospinal fluid (CSF), using a set of commercially available assays, of 71 patients with DLB, 67 patients with AD and 41 nondemented controls (NDC) for their differential diagnostic relevance. Patients with DLB showed significantly lower tau protein values compared to AD but with a high overlap of values. More prominent differences were observed in the comparison of DLB patients with all three clinical core features and AD patients. Abeta42 levels were decreased in the DLB and AD groups versus NDC, without significant subgroup differences. S-100B levels were not significantly different between the groups. Tau protein levels in CSF may contribute to the clinical distinction between DLB and AD, but the value of the markers is still limited especially due to mixed pathology. We conclude that more specific markers have to be established for the differentiation of these diseases. Copyright (C) 2005 S. Karger AG, Basel
Religions-Proceß des Prediger Schulz zu Gielsdorf [et]c. nebst dessen eigenen, gerichtlich übergebenen Vertheidigungs-Schrift seiner Lehren
Autopsie nach dem Ex. der ULB Sachsen-AnhaltVorlage des Erscheinungsvermerks: 1792. - Angabe des Erscheinungsortes und Verlages nach GValt, Bd.116, S.18
Tetramorium rhodium S., Radchenko & Schulz, 2007, Status revised
7. Tetramorium rhodium Emery, 1922 Status revised (figs 50-53) Tetramorium caespitum var. rhodia Emery, 1922: 277; first available use of Tetramorium caespitum ssp. caespitum var. rhodia Emery, 1915: 3 ([[worker]]); TYPE MATERIAL: SYNTYPE [[workers]], “ Rodes ” [GREECE] [/] “ Kattabea ” [-] “ Tetr. caesp.” [/] “ var. rhodia Emery ” (2[[workers]] / MHNG, 2[[workers]] MSNG); Tetramorium caespitum rhodia: Emery 1925: 179; Raised to species rank hereby. Redescription of worker (figs 50-53.). Medium to large size, CS 832 [720, 895]. Whole body and appendages black. Head square, CL/CW 0.99 [0.98, 1.02], with somewhat convex sides, slightly concave occipital margin and rounded occipital corners. Eyes small, EYE 0.173 [0.163, 0.184]. Frons moderately wide, FR/CS 0.38 [0.36, 0.40], frontal lobe as wide as frons, FL/FR 1.0 [1.00, 1.02]. Scape short, SL/CS 0.73 [0.71, 0.75], with short dorsal carina basally, well visible parallel costulae extending scape. Promesonotal dorsum convex, metanotal groove shallow, but distinct. Propodeal teeth moderately long. Petiolar node cubic in profile, NOH/ NOL 0.84 [0.76, 0.97], petiole relatively low, PEH/NOL 1.50 [1.38, 1.73]. General appearance coarsely rugose, ground surface coarsely microreticulate, dull. Head dorsum and occiput longitudinally rugose and coarsely microreticulate, its sides rugoso-reticulate and microreticulate. Alitrunk dorsum rugoso-reticulate and coarsely microreticulate, mesopleuron coarsely microreticulate. Dorsum of petiolar node rugoso-reticulate and microreticulate, dorsum of postpetiole longitudinally rugulose and microreticulate. Polygonal striation continuous on 1st gastral tergite, posteriorly disrupted. Basal part of first gastral tergite microreticulate (see fig. 7.), MRG 319.7 ±126.5 [50, 500]. Ventral surface of head with several short and moderately long, straight, or few C-shape setae arising posteriorly to buccal cavity (see fig. 5.). Gynes and Males are unknown. Material examined (3 nest series including 18 workers). CYPRUS - Platres 1km E Mandria, 900mH, Prov. Limassol, 30.03.1994. nr.13. leg. Sanetra (3[[workers]]); TURKEY - Denizli, Yahsiler, 35 km SEE Karacasu, 30 km SW Denizli 800 mH Kiefernwald, 20.05.93. nr.886, leg Schulz (6[[workers]] / HNHM); Izmir, 10km SE. Beydag, 50km NE. Aydin, 600mH, Bachlauf, Bewaldet, 20.05.1993. nr. 879, leg. Schulz (1[[worker]] / MHNG, 8[[workers]] HNHM). Morphometerics: (22 workers were metrically investigated). Diagnosis. Workers of T. rhodium differ from related species by the lack of psammophore, relatively small eyes, (EYE, Table 1.), very short and very feebly costulate scape (SL/CS, Table 1.), cubic petiolar node and moderately wide frons (FR/CS, Table 1.). Workers of T. rhodium mostly resemble those of, T. syriacum, T. sanetrai n. sp. and T. chefketi. Workers of T. rhodium well differ from those of T. syriacum by their narrower frons, FR/CS (Table 1.), from those of T. chefketi by their shorter scape SL/CS (Table 1.). Tetramorium rhodium and T. sanetrai n. sp. are very similar in both, general appearance and metric characters. For separation between T. rhodium and T. sanetrai n. sp. see differential diagnosis of T. sanetrai n. sp. below. For further combination of morphometric characters see Table 1-2. Distribution. This species seems to be widespread over Asia Minor, Rhodes and Cyprus.Published as part of Csösz S., Radchenko, A. & Schulz, A., 2007, Taxonomic revision of the Palaearctic Tetramorium chefketi species complex (Hymenoptera: Formicidae)., pp. 1-38 in Zootaxa 1405 on pages 27-2
Tetramorium anatolicum S., Radchenko & Schulz, 2007, New species
2. Tetramorium anatolicum Csösz & Schulz, New species (figs 18-24) Description of Worker (figs 21-24). Morphometric data of holotype worker: CL: 720; CW: 695; FR: 245; FL: 265; SL: 550; ML: 770; MW: 430; PEW: 200; PEH: 240; NOH: 140; NOL: 115; PEL: 155; PPW: 250; PPL: 155; PPH: 220; SPL: 80; SPSP: 140; EL: 145; EH: 100; ED: 190; Small size, CS 702 [635, 743]. Whole body and appendages light brown to brown. Head slightly longer than broad, CL/CW 1.02 [0.99, 1.05], with very feebly convex or straight sides and occipital margin, and rounded occipital corners. Eyes small, EYE 0.176 [0.167, 0.182]. Frons moderately narrow, FR/CS 0.37 [0.35, 0.39], frontal lobes usually wider, FL/FR 1.02 [1.0, 1.08]. Scape moderately long, SL/CS 0.78 [0.76, 0.81], without longitudinal dorsal carina basally, smooth and shiny. Promesonotal dorsum convex, metanotal groove shallow, but visible. Propodeal teeth moderately long, thin and acute. Petiolar node trapezoidal in profile, NOH/NOL 1.15 [1.0, 1.30], petiole relatively high, PEH/NOL 2.01 [1.74, 2.30]. General appearance finely rugose, or rugulose. Head dorsum longitudinally rugulose, ground surface feebly microreticulate, shiny. Alitrunk dorsum longitudinally rugulose and finely microreticulate. Mesopleuron usually feebly rugulose and microreticulate. Dorsum of petiolar node rugulosoreticulate and microreticulate, dorsum of postpetiole feebly rugulose and microreticulate. Polygonal striation usually continuous on 1st gastral tergite, sometimes slightly disrupted posteriorly (see fig. 8.). Ventral surface of head with several short and few moderately long, straight, or few C-shape setae posteriorly to buccal cavity (see fig. 5.). Description of Gyne (figs 18-20). Medium to small size, CS 1012 [980, 1055]. Whole body and appendages dark brown to black. Head wider than long, CL/CW 0.93 [0.90, 0.98], with feebly convex sides, straight occipital margin and rounded occipital corners. Frons moderately narrow, FR/CS 0.37 [0.36, 0.40], frontal lobes as wide as frons, or slightly wider, FL/FR 1.01 [1.0, 1.03]. Scape moderately long, SL/CS 0.75 [0.71, 0.77], without longitudinal dorsal carina basally, smooth and shiny. Head wider than scutum, MW/CS 0.96 [0.92, 1.01]. Propodeal teeth moderately long. Dorsal crest of petiolar node in frontal view straight. Petiolar node dorsum steeply rounded backward. Petiole and postpetiole relatively narrow, WAIST 0.85 [0.83, 0.87]. General appearance rugulose, ground surface microreticulate, dull. Head dorsum, occiput and sides rugosoreticulate, ground surface microreticulate. Frons longitudinally rugulose and microreticulate. Scutum longitudinally rugose, anteriorly smooth, scutellum medially more or less smooth; laterally finely rugulose. Sides of alitrunk ruguloso-reticulate and microreticulate, katepisternum smooth and shiny ventrally. Dorsum of petiolar node and postpetiole reticulate, petiolar node smooth medially. Polygonal striation disrupted on 1st gastral tergite, sometimes continuous basally. Ventral surface of head with several short and few longer, straight or “C”-shape setae, arising posterior to buccal cavity. Description of Male. Whole body and appendages brownish black. ead with convex sides, round occipital margin and widely rounded occipital corners. Scutum wider than head. Propodeal teeth very short, propodeum nearly rounded in profile. Dorsal crest of petiolar node with sharp transversal edge, slightly emarginated in frontal view. Head, alitrunk and waist rugulose, ground surface reticulate to microreticulate, dull. Scutum finely rugulose, antero-laterally smooth and shiny. Scutellum transversally rugulose and microreticulate. Sides of alitrunk finely rugose and microreticulate. Dorsum of petiolar node finely reticulate and microreticulate. Postpetiole shiny, feebly striate. Polygonal striation disrupted on 1st gastral tergite. Material examined: (6 nest series including 52 workers, 3 gynes and 1 male) HOLOTYPE [[worker]]: TURKEY - Erzurum, 5km SW Aydogdu 20km SW Göle, 1400 mH nr.1148 leg. Schulz26.06.1993 (1[[worker]] / HNHM); PARATYPES: TURKEY - Digor 1650 mH13.06.1991 leg. Lˆbl (4[[workers]] / HNHM, 4[[workers]], 1[[queen]] MHNG); Erzurum, 5km SW Aydogdu 20km SW Göle, 1400 mH nr.1148 leg. Schulz26.06.1993 (5[[workers]], 1[[male]] / HNHM, 2[[workers]], 1[[queen]], PCAS); Van, 5km SE Dedeli 30km SE Patnos 1700mH, Hochsteppe20.06.1993. nr.1104. leg. Schulz (3[[workers]] PCAS); Van-5km Van, 5km SE Dedeli 30km SE Patnos 1700mH, Hochsteppe20.06.1993. nr.1102. leg. Schulz (9[[workers]] PCAS, 6[[workers]] SMNK); Van, 5km SE Dedeli, 30km SE Patnos, 1700 mH Hochsteppe nr. 1104 leg. Schulz20.06.1993 (6[[workers]] / HNHM, 3[[workers]] / PCAS); Van, 5km SE Dedeli, 30km SE Patnos, 1700 mH Hochsteppe nr. 1106 leg. Schulz20.06.1993 (3[[workers]], 1[[queen]] / HNHM, 6[[workers]] / PCAS, 3[[workers]] / SMNK). Morphometrics: (38 workers and 3 gynes measured). Diagnosis. Workers of T. anatolicum n. sp. can be separated from related species by the lack of psammophore, relatively small eyes, (EYE, Table 1.), moderately long and smooth scape (SL/CS, Table 1.), without a dorsal carina basally, relatively fine and parallel body sculpture and trapezoidal petiolar node (NOH/NOL and PEH/NOL, Table 1.). Workers of T. anatolicum n. sp. are mostly similar to T. exile n. sp., but differs by its relatively shorter scape and somewhat wider frons (SL/CS and FR/CS, Table 1.). Discriminant D(2a) function proves the separation between T. anatolicum n. sp. and T. exile n. sp. (see differential diagnosis of T.exile n. sp.). Workers of T. anatolicum n. sp. may look similar to those of T. chefketi, but can be distinguished by their lighter colour and shape of petiolar node: in T. anatolicum n. sp. it is relatively high and short, trapezoidal, in profile, while in T. chefketi it is relatively low and longer, cubic in profile, (PEH/NOL and NOH/NOL, Table 1.). Discriminant D(3a) function proves the separation between T. anatolicum n. sp. and T. chefketi (see differential diagnosis of T.exile n. sp.). Gynes of T. anatolicum n. sp. can be distinguished by the lack of psammophore, moderately long, smooth scape (SL/CS, Table 2.), without a dorsal carina basally, wide scutum (MW/CS, Table 2.), relatively narrow petiole and postpetiole (WAIST, Table 2.), and partly smooth katepisternum. For further combination of morphometric characters see Table 1-2. Distribution. It is known only from Turkey. Etymology. This adjective [anatolicum (neutrum)] refers to the known distribution of this species in Anatolian part of Turkey.Published as part of Csösz S., Radchenko, A. & Schulz, A., 2007, Taxonomic revision of the Palaearctic Tetramorium chefketi species complex (Hymenoptera: Formicidae)., pp. 1-38 in Zootaxa 1405 on pages 13-1
Die Sparkassen und die staatliche Sparförderung
Kopper C. Die Sparkassen und die staatliche Sparförderung. In: Schulz G, ed. Die Entstehung der modernen Sparkasse. Sparkassen in der Geschichte / Forschung. Vol 23. Stuttgart: S-Communications Services GmbH; 2022: 165-180
Tetramorium sanetrai S., Radchenko & Schulz, 2007, New species
8. Tetramorium sanetrai Schulz & Csösz New species (figs 54-60) Description of Worker (figs 57-60.). Morphometric data of holotype worker: CL: 720; CW: 695; FR: 245; FL: 265; SL: 550; ML: 770; MW: 430; PEW: 200; PEH: 240; NOH: 140; NOL: 115; PEL: 155; PPW: 250; PPL: 155; PPH: 220; SPL: 80; SPSP: 140; EL: 145; EH: 100; ED: 190; Small to medium size, CS 740 [683, 783]. Whole body and appendages dark brown to black. Head nearly square, CL/CW 1.01 [0.98, 1.04], with very feebly convex sides, straight occipital margin and rounded occipital corners. Eyes small, EYE 0.172 [0.164, 0.185]. Frons moderately narrow, FR/CS 0.37 [0.36, 0.38], frontal lobes as wide as frons, FL/FR 1.0 [1.0, 1.02]. Scape short, SL/CS 0.74 [0.72, 0.75], without, or with very short dorsal carina basally, moderately shiny, or very feebly costulate distally. Pronotum with weakly marked humeri formed by stronger rugae. Promesonotal dorsum slightly convex, metanotal groove rather deep. Propodeal teeth rather long. Petiolar node cubic, robust, with broad, slightly convex node in profile, NOH/NOL 0.89 [0.83, 0.97], petiole relatively low and long, PEH/NOL 1.54 [1.47, 1.63]. General appearance coarsely rugose, ground surface microreticulate, dull. Head dorsum longitudinally rugulose and feebly microreticulate. Alitrunk dorsum rugoso-reticulate and microreticulate. Mesopleuron usually coarsely rugoso-reticulate and microreticulate. Dorsum of petiolar node and dorsum of postpetiole rugoso-reticulate and microreticulate. Polygonal striation continuous on 1st gastral tergite (see fig. 8.). Ventral surface of head with several short and few moderately long, straight, or few C-shape setae arising posterior to buccal cavity (see fig. 5.). Description of Gyne (figs 54-56.). Small size, CS 986 [973, 995]. Whole body and appendages black. Head clearly wider than long, CL/CW 0.89 [0.86, 0.90], with feebly convex sides, straight occipital margin and rounded occipital corners. Frons moderately narrow, FR/CS 0.38 [0.37, 0.38], frontal lobes as wide as frons, FL/FR 1.0 [1.0, 1.0]. Scape very short, SL/CS 0.67 [0.66, 0.68], without dorsal carina basally, moderately smooth and shiny. Head wider than scutum, MW/CS 0.94 [0.94, 0.95]. Propodeal teeth long. Dorsal crest of petiolar node straight in frontal view; node with flattened dorsal plate in profile. Petiole and postpetiole relatively narrow, WAIST 0.98 [0.97, 0.99]. General appearance coarsely rugose, ground surface microreticulate, dull. Head dorsum, occiput and frons longitudinally rugose, ground surface feebly microreticulate. Scutum and scutellum usually longitudinally rugose, lateral and antero-medial surfaces of scutum smooth and shiny, scutellum more or less smooth medially. Sides of alitrunk, including anepisternum and katepisternum, rugoso-reticulate and microreticulate, ventral part of katepisternum always rugulose, or microreticulate. Dorsum of petiolar node coarsely reticulate and microreticulate, medially shiny, dorsum of postpetiole coarsely reticulate and microreticulate. Polygonal striation disrupted on 1st gastral tergite, superficially microreticulate basally. Ventral surface of head with several short and few longer, straight or “C”-shape setae, arising posterior to buccal cavity. Description of Male. Whole body and appendages brownish black. Head with convex sides, rounded occipital margin and widely rounded occipital corners. Scutum wider than head. Propodeal teeth very short, propodeum slightly angulate in profile. Dorsal crest of petiolar node with sharp, slightly emarginated, with transversal edge in frontal view. Head and waist rugulose to reticulate, ground surface microreticulate, dull. Scutum finely rugulose, antero-laterally smooth and shiny. Scutellum rugulose and microreticulate. Sides of alitrunk finely rugose and microreticulate. Ventral part of katepisternum smooth and shiny. Dorsum of petiolar node finely reticulate and microreticulate. Postpetiole finely striate, shiny. Polygonal striae hardly visible on 1st gastral tergite. Material examined (5 nest series including 43 workers, 11 gynes and 12 males). HOLOTYPE [[worker]]: ITALY - Calabria Prov.Catanzaro, 3 km NW Umbriatico, 350 mH, 19.05.1994, nr. 1305 leg. A. Schulz, R. Güsten, M. Sanetra (1[[worker]] / HNHM); PARATYPES: ITALY - Catanzaro, 3 km NW Umbriatico, 350 mH, Calabria Prov.19.05.1994, nr. 1305 leg. Schulz, Güsten, Sanetra (2[[workers]] / HNHM); Catanzaro, 3km NW. Umbriatico, 350mH, Calabria, Prov.19.05.1994, Nr. 1305 & 1309 leg. A. Schulz, R. Güsten, M. Sanetra (2[[workers]] / HNHM, 3[[workers]], 1[[queen]], 1[[male]] / PCAS, 3[[workers]], 1[[queen]] / SMNK); Cosenza, 1km NW. Frascineto, 500mH, Calabria, Prov.21.05.1994, Nr. T350 & 1366 leg. A. Schulz, R. Güsten, M. Sanetra (2[[workers]], 2[[queens]], 1[[male]] / HNHM, 2[[workers]], 1[[queen]], 1[[male]] / MCSN, 1[[worker]], 1[[queen]], / PCAS); Foggia, Gargano N. 528, ca. 2 km NE Abzweig n. Carpino, 700 mH Puglia Prov.23.05.1994, nr. T353 leg. R Güsten, M. Sanetra (3[[workers]] / HNHM, 3[[workers]] / MCSN, 3[[workers]] / PCAS); Foggia, Gargano N. 528, ca. 2 km NE Abzweig n. Carpino, 700 mH Puglia Prov.23.05.1994, nr. 383 leg. R Güsten, M. Sanetra (3[[workers]], 2[[queens]], 3[[males]] / HNHM, 6[[workers]], 2[[queens]], 3[[males]] / PCAS, 3[[workers]], 1[[queen]], 2[[males]] / SMNK); Morphometrics: (15 workers and 3 gynes measured). Diagnosis. Workers of T. sanetrai n. sp. can be separated from related species by the absence of psammophore, relatively coarse body sculpture, cubic petiolar node (NOH/NOL and PEH/NOL, Table 1.) and very short scape (SL/CS, Table 1.). Workers of T. sanetrai n. sp. mostly resemble those of T. rhodium and T. alternans. Tetramorium alternans has microreticulate sculpture on dorsum of petiole and postpetiole with very feeble rugulae, and microreticulate, in contrast with T. sanetrai n. sp. dorsum of petiolar node and postpetiole rugoso-reticulate and microreticulate. Differentiation between T. sanetrai n. sp. and T. rhodium is based on microreticulation of the body including gaster and scape sculpture. Tetramorium rhodium has stronger microreticulation between the primary ornamentation, best visible on head, petiole and postpetiole dorsum, which is strongly and irregularly rugose with densely microreticulate ground surface. In T. sanetrai n. sp. especially the dorsal surface of petiole is partially unsculptured and shining between the rugulae. The scape of T. rhodium is strongly sculptured, parallel costulae cover the whole surface of scape, in contrast to T. sanetrai n. sp. the scape is smooth and shinning at least proximally, distal end sometimes very feebly costulate. First gastral tergite of T. rhodium is basally microreticulate, that of T. sanetrai n. sp. is never microreticulate, but polygonally striate. Moreover, CS/PEW and CS/PPW give appropriate discrimination between T. sanetrai n. sp. and T. rhodium (Table 1.). For separation between T. sanetrai n. sp. and T. rhodium the following Discriminant D(5) function is provided: 0.114 FR - 0.016 CS + 0.043 SL - 0.026 PEW - 0.086 PPW - 13.907 results of D(5) analysis: T. sanetrai n. sp. D(5) = -2.448 ±0.833 [-3.977, -1.137] (n= 15), T. sanetrai n. sp. holotype D(5) = -1.257, p<0.001. T. rhodium D(5) +2.425 ±1.155 [+4.643, +1.155] (n= 22), T. rhodium syntype series D(5) mean = +2.652 (n= 4). The less complicate Discriminant D(3b) function gives separation: D(3b) = 0.118 MW - 0.121 PEH - 0.084 PPH - 4.585. T. sanetrai n. sp. D(3b) = -2.643 ±0.901 [-4.022, -0.882] (n= 15), T. sanetrai n. sp. holotype D(3b) = -1.302, p<0.001. T. rhodium D(3b) = +2.643 ±1.449 [-0.619, +4.595] (n= 22), T. rhodium syntype series D(3b) mean +3.665 (n= 4). Petiole and frons characters (NOH/NOL, PEH/NOL, FR/CS, Table 1.) give appropriate separation between T. sanetrai n. sp. and T. alternans. For separation between T. sanetrai n. sp. and T. alternans the following Discriminant D(2b) function is provided below: T. sanetrai n. sp. vs. T. alternans D(2b)= 0.093 FR - 0.148 NOL - 2.941 results of D(2b) analysis. T. sanetrai n. sp. D(2b) = -2.647 ±0.866 [-4.206, -0.982] (n= 15), T. sanetrai n. sp. holotype D(2b) = - 1.528, p<0.001; T. alternans D(2b) +2.647 ±0.878 [+1.069, +4.647] (n= 34), T. alternans lectotype D(2b) = +1.969, p<0.001, T. kahenae lectotype D(2b) = +1.070, p =0.01. Gynes of T. sanetrai n. sp. can be distinguished by lacking of psammophores, smooth scape, wide scutum, (MW/CS Table 2.) relatively narrow petiole and postpetiole, (WAIST Table 2.) and rugo-reticulate katepisternum. Gynes of T. sanetrai n. sp. mostly resemble those of T. chefketi, but scape length (SL/CS, Table 2.) gives discrimination between them. For further combination of morphometric characters see Table 1-2. Distribution. Based on the studied material this species seems to be endemic to the South Italian mountains. Etymology. This species [sanetrai] is dedicated to Matthias Sanetra for his fundamental work with the genus Tetramorium.Published as part of Csösz S., Radchenko, A. & Schulz, A., 2007, Taxonomic revision of the Palaearctic Tetramorium chefketi species complex (Hymenoptera: Formicidae)., pp. 1-38 in Zootaxa 1405 on pages 28-3
Welche Einstellungen haben Lehrende zur Lehre?
Kamphans M, Funger A, Ernst C. Welche Einstellungen haben Lehrende zur Lehre? In: Cremer-Renz C, Jansen-Schulz B, eds. Innovative Lehre – Grundsätze, Konzepte, Beispiele der Leuphana Universität Lüneburg. Bielefeld: UniverstitätsVerlag Webler, S.; 2010
Seiner Hochehrwürden, dem Herrn M. Friedrich Heinrich Starken hochverordneten Superintendenten und Pastori Primario zu Bitterfeld bey dem erfreulichen Antritte dieses Amtes am 1. Januar 1800.
ehrfurchtsvoll gewidmet von den sämmtlichen Predigern der Inspection [C. G. Blüthner, Pastor in Alt-Jessnitz. M. A. W. Hofmann, Pastor in Sandersdorf. M. J. G. Köpping, Diaconus in Brena. M. C. G. Martius, Pastor in Niemeck. M. J. A. Mulert, Pastor in Crina. M. F. Ch. Nitzsche, Past. sen. in Roitzsch. J. A. Nitzsche, Past. subst. [in Roitzsch.] G. L. Richter, Pastor in Mühlbeck. W. G. Richter, Pastor in Pouch. M. J. G. Rieck, Pastor in Brena. M. J. Ch. Schmidt, Pastor in Priorau. F. G. Schulz, Diaconus in Bitterfeld. C. A. Schulze, Past. sen. in Rösa. M. C. G. Schulze, Pastor subst. [in Rösa.] C. F. Schulze, Pastor in Sausedlitz. M. J. G. Seyfert, Pastor in Beyersdorf. S. T. Siebold, Pastor in Petersroda. C. A. Wachsmuth, Pastor in Pösigck. J. S. Walther, Pastor in Reuden. M. S. G. Wegner, Pastor in Burgkemnitz. M. C. F. G. Werner, Pastor in Capella]Autopsie nach Exemplar der ULB Sachsen-AnhaltVorlageform des Erscheinungsvermerks: Leipzig, gedruckt in der Sommerschen Buchdruckerey
Novel insights into somatostatin receptor physiology
The experimental data reviewed in the present paper deal with the molecular events underlying the
agonist-dependent regulation of the distinct somatostatin receptor subtypes and may suggest
important clues about the clinical use of somatostatin analogs with different pattern of receptor
specificity for the in vivo targeting of tumoral somatostatin receptors. Somatostatin receptor subtypes
are characterized by differential b-arrestin trafficking and endosomal sorting upon agonist binding
due, at least in part, to the differences in their C-terminal tails. Moreover, the subcellular expression
pattern of somatostatin receptor subtypes and their activity in response to agonist treatment are
affected by intracellular complements, such as proteins involved in intracellular vesicle trafficking.
Different somatostatin analogs may induce distinct conformations of the receptor/ligand complex,
preferentially coupled to either receptor signaling or receptor endocytosis
- …
