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  • 1985-1989  (15)
  • 1970-1974  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 513 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-6052
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The polarization of theΛ 0 hyperon produced inK − p interactions at 110 GeV/c shows a strong dependence on the transverse momentump t of theΛ 0 and no significant dependence onx F . The polarization for largep t is negative in the proton hemisphere and positive in the kaon hemisphere. In theproton hemisphere it is compared with the results of otherK − p experiments at lower energies as well as with reactions induced byp, $$\bar p$$ , π+, π+ andK +. The comparison is performed separately forK − p→Λ 0 KK+pions andK − p→Λ 0+pions showing an analogous behaviour in the former channel. In thekaon hemisphere the comparison with otherK − p experiments at lower energy shows ap t -dependence of theΛ 0 polarization which changes with energy. The experimental results are discussed in terms of current quark models and of the Mueller-Regge phenomenology. The model predictions reproduce the trend of the data qualitatively well but fail in describing some details.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-6052
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Results are presented on inclusive production of ∑+(1385) and ∑−(1385) inK − p interactions at 110 GeV/c. The inclusive and topological cross sections have been estimated and compared with published results at lower energies. The inclusive cross section of ∑+(1385) seems to decrease with c.m. energy, while that of the ∑−(1385) is nearly constant. The mean charged multiplicity associate to Σ(1385) increases with c.m. energy. The ∑+(1385) is produced both in the target fragmentation region and in the central region where ∑−(1385) is predominantly produced in the central region. Approximately 16% of the Λ's stem from the decay of ∑±(1385) and the kinematic distributions of these Λ's are not very different from the inclusive Λ's.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1434-6052
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We present data on inclusive production ofK + andK S 0 mesons in a 70 GeV/cK + p experiment performed in BEBC filled withH 2. Cross sections and inclusive Feynman-x distributions for identifiedK +'s andK S 0 's are presented. The spectra of “prompt” non-diffractiveK S 0 are determined by subtraction of the decay products of prominent resonances and diffractive contributions. These data, contrary to the overall inclusive spectra, allow to differentiate between some fragmentation models for soft hadron-hadron interactions.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-6052
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Results on inclusive ϕ production inK − p interactions at 110 GeV/c are presented. The production cross section is found to be larger than in πp andpp interactions at similar energies, suggesting OZI allowed $$s\bar s$$ fusion to be the dominant mechanism in ϕ production. Thex distributions of ϕ and $$\bar K^{*0} $$ are found to be similar to each other over the entirex range suggesting an overall strangeness suppression factor of 0.20±0.04 in the sea to be the dominant source of the difference in the cross section for ϕ and $$\bar K^{*0} $$ . There is no evidence of a narrowφπ − state around 2.1 GeV/c2 as suggested byK + experiments, but there is some excess of events in the region 1.94−1.98 GeV/c2 consistent with theF-meson mass as observed ine + e − experiments.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 211 (1985), S. 285-294 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Ciliated cells of the ductuli efferentes show at their apex a discrete endocytic apparatus composed of small vesicles connected to or subjacent to the apical plasma membrane, small apical membranous tubules, and pale multivesicular bodies. Deeper in the cytoplasm, there are acid phosphatase-positive denser, multivesicular bodies and secondary lysosomes showing an electron-dense cortex and a crystalline, paler stained core. Cationic ferritin and concanavalin A-ferritin used to demonstrate adsorptive endocytosis, when injected into the rete testis, rapidly reached the lumen of the ductuli efferentes. At 1 min after injection, these tracers were seen bound to the apical plasma membrane of ciliated cells and within small endocytic vesicles and by 5 min in narrow apical tubules. At 15 and 30 min after injection, the tracers appeared in pale multivesicular bodies while at 1 hr they were found within dense multivesicular bodies. At 2 hr and longer time intervals these tracers accumulated within secondary lysosomes. Native ferritin, concanavalin A-ferritin in the presence of α-methyl-D-mannoside, and horseradish peroxidase or albumin-colloidal gold complexes were used to analyze fluid-phase endocytosis. At various intervals following their injection into the rete testis, these tracers presented a distribution identical in all respects to that described for cationic ferritin and concanavalin A-ferritin. In the present work, none of the above tracers were transported to the abluminal aspect of the ciliated cells. These cells, like the nonciliated epithelial cells of the ductuli efferentes are thus involved in adsorptive as well as in fluid-phase endocytosis.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 169 (1971), S. 613-625 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In sections of thymus stained with the tannic acid-phosphomolybdic acid-amido black (TPA) technique, the epithelial reticular cells can readily be identified by the well-stained tonofibrils in their cytoplasm. In the cortex, flattened epithelial reticular cells form a continuous layer on the inner surface of the capsule and along the interlobular septa. Within the cortex proper, stellate epithelial reticular cells are widely dispersed as a loose network. In the medulla, two zones, referred to as “outer” and “inner” medulla, are distinguished. The outer medulla, like the cortex, contains epithelial reticular cells, but these are more voluminous, are more richly provided with tonofibrils and form a denser network than in the cortex. In the inner medulla no epithelial reticular cells can be seen but instead connective tissue cells and fibers make up the supporting framework. A layer of flattened epithelial reticular cells demarcates the outer from the inner medulla. This layer of cells also extends along the outer surface of blood capillaries seen in the outer medulla and cortex. Around the larger blood vessels, this layer of epithelial reticular cells is separated from the vessel wall by a connective tissue perivascular space. Hence, the inner medulla is continuous with the perivascular spaces and, like them, is supported by connective tissue. Thus, the epithelial reticular cells constitute the supporting framework of the cortex and outer medulla and separate these regions from the connective tissue of the capsule, interlobular septa, blood vessels and inner medulla.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 221 (1988), S. 591-598 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The cytochemical distribution of two different acid phosphatases, nicotinamide adenine dinucleotide phosphatase (NADPase) and cytidine monophos phatase (CMPase), was analyzed within the Golgi apparatus, acrosomic system, and chromatoid body of early spermatids. Within the saccules composing the Golgi cortex, the phosphatases were localized in specific and nonoverlapping compartments: the cis-tubular network, or cis-element, and the first underlying saccule were unreactive for both enzymes, the following four to five saccules were reactive for NADPase, and the last three saccules were reactive for CMPase. Vesicles of various sizes and short membranous tubules, present near the edges of saccules and in the medulla of the Golgi apparatus, were NADPase- and/or CMPase-positive. The acrosomic system showed a weak but significant NADPase reactivity and a strong CMPase reactivity. The vesicles associated with the chromatoid body were reactive for NADPase and/or CMPase. The combined observations indicate that the two cytochemically distinct compartments of the Golgi cortex, the NADPase- and CMPase-positive saccules, independently contribute to the formation of the acrosomic system and the vesicular component of the chromatoid body.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 221 (1988), S. 482-493 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Underlying the epithelium of the vas deferens there is a complex basement membrane showing a thick lamina densa separated from the plasma membrane of epithelial cells by a lamina lucida. On the connective tissue side of the lamina densa, there are plaques composed of a material that is similar to that of the lamina densa but is more compact and has a greater electron density. This material also forms plaques at a short distance from the lamina densa, where it appears as irregular nodular masses. The plaques are bridged by striated anchoring fibrils (SAF) that are variable in structure. Some SAF are long (0.5-0.6 μm) and bilaterally symmetrical, with a central fusiform segment and, on each side, coarsely banded segments. While the fusiform segment presents 5 or 6 diffuse cross striations, the coarsely banded segments show distinct bands labeled B1-B4. Shorter SAF show a coarsely banded segment alone or a coarsely banded segment plus a fusiform segment. Some SAF also branch at the level of the fusiform segments, in which case they from star-shaped structures with three or more branches that have their extremities inserted into plaques. The plaques, as well as the lamina densa, are immunohistochemically reactive to type IV collagen, laminin, and heparan sulfate proteoglycan, whereas the SAF are not immunoreactive to these substances. SAF and plaques, considered as integral components of this basement membrane, form a series of arches or open tunnels traversed by collagen fibrils. It is thus apparent that these elements contribute to the attachment of the basement membrane and the overlying epithelium to the underlying dense connective tissue of the lamina propria.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 140 (1974), S. 27-45 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Osmication in an unbuffered aqueous solution of osmium tetroxide allows the forming face of the Golgi apparatus to be labeled in many cell types. This property was utilized to study the spatial configuration of this organelle by examining stereopairs of the same field taken at 1,000 KV after tilting a thick (1 to 7 μUm) section of - 7° or + 7° from the original (0°) position. When examined in 1 μm thick sections at magnifications ranging from 13,000 to 18,000 times, the osmic acid-impregnated element of the Golgi apparatus of ganglion nerve cells, Leydig cells or Sertoli cells takes the appearance of a single layered polygonal network of tubules. This network can only be seen at electron microscope magnifications and is referred to as the primary network or structure of the forming face of the Golgi apparatus. When 2 to 7 μm thick sections are examined under progressively lower magnifications, the details of the primary structure remain discernible but become less conspicuous. The osmiophilic portion of the Golgi apparatus now extends over large areas of the cytoplasm to form an extensive continuous structure. This structure which is in the range of visibility of the light microscope is referred to as the secondary network or structure of the forming face. In ganglion nerve cells, the secondary structure consists of a perinuclear network showing slender projections reaching the nucleus and wider expansions approaching the cell surface; in the Leydig cells it appears as an ovoid structure located at one pole of the nucleus whereas in Sertoli cells it forms a cylindrical structure located in the main shaft of the cytoplasm and extending from the nucleus towards the lumen of the seminiferous tubule. Thus the forming face of the Golgi apparatus displays a primary structure; the tubular roughly polygonal network, which is similar in the three cell types and a secondary structure which varies from cell to cell.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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