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  • Life and Medical Sciences  (5)
  • 2010-2014
  • 2005-2009
  • 1985-1989  (5)
  • 1955-1959
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 198 (1988), S. 189-204 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The fine structure of the male germinal cells in testes of two salps, Thalia democratica and Cyclosalpa affinis, is identical. The earliest germ cells seen were spermatocytes, located at the periphery of the testis and sometimes connected by cytoplasmic bridges. They are spherical with an anucleolate nucleus, a pair of centrioles, aboundant free ribosomes, sparse rough endoplasmic reticulum, and about five mitochondria. No Golgi complex was seen. The earliest spermatids, though similar to the spermatocytes, are smaller and have only one centriole. Spermatids develop (1) singly, (2) joined by cytoplasmic bridges, or (3) in syncytia. The next stage has a flagellum, a single large mitochondrion with dense material in some intracristal spaces, and a patch of highly condensed chromatin in the nucleus adjacent to the centriole. Subsequently the nucleus and the spermatid elongate. During elongation (1) the mitochondrion remains lateral to the nucleus and the amount of intracristal material enlarges, (2) the central core of condensed chromatin increases, and (3) the remainder of the chromatin becomes organized into dense strands. When elongation is 75% complete, the dense strands of chromatin appear to coalesce, to become homogeneous and denser than the core of chromatin, and the mitochondrion transforms into dense tubules. Finally, the mitochondrion wraps around the nucleus and extends its entire length, ultimately becoming a single tubule spiraled about 45 times around the nucleus. The mature sperm head is 18 μm long, tapering from 0.8 μm posteriorly to a tip about 0.14 μm wide. There is no acrosome. The single (distal) centriole of the sperm gives rise to a 9+2 flagellum with a fuzzy coat and dense material peripheral to each of the nine doublets. Spermiogenesis in T. democratica and C. affinis is similar to that in ascidians, and the sperm share many features with sperm of colonial ascidians in the suborder Didemnidae. The results, therefore, suggest that salps are closely related to ascidians and support the view that colonial ascidians gave rise to salps.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 198 (1988), S. 205-217 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Natural maturation of the oocytes of Oxycomanthus japonicus can be predicte in advance, and the multiple ovaries permit unintrusive serial biopsies. Ovaries were fixed for transmission electron micrscopy at 15-min intervals before, during, and after oocyte maturation. The start of maturation of each oocyte is signaled by the breakdown of the germinal vesicle and the disruption of a macula adhaerens associating the oocyte with nongerminal cells of the ovary. This disruption is followed by an ovulation of the oocyte into the ovarian lumen. Ovulation takes about 1 hr, and a continuous vitelline coat is produced around the oocyte during this interval. Within the oocyte cytoplasm, patches of nuage and the annulate lamellae disappear at 30 and 45 min after the start of oocyte maturation, respectively. Micropapillae become transiently abundant at the oocyte surface both at the time of germinal vesicle breakdown and around the time when the first and second polar bodies are produced. Oocyte maturation takes about 2 hr from start to finish, and the emission of the second polar body marks the beginning of the stage of the ovum. Within the cytoplasm of the ovum, the haploid chromosomes develop into chromosome-containing vesicles, which later fuse into a single female pronucleus. Pronuclear ova are retained in the ovarian lumen for about 1 hr and are then spawned into the surrounding seawater, where fertilization takes place.
    Additional Material: 24 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 124 (1985), S. 457-466 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Human fetal bone marrow (FBM) cells were examined for the ability to form colonies in the absence of exogenous colony-stimulating factor (CSF) in double layer agar, methylcellulose (MC), and in agar-MC (agar underlayer, MC overlayer) culture systems. Without exogenous CSF, macrophage colonies (M-CFC) were formed in a combined culture of agar and MC. Aggregates of 5-40 cells were observed on day 7. Gradually, large compact colonies which survived for 10-12 weeks of cultivation, were formed. They were composed of mononuclear monocytes and multinucleated cells. M-CFC progenitors were nonadherent, but their progeny became adherent during differentiation within the colony. Colony formation was cell-dose-dependent. Depletion of monocytes increased the number of colonies in agar-MC cultures and stimulated the development of some macrophage colonies in MC. Survival of monocyte progenitors was not dependent on CSF. Neither was their proliferation nor partial differentiation in agar-MC cultures. CSF increased M-CFC colony efficiency, however, if it was present when cultures were initiated. Addition of CSF to M-CFC growing for 2-5 weeks in CSF-deprived medium stimulated monocytes proliferation and transformation into macrophages. Epithelioid cells, and increase in the number of giant multinucleated cells, and granulocyte multiplication were also observed. The absolute dependence of macrophage colony formation on CSF described by others might be a result of inadequate culture conditions due to agar rather than an intrinsic physiological requirement.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 24 (1989), S. 439-451 
    ISSN: 0148-7280
    Keywords: epdidymis ; glycoproteins ; caudal fluid ; spermatozoa ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Glycoproteins from luminal fluid of the mouse cauda epiciidymidis have been compared with glycoproteins from Triton X-100 extracts of mouse spermatozoa from varying regions of the epididymis, using lectins with specific affinity for different sugar residues. Concanavalin A recognizes 11 glycocomponents on Western blots of fractionated caudal fluid; wheat germ agglutinin (WGA) binds 12 proteins; Ulex europaeus agglutinin (UEA) binds seven; and Dolichos biflorus agglutinin (DBA) recognizes nine. Several of these glycoproteins display an affinity for more than one lectin, indicating a diversity in their exposed carbohydrate residues; whereas other proteins bind only one of the four lectins used. The results also show that some glycoproteins exhibit a higher affinity for particular lectins. Eight glycoproteins of similar mobility and lectin-binding characteristics are detected in Triton X-100 extracts of spermatozoa from different regions of the epididymis and in caudal fluid. The lectin affinity of some proteins appears or increases in spermatozoa from distal epididymal regions (54 kD, 32 kD), whereas the lectin affinity of others decreases (29 kD, 40 kD). There are differences in lectin affinities between proteins in sperm extracts and in caudal fluid. Some proteins show an affinity for three or four lectins in caudal fluid, but proteins of similar electrophoretic mobility in sperm extracts bind only one or two of the lectins. These data show that glycoproteins of similar mobility are present in caudal fluid and in Triton-X-100 sperm extracts, implying a potential interaction between caudal fluid components and epididymal sperm.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 8 (1987), S. 375-387 
    ISSN: 0192-253X
    Keywords: urease ; isozymes ; clones ; null mutants ; soybean ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The soybean (Glycine max [L.] Merr.) contains two urease isozymes whose expression is regulated in a tissue-specific and temporal manner. The ubiquitous urease is expressed in all tissues examined (leaf, embryo, seed coat, cell culture); the embryo-specific urease is synthesized exclusively in the developing embryo. The embryo-specific urease accumulates during seed development while the ubiquitous urease is found in highest levels during early development of both leaves and seeds. We have isolated mutants which fall in three phenotypic classes lacking one or both urease isozyme activities. Genetic analysis has thus far identified three unlinked loci which control the expression of urease(s). Genomic and cDNA clones of urease structural genes have also been recovered and we are working to assign these to genetic loci by sequence and RFLP analyses. That the ubiquitous urease isozyme is expressed in cell culture makes it possible to include cell culture in physiological and developmental studies. Additionally, we have developed direct selections for urease-negative mutants, and their revertants, in cell culture. These selections will facilitate the study of the expression of cloned urease genes in genetically transformed tissue.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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