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  • 1990-1994  (2)
  • 1970-1974  (1)
  • Life and Medical Sciences  (3)
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  • 1990-1994  (2)
  • 1970-1974  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Developmental Dynamics 196 (1993), S. 11-24 
    ISSN: 1058-8388
    Keywords: Homeobox genes ; Xenopus laevis ; Anteroposterior axis ; Limb bud ; Paralog ; Retinoic acid ; Embryogenesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We report on the Xenopus homolog of the Hox 2.4 gene. This gene occupies the next to 5′-most position in the Xenopus Hox 2 complex. Hox 2.4 RNA is first detected at the early neurula stage, reaching a peak at the early tailbud stage, and is localized in the middle and posterior portions of the embryos Antibodies raised against a fusion protein show expression of Hox 2.4 protein in Xenopus embryos in a band located in the mid spinal cord. Thus, the protein is expressed in a narrower domain than that of Hox 2.4 mRNA. The Xenopus Hox 2.4 antibody cross-reacts readily with mouse embryonic tissue, where the protein is detected in migrating neural crest cells, the dorsal portion of the spinal cord, somites, lateral plate mesoderm, and in the forelimb bud. The Xenopus Hox 2.4 intron shares considerable sequence identity with the intron in the mouse homolog. A reporter gene containing an element from this intron which can bind homeodomain proteins is activated following microinjection into Xenopus embryos. The short distance between the end of the Hox 2.4 cDNA and the start site of the neighboring gene in the complex raises the possibility that this transcriptional element might be shared by two Hox genes. © 1993 wiley-Liss, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The fine structure of testicular interstitial cells from mice submitted to different experimental conditions is described. Following treatment with methallibure (I.C.I. 33,828; 1-α-methylallylthiocarbamoyl-2-methylthiocarbamoylhydrazine), a selective inhibitor of hypophyseal gonadotropic activity, interstitial cells acquire a quiescent appearance characterized by: (1) accentuated segregation of agranular endoplasmic reticulum from other cytoplasmic organelles and inclusions, (2) increased depots of lipid droplets. A single injection of interstitial-cell-stimulating hormone (ICSH or LH) induces prominent changes in the ultrastructure and distribution of cell inclusions and organelles that are seemingly related to augmented secretory activity. The cell surface shows a striking development of cytoplasmic processes that interdigitate with similar processes from adjacent cells. Intercellular spaces form a system of interfacial channels providing a direct connection of the interstitial cell surface with blood vessels and the myoid layer of seminiferous tubules. Gonadotropic stimulation causes an increased number of free ribosomes and expansion of the Golgi complex and rough endoplasmic reticulum. There is a marked depletion of lipid droplets and formation of lipofuscin granules.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 194 (1992), S. 21-32 
    ISSN: 0002-9106
    Keywords: Hox gene complexes ; Colinearity ; Homeobox ; Axis formation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We show that Xenopus laevis has a Hox 2 complex, and that this complex is strongly conserved with the mammalian one, both in structure and in the rules of spatial and temporal sequential expression of its genes during the early stages of development. Lithium chloride and retinoic acid, two reagents known to alter axial patterning of the body when applied to Xenopus embryos, produce, respectively, embryos with reduced posterior but exaggerated anterior structures and embryos with truncation of anterior structures. We report here on the effect of these reagents on the expression of Hox 2 genes in the Xenopus embryo. LiCl has a dramatic effect on Hox genes, suppressing the expression of these genes during gastrulation and early neurulation. However, later on expression of these genes reaches significant levels, suggesting the existence of two phases in the control of Hox gene expression. Retinoic acid increases the steady state level of transcripts from Hox genes with the greatest effect on Hox 2.7, the most anterior of the genes studied. This suggests that the results obtained in EC cells (Simeone et al., 1990, 1991) reflect what occurs in vivo. Neither LiCl nor RA change the sequential order of the onset of expression of the genes, showing that these reagents do not perturb the molecular mechanisms used to establish the sequential activation of the genes of the Hox complexes. © 1992 Wiley-Liss, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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