Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Developmental Genetics 4 (1983), S. 159-165 
    ISSN: 0192-253X
    Keywords: trisomy ; monosomy ; aneuploidy ; chimeras ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Mouse trisomy 15 ↔ 2n aggregation chimeras have been produced and analyzed at 19 days of gestation. We have found that these chimeras are viable and in most instances normal in external appearance, unlike trisomy (Ts)-15 embryos which are severely growthretarded and die midway through gestation. Trisomic cells were found in all tissues of fetal chimeras, with proportions not significantly different from those of the controls in kidney, heart, liver, and brain, but significantly reduced in thymus and spleen. Ts-15 cells do not, therefore, exhibit a proliferative advantage during fetal development of tissues susceptible to Ts-15-related lymphoid malignancies. However, the presence of Ts-15 cells in the placenta may be associated with placental overgrowth. One fetus containing a monosomy 3 cell population was also observed, the first term fetal chimera with monosomic cells that has been detected.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0192-253X
    Keywords: dedifferentiation ; Dictyostelium ; aggregation ; mutant ; Life and Medical Sciences ; Genetics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: During slime mold development, cells acquire the capacity to rapidly recapitulate morphogenesis in roughly a tenth the original time. When developing cells are disaggregated and refed, they completely loss this capacity in a rapid and synchronous step referred to as the “erasure event.” The erasure event sets in motion a program of dedifferentiation during which developmentally acquired functions are lost at different times. In this report, we describe the phenotype of HI4, which is a mutant partially defective in the dedifferentiation program but normal in all aspects of growth, morphogenesis, and rapid recapitulation. HI4 cells progress through the erasure event, losing in a relatively normal fashion (I) the capacity to rapidly recapitulate later stages of morphogenesis, (2) the capacity to release a cAMP signal, and (3) the capacity to respond chemotactically to a cAMP signal. However, erased HI4 cells abnormally retain the capacity to rapidly reaggregate, even though they have lost chemotactic functions. Erased HI4 cells also abnormally retain EDTA-resistant cohesion (contact sites A) and the surface glycoprotein gp80. It appears that erased HI4 cells rapidly reaggregate owing to random collisions followed by tight cell cohesion.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...