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Universlty of Manitoba, ln Partîal Fulfiìlment - MSpace at the ...

Universlty of Manitoba, ln Partîal Fulfiìlment - MSpace at the ...

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261<br />

<strong>ln</strong> <strong>the</strong>se tables <strong>the</strong> contrors and <strong>the</strong> experimentar embryos w¡thout<br />

neural dèfects show extensive separ<strong>at</strong>ion between somites and neural<br />

m<strong>at</strong>erial; <strong>the</strong>re Issome separ<strong>at</strong>ion between notochord and neural m<strong>at</strong>erial<br />

by Stêge 20 in two embryos ('ZC Zl , 428 73). The embryos wìth neural<br />

defects also show extensive separ<strong>at</strong>¡on from somites, with separ<strong>at</strong>ion<br />

from notochord (especially <strong>ln</strong> myelosct isis after Stage ,t7) ¡and somite<br />

defects (especial ly ín myelodysptasia after Stage l6). There is no<br />

close associ<strong>at</strong>ion between <strong>the</strong> rength <strong>of</strong> ectoderm discontinuíty from<br />

neural tissue and <strong>the</strong> type <strong>of</strong> neural tesion<br />

.<br />

Figsi. 112-119 compare <strong>the</strong> percentage lengths <strong>of</strong> neural defects in<br />

regions B,c, D and E <strong>of</strong> each âffected experimental embryo with <strong>the</strong> correspondîng<br />

percentage I engths <strong>of</strong>:<br />

(a) ectoderm d iscont inu ity<br />

(b) somite separ<strong>at</strong>ion from neural tîssue<br />

(c) notochord separ<strong>at</strong>ion from neural tissue<br />

(d) local somi te defects.<br />

These figures demonstr<strong>at</strong>e <strong>the</strong> percentage distribution in <strong>the</strong> four<br />

regions <strong>of</strong> embryonic cord <strong>of</strong> myeloschisis irom Stage lJ and myelodysplasia<br />

from Stage 16. Horvever as region B is much larger than all <strong>the</strong> o<strong>the</strong>r<br />

regîons <strong>the</strong> size <strong>of</strong> each region in rel<strong>at</strong>ion to a whole embryo is disproportion<strong>at</strong>e.<br />

The assocî<strong>at</strong>ion <strong>of</strong> myeloschisis with notochord sãpar<strong>at</strong>ion<br />

after Stage 1/,and <strong>of</strong> myelodysplasia with somite defects after Stage l6<br />

are clearly i I lustr<strong>at</strong>ed.<br />

.An analysis <strong>of</strong> variance could not be performed with <strong>the</strong>se figures<br />

as so many <strong>of</strong> <strong>the</strong> histologîcar fe<strong>at</strong>ures showed zero varues in both<br />

exper imenta I and control embryos.

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