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1               In severe cases embryos appear unsegmented.
2 es into rhombomeres, the spinal cord remains unsegmented.
3 e in nature has always been characterized as unsegmented.
4 es previously considered to be predominantly unsegmented, and in doing so expanded the number of know
5            Investigating trunk elongation in unsegmented animals facilitates examination of mechanism
6 the ancestral panarthropod head and brain is unsegmented, as in C. catenulum.
7 We examined coordination of locomotion in an unsegmented, ciliolocomoting gastropod, the sea slug Ple
8  uniform Wingless activity are added back to unsegmented embryos (wingless- engrailed-).
9                                              Unsegmented embryos are much shorter than wild type.
10 rae were replaced by a ventrally-positioned, unsegmented endoskeleton.
11 (Jingmenvirus) related to the prototypically unsegmented Flaviviridae.
12 an Cardiodictyon catenulum, which reveals an unsegmented head and brain comprising three cephalic dom
13  Lox22-Otx RNA is primarily restricted to an unsegmented head domain, including tissues in the foregu
14 n peripheral ectoderm or endoderm, or in the unsegmented head region (prostomium).
15 od to extract vascular objects directly from unsegmented images without the need for machine learning
16                                              Unsegmented lesions either were adjacent to high urine a
17   During segmentation of vertebrate embryos, unsegmented mesenchymal mesoderm is divided into epithel
18 e neural tube, and dramatically expanded the unsegmented mesenchymal PSM while blocking somitogenesis
19 tebrates have a relatively extensive zone of unsegmented mesenchyme (i.e., presomitic mesoderm) inter
20                                          The unsegmented, mud-dwelling echiuran spoon worms and the g
21 ts prosoma is situated behind a pair of oval unsegmented neuropils that are directly connected to pai
22                            The cells exhibit unsegmented nuclei, have Gr-1(dim)Ly-6G(dim)CD11b(+) phe
23 that was either coextensive with the target (unsegmented) or appeared segmented from it due to a gap
24  5-6 embryos and subsequently in somites and unsegmented paraxial and lateral plate mesoderm overlapp
25 anisms the gene is specifically expressed in unsegmented paraxial mesoderm and its immediate progenit
26 -helix transcription factor expressed in the unsegmented paraxial mesoderm and throughout epithelial
27 ecause when pieces of dorsal neural tube and unsegmented paraxial mesoderm are combined in tissue cul
28 analysis of lunatic fringe expression in the unsegmented paraxial mesoderm of chick embryos.
29 ntation in vertebrates first arises when the unsegmented paraxial mesoderm subdivides to form paired
30 ically expressed in developmentally immature unsegmented paraxial mesoderm, causes complete failure o
31            Both genes are transcribed in the unsegmented presomitic mesoderm (PSM), newly formed somi
32 ls cyclic initiation of transcription in the unsegmented presomitic mesoderm (PSM).
33 ective somites cause them to detach from the unsegmented presomitic mesoderm [1-3].
34 ntrols the periodic cleavage of somites from unsegmented presomitic mesoderm during vertebrate segmen
35 tation clock') intrinsic to the cells in the unsegmented presomitic mesoderm, and is manifested in cy
36    Somites form by an iterative process from unsegmented, presomitic mesoderm (PSM).
37                             Importantly, the unsegmented region does not generate additional tissue v
38                                         With unsegmented retinal angiograms, the sensitivity and spec
39 nce space by a viral genome (in this case an unsegmented RNA) can reach a point of the space in which
40  was done to predict RNFL thickness from raw unsegmented scans using conventional RNFL thickness meas
41     We show that parts emerge from initially unsegmented sequences, that their distribution becomes c
42 nsion of the hindbrain at the expense of the unsegmented spinal cord.
43                  Segmentations of 36 further unsegmented target images of developing brains yielded v
44 d have arisen from an ancestral limb with an unsegmented tarsus.
45 ntially bud off from the anterior end of the unsegmented tissue, laying down an exquisite repetitive
46 scillatory Her1 protein production along the unsegmented tissue.
47 ern of double segment periodicity in overtly unsegmented tissue.
48 he posterior end of the embryo containing an unsegmented tissue.
49 ves of clock gene expression sweeping in the unsegmented tissue.
50  segmented vertebral column as well as other unsegmented tissues.
51      VAPiD supports annotation of nearly all unsegmented viral genomes.
52 have to be discovered by learners exposed to unsegmented wholes.