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1 development and fail to form normal anterior embryonic structures.
2 ng patterning and development of a number of embryonic structures.
3 possible link between the formation of these embryonic structures.
4 of genes that are required for formation of embryonic structures.
5 nd group affect formation of ventroposterior embryonic structures.
6 l crest-dependent morphogenesis of essential embryonic structures.
7 onse maximum and the specification of apical embryonic structures.
9 sional coordinate system in order to pattern embryonic structures and create the complex shape of the
13 roducible pattern that interfaces with other embryonic structures and tissues, but the sources and id
14 work suggested that the EVL was a transient embryonic structure, and that maturation of the epidermi
15 peritoneal folds (PPFs), which are transient embryonic structures, are the source of the diaphragm's
16 Hox genes act to differentiate and pattern embryonic structures by promoting the proliferation of s
17 ential for the normal development of diverse embryonic structures (e.g. eye, heart, nervous system, u
18 apical ectodermal ridge (AER) is a transient embryonic structure essential for the induction, pattern
20 tingly, the notochord appears to be the only embryonic structure in Ciona activating the PCP pathway.
24 essential for specification of dorsoanterior embryonic structures, including notochord, prechordal me
25 h(-/-) mutant mouse, the development of many embryonic structures, including the limb, is severely co
26 ulations, culminating in defects to anterior embryonic structures, including the pharyngeal arches, h
29 nt differentiation of Mullerian and Wolffian embryonic structures into female-typical or male-typical
31 edial (MGE) ganglionic eminences, subpallial embryonic structures, is required for generation of tele
32 cortical interneurons arise from a transient embryonic structure known as the medial ganglionic emine
33 These abnormalities include truncation of embryonic structures, limb bud malformation, partial dup
35 ignaling in coordinating the growth of extra-embryonic structures necessary to support development wi
36 production (E16.5) of interneurons from this embryonic structure occurs 3 d later in development.
38 evelopment, compartmentalization of an early embryonic structure produces blocks of cells with distin
39 Because Uch-L3 transcripts were present in embryonic structures relevant to the s(1Acrg) phenotype,
40 ation of the notochord is unaffected and the embryonic structures rostral to the forelimb are relativ
42 f human pharyngeal arch 1 (PA1), a conserved embryonic structure that develops into the palate and ja
44 n vertebrates, the sclerotome is a transient embryonic structure that gives rise to various tissue su
47 incipally derived from the branchial arches, embryonic structures that exhibit proximodistal polarity
48 f mesoderm into somites, which are transient embryonic structures that form down each side of the neu
50 the pleuroperitoneal folds (PPFs), transient embryonic structures that give rise to the connective ti
53 development for proper patterning of dorsal embryonic structures, whereas Tlr is required later duri
54 istic of the medial ganglionic eminence, the embryonic structure which gives rise to the globus palli
55 organs in the vertebrate head, are important embryonic structures whose development has not been well