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1 oprioceptor muscle targets: pSNs innervating hypaxial and axial muscles depend critically on Etv1 for
2 namic cell movements that generate posterior hypaxial and fin muscles, and demonstrate flexibility in
3            Finally, we provide evidence that hypaxial and myotomal gene expression is mispatterned in
4 d from pectoral fin level somites to forming hypaxial and specifically appendicular muscle.
5 Its structures are categorized as epaxial or hypaxial based on their adult position and innervation.
6 differentially restricted to the epaxial and hypaxial body domains, respectively.
7 hypaxial, eventually leading to an excess of hypaxial body wall muscle.
8 tes that the lymph heart originates from the hypaxial compartments of somites 34-41.
9 yogenesis in the mouse embryo, including the hypaxial dermomyotomal cells that give rise to the abdom
10 1-Sim1 expression boundary marks the epaxial-hypaxial dermomyotomal or myotomal boundary.
11  Pax3 positive myoblasts delaminate from the hypaxial dermomyotome of limb level somites and migrate
12 the somitic environment, Hh signals restrict hypaxial development and promote epaxial muscle formatio
13 th begins earlier in the epaxial than in the hypaxial domain, but that after an initial lag phase, bo
14 myotome specifically, and in the epaxial and hypaxial domains of the body generally, are governed by
15         Myotome formation in the epaxial and hypaxial domains of thoraco-lumbar somites was analyzed
16 and a shift in myoblast fate from epaxial to hypaxial, eventually leading to an excess of hypaxial bo
17  the medio-lateral boundaries of epaxial and hypaxial gene expression.
18 the expression domain of the lead-lateral or hypaxial marker Sim1.
19 ons are initially part of the Foxd3 lineage, hypaxial melanocytes lose Foxd3 at late stages upon sepa
20 b promotes the medial motor column (MMC) and hypaxial motor column (HMC) fates while inhibiting the l
21 ing Lhx3 downregulation in stem-cell-derived hypaxial motor neurons.
22 e left or right nMLF activates the posterior hypaxial muscle and produces a graded ipsilateral tail d
23  including somite organization, migration of hypaxial muscle anlagen toward the ventral abdomen, and
24                              Shh function in hypaxial muscle appears to be spatially restricted to th
25 ll formation in Xenopus laevis is similar to hypaxial muscle development in chickens and mice.
26  indicate that a primary function of lbx1 in hypaxial muscle development is to repress myoD, allowing
27 pus laevis, which, due to its unique mode of hypaxial muscle development, allows us to examine myobla
28 rest cells migrate, where it is required for hypaxial muscle development.
29 from a lack of myoblast proliferation in the hypaxial muscle domain.
30 e entire stream contributes to the posterior hypaxial muscle indicating that muscle precursors are no
31 or neurons and their division of epaxial and hypaxial muscle into four distinct quadrants as a refere
32  maintaining the balance between epaxial and hypaxial muscle mass.
33                                  Epaxial and hypaxial muscle precursors can be attributed to distinct
34                    In zebrafish, a subset of hypaxial muscle precursors from the anterior somites und
35 ctor (SF) are necessary for the migration of hypaxial muscle precursors in mice.
36 1 and Pax3 are co-expressed in all migrating hypaxial muscle precursors, raising the possibility that
37 r the lateral, but not ventral, migration of hypaxial muscle precursors.
38 Rbeta2 positively regulates Tbx3 a marker of hypaxial muscle, and negatively regulates Tbx6 via Rippl
39 have been shown to give rise specifically to hypaxial muscle, including the appendicular muscle that
40 in progenitors of epaxial muscle, dermis and hypaxial muscle, respectively.
41  of this stream contributes to the posterior hypaxial muscle.
42 cranial sensory organs and ganglia, kidneys, hypaxial muscles and several other organs in vertebrates
43 equired for the correct morphogenesis of the hypaxial muscles in which met is expressed.
44  and hence the formation of distinct epaxial-hypaxial muscles is not understood.
45 ding epaxial muscles (deep back muscles) and hypaxial muscles of the body wall (intercostal muscles,
46 orphogenetic basis for formation of specific hypaxial muscles within the zebrafish embryo and larvae.
47 eural tube and neural crest defects and lack hypaxial muscles.
48  displayed malformations of some but not all hypaxial muscles.
49 ome that are fated to form the non-migratory hypaxial muscles.
50 l myotome and there is normal development of hypaxial muscles.
51 gnals necessary for the specification of the hypaxial musculature by ablating them or transplanting t
52 these rib motions, active contraction of the hypaxial musculature may be at least partly responsible.
53 gratory muscle precursors giving rise to the hypaxial musculature.
54 muscle precursors giving rise to the ventral hypaxial musculature.
55 face ectoderm to induce the formation of the hypaxial musculature.
56 and, in the limb bud, Hh signaling represses hypaxial myoblast differentiation.
57 terior border, somite chevron morphology and hypaxial myoblast migration.
58 ck Lbx1 gene that is specific to prospective hypaxial myoblasts at occipital, cervical and limb level
59 o have different roles on differentiation of hypaxial myoblasts of amniotes.
60                                 We find that hypaxial myoblasts respond similarly to Hh manipulations
61 somites that leads to a paucity of migratory hypaxial myoblasts.
62  differences between pre- and post-migratory hypaxial myoblasts.
63 biting all further growth of the epaxial and hypaxial myotome.
64  compensate for deficiencies of the lateral (hypaxial) myotome.
65   Muscle precursor cells for the epaxial and hypaxial myotomes are predominantly located in the dorso
66 ssed not only in the epaxial but also in the hypaxial myotomes, while it is maintained in the AER.
67 ralward growth directions of the epaxial and hypaxial myotomes.
68 MyoD in the epaxial myotomes, but not in the hypaxial myotomes.
69 rtments, which correspond to neither epaxial/hypaxial nor primaxial/abaxial subdivisions.
70 t independent cues converge on the migratory hypaxial precursors in the dermomyotomal lip after they
71  epaxial muscle precursors of the body, some hypaxial precursors of the body, some facial muscles and
72 fish duplicate of Pax3, is restricted to the hypaxial region of anterior somites that generate migrat
73 partment boundary, foreshadowing the epaxial-hypaxial segregation of muscle.
74 ndence on epaxial signals and suppression by hypaxial signals places En1 into the epaxial somitic pro
75 ion for a new hypothesis for Shh function in hypaxial skeletal muscle development.
76                                              Hypaxial skeletal muscles develop from migratory and non
77 egregated, separately innervated epaxial and hypaxial skeletal muscles.
78 f the somite is destined to give rise to the hypaxial skeletal musculature.
79 om cells expressing Pax3 specifically in the hypaxial somite and their migratory derivatives.
80 ) embryos, MyoD is activated normally in the hypaxial somite, but MyoD-expressing cells are disorgani
81 l, limb muscle SP cells are derived from the hypaxial somite.
82 rs that drive Myf5 expression in epaxial and hypaxial somites, branchial arches and central nervous s
83 ogenitors in the presomitic mesoderm and the hypaxial somites.
84 uous dermomyotome and myotome, whose epaxial-hypaxial subdivision and hence the formation of distinct
85                                  The epaxial/hypaxial terminology is also used to describe regions of
86 atic losses were observed in the epaxial and hypaxial trunk muscles that are proximal to the vertebra