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1 e lateral plate mesoderm - the heart and the pectoral fin.
2 ETs) on the surfaces of adult male zebrafish pectoral fins.
3 in the developing brain, jaw structures and pectoral fins.
4 eral plate mesoderm for specification of the pectoral fins.
5 postfertilization, four nerves innervate the pectoral fins.
6 n fold defect, which also displays malformed pectoral fins.
7 otoreceptor cell layer, branchial arches and pectoral fins.
8 24 function results in viable fish that lack pectoral fins.
9 d formation, leading to the complete loss of pectoral fins.
10 midline mesendodermal tissues and absence of pectoral fins.
11 vous system, adaxial mesoderm, cartilage and pectoral fins.
12 -slaps were initiated by an adduction of the pectoral fins, a manoeuvre that changed a thresher shark
16 including boxer, dackel and pincher, affect pectoral fins and axonal trajectories in the brain, as w
17 rphants and mutants (heartstrings; hst) lack pectoral fins and exhibit a persistently elongated heart
18 sive lethal mutant heartstrings, which lacks pectoral fins and exhibits severe cardiac dysfunction, b
19 through the constant "flapping" of wing-like pectoral fins and minimizes heat loss through a series o
20 in a variety of tissues including the brain, pectoral fins and pigment cells as well as pharyngeal ar
21 ideos and amputation experiments reveal that pectoral fins and their ETs are used for male spawning.
23 n the distal portion of developing zebrafish pectoral fins, and respond to the same functional cues a
25 and, for sharks, the functions of dorsal and pectoral fins are considered well divided: the former as
26 rphological and behavioral diversity and use pectoral fin-based propulsion with fins ranging in shape
27 alb2b, crx, neurod, rs1, sox4a and vsx1) and pectoral fin bud (klf2b and EST AI722369) as candidate t
28 four specific, viable phenotypes: failure of pectoral fin bud initiation, deletion of the 6th pharyng
31 lic neural crest, the pharyngeal arches, the pectoral fin buds and the gut in contrast to its paralog
33 the developmental mechanisms present in the pectoral fins, but re-iterated at a posterior location.
34 es display regenerative defects in amputated pectoral fins, caused by impaired blastemal proliferatio
37 rmalities, pericardial edema, failed jaw and pectoral fin development, and the absence of differentia
41 tetrapods, hox gene expression in zebrafish pectoral fins during the distal/third phase is dependent
42 uired to guide spinal nerves innervating the pectoral fins, equivalent to the tetrapod forelimbs.
43 how a strikingly unique morphology where the pectoral fin extends anteriorly to ultimately fuse with
45 rst zebrafish mutant identified in which the pectoral fins fail to make the transition from an apical
46 e is sufficient for lateral fast somitic and pectoral fin fibre formation from the lateral compartmen
47 d in the developing atrium, ventricle and in pectoral fin fields, but its genetic targets are still b
48 ined sensory physiology and mechanics of the pectoral fins, forelimb homologs, in the fish family Lab
49 ficient in retinoic acid (RA) signaling, the pectoral fins (forelimbs) are lost while both chambers o
51 that anterior and posterior portions of the pectoral fin have different genetic underpinnings: canon
53 from tissues along the AP axis of uninjured pectoral fins identified many genes with region-specific
54 ganizes the distal cells of the fin fold and pectoral fins in order to promote the morphogenesis of t
57 nnervation to the tetrapod forelimb and fish pectoral fin is assumed to share a conserved spinal cord
58 ogs are specifically enriched at the jaw and pectoral fin joints of zebrafish, stickleback, and gar,
59 precocious commitment of cells derived from pectoral fin level somites to forming hypaxial and speci
60 ts is observed in the differentiation of the pectoral fin mesenchyme: small fin buds form in a delaye
63 od gene delays and reduces early somitic and pectoral fin myogenesis, reduces miR-206 expression, and
64 ioceptive capabilities, and suggest that the pectoral fins need to be considered as possible proprioc
67 nes, expression of hoxa/d genes in zebrafish pectoral fins occurs in three distinct phases, in which
68 s, is expressed in the posterior half of the pectoral fin of skate, shark, and zebrafish but in the a
74 Transgenic overexpression of hand2 in all pectoral fin rays did not affect formation of the prolif
75 osensory abilities of afferent nerves in the pectoral fin rays, limb structures used by many fish spe
76 s for all three traits, lateral-line scales, pectoral-fin rays and pelvic-fin rays, previously found
77 l fin also regenerates but, in contrast with pectoral fins, regeneration can resume after release fro
78 link between multiple phenotypic characters: pectoral fin shape, swimming behavior, fin ray stiffness
79 cestral patterns of gene expression in skate pectoral fins, shedding light on the molecular mechanism
80 ield cell convergence and truncations in the pectoral fin skeleton, resembling aspects of the forelim
82 s premature differentiation of the zebrafish pectoral fins, which are analogous to the forelimbs of t
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