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1 em likely predisposed for the evolution of a syrinx.
2 major driving force in the evolution of the syrinx.
3 sounds using a unique vocal organ called the syrinx.
4 the spinal cord could be misinterpreted as a syrinx.
5 x, but are commonly generated in the excised syrinx.
6 feedback by deafening or denervation of the syrinx.
7 d unilateral or bilateral denervation of the syrinx.
8 th transitions in the dynamical state of the syrinx.
9 ed by rostrad movement and stretching of the syrinx.
10 he opposite end, birds phonate only with the syrinx.
11 origins of the novel avian vocal organ, the syrinx.
12 are generated in the avian vocal organ, the syrinx.
13 tated the origin of vocal folds in the avian syrinx.
14 easurements of the patients with and without syrinx, according to the S/C ratio, were statistically c
15 ontrol of labia and membrane position in the syrinx; adaptations that set them apart from closely rel
17 nt developmental tissues, vocal folds in the syrinx and larynx have similar tissue composition and ar
18 eristics, including the spinal region of the syrinx and the absence of OSAHS, correlated with spontan
22 and the few reported fossilized parts of the syrinx are geologically young (from the Pleistocene and
24 tive biomechanical model of the vocal organ (syrinx) as the low-dimensional target for these mappings
25 in artificially induced sound in the intact syrinx, but are commonly generated in the excised syrinx
26 re can induce partial masculinization of the syrinx, but other factors must be important in mediating
27 with syrinx group 1 and the patients without syrinx, but the AP length of posterior fossa was statist
28 thermore, in vitro experiments show that the syrinx can produce a sequence of oscillatory states that
30 The endoscopic images of the intact songbird syrinx during spontaneous and brain stimulation-induced
32 first remains, to our knowledge, of a fossil syrinx from the Mesozoic Era, which are preserved in thr
34 nce in the measurements of the patients with syrinx group 1 and the patients without syrinx, but the
35 lly significantly lower in the patients with syrinx group 2 than the patients without syrinx (p = 0.0
38 well as CT imaging of the Vegavis and Eocene syrinxes, informs both the reconstruction of ancestral s
42 How sound is generated in the hummingbird syrinx is largely unknown despite their complex vocal be
43 at the cranial end of the airway, the avian syrinx is located at the base of the airway at the split
44 ocated at the tracheobronchial junction, the syrinx is responsible for avian vocalization, but it is
46 (e.g., HVC, dopaminergic cell groups, or the syrinx) is required to enhance the quality of song (i.e.
47 g mechanism in the songbird vocal organ, the syrinx, is based on indirect evidence and theoretical tr
50 radiologically defined as >50% reduction in syrinx length or maximal axial diameter on T1-weighted M
52 isms existed in the volume of nXIIts, and in syrinx mass and size of muscle fibers, but not in motone
54 zed condition in archosaurian taxa without a syrinx, may indicate that a complex syrinx was a late ar
55 There are between-species differences in syrinx measurements, despite similar overall morphology.
56 hat a key element in selection for the early syrinx might be the position of this vocal structure: al
65 d-contrast X-ray computed tomography (CT) of syrinx structure in twelve extant non-passerine birds, a
66 l parameters describing the vocal organ, the syrinx, such as material properties of syringeal element
67 he hypoglossal nucleus, which innervates the syrinx (the avian vocal organ) but possesses no known pr
73 nlinear properties of their vocal organ, the syrinx, to insert subharmonic transitions in their song.
75 ithout a syrinx, may indicate that a complex syrinx was a late arising feature in the evolution of bi
79 rinx were divided into 2 groupd according to syrinx width/cord width (S/C) ratios: group 1 - S/C rati
80 monachus, we replaced the vocal source, the syrinx, with a small speaker that generated a broad-band