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1 cluding enlargement of the internal auditory meatus.
2 livocochlear bundle in the internal auditory meatus.
3 ations in formation of the external acoustic meatus.
4  levels of IL-13 and periostin in the middle meatus.
5 of the urine stream as it exits the urethral meatus.
6 ies were derived from cultures of the middle meatus.
7 EMG and expulsion of urine from the urethral meatus.
8 ayer is contributed by the external acoustic meatus, a derivative of the first pharyngeal cleft.
9 n between formation of the external acoustic meatus and formation of the tympanic ring, a first arch-
10 at three nasal sites (anterior naris, middle meatus, and sphenoethmoidal recess).
11 n and morphogenesis of the external acoustic meatus, and that expression of the Hoxa-2 and goosecoid
12 nerve in the fundus of the internal auditory meatus by trephining the medial modiolar wall of the coc
13                       Cultures of the middle meatus cannot be used as a surrogate for a maxillary sin
14  by organisms that migrate from the urethral meatus-catheter interface along the external surface of
15 or staphylococcal colonization of the middle meatus in healthy adults.
16 ring the anatomical location of the urethral meatus, it is surprising that urine is normally sterile.
17 tively smooth central channels of the dorsal meatus map onto the dorsal MOB, whereas the highly convo
18 in the study rolled a Dacron swab across the meatus three times (method 1).
19 nclusion, inoculation of WT male mice in the meatus urethra with a human serovar of C. trachomatis re
20  conclusion, inoculation of male mice in the meatus urethra with C. trachomatis MoPn results in an in
21 , we inoculated C3H/HeN (H-2(k)) mice in the meatus urethra with C. trachomatis serovar D.
22 sion model, male mice were inoculated in the meatus urethra with Chlamydia muridarum and they were ca
23 eN (H-2(k)) male mice were inoculated in the meatus urethra with doses ranging from 10(1) to 10(7) in
24 of infection, we inoculated male mice in the meatus urethra.