ライフサイエンスコーパス: auricle

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1 e into the specialized tissues of ligule and auricle.

2 clearly delineated, leading to an undulating auricle.

3 ial Purkinje cells of the lateral cerebellar auricle.

4 rs of the Kn1 family, affects the ligule and auricle.

5 undary even in the absence of the ligule and auricles.

6 e ligule, and two wedge-like structures, the auricles.

7 The auricles act as a hinge, allowing the leaf blade to proj

8 ade/sheath boundary and the boundary between auricle and blade is not clearly delineated, leading to

9 in proximal to distal order, sheath, ligule, auricle and blade.

10 leless3-O (Lg3-O) transforms the leaf blade, auricle and ligule into sheath around the midrib region.

11 Mb is absent from heart auricle and oxidative skeletal muscle of all species.

12 cessive liguleless1 mutants lack ligules and auricles and have upright leaves.

13 th bilateral cleft lip and palate, malformed auricles, and bilateral ectrodactyly of his hands and fe

14 d sheath are two wedge-shaped tissues called auricles, and the ligule, an epidermally derived fringe.

15 The ligule and the associated auricle are dispensable structures, amenable to genetic

16 iguleless1 (Ig1) gene expression, ligule and auricle are not formed, and the blade-sheath boundary do

17 The maize ligule and auricle are structures on the maize leaf that develop at

18 iguleless2-reference (lg2-R), the ligule and auricles are often absent or positioned incorrectly and

19 econstruction which largely mimic the native auricle both biomechanically and histologically, even af

20 between blade and sheath are the ligule and auricles, both of which are absent in the recessive ligu

21 rrowing the region from which the ligule and auricle develop in a typical maize leaf.

22 type, such as ligule position, inhibition of auricle development, and sheath thickness showed autonom

23 alized BR signaling is involved in promoting auricle development, consistent with the zmbri1-RNAi phe

24 nown to be uniquely necessary for ligule and auricle development.

25 of leaf support tissues, and for restricting auricle expansion at the midrib.

26 before the first visible sign of ligule and auricle formation.

27 green, upright, and twisted, with decreased auricle formation.

28 ave identified a new dominant mutation, Wavy auricle in blade1 (Wab1), which affects patterning in bo

29 The dominant mutant Wavy auricle in blade1 (Wab1-R) produces ectopic auricle tiss

30 1 and lg2 play different roles in the ligule-auricle induction mechanism.

31 ) to transmit and receive a make-ligule-make-auricle inductive signal.

32 h-like with ectopic ligule (ectopic ligule), auricle-like, macro-hairless blade and wild-type blade.

33 cement, sheath-like with ectopic ligule, and auricle-like.

34 The ligule and auricle mark the boundary between distal blade and proxi

35 ry disruption, shorter ligule, and disrupted auricle morphology of RNAi lines resemble KNOTTED1-LIKE

36 n of the BES1-YFP reporter was strong in the auricle region of developing leaves, suggesting that loc

37 Specialized ligule and auricle structures form at the blade-sheath boundary.

38 ge the shape and position of both ligule and auricle, thus disturbing the overall pattern of the leaf

39 s eta1 individuals have a wavy overgrowth of auricle tissue and the blade/sheath boundary is diffuse.

40 auricle in blade1 (Wab1-R) produces ectopic auricle tissue in the blade and increases the domain of

41 specific regions of the circulatory system (auricle, ventricle, cristae aorta, anterior aorta) and t

42 cifies the precise position where ligule and auricle will develop.

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