ライフサイエンスコーパス: fore-

1 side of the body (e.g., right hind and right fore).

2 and ForG the inner territory, whereas ForA, ForE, and ForH are more strongly recruited to the extern

3 hree Diaphanous-related formins (DRFs) ForA, ForE, and ForH are regulated by the RhoA-like GTPase Rac

4 Masker' based on image entropy to tackle the fore- and background segmentation (masking) task in hist

5 graphic frequency with the morphology of the fore- and hind limbs of extant and fossil proboscideans

6 ; R. balochistanensis has virtually complete fore- and hind limbs.

7 Eml5 transcripts can be detected in fore- and hindbrain structures from embryonic day 13 onw

8 expanded structures in the fat pads of their fore- and hindfeet, but for three centuries these have b

9 ouse cerebellum, midbrain, nasal process and fore- and hindlimb buds.

10 Using Tbx5 and Tbx4 as fore- and hindlimb field markers, respectively, we have

11 Furthermore, we found that both fore- and hindlimb fields arise gradually during gastrul

12 rebro-olivocerebellar paths originating from fore- and hindlimb motor cortex has implications for the

13 trating that LAPNs secure alternation of the fore- and hindlimb pairs during overground stepping.

14 creases in horizontal bar test catalepsy and fore- and hindlimb paw retraction latencies.

15 ud occurs in the anterior mesenchyme of both fore- and hindlimb.

16 correlated with altered coordination of the fore- and hindlimbs and impaired balance.

17 specify the differential development of the fore- and hindlimbs are unknown.

18 ages, pectoral and pelvic fins in fishes and fore- and hindlimbs in tetrapods.

19 ty and integration of both the heads and the fore- and hindlimbs of abnormal cyclopic trisomy 18 and

20 th and a 30% decrease in inflammation in the fore- and hindlimbs of mdx mice.

21 t T10-T11) hemisections, coordination of the fore- and hindlimbs was altered and/or became less consi

22 tensive anterior digit abnormalities of both fore- and hindlimbs, while all double Bmp4(tm1); Alx4(tm

23 phrenic nerve, and the dorsal motor nerve in fore- and hindlimbs.

24 distinct structures, such as the vertebrate fore- and hindlimbs.

25 tal digit duplications were seen in both the fore- and hindlimbs.

26 birth, despite the complete absence of both fore- and hindlimbs.

27 so exhibit syndactyly (digit fusions) of the fore- and hindlimbs.

28 Fore- and hindpaw withdrawal latencies from a 30 degrees

29 tinct Tarachoptera, with dense scales on the fore- and hindwings, while the other is an early lineage

30 individual insects, such as left and right, fore- and hindwings.

31 a-receptors, in adjacent coronal sections in fore- and midbrain and in sagittal sections, were labell

32 O binding to mu-opioid receptors in selected fore- and midbrain regions of chickens subject to varyin

33 tivity was evident in several regions of the fore- and midbrain, in support of putative homologies to

34 n-segmental and homologous to the vertebrate fore- and midbrain.

35 thalamus at the expense of the ZLI and other fore- and/or mid-brain regions.

36 agonal limb pairs (e.g., right hind and left fore) are more closely related in time than those of the

37 ssion of both genes was found in adult mouse fore- but not mid- or hindbrain.

38 ru imposed strong balancing selection on the Fore, essentially eliminating PRNP 129 homozygotes.

39 isorder characterised predominantly by upper(fore) limb defects and heart abnormalities.

40 Cross-species assessment of upper/fore- limb and lower/hind- limb motor units using object

41 evelopmental defects in the formation of the fore-, mid- and hindbrain and somites of E- embryos at 2

42 dermal cell lineages and a gut consisting of fore-, mid- and hindgut.

43 ormation of large hemorrhages throughout the fore-, mid-, and hindbrain by E11.5.

44 pmental control genes defining the segmental fore-, mid-, and hindbrain suggests that those character

45 ar mechanisms in three regions of the brain (Fore-, Mid-, and Hindbrain) during the interaction of th

46 nd oligodendrocytes, which populate the host fore-, mid-, and hindbrain.

47 module distinct from, and ancestral to, the fore-, mid-, and hindbrain.

48 pattern is formed from three broad domains: fore-, mid-, and hindgut that have distinct functional,

49 he model proceeds to form 6-14 somite pairs, fore-/mid-/hindbrain, a looping heart tube, optic buds,

50 l breast milk samples, with a gradient from "fore" milk to "hind" milk.

51 Electrical stimulation of the ipsilateral fore- or hindimbs or somatotopically corresponding parts

52 ssion domains in the heart and the exclusive fore- or hindlimb expression of Tbx5 and Tbx4, respectiv

53 o-Ruby or Fluoro-Emerald) were made into the fore- or hindlimb parts of the motor cortex where stimul

54 ding (spino-olivocerebellar) paths targeting fore- or hindlimb-receiving parts of the C1 zone.

55 are, in marked contrast to younger unexposed Fore, predominantly PRNP 129 heterozygotes.

56 isms of aggregate formation have come to the fore, suggesting that nucleation-dependent aggregation m

57 quantum simulators has recently come to the fore: they generally require less memory than their clas

58 usly shown that combining Fourier rebinning (FORE) with 2-dimensional (2D) statistical image reconstr