ライフサイエンスコーパス: tecta

1 days after a unilateral stab injury to optic tecta.

2 ell death were also confirmed in the injured tecta.

3 cation that individual cells project to both tecta.

4 medial/ventrolateral thalamus, and the tenia tecta.

5 yndrome may be due to haploinsufficiency for TECTA.

6 EF2 phosphorylation is widespread in tadpole tecta.

7 re imbedded and that CEACAM16 interacts with TECTA.

8 A missense mutation in Tecta, a gene that encodes for the alpha-tectorin protei

9 tion occurred in the indusium griseum, tenia tecta and fasciola cinerea within 5 days post-METH expos

10 ronal degeneration was detected in the tenia tecta and other regions of the anterior limbic system of

11 Previous studies have shown that TECTA and TECTB are both required for formation of the s

12 g that it may stabilize interactions between TECTA and TECTB.

13 to both ipsilateral and contralateral optic tecta and to an array of three nuclei in the auditory th

14 formed by two glycoproteins, alpha-tectorin (Tecta) and beta-tectorin (Tectb).

15 homopolymeric glycoproteins alpha-tectorin (TECTA) and glycoprotein 2 (GP2).

16 the dorsal peduncular cortex, ventral tenia tecta, and anterior olfactory tubercle and piriform cort

17 een in the dorsal endopiriform, dorsal tenia tecta, bed nucleus, and the red nucleus.

18 alpha-Tectorin (TECTA), beta-tectorin (TECTB), and carcinoembryonic anti

19 These findings were exaggerated in Tecta(C1509G/C1509G) mice, where the tectorial membrane

20 ncy hearing loss in a Spanish family and the Tecta(C1619S/+) mouse for a zonadhesin-like (ZA) domain

21 quency hearing loss in a Belgian family, the Tecta(C1837G/+) mouse for a ZP-domain mutation underlyin

22 Missense mutations in Tecta cause dominant forms of non-syndromic deafness and

23 In humans, the Y1870C missense mutation in TECTA causes a 50- to 80-dB hearing loss.

24 l subiculum of the hippocampus, dorsal tenia tecta, claustrum, lateral septum, dorsal striatum, nucle

25 Electrically elicited responses from Tecta(DeltaENT/DeltaENT) mice were markedly similar to a

26 lacements from the cochleae of wild-type and Tecta(DeltaENT/DeltaENT) mice, in which stereocilia are

27 orted in humans, with mutations in different Tecta domains causing mid- or high-frequency hearing imp

28 Tecta from frogs with different degrees of plasticity sh

29 cular macula is dependent on tectorin alpha (tecta) function, which is disrupted in the rolling stone

30 Mutations in the human TECTA gene can cause either dominant (DFNA8/12) or reces

31 merous pathogenic mutations in both UMOD and TECTA genes.

32 nucleus; in the induseum griseum and taenia tecta; in the olfactory tubercle; in CA1-CA3, the hilus

33 in the ventricular zone (VZ) of the injured tecta indicated an astroglial precursor response.

34 lyzed and compared with samples from control tecta injected with cytochrome C.

35 CRF-like immunoreactivity included the tenia tecta, inner layers of cingulate cortex, lateral septum,

36 Tecta is a modular, non-collagenous protein of the tecto

37 Alpha-tectorin (encoded by Tecta) is a component of the tectorial membrane, an extr

38 alpha-Tectorin (Tecta) is a major constituent of the tectorial membrane

39 ted as models for human Tecta mutations; the Tecta(L1820F,G1824D/+) mouse for zona pellucida (ZP) dom

40 1/subiculum of hippocampus; claustrum, tania tecta, lateral septum, substantia innominata, and medial

41 imbic and dorsopeduncular cortices and tenia tecta) mPFC lesions were trained in a multiple-choice di

42 Despite elevated auditory thresholds, the Tecta mutant mice all exhibit an enhanced tendency to ha

43 ing a previously unrecognised consequence of Tecta mutations.

44 mutant mice were created as models for human Tecta mutations; the Tecta(L1820F,G1824D/+) mouse for zo

45 In En-infected tecta, nasal retinal axons form an abnormally diffuse pr

46 In intact tadpole tecta, NMDAR activation leads to phosphorylation of a su

47 vasculosum of the lamina terminalis, taenia tecta, nucleus accumbens, lateral septum, endopiriform n

48 , and ventrolateral orbital cortices, taenia tecta, nucleus accumbens, paraventricular nucleus of the

49 sine binding was significantly higher in the tecta of adults than in those of tadpoles.

50 esis of an asymmetric modulation between the tecta of both hemispheres.

51 I-labeled retinotectal fibers in whole-mount tecta of embryos pretreated with a polysialic acid-speci

52 quency tuning that are observed in the optic tecta of owls raised with abnormal auditory experience.

53 ous studies have demonstrated that the optic tecta of the left and right brain halves reciprocally in

54 In adult tecta, only NARPP-21 and -50 were phosphorylation.

55 n of the ventricular surface in FGF2-treated tecta outpaces the expansion of the pial surface, creati

56 , fasciola cinereum, induseum griseum, tenia tecta, presubiculum, and parasubiculum), and in the sept

57 d encode diaphanous (HDIA1), alpha-tectorin (TECTA), the transcription factor POU4F3, connexin 26 (GJ

58 transgenic mice with the Y1870C mutation in Tecta, the tectorial membrane's matrix structure is disr

59 retrograde labels are injected into opposite tecta, there is no indication that individual cells proj

60 ot well understood in species whose midbrain tecta undergo a protracted anterior to posterior develop

61 ous studies, establish an allelic series for Tecta unequivocally demonstrating an association between

62 NOS in doubly innervated Rana tadpole optic tecta using L-N(G)-nitroarginine methyl ester in Elvax.

63 ne expression in ectopic eyes and denervated tecta was analyzed over time using in situ hybridization

64 lture system for neurons from larval Xenopus tecta, we show that blocking NMDA receptors or preventin

65 ater, chicken embryos were killed, and optic tecta were dissected and processed for histochemical det

66 Notably, neurons in rewired tecta were predominantly binocular and showed matching d

67 Notably, neurons in rewired tecta were predominantly binocular and showed matching d

68 In contrast, in adult tecta, where synaptic plasticity is reduced, this phosph

69 osomal preparations after treatment of whole tecta with pharmacological agents.

70 zures had somatic degeneration in the taenia tecta within 3 days of amphetamine exposure.

71 TMs from Tecta(Y)(1870C/+) mice showed little volume change in re

72 In Tecta(Y)(1870C/+) mice, the tectorin content of the TM w

73 hear impedance was reduced by 10+/-1.6 dB in Tecta(Y)(1870C/+) mice.

74 mmol/L in wild-types to -2.1+/-0.7 mmol/L in Tecta(Y)(1870C/+) TMs.

75 ) mice is significantly sharper than that of Tecta(Y1870C/+) mice, even though TM stiffnesses are sim

76 Thus, using Tecta(Y1870C/+) mice, we have genetically isolated a sec

77 the basal cochlear turn, nanoscale pores of Tecta(Y1870C/+) TMs are significantly larger than those