ライフサイエンスコーパス: tecta

1 re imbedded and that CEACAM16 interacts with TECTA.

2 days after a unilateral stab injury to optic tecta.

3 ell death were also confirmed in the injured tecta.

4 cation that individual cells project to both tecta.

5 medial/ventrolateral thalamus, and the tenia tecta.

6 yndrome may be due to haploinsufficiency for TECTA.

7 EF2 phosphorylation is widespread in tadpole tecta.

8 alpha-Tectorin (TECTA), a glycosylphosphatidylinositol (GPI)-anchored EC

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

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

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

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

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

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

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

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

17 , and Prm1), a paralogous somatic cell gene (TectA), and a mitochondrial gene commonly used for phylo

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

19 undant in anterior olfactory nucleus, taenia tecta, and lateral septum.

20 werful input from the piriform cortex, tenia tecta, and the BLA but only very weak input from the OB.

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

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

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

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

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

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

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

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

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

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

31 extrahippocampal regions including the tenia tecta, diagonal band, and retromammillary nucleus, but a

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

33 Tecta from frogs with different degrees of plasticity sh

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

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

36 merous pathogenic mutations in both UMOD and TECTA genes.

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

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

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

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

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

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

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

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

45 1/subiculum of hippocampus; claustrum, tania tecta, lateral septum, substantia innominata, and medial

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

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

48 ing a previously unrecognised consequence of Tecta mutations.

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

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

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

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

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

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

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

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

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

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

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

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

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

62 In Tecta/Tectb(-/-) double knockout mice, in which the TM i

63 ial membrane (TM) from the organ of Corti in Tecta/Tectb(-/-) mice affects the biophysical properties

64 Tecta/Tectb(-/-) mice have highly elevated hearing thres

65 turation of hair cells is also unaffected in Tecta/Tectb(-/-) mice, and the resting open probability

66 onics, are symmetrical in both wild-type and Tecta/Tectb(-/-) mice, indicating that the TM does not b

67 channel resting P(o) in vivo is also high in Tecta/Tectb(-/-) mice, indicating that the TM is unlikel

68 pendent otoacoustic emissions in vivo in the Tecta/Tectb(-/-) mice.

69 ting adaptation to repetitive stimulation in Tecta/Tectb(-/-) mice.

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

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

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

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

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

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

76 MYO6, MYO7A, PTPRQ, and TECTA variants were present in 8.9% of ARHL cases but le

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

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

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

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

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

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

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

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

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

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

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

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

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

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