ライフサイエンスコーパス: MGN

1 Of the specific diseases, FSGS and MGN recurred more commonly (20.2% and 20.3%, respectivel

2 ons of lesions of normal retinal targets and MGN afferents.

3 gated the full extent of connections between MGN and AI, R, RT, RTp, and STGr using retrograde and an

4 On each MGN biopsy positive by IF, 14/19 showed absence of depos

5 s and morphological data were determined for MGN muscles and eighty-two single motor units in muscles

6 s studies have examined the projections from MGN to auditory cortex, but most have focused on the cau

7 ic force (Fo) of whole medial gastrocnemius (MGN) muscles in old compared with adult rats.

8 and/or necrosis in > or = 50% of glomeruli (MGN with segmental proliferation and/or necrosis in > 50

9 pathology of membranous glomerulonephritis (MGN) in patients with systemic lupus erythematosus (SLE)

10 of recurrent membranous glomerulonephritis (MGN) in renal allografts.

11 nti-GBM), and membranous glomerulonephritis (MGN).

12 nd CR as surrogates for long-term outcome in MGN.

13 ng-term prognosis in membranous nephropathy (MGN), variability in proteinuria levels and lag between

14 ional microarray screen comparing the normal MGN to "rewired" MGN, in which normal auditory afferents

15 first characterized the inputs to the normal MGN, and the most effective combination of neonatal lesi

16 slices of A1 and medial geniculate nucleus (MGN) in mouse from postnatal day 1 (P1) to P13.

17 ), but not in the medial geniculate nucleus (MGN) of rats that explore a novel-complex environment in

18 ansmission in the medial geniculate nucleus (MGN) to lateral nucleus of the amygdala (LA) pathway, a

19 elay nucleus, the medial geniculate nucleus (MGN), and principal visual relay nucleus, the lateral ge

20 sion (MGm) of the medial geniculate nucleus (MGN), the posterior intralaminar nucleus (PIN), and the

21 jections from the medial geniculate nucleus (MGN).

22 to innervate the medial geniculate nucleus (MGN).

23 vision of the cat medial geniculate nucleus (MGN).

24 to innervate the medial geniculate nucleus (MGN).

25 to innervate the medial geniculate nucleus (MGN).

26 und that, after extensive deafferentation of MGN, other axonal systems in addition to retinal axons p

27 in 4 months post-transplant with evidence of MGN and on follow-up biopsies, compared to a biopsy cont

28 ojections correlates well with the extent of MGN deafferentation, but not with extent of removal of n

29 /or necrosis in > 50%, WHO Vc > or = 50%, or MGN with superimposed diffuse endocapillary proliferatio

30 projections to the LA originating from PIN, MGN, and Sg, we also found substantial projections from

31 tients with biopsy-proven idiopathic/primary MGN who achieved a remission after a period of nephrotic

32 opsy features aids in diagnosis of recurrent MGN before patients develop significant proteinuria.

33 group of eight transplants without recurrent MGN.

34 consistent with the idea that ectopic retino-MGN projections develop by sprouting of axon collaterals

35 s required for the induction of novel retino-MGN projections.

36 The diameters of retino-MGN axons suggest that more than one type of retinal gan

37 seems necessary for the formation of retino-MGN connections.

38 We found that the extent of retino-MGN projections correlates well with the extent of MGN d

39 The resulting extent of retino-MGN projections was estimated for each case at adulthood

40 These retino-MGN projections also show retinotopic organization.

41 Data from this screen indicate that rewired MGN acquires some patterns of gene expression that are p

42 screen comparing the normal MGN to "rewired" MGN, in which normal auditory afferents are ablated and

43 SLE MGN has a heterogeneous course and outcome, and this var

44 Twenty-eight patients had SLE MGN with endocapillary proliferation and/or necrosis in

45 Fifteen patients had SLE MGN with segmental endocapillary proliferation and/or ne

46 Thirty-six patients had "pure' SLE MGN without (WHO Va) or with (WHO Vb) mesangial hypercel

47 istory and/or a response to therapy than SLE MGN with less widespread glomerular inflammation and/or

48 e medial geniculate nucleus of the thalamus (MGN) and the basolateral complex of the amygdala (BLA) a

49 The MGN input to RTp distinguished this rostral extension of

50 The MGN projections to SPNs strengthen between P2 and P13 an

51 al studies indicate that neurons in both the MGN and BLA exhibit associative plasticity of spike firi

52 eceive functional excitatory inputs from the MGN as early as P2.

53 ease in both CS-elicited spike firing in the MGN and conditional freezing behavior in vehicle-treated

54 increases in CS-elicited spike firing in the MGN and conditional freezing to the auditory CS.

55 ch are expressed in similar gradients in the MGN and LGd, can be used to pattern novel retinal projec

56 ustering and eye-specific segregation in the MGN arise as a refinement of initially diffuse and overl

57 entation of retinal terminal clusters in the MGN closely match those of relay cell dendrites arrayed

58 minate in discrete eye-specific zones in the MGN of rewired wild-type and ephrin-A2/A5 knockout mice.

59 whether the development of plasticity in the MGN requires the BLA.

60 In the MGN, as in the LGd, terminations from the two eyes show

61 iptional repressor expressed strongly in the MGN, was found to be positively regulated by activity in

62 o be positively regulated by activity in the MGN.

63 avoid areas of high ephrin expression in the MGN.

64 to pattern novel retinal projections in the MGN.

65 representation of the ipsilateral eye in the MGN.

66 ther sets of axons for terminal space in the MGN.

67 arrayed within fibrodendritic laminae in the MGN.

68 type of retinal ganglion cells innervate the MGN under a lesion paradigm that spares the visual corte

69 lated and novel retinal inputs innervate the MGN.

70 us, by injecting retrograde tracers into the MGN of normal and neonatally operated adult ferrets, res

71 l projections from the dorsal portion of the MGN (MGd) and the lateral posterior thalamic nucleus (LP

72 c inputs from the ventral subdivision of the MGN (MGv; the primary/lemniscal auditory pathway).

73 al targets along with deafferentation of the MGN are two concurrent factors required for the inductio

74 in the dorsal superficial subdivision of the MGN nucleus is very similar to that in other thalamic nu

75 odes implanted in the medial division of the MGN of conscious and freely moving rats.

76 rt of the LA, whereas the caudal part of the MGN projects to the caudal part of the LA.

77 thin the normal cellular organization of the MGN, which does not differentiate into eye-specific cell

78 ing increase in the synaptic efficacy of the MGN-LA pathway attributable to fear-conditioning itself,

79 lecules were synthesized and modified on the MGN surface for targeted MRI detection.

80 l inputs from multisensory areas outside the MGN (30% in RTp vs. 1-5% in core areas).

81 A, such that projections from throughout the MGN terminate in the anterior part of the LA, whereas th

82 We find that retinal projections to the MGN are arranged in scattered clusters.

83 to retinal axons project ectopically to the MGN.

84 Clustering of retinal projections within the MGN and eye-specific segregation involve progressive rem

85 For old rats, whole MGN muscle Fo was 29% less than the value of 11.2 N meas