ライフサイエンスコーパス: retinoschisis

1 as devoid of MG rip apart, a defect known as retinoschisis.

2 nal thickness decreases with age in X-linked retinoschisis.

3 n impairment in young males, called X-linked retinoschisis.

4 etinal hole, and typical degenerative senile retinoschisis.

5 come from a recent investigation in X-linked retinoschisis, a currently untreatable retinopathy.

6 s mutated, as it occurs in X-linked juvenile retinoschisis, a disease that results in morphological a

7 nked retinoschisis gene (RS1) cause X-linked retinoschisis, a form of progressive blindness.

8 riteria included a family history of macular retinoschisis, a known genetic abnormality associated wi

9 Most cases of X-linked juvenile retinoschisis and degenerative retinoschisis never requi

10 eted protein implicated in X-linked juvenile retinoschisis and essential for the structural and funct

11 uch as macular Berlin's edema, midperipheral retinoschisis, and choroidal and retinal detachment migh

12 choroidal melanoma; and intraretinal edema, retinoschisis, and retinal thinning overlying irradiated

13 tosa, Leber's congenital amaurosis, X-linked retinoschisis, Best's disease, Stargardt's disease, and

14 e discovery that retinal folds and traumatic retinoschisis can very rarely occur after crush head inj

15 ERG waveform that is characteristic of human retinoschisis disease and that implicates a synaptic tra

16 This new locus (RP23) encompasses the retinoschisis disease gene; therefore, XLRS1 was screene

17 he coding region of the gene responsible for retinoschisis do not cause RP23.

18 , loss-of-function mutations in the X-linked retinoschisis gene (RS1) cause X-linked retinoschisis, a

19 was amplified with primers specific for the retinoschisis gene (XLRS1), and the products were screen

20 holog (Xlrs1) of the human X-linked juvenile retinoschisis gene (XLRS1).

21 nine hydroxylase, paired box 6, the X-linked retinoschisis gene and TSC2/tuberin.

22 ulitis, whereas congenital disorders such as retinoschisis had the worst.

23 therapy will benefit patients with X-linked retinoschisis in a forthcoming clinical trial.

24 -photoreceptor phenotype similar to X-linked retinoschisis in young males.

25 ings feature residues implicated in X-linked retinoschisis, indicating the importance of correct asse

26 Thus, X-linked retinoschisis is caused by abnormalities in a putative s

27 X-linked retinoschisis is characterized by microcystic-like chang

28 treomacular traction syndrome, macular hole, retinoschisis, macular edema, central serous chorioretin

29 An X-linked retinoschisis mouse (Rs1h-KO) model was created by subst

30 a known genetic abnormality associated with retinoschisis, myopic traction maculopathy, epiretinal m

31 nked juvenile retinoschisis and degenerative retinoschisis never require any type of surgical interve

32 ore, our data suggest that X-linked juvenile retinoschisis originates from abnormalities in a photore

33 ss and volume measurements were increased in retinoschisis patients compared to controls.

34 ss and volume measurements were decreased in retinoschisis patients compared to controls.

35 s and volumes were consistently increased in retinoschisis patients relative to controls.

36 The mean age of the retinoschisis patients was 26.4 years.

37 Foveal schisis was observed in 81% of retinoschisis patients.

38 inal detachment, typical degenerative senile retinoschisis, peripheral laser coagulation scars, ora t

39 actors can contribute to the severity of the retinoschisis phenotype.

40 X-linked retinoschisis results in visual loss in early life with

41 5 years of age underwent genotyping, and the retinoschisis (RS1) mutations were classified as less se

42 A macular retinoschisis was detected in 5 eyes (31%), decreased el

43 three eyes of 33 male patients with X-linked retinoschisis were gleaned from a SD OCT database at the

44 ructural features of human X-linked juvenile retinoschisis with dissection through, and disorganizati

45 ble option in the treatment of patients with retinoschisis without causing significant cellular damag

46 family (a total of 18 members)with X-linked retinoschisis (XLRS) and detected a novel mutations of c

47 istent with human clinical X-linked juvenile retinoschisis (XLRS) in showing schisis cavities, which

48 X-linked retinoschisis (XLRS) is a form of macular degeneration w

49 X-linked retinoschisis (XLRS) is an inherited form of macular deg

50 The human retinal synaptic disease X-linked retinoschisis (XLRS) is characterized by impaired visual

51 X-linked Retinoschisis (XLRS) is one of the most common macular d

52 e cone system typically observed in X-linked retinoschisis (XLRS) represents a relatively greater def

53 Individuals with X-linked retinoschisis (XLRS) show a comparatively greater reduct

54 oschisin gene, RS-1, cause juvenile X-linked retinoschisis (XLRS), a dystrophy characterized by delam

55 at encode retinoschisin (RS1) cause X-linked retinoschisis (XLRS), a form of juvenile macular and ret

56 ions in the RS1 gene cause X-linked juvenile retinoschisis (XLRS), a hereditary retinal dystrophy.

57 X-linked juvenile retinoschisis (XLRS), a leading cause of juvenile macula

58 architecture with mutations causing X-linked retinoschisis (XLRS), a monogenic form of macular degene

59 tations in the NR2E3 gene, juvenile X-linked retinoschisis (XLRS), and some other retinal dystrophies