ライフサイエンスコーパス: nonfamilial

1 ybrid") cells made from mitochondrial DNA of nonfamilial AD subjects show antioxidant-reversible lowe

2 e used to reconstruct evolutionary stages of nonfamilial adenocarcinoma.

3 APC gene mutations in 16 sporadic JNAs from nonfamilial adenomatous polyposis patients using immunoh

4 f Alzheimer's patients, including those with nonfamilial Alzheimer's disease, but it has been unclear

5 r of first-degree relatives screened between nonfamilial and sarcomere-positive groups.

6 tions, as well as in those with familial and nonfamilial ARVD/C.

7 our suppressor gene(s) frequently deleted in nonfamilial breast and other cancers.

8 ation study to identify genes that influence nonfamilial breast cancer risk using a collection of Ger

9 study of this disease and the role of p53 in nonfamilial breast cancer.

10 city to identify individuals at high risk of nonfamilial cancer, and prediagnostic signs and symptoms

11 of single-nucleotide substitutions (SNS) in nonfamilial cancers is strongly debated.

12 d familial cases, and present in 0.5% of the nonfamilial cases and in <0.05 of a control population.

13 rol subjects, and 13 patients with sporadic, nonfamilial cerebral cavernous malformation (CCM).

14 s more common in patients with nongenetic or nonfamilial DCM than in patients with genetic or familia

15 In contrast, among grandchildren with nonfamilial depression, ie, depressed parents with no de

16 correlation of 0.59 (95% CI, 0.15-0.84) for nonfamilial environment.

17 ssion of other axis I DSM-IV disorders or of nonfamilial environmental factors.

18 are needed to clarify the potential role of nonfamilial factors.

19 nsion, but the molecular basis of the common nonfamilial forms is unknown.

20 loss of metals in WT SOD may be involved in nonfamilial forms of ALS.

21 tension and may implicate the pathway in the nonfamilial forms of the disease.

22 story of FSGS as well as in individuals with nonfamilial FSGS.

23 hat most idiopathic DCM, whether familial or nonfamilial, has a genetic basis, in which case a geneti

24 robands with no sarcomere mutation, that is, nonfamilial HCM.

25 PCSK9 reduced LDLR abundance by 39 +/- 8% in nonfamilial hypercholesterolemia (non-FH) and by 45 +/-

26 ng atorvastatin (21 subjects) and those with nonfamilial hypercholesterolemia who were receiving trea

27 volunteers and in subjects with familial or nonfamilial hypercholesterolemia.

28 of both granule proteins were lower than in nonfamilial hypereosinophilic syndrome (HES).

29 , although none of the five individuals with nonfamilial IM had mutations in this gene.

30 ich COL4A1 mutations contribute to sporadic, nonfamilial, intracerebral hemorrhages (ICHs).

31 unrelated females with clinical features of nonfamilial IP with constitutional de novo reciprocal X;

32 Sporadic, nonfamilial kidney cancer includes clear cell kidney can

33 Patients with nonfamilial MDD had significantly larger left-sided but

34 ereas 10 had no clear family history of MDD (nonfamilial MDD).

35 rvival and tumor development in 43 to 60% of nonfamilial melanomas.

36 id samples from 61 patients; 35 adenomas, 10 nonfamilial multiple gland neoplasia, 3 familial primary

37 34 of 35 cases of adenoma, 9 of 10 cases of nonfamilial multiple gland neoplasia, and identified a m

38 of 11 familial neuroblastomas and 68 of 336 nonfamilial neuroblastomas (20.2%) at multiple 16p polym

39 s gene may contribute to the pathogenesis of nonfamilial neuroblastomas.

40 Alzheimer's disease (AD) is primarily nonfamilial or sporadic (SAD) in origin, although severa

41 The nonfamilial or sporadic AD (SAD), the most prevalent for

42 ity by regulating the calcium homeostasis in nonfamilial or sporadic Alzheimer's disease.

43 inases has been linked to the development of nonfamilial or sporadic breast cancer.

44 aneously define the cause of the more common nonfamilial, or sporadic, form of MFH-a tumor that const

45 Ts, we determined the exomic sequences of 10 nonfamilial PanNETs and then screened the most commonly

46 t, presence of cardiovascular comorbidities, nonfamilial pattern of disease, PR interval prolongation

47 ormed, and cases of initial neck surgery for nonfamilial primary hyperparathyroidism were selected fo

48 multiple gland neoplasia (double adenoma and nonfamilial primary hyperplasia) is problematic and resu

49 cancer (3.1%) than in those with late-onset, nonfamilial prostate cancer (0.6%) (P=2.0x10(-6)).

50 ancer may have a more aggressive course than nonfamilial prostate cancer, and that clinical and/or pa

51 various forms of acquired as well as primary nonfamilial pulmonary hypertension.

52 A mutations are not commonly associated with nonfamilial recurrent fevers of unknown etiology.

53 ociated with witnessing domestic violence or nonfamilial sexual abuse and larger than those associate

54 families and a second group of 137 men with nonfamilial SLE were evaluated.

55 ajor goal is the accurate modeling of common nonfamilial "sporadic" forms of brain disorders.

56 atic cell reprogramming may afford models of nonfamilial "sporadic" neurologic disorders, which are l

57 iatric disease, which exists in familial and nonfamilial (sporadic) forms.

58 e-case WM and 46 mixed WM/BCD kindred and 28 nonfamilial (sporadic) WM patients, using logistic regre

59 Adjusted predictors of nonfamilial status were older age (odds ratio, 1.04; 95%

60 story and no sarcomere mutations represent a nonfamilial subgroup of HCM.

61 and potential clinical implications of this nonfamilial subgroup of HCM.

62 Approximately 40% of HCM probands have a nonfamilial subtype, with later onset and less severe cl

63 ediatric MDD that may differ in familial and nonfamilial subtypes of MDD.

64 Sequencing of DNA from patients with nonfamilial TAAD and from premature-onset CAD patients i

65 d in 176 consecutive subjects with sporadic (nonfamilial) "TRAPS-like" symptoms.