ライフサイエンスコーパス: developmental anomaly

1 variants considered to have caused the fetal developmental anomaly.

2 iption factor and their role in causing this developmental anomaly.

3 termed coronal synostosis, is a common human developmental anomaly.

4 sm for arsenic in the etiology of cancer and developmental anomalies.

5 They are sometimes accompanied by other developmental anomalies.

6 racterized by broad spectrum, multifactorial developmental anomalies.

7 paper basket' diagnosis for anterior segment developmental anomalies.

8 h that can be extended to other diseases and developmental anomalies.

9 ion pattern of ncRNA in the human heart with developmental anomalies.

10 vents to occur at specified times results in developmental anomalies.

11 ant neuronal activity and could be masked by developmental anomalies.

12 rmalities and deafness) syndrome of multiple developmental anomalies.

13 ntial for involvement in renal/urinary tract developmental anomalies.

14 suffiency causes more widespread human neuro developmental anomalies.

15 physician to scrutinize adjacent regions for developmental anomalies.

16 ge imbalance of specific genes with specific developmental anomalies.

17 ormation were impaired, resulting in several developmental anomalies.

18 me with hypomelanosis of Ito associated with developmental anomalies.

19 isease characterized by bone marrow failure, developmental anomalies, a high incidence of myelodyspla

20 auses are known for many syndromes involving developmental anomalies, a large number of individuals w

21 suppressor P1/HC-Pro in plants causes severe developmental anomalies accompanied by defects in both s

22 Tooth agenesis is one of the most common developmental anomalies affecting function and esthetics

23 riations cause a wide phenotypic spectrum of developmental anomalies affecting the brain (hypothalami

24 a-uterine fractures, and multiple congenital developmental anomalies affecting the brain, lungs, and

25 These mice display a number of developmental anomalies analogous to those in DS, includ

26 r Gorlin syndrome, which is characterized by developmental anomalies and a predisposition to skin and

27 whether cellular exposures that induce both developmental anomalies and cancer alter miRNAs.

28 lation of TGF-beta family signaling leads to developmental anomalies and disease, whereas enhanced TG

29 ising from pre- and/or early postnatal brain developmental anomalies and/or early brain insults.

30 tal heart defects (CHDs) are the most common developmental anomaly and are the leading non-infectious

31 pits, odontogenic keratocysts, skeletal and developmental anomalies, and ectopic calcification.

32 individuals who have diverse yet overlapping developmental anomalies, and who all have de novo missen

33 These neural crest-derived developmental anomalies are associated with altered expr

34 Neural tube defects and other developmental anomalies are more common in infants born

35 these data indicate that other neurological developmental anomalies associated with dosage-sensitive

36 We are investigating the molecular basis of developmental anomalies associated with human PITX2 muta

37 To contextualize developmental anomalies associated with Mendelian metabo

38 variety of radiolucent mandibular lesions or developmental anomalies can lead to erroneous interpreta

39 Although a remote antecedent event or even a developmental anomaly cannot entirely be ruled out, our

40 ) is a heterogeneous craniofacial and neural developmental anomaly characterized in its most severe f

41 Heterotopic pancreas is a rare developmental anomaly defined as pancreatic tissue found

42 ile, but CycF(-/-) animals, with a myriad of developmental anomalies due in large part to failures in

43 reaction creates a ripple effect propagating developmental anomalies during the subsequent course of

44 over, Tbx1-/- mice displayed a wide range of developmental anomalies encompassing almost all of the c

45 in the homeobox gene, MSX1, causes a common developmental anomaly, familial tooth agenesis.

46 We also observed developmental anomalies in a proportion of heterozygous

47 ytogenetic damage, which was correlated with developmental anomalies in both vegetative and reproduct

48 Tooth agenesis is one of the most common developmental anomalies in humans.

49 sine into RNA and can cause severe and fatal developmental anomalies in humans.

50 we quantified the frequency and severity of developmental anomalies in otoliths of delta smelt (Hypo

51 Ectopic DCL1 largely alleviated developmental anomalies in P1/HC-Pro plants but did not

52 olt-Oram syndrome, which is characterized by developmental anomalies in the heart and forelimbs.

53 The genetic basis for the wide range of developmental anomalies in the heart, glands and facial

54 o defective maturation of dendritic cells or developmental anomalies in the peripheral T cell compart

55 pping virtual subpanels for anterior segment developmental anomalies including glaucoma (ASDA; 59 gen

56 us DeltaNp63(gfp/gfp) animals exhibit severe developmental anomalies including truncated forelimbs an

57 resents clinically with the full spectrum of developmental anomalies (including tooth anomalies), is

58 ERBB3 or ERBB2 leads to a broad spectrum of developmental anomalies, including intestinal dysmotilit

59 However, multiple endocrine deficiencies and developmental anomalies inherent in these models confoun

60 resulting, for example, from prematurity or developmental anomalies - is a risk factor for the devel

61 ming clear that genetic mutations that cause developmental anomalies may result in cardiac dysfunctio

62 r bone marrow failure, B and NK lymphopenia, developmental anomalies, microcephaly, and/or intrauteri

63 Ocular developmental anomalies (ODA) such as anophthalmia/micro

64 ual differentiation are prime candidates for developmental anomalies of multiple LGU organs, but insu

65 d deletion of these genes in mice results in developmental anomalies of multiple organs that recapitu

66 These results, along with the developmental anomalies of Pds5B(-/-) mice, the presence

67 Triploid fetuses had clear gross developmental anomalies of the brain.

68 Developmental anomalies of the carotid and aortic arch w

69 opment and its dysfunction leads to SNHL and developmental anomalies of the cochlea in humans and mic

70 eatures of NS are characterized by 1 or more developmental anomalies of the eyelids (involving the po

71 show that the loss of BF-1 leads to multiple developmental anomalies of the eyes.

72 en diethylstilbestrol (DES) in utero induces developmental anomalies of the female reproductive tract

73 yngeal cancer, skin telangiectases, and mild developmental anomalies of the hair, teeth, and nails.

74 I) is a form of open-angle glaucoma in which developmental anomalies of the iris and irido-corneal an

75 ongenital lung malformations (CLMs) are rare developmental anomalies of the lung, including congenita

76 Lymphatic malformations (LMs) are developmental anomalies of the lymphatic system associat

77 It is often associated with other developmental anomalies of the urinary tract, emphasisin

78 lterations in epidermal differentiation, and developmental anomalies of various ectodermal appendages

79 chsprung disease (HSCR) is the most frequent developmental anomaly of the enteric nervous system, wit

80 Holoprosencephaly (HPE) is a common developmental anomaly of the human forebrain and midface

81 Holoprosencephaly (HPE) is the most common developmental anomaly of the human forebrain, and in its

82 Holoprosencephaly (HPE) is the most common developmental anomaly of the human forebrain; however, t

83 y be only occasionally, if ever, an isolated developmental anomaly of the inner ear.

84 so interferes with miRNA pathways, eliciting developmental anomalies partially phenocopying ago1 muta

85 ella syndrome (CRS) remains a major cause of developmental anomalies, particularly blindness and deaf

86 hat this deficit does not arise from retinal developmental anomalies, photoreceptor degeneration, or

87 Gorlin syndrome), which is characterized by developmental anomalies, radiation hypersensitivity and

88 tants in zebrafish embryos recapitulates the developmental anomalies seen in the patients.

89 ng cures for long-term problems of a complex developmental anomaly such as Hirschsprung's disease wil

90 ufman syndrome (MKKS, MIM 236700) is a human developmental anomaly syndrome comprising hydrometrocolp

91 McKusick-Kaufman syndrome is a human developmental anomaly syndrome comprising mesoaxial or p

92 The remainder are associated with other developmental anomalies termed syndromic deafness.

93 ression of SmoM2 in Xenopus embryos leads to developmental anomalies that are consistent with known r

94 ufficiency of TFII-I proteins causes various developmental anomalies that are often associated with W

95 ight a key role for NOTCH1 across a range of developmental anomalies that include cardiac defects and

96 ipal candidate gene for DiGeorge syndrome, a developmental anomaly that affects the heart, thymus, pa

97 nt abnormalities in skull shape, is a common developmental anomaly that disrupts this process.

98 in band 13q32 where deletion leads to major developmental anomalies (the 13q32 deletion syndrome).

99 Portal annular pancreas is a rare pancreatic developmental anomaly which is often overlooked at imagi

100 whose mutations cause STAR syndrome, a human developmental anomaly whose features include toe syndact

101 re found to have reduced head volume and eye developmental anomalies with chorioretinal dysplasia.