ライフサイエンスコーパス: fertilized egg

1 the calcium wave reaches the antipode in the fertilized egg.

2 specifies the germline of descendants in the fertilized egg.

3 organisms that allow mRNA delivery into the fertilized egg.

4 all fraction of the total amount of PLC in a fertilized egg.

5 such as the notochord and neural tube to the fertilized egg.

6 ed specifically to the vegetal cortex of the fertilized egg.

7 nates sperm-derived mitochondrial DNA from a fertilized egg.

8 ertilized egg, but not to the surface of the fertilized egg.

9 ing to deformation and rapid ejection of the fertilized eggs.

10 jection of zinc-finger nucleases (ZFNs) into fertilized eggs.

11 s in 168 day old larvae as compared to newly fertilized eggs.

12 pollen tube growth, and decreased numbers of fertilized eggs.

13 mRNA, encoding GFP-tagged beta-catenin, into fertilized eggs.

14 showed that CrANT is expressed in sperm and fertilized eggs.

15 ytosis, and preventing sperm from binding to fertilized eggs.

16 ites, and is subsequently microinjected into fertilized eggs.

17 ed eggs and females develop as diploids from fertilized eggs.

18 mRNA, eGFP mRNA, and single guide RNAs into fertilized eggs.

19 unfertilized oocytes, but not to the zona of fertilized eggs.

20 re inherited differently in unfertilized and fertilized eggs.

21 that are restricted to the vegetal cortex of fertilized eggs.

22 on of F-actin and are defective in producing fertilized eggs.

23 In addition, they do not bind to fertilized eggs.

24 However, in fertilized eggs, activation of the Mos/MEK/p42 MAPK path

25 uctures called P granules are present in the fertilized egg and are segregated into each of the germl

26 is present in both the unfertilized and the fertilized egg and contributes to the initial phase of P

27 GLUT1) is a major glucose transporter of the fertilized egg and preimplantation embryo.

28 ing through the cellular lineage between the fertilized egg and the cancer cell, each composed of spe

29 and are haploid, while females develop from fertilized eggs and are diploid.

30 become localized to the vegetal cytoplasm of fertilized eggs and are incorporated into muscle lineage

31 nesis, in which diploid females develop from fertilized eggs and haploid males develop from unfertili

32 s, in which females develop as diploids from fertilized eggs and males develop parthenogenetically as

33 ed cytomegalovirus (CMV)-CTCF construct into fertilized eggs and mouse oocytes, respectively.

34 chromosomes while diploid females arise from fertilized eggs and receive both maternal and paternal c

35 f microtubules in the cortex of activated or fertilized eggs and resulted in defects in the dorsovent

36 s uniformly distributed in oocytes and newly fertilized eggs, and becomes localized asymmetrically in

37 on genes were separately electroporated into fertilized eggs, and their regulatory activities were mo

38 Embryogenesis, from the time fertilized eggs are deposited in an eggcase (called a co

39 erference, the anterior cortical membrane of fertilized eggs became very fluid during meiosis and sub

40 inase activity was specifically inhibited in fertilized eggs by a truncated form of the Xenopus Cdk i

41 ine shows that the cellular machinery of the fertilized egg cannot demethylate the second maternal ge

42 onstrate that injection of HrPax-37 RNA into fertilized eggs causes ectopic expression of the dorsal

43 Here we show that whereas oocytes and fertilized eggs could utilize Sp1-dependent promoters, t

44 fficient in mutating Dot1L when expressed in fertilized eggs, creating essentially Dot1L knockout emb

45 transient, whereas BAPTA/AM-treated ICSI or fertilized eggs cultured in Ca(2+)-free medium remained

46 How does a fertilized egg decode its own genome to eventually devel

47 rtilized eggs develop as haploid males while fertilized eggs develop as diploid females, so the entir

48 use unfertilized eggs develop as males while fertilized eggs develop as females.

49 Fertilized eggs develop poorly into blastocysts, which r

50 In addition, all successfully fertilized eggs die before the 2-cell stage due to persi

51 curred, in the absence of Ca(2+) influx, the fertilized eggs failed to emit the second polar body, re

52 urate and cost-effective selection of normal fertilized eggs for embryo transfer.

53 sayed nests, and multiple sneakers sometimes fertilized eggs from a single female.

54 he transgene cassette was microinjected into fertilized eggs from B6C3 (C3H x C57BL/6) females mated

55 Fertilized eggs from FVB mice were injected with a const

56 strongly co-expressed with Xeed mRNA in the fertilized egg, further suggesting that their encoded pr

57 box RNA was found in maturing oocytes and in fertilized eggs; however, the abundance of Sebox RNA is

58 ales sequentially to two males and collected fertilized eggs in a temporal series.

59 Sneaker males had fertilized eggs in approximately 50% of the assayed nest

60 ximately 12 microm) while it develops from a fertilized egg into a tadpole [2].

61 to run at maximum velocity, subdividing the fertilized egg into smaller and smaller cells.

62 y develop into uniparental haploid males and fertilized eggs into biparental diploid females.

63 n into wild-type ova and implantation of the fertilized eggs into foster mothers.

64 ne of two ways: as a "conversion" of diploid fertilized eggs into haploid males or as embryonic morta

65 Optimal development of fertilized eggs into preimplantation embryos is essentia

66 physiological function of activated cPKCs in fertilized eggs is to sustain long-lasting Ca2+ oscillat

67 D choreography of reductive divisions of the fertilized egg, known as cleavage patterns.

68 Incubation at high altitude of fertilized eggs laid by high altitude hens also restrict

69 By contrast, incubation at sea level of fertilized eggs laid by high altitude hens not only rest

70 ata show that incubation at high altitude of fertilized eggs laid by sea level hens markedly restrict

71 Single fertilized eggs monitored for Ca(2+) had a mean increase

72 Since groups of fertilized eggs normally oscillate asynchronously, synch

73 n the sMic lineage: microinjection into a Sp fertilized egg of an RNA that contains the GFP open read

74 olutionary changes in developmental mode, we fertilized eggs of a direct-developing sea urchin, Helio

75 the rejection of BMC grafts, we transfected fertilized eggs of FVB mice with a vector containing DNA

76 I cDNA, and the fusion gene microinjected to fertilized eggs of the FVB-N mouse strain.

77 lobase human SP-C promoter and injected into fertilized eggs of the FVB/N mouse strain.

78 iable in generating hundreds or thousands of fertilized eggs on a roughly weekly schedule.

79 p42 MAPK are critical for the progression of fertilized eggs out of meiosis and through the first mit

80 In fertilized eggs rapamycin treatment increased the transl

81 aevis egg (approximately 1.2 mm diameter), a fertilized egg rapidly proceeds through mitosis in a spa

82 ivity in mouse oocytes and one-cell embryos (fertilized eggs) renders them incapable of utilizing Gal

83 function appears to be unique to oocytes and fertilized eggs, suggesting that it provides a safeguard

84 To demonstrate this, we fertilized eggs that had been depleted of both XTcf3 and

85 In fertilized eggs, the Nasonia sperm brought in paternally

86 The development of a single-celled fertilized egg, through the blastocyst stage of a ball o

87 The zygotic transition, from a fertilized egg to an embryo, is central to animal and pl

88 nteract with the extracellular matrix of the fertilized egg to form the block to polyspermy.

89 roteins of Xenopus laevis was generated from fertilized egg to neurula embryo.

90 chemical explanation of development from the fertilized egg to the adult requires an understanding of

91 transcriptional processes occurring from the fertilized egg to the adult stage.

92 Amoeboid sperm crawl around fertilized eggs to the spermatheca--a convoluted tube wh

93 In insects, the fertilized egg undergoes a series of rapid nuclear divis

94 to the sea urchin embryo by RNA injection of fertilized eggs was examined.

95 on by injection of zebrafish Hmox1 mRNA into fertilized eggs was found to be sufficient for a dystrop

96 Fertilized eggs were compressed to change the orientatio

97 ormally transient structure derived from the fertilized egg, were often associated with the arrested

98 Upon injection into newly fertilized eggs, wild-type Cdc25A shortened the cell cyc

99 hibition of gelsolin expression by injecting fertilized eggs with a specific morpholino oligonucleoti

100 g-term cell cycle inhibition was observed in fertilized eggs with the CaMKII antagonist myrAIP (50 mi

101 The transition from oocyte to fertilized egg (zygote) involves many changes, including

102 we show that a significant number of normal fertilized eggs (zygotes) can be obtained for reprogramm

103 control of the transcriptomic homeostasis in fertilized eggs, zygotes and two-cell embryos.