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1 n a block to lymphomyeloid development at an early developmental stage.
2 e fly ortholog, dre4, causes lethality at an early developmental stage.
3 neity among venous endothelial cells at this early developmental stage.
4 ing expression of the expanded CGG RNA at an early developmental stage.
5 , the onset of these phenotypes occurs at an early developmental stage.
6 fied pigment cell precursors at a relatively early developmental stage.
7 oduction, in that the ONL appeared normal in early developmental stages.
8 propriate cDNA collections, particularly for early developmental stages.
9 d to suppress beta-globin gene expression at early developmental stages.
10 pecific gene expression events at these very early developmental stages.
11 e survival requirements for neurotrophins at early developmental stages.
12 s, even more simple versions are used during early developmental stages.
13 sure on a seasonal or daily basis, or during early developmental stages.
14  of L1-80 contribute to brain development at early developmental stages.
15 ulation imbalance is present already at very early developmental stages.
16 specify proper cellular arrangements at very early developmental stages.
17 especially at crucial metabolically draining early developmental stages.
18 a free form up to 9.85mg/g dry matter at the early developmental stages.
19 ce, indicating an immediate activity even at early developmental stages.
20 w major-effect additive and dominant QTLs in early developmental stages.
21 tners for nutrient supply, especially during early developmental stages.
22 tes local oxygen to below baseline levels at early developmental stages.
23 ting only transiently, as cells pass through early developmental stages.
24 polarity by inhibiting dendrite outgrowth at early developmental stages.
25 ession and function of guidance molecules at early developmental stages.
26 es of polycomb repressive complexes (PRC) in early developmental stages.
27 gammadelta-transgenic mice at two sequential early developmental stages.
28 SI), the damage being most severe during the early developmental stages.
29 y gland sensory innervation of both sexes at early developmental stages.
30 etween two regulators are overrepresented in early developmental stages.
31 , leaves are not positioned at random during early developmental stages.
32 xhibit distinct molecular characteristics at early developmental stages.
33 aevis, a vertebrate well suited for study of early developmental stages.
34 ner cell mass and the epiblast of embryos at early developmental stages.
35 lis expressed sequence tags (ESTs) from four early developmental stages.
36  been shown to cause cardiac toxicity during early developmental stages across fishes.
37                                           At early developmental stages, alpha4 protein and mRNA were
38 ement membrane component changes through the early developmental stage and age-dependent changes in t
39  via gap junction at a rate similar to their early developmental stage and comparable to other brain
40 how strong neural responses to odors at this early developmental stage and highlight nasal airflow as
41  by (1) increasing time spent in susceptible early developmental stages and (2) suppressing tadpole i
42 ignaling promotes cardiac differentiation at early developmental stages and inhibits it later.
43 eavily expressed in neuronal growth cones at early developmental stages and its activation engages sm
44 est signals are enriched in the notochord at early developmental stages and myoblast/myocytes at late
45 n manipulated MITF RNA and protein levels at early developmental stages and observed decreased expres
46                  We isolated thymocytes from early developmental stages and observed that suspensions
47 anatomy and molecular studies to clarify the early developmental stages and position of corona initia
48 le of these transcription factors beyond the early developmental stages and provide mechanistic links
49        All these features are more severe in early developmental stages and show substantial recovery
50           Annual plants grow vegetatively at early developmental stages and then transition to the re
51 in-12 in AC/VU cell fate specification at an early developmental stage, and functions downstream of f
52 olution, particularly for genes expressed at early developmental stages, and resulting in high specia
53 x1, expressed in the presumptive midbrain at early developmental stages, and the hindbrain at later s
54                                              Early developmental stages are highly sensitive to stres
55                                              Early developmental stages are ideal targets for amphibi
56  significant decrease in etsrp expression at early developmental stages as measured by quantitative r
57 luences neurogenesis in the left habenula at early developmental stages as well as neurotransmitter p
58 al immunoblots of total proteins at selected early developmental stages, as well as EMSA of egg and 1
59 ived from ESCs correspond consistently to an early developmental stage at which the yolk sac and feta
60  alpha-1 was broadly expressed in the gut at early developmental stages, at which times soluble GFR a
61 nown whether these channels are expressed at early developmental stages, before gliogenesis or angiog
62 nd lingual sides of the cervical loop during early developmental stages, both at the gross and ultras
63 Xenopus can normally regenerate its limbs at early developmental stages but loses the ability during
64 e, dyads were observed to be functional from early developmental stages, but exhibited an impaired ab
65 ozygous matings produced Xrcc1-/- embryos at early developmental stages, but not Xrcc1-/- late-stage
66 anscriptionally inhibits let-7 biogenesis at early developmental stages, but the mechanisms by which
67                 Many TDMRs are methylated at early developmental stages, but unmethylated later, sugg
68 -reducing root nodules, may be favored at an early developmental stage by lumichrome, a previously un
69 lial cells regulate the number of neurons at early developmental stages by dynamically influencing ne
70 at broad ectopic activation of Notch at very early developmental stages causes induction of prosensor
71 sion of lamp in limbic regions, beginning in early developmental stages, combined with the results of
72 use heart, BIN1 localizes along Z-lines from early developmental stages, consistent with roles in ini
73 ttranscriptional control, MB neurons born at early developmental stages contain more abundant Chinmo
74 evidence shows that alterations occurring at early developmental stages contribute to symptoms manife
75  regulator of strawberry fruit ripening from early developmental stages, controlling abscisic acid bi
76 d BEST1 expression in the periphery, from an early developmental stage, could provide a mechanism tha
77 been limited to either superficial layers or early developmental stages due to tissue turbidity.
78                                           At early developmental stages (E10.5, E15.5), FgfrL1-defici
79 tral domains of the neuroepithelial layer at early developmental stages (E2.5-E4).
80                                           In early developmental stage (EDS) cells (from 7+3d to 7+5d
81 od is well established, its influence during early developmental stages-especially in response to exp
82  promelas) exposed to CAFO ditchwater during early developmental stages exhibited significantly skewe
83 ll behaviour, with increased self-renewal at early developmental stages, followed by expanded neuroge
84  down-regulation of microexon inclusion from early developmental stages, followed by other transcript
85 cusing on the immunostimulation of different early developmental stages for gaining a more comprehens
86 , the increase was smaller and restricted to early developmental stages for rats.
87                                           At early developmental stages, glutamatergic synapses are s
88 liferative effects only on cardiomyocytes in early developmental stages, glycogen synthase kinase-3 a
89    High-dose cranial irradiation (CI) during early developmental stages has been linked to metabolic
90 pulating endosperm proliferation at a rather early developmental stage in crops.
91  phosphorylation of tau at tyr18 occurred at early developmental stages in mouse but was absent in th
92                 These genes are expressed at early developmental stages in the embryonic nervous syst
93 rk, we found that MarvelD3 is expressed from early developmental stages in the exocrine and endocrine
94 at the extensive abnormalities formed during early developmental stages in the peripheral nervous sys
95 t plants became hypersensitive to ABA in the early developmental stages, including seed germination a
96  knockout mutants were albino and died at an early developmental stage, indicating that ZL1 is crucia
97                      Parasites blocked at an early developmental stage inside hepatocytes elicit a pr
98 echanism by which endoglin functions at this early developmental stage is currently unknown.
99  quantification of the mutant viruses at the early developmental stage is even more challenging, as t
100 t its function in bone formation beyond this early developmental stage is unknown.
101  here that the level of VRN-1 transcripts in early developmental stages is critical for flowering ini
102 p63-deficient mice does not progress past an early developmental stage: it lacks stratification and d
103 fying small RNAs in different cell layers of early developmental stage maize anthers that are importa
104 ultured hiPSC-derived neurons, characterized early developmental stages, measured electrophysiologica
105            We hypothesized that plasma of an early developmental stage, namely umbilical cord plasma,
106 contributing cells to the arterial valves at early developmental stages, NCC persistence in the valve
107 acquisition of stimulus-evoked exocytosis at early developmental stages occurs independent of both po
108               Such 3-D hECTs recapitulate an early developmental stage of human myocardium and promis
109  suggest that MFO activity is an index of an early developmental stage of the respiratory system.
110 istinguish the effects of stressors on three early developmental stages of each of three species: (i)
111 ial distribution and speciation of Se in the early developmental stages of fish, which provide import
112 as to assess the impact of bifenthrin on the early developmental stages of Longfin Smelt.
113 ntrinsically hindered the transition between early developmental stages of NK cells, whereas overexpr
114 nt implications for the understanding of the early developmental stages of self-awareness, self-regul
115  and generation of L1-80 coincide in time at early developmental stages of the cerebral cortex.
116 oblotting assays to characterise PABP in the early developmental stages of the clam Spisula solidissi
117 ransactivator (tTA) that causes lethality in early developmental stages of the heterozygous progeny b
118 yndromes, which are generally exerted during early developmental stages of the host: male feminizatio
119 uring development and provide little hint at early developmental stages of the rich functional divers
120 ffect the internal concentrations already in early developmental stages of the ZFE.
121                      They also show that the early developmental stages of these T cells are not gove
122 culties in histologically defining nuclei at early developmental stages, our understanding of the mec
123                                           At early developmental stages, physiologically high PI3K-Ak
124                                           At early developmental stages, PN types with adjacent birth
125          Thus, pnr has dual function, during early developmental stages pnr is involved in axial patt
126                      This indicates that, at early developmental stages, Ptch2 functions to suppress
127 eover, though the block of Shh signalling at early developmental stages results in the loss of chick
128                                           At early developmental stages, rnf-145 in the cis-Golgi net
129        The transcript was widely detected in early developmental stages, showing the highest expressi
130 sodermal and endodermal cell populations and early developmental stages, shows that the genes associa
131                                           At early developmental stages somatostatin receptors couple
132                                         From early developmental stages, sonic hedgehog (Shh) and ind
133 e competitive advantage of the gamma gene at early developmental stages, stable transgenic mouse line
134 und that ciliary assembly occurs only during early developmental stages, supporting the idea that mat
135   We found that promoters that are active in early developmental stages tend to be CG rich and mainly
136                          We show that during early developmental stages the strong expression of endo
137  vasculature scaffold in the RMS and, during early developmental stages, the RMS contains only a few
138 equence evolution, especially for genes from early developmental stages, thereby leading to animal sp
139 hile granule cell cilia are essential during early developmental stages, they become infrequent upon
140 romoter 1 of the KOR gene and expressed from early developmental stages through adult life.
141 LEC1 gene and showed that it functions at an early developmental stage to maintain embryonic cell fat
142 ial subpallium-derived amygdalar nuclei from early developmental stages to adult.
143  are subjected to metabolic regulation, from early developmental stages to adulthood.
144 transformation from a near-spherical form at early developmental stages to an oblate spheroid with a
145  shows how cells can become committed during early developmental stages to execute a specific fate mu
146  sympathetic neuron development; Fz3 acts at early developmental stages to maintain a pool of dividin
147 rovides the high sensitivity required during early developmental stages to trigger editing of any aut
148 associated with practice accumulation during early developmental stages up to age 12 years.
149 terenol, forskolin, and 8-bromo-cAMP in very early developmental stage (VEDS) cardiomyocytes (from 7+
150 ions between sensory axons and skin cells at early developmental stages, we conducted a detailed anal
151                     When CCR7 was studied at early developmental stages, we detected a progressive in
152                        In mice at equivalent early developmental stages, we find that auditory experi
153               Sex-biased genes identified at early developmental stages were generally consistently m
154                                           At early developmental stages when GABAergic inputs dominat
155 aving localized NT-3 and trk C expression at early developmental stages when retinal neuroepithelial
156 , exon 18b is predominantly expressed during early developmental stages, while exon 18a is prevalent
157          However, null mutant mice die at an early developmental stage with severe malformations, and

 
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