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1 ycemic phenotype in pdx1-knockdown zebrafish pronephros.
2 d in the neural tube and disorganized in the pronephros.
3  the development of proximal elements of the pronephros.
4 evelopment and differentiation in retina and pronephros.
5 rentiation program of distal segments in the pronephros.
6  in organs such as Kupffer's vesicle and the pronephros.
7 ed terminal differentiation of the amphibian pronephros.
8 s derived from other germ layers such as the pronephros.
9 the formation of motile sensory cilia in the pronephros.
10 as caused by impaired differentiation of the pronephros.
11 detected in a small region of the developing pronephros.
12 zed its function in the developing amphibian pronephros.
13 nt hematopoietic sites such as the thymus or pronephros.
14 entially new methods of gene delivery to the pronephros.
15 l derivatives such as vasculature, blood and pronephros.
16 ogenesis of the larval amphibian kidney, the pronephros.
17 he first kidney to form in the embryo is the pronephros.
18 duce the formation of somitic muscle and the pronephros.
19 te the role for pax2.1 in development of the pronephros.
20 ishment of the Xenopus embryonic kidney, the pronephros.
21 ive mutations that affect development of the pronephros.
22 ected in the developing nephric duct and the pronephros.
23 he neural crest, central nervous system, and pronephros, all defects that were rescued by a Cby-GFP c
24 vis embryos to manipulation make the Xenopus pronephros an attractive system in which to study organo
25 nal glomerulus but retention of a functional pronephros, an arrangement similar to the aglomerular ki
26 ations that perturb the entire length of the pronephros and body axis curvature.
27  also expressed in other organs, such as the pronephros and liver primordium.
28 rx2a transcripts localized to the developing pronephros and maturing MCCs, and loss of function alter
29 s, podocytes are stationary in the zebrafish pronephros and neither migrate nor change their branchin
30 ongly affect cilia motility in the zebrafish pronephros and neural tube.
31 matically extends its effect to head, heart, pronephros and pronephric duct mesoderm inducing early b
32 ion of the late distal tubule of the Xenopus pronephros and regulates renal epithelial cell different
33 e distribution of top clonotypes showed that pronephros and spleen B cells constitute distinct compar
34 cy of anti-VHSV clonotypes decreased both in pronephros and spleen, raising questions about B cell ci
35  exclusive from the dorsal mesoderm whereas, pronephros and tail originate from both dorsal and ventr
36               The simple organisation of the pronephros and the amenability of Xenopus laevis embryos
37        The two most anterior structures, the pronephros and the mesonephros, are transitory and large
38 strate that vascularization of the zebrafish pronephros and the onset of glomerular filtration occurs
39  physiological degeneration of the amphibian pronephros and to the development of the cement gland an
40 CDC11 leads to defective ciliogenesis in the pronephros and within the Kupffer's vesicle and results
41            Ssbp2 is expressed in the Xenopus pronephros, and knockdown prevents normal morphogenesis
42 e mesoderm fated to become the nephric duct, pronephros, and mesonephros.
43 otch signalling patterns the early X. laevis pronephros anlagen, a function that might be conserved i
44 the medio-lateral axis of the dorso-anterior pronephros anlagen, permitting the glomus and tubules to
45 gnalling in the dorso-anterior region of the pronephros anlagen.
46 echanisms that regulate cell fate within the pronephros are poorly understood but are important for t
47 form of urine, while emphasizing the Xenopus pronephros as a model for physiology and disease.
48 postfertilization and distension/dilation of pronephros at 5 d postfertilization (dpf).
49 ection led to extensive modifications of the pronephros B cell repertoire, implicating several VH sub
50 es are primarily expressed in the spleen and pronephros (bone marrow equivalent), and ontogenically,
51 neage assignment in the developing zebrafish pronephros by repressing Tfap2a activity.
52  versus transporting epithelial cells in the pronephros by way of a genetic pathway involving repress
53  In this work, we test whether the zebrafish pronephros can be used as an assay system for the develo
54                                          The pronephros consists of two nephrons with fused glomeruli
55                                          The pronephros-derived glands that synthesize Stc1a interact
56 ces lmx1b in a genetic hierarchy involved in pronephros development and suggests that it is the balan
57  essential and novel mechanisms that control pronephros development in the zebrafish.
58               Notch signaling is involved in pronephros development in Xenopus and in glomerulogenesi
59 MX1B and ABRA act in a common pathway during pronephros development.
60 es and is enriched in neural tissues and the pronephros during later embryogenesis.
61  days in ovo, the mesonephros as well as the pronephros failed to develop on the experimental side.
62 ecific gene expression in the portion of the pronephros fated to form its vascular structure, the glo
63 he kidney, such as tnnt2a, or elimination of pronephros fluid output through knockdown of the intrafl
64 h the normal pattern of Pax-2 expression and pronephros formation.
65 sh development was consistent with a role in pronephros formation.
66  after focal destruction, such that a normal pronephros forms after laser-mediated removal of the wt1
67 ired and sufficient for the induction of the pronephros from the chick IM.
68  gene ift88, was not associated with ectopic pronephros gene expression, thus suggesting a unique rol
69 zebrafish altered proximal and distal tubule pronephros growth suggesting a possible role of thymosin
70 iously described in spleen, was confirmed in pronephros in all infected fish, strongly correlated to
71  whether paraxial mesoderm is sufficient for pronephros induction, stage 7 or earlier chick lateral p
72                              The fish larval pronephros is a relevant kidney in which to pursue many
73                                  The Xenopus pronephros is a simple paired organ; each nephron consis
74                                The zebrafish pronephros is also associated with the corpuscles of Sta
75                                          The pronephros is the first to form and is the functional em
76                                         Fish pronephros is the site of B cell differentiation and the
77 renal cyst formation because its kidney (the pronephros) is simple and genes that cause cystic kidney
78           The zebrafish embryonic kidney, or pronephros, is a simplified yet conserved genetic model
79                                       In the pronephros, kcnj1 transcript expression was restricted t
80  cyp2k22 and slco1f4 was demonstrated in the pronephros; lipca was detected in the liver, and sult2st
81 nd synergist cyst formation in the zebrafish pronephros model.
82 s, angiogenesis of intersomitic vessels, and pronephros morphogenesis.
83                             In the zebrafish pronephros, multiciliated cells (MCCs) are specialized f
84 ent of other mesoderm derivatives, including pronephros, muscle and lateral plate is not disrupted.
85 malian metanephros and also in the primitive pronephros of fish and amphibian larvae.
86                To address this question, the pronephros of translucent zebrafish larvae (casper) expr
87 be so derived from the hematopoietic kidney (pronephros) of a red-blooded Antarctic rockcod, Notothen
88 l mesoderm and IM before stage 8 developed a pronephros on the control side only.
89 porter traits at the final tier of zebrafish pronephros ontogeny.
90                                       In the pronephros, our approach quantified the clonotype freque
91                                The zebrafish pronephros provides a conserved model to study kidney de
92                                The zebrafish pronephros provides an excellent in vivo system to study
93                 Progenitors of the zebrafish pronephros, red blood and trunk endothelium all originat
94 iption factors irx3b and sim1a that mitigate pronephros segment patterning.
95  in many physiological functions, influenced pronephros segmentation.
96  kidney dysfunction as the embryonic kidney (pronephros) shares considerable molecular and morphologi
97  and functional analysis of newly identified pronephros-specific genes are also described.
98 ibuted in a ;salt-and-pepper' fashion in the pronephros, suggesting that a lateral inhibition mechani
99 ate-1, and Delta-1 in the developing Xenopus pronephros suggests a role for this pathway in cell fate
100                                          The pronephros, the major hematopoietic organ in the adult f
101 acterised by the successive formation of the pronephros, the mesonephros and the metanephros.
102  in the epithelial structures of the Xenopus pronephros, the tubules and the duct, but not the glomus
103 es recent progress in applying the zebrafish pronephros to issues of human health and development.
104 e partially redundant functions to establish pronephros tubule epithelium polarity.
105 rmined the precise timing of these events in pronephros tubulogenesis.
106                         Morphogenesis of the pronephros was examined in UV-ventralized and lithium-do
107                     To determine whether the pronephros was induced by adjacent tissues and, if so, t
108              In the current study, the chick pronephros was used as a model system to identify tissue
109                                  The Xenopus pronephros was used as a paradigm to address this questi
110  the experiments presented here, the Xenopus pronephros was used as a simple model system to examine
111            The Xenopus embryonic kidney, the pronephros, which consists of a single large nephron, ha
112 ession patterns of the embryonic kidney, the pronephros, will be described and compared to the more c

 
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