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1             This results in the formation of Malpighian calcium-Pi stones, while RNAi-mediated knockd
2 similar 14-d turnover times for the (SC) and Malpighian epidermis, the number of corneocytes results
3 ensin-1 and -2 peptides are localized to the Malpighian layer of the epidermis and/or stratum corneum
4        GmHs1-1 is primarily expressed in the Malpighian layer of the seed coat and is associated with
5                                       In the Malpighian (renal) tubule of Drosophila melanogaster, TA
6 )(+)]i and fluid transport by the Drosophila Malpighian (renal) tubule.
7 ated by capa peptide signaling in the insect Malpighian (renal) tubules is a key physiological mechan
8 es transepithelial ion and water flux in the Malpighian (renal) tubules of the fly, which are in dire
9 ide-stimulated fluid transport by Drosophila Malpighian (renal) tubules.
10 tes epithelial fluid transport by Drosophila Malpighian (renal) tubules.
11 amily, perform osmolyte transport within the Malpighian tubule and hindgut.
12  preventing osmolyte accumulation within the Malpighian tubule and hindgut.
13 phila causes lethal abnormalities in muscle, Malpighian tubule and trachea formation.
14 e invaginating posterior midgut, evaginating Malpighian tubule buds, elongating hindgut, invaginating
15 Specifically, wal affects evagination of the Malpighian tubule buds, fas and thr affect bud extension
16        Ultrastructural examination of larval Malpighian tubule cells depleted for NS1 showed a loss o
17  genes, into a genetic pathway that controls Malpighian tubule development.
18 epolarize the transepithelial voltage of the malpighian tubule in concentrations of less than 10(-9)
19                               The Drosophila Malpighian tubule is a model system for studying genetic
20                                          The Malpighian tubule is a particularly excellent model to s
21 nd one novel gene, walrus (wal), that affect Malpighian tubule morphogenesis.
22 ing the two hormones (Urinate, Urn8) reduces Malpighian tubule secretion and restricts organismal flu
23 FS2 increased fly life span, suggesting that Malpighian tubule stones are a key element whereby high
24 od (hemolymph) Pi and decreases formation of Malpighian tubule stones in flies cultured on high Pi me
25 les induces expression of MFS2 and increases Malpighian tubule stones suggesting that bnl is the endo
26 r, some secretory epithelia (choroid plexus, Malpighian tubule, rectal gland, etc.) have "backwards"
27 expected complexity in the physiology of the Malpighian tubule.
28 gans such as the mammalian kidney and insect Malpighian tubule/hindgut requires a region of hypertoni
29                    In Drosophila, the renal (Malpighian) tubule displays the highest per-cell transpo
30 ost abundantly expressed in the adult renal (Malpighian) tubule rather than in neuronal tissues.
31 ion and homeostasis of the Drosophila renal (Malpighian) tubule.
32  origin of stem cells found in the excretory Malpighian tubules ('renal stem cells') has not been est
33 urprisingly strong reduction also in gut and Malpighian tubules (kidney) volume.
34                                          The Malpighian tubules (MT), of chill susceptible Drosophila
35 Mas-DH by incubating it in vitro with larval Malpighian tubules (Mt), the target organ of the hormone
36    Like other insects, secretion by mosquito Malpighian tubules (MTs) is driven by the V-type H(+)-AT
37 to the peri-ureter region of the kidney-like Malpighian tubules (MTs).
38         Finally, we highlight the use of the Malpighian tubules and hindgut as accessible models of h
39 , composed of the kidneys in mammals and the Malpighian tubules and hindgut in insects, can increase
40  a recent surge in interest, research on the Malpighian tubules and hindgut of Drosophila have uncove
41 adult Drosophila renal system, consisting of Malpighian tubules and nephrocytes, which shares similar
42 ins two organ systems acting in concert: the Malpighian tubules and the hindgut perform essential rol
43 f their organs, in which part of their renal/Malpighian tubules are bound to the surface of the rectu
44 ted that several differentiated cells in the malpighian tubules arise from these stem cells.
45  leptophragmata, in the distal region of the Malpighian tubules associated with the rectal complex.
46 s of ALAT1 or ALAT2 in fat body, thorax, and Malpighian tubules compared with dsRNA firefly luciferas
47  Further analysis of the role of cv-c in the Malpighian tubules demonstrates that its activity is req
48                                  In Diptera, Malpighian tubules derive from ectodermal cells that eva
49 cv-c activity, tubulogenesis in the renal or Malpighian tubules fails and they collapse into a cyst-l
50 adult eye, larval salivary glands and larval Malpighian tubules for each of three different chromosom
51      Cells of Chironomus salivary glands and Malpighian tubules have junctions of the "septate" kind.
52                             Adult Drosophila Malpighian tubules have low rates of cell turnover but a
53           The kidneys in vertebrates and the malpighian tubules in Drosophila accomplish these functi
54 a stable boundary between midgut and hindgut/Malpighian tubules is not established during early embry
55                                              Malpighian tubules mutant for raw or rib are wider and s
56 ic bud and metanephric mesoderm, whereas the malpighian tubules of Drosophila develop from the hindgu
57 ts expression was high in the integument and Malpighian tubules of last instar larvae and adults.
58 rease cAMP production and fluid secretion in Malpighian tubules of several insect species.
59 hat strongly inhibits fluid secretion by the Malpighian tubules of this insect.
60        Together, these data show that beetle Malpighian tubules operate by a fundamentally different
61 c pathways in mosquito fat body, midgut, and Malpighian tubules prior to and after blood feeding.
62 ce fluid secretion or depolarizations in the malpighian tubules suggest that there may be more than o
63  is the only endogenous insect ADF acting on Malpighian tubules to be sequenced, and the first coleop
64 cently, multipotent stem cells in Drosophila malpighian tubules were identified, and it was demonstra
65      Expression is high in gut, ovaries, and Malpighian tubules where immunofluorescence microscopy r
66 ulate fluid secretion from the renal organs (Malpighian tubules) and hindgut contractions by activati
67  as of various tubules (e.g., nephric ducts, Malpighian tubules), as it is driven by cell rearrangeme
68 cell types, including the posterior hindgut, Malpighian tubules, anal plate, garland cells, and a sub
69                                              Malpighian tubules, analogous to vertebrate nephrons, pl
70 heral tissues such as the epidermis, midgut, Malpighian tubules, and fat body, i.e., tissues known to
71 er alimentary canal (salivary gland, midgut, Malpighian tubules, and hindgut), we have verified the e
72 ed in the nervous tissue of the synganglion, Malpighian tubules, and muscle.
73  developing midgut endoderm, the hindgut and Malpighian tubules, and the epidermis and central nervou
74  NO-stimulated fluid secretion in Drosophila Malpighian tubules, both when applied in the form of a N
75  showing highly abundant expression in adult Malpighian tubules, ClC-c, did not impact depolarization
76 al trunk of larval tracheal airways or adult Malpighian tubules, downregulation of Yki signaling trig
77 cules in the salivary glands, midgut, ovary, Malpighian tubules, haemolymph and the tick cell line IR
78 gh byn is not expressed in the midgut or the Malpighian tubules, it is required for the formation of
79 the endodermal midgut and ectodermal hindgut/Malpighian tubules, maintain populations of dividing ste
80 ypti body parts (head, thorax, abdomen, gut, Malpighian tubules, ovaries), gut regions (crop, provent
81 otting revealed low levels of readthrough in malpighian tubules, ovary, and testis but abundant readt
82 itzi, and that it is distributed in ovaries, malpighian tubules, salivary glands and midguts of the t
83 es the formation of zinc storage granules in Malpighian tubules, where 3-hydroxykynurenine and xanthu
84 tected in clock-containing tissues including Malpighian tubules, where it mediates both light-depende
85 in-dependent detoxification by desert locust Malpighian tubules.
86  results in the absence of stem cells in the Malpighian tubules.
87 tis, larval male gonads, adult intestine and Malpighian tubules.
88 e basal surfaces of the digestive system and Malpighian tubules.
89 tanding of the development and physiology of Malpighian tubules.
90  the corpus allatum (CA), gastric cecum, and malpighian tubules.
91 ead, ovaries, gut, cuticle plus fat body and malpighian tubules.
92 ses in tissues such as the gut, trachea, and malpighian tubules.
93  increase the rate of fluid secretion by the malpighian tubules.
94 heral nervous systems, and the ureter of the Malpighian tubules.
95 h same manner as they alter the shape of the Malpighian tubules.
96  constrictions and for the elongation of the Malpighian tubules.
97                                   The renal (Malpighian) tubules can secrete fluid faster on a per-ce
98 nhibits a Kir channel cloned from the renal (Malpighian) tubules of Aedes aegypti (AeKir1).
99 three main tissues - the transporting renal (Malpighian) tubules, the reabsorptive hindgut and the en
100 y MFS2 as a key Pi transporter in fly renal (Malpighian) tubules.