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1 similar 14-d turnover times for the (SC) and Malpighian epidermis, the number of corneocytes results
2 ensin-1 and -2 peptides are localized to the Malpighian layer of the epidermis and/or stratum corneum
6 ated by capa peptide signaling in the insect Malpighian (renal) tubules is a key physiological mechan
7 es transepithelial ion and water flux in the Malpighian (renal) tubules of the fly, which are in dire
13 e invaginating posterior midgut, evaginating Malpighian tubule buds, elongating hindgut, invaginating
14 Specifically, wal affects evagination of the Malpighian tubule buds, fas and thr affect bud extension
17 epolarize the transepithelial voltage of the malpighian tubule in concentrations of less than 10(-9)
20 r, some secretory epithelia (choroid plexus, Malpighian tubule, rectal gland, etc.) have "backwards"
22 gans such as the mammalian kidney and insect Malpighian tubule/hindgut requires a region of hypertoni
25 origin of stem cells found in the excretory Malpighian tubules ('renal stem cells') has not been est
27 Mas-DH by incubating it in vitro with larval Malpighian tubules (Mt), the target organ of the hormone
28 , composed of the kidneys in mammals and the Malpighian tubules and hindgut in insects, can increase
30 s of ALAT1 or ALAT2 in fat body, thorax, and Malpighian tubules compared with dsRNA firefly luciferas
31 Further analysis of the role of cv-c in the Malpighian tubules demonstrates that its activity is req
33 cv-c activity, tubulogenesis in the renal or Malpighian tubules fails and they collapse into a cyst-l
34 adult eye, larval salivary glands and larval Malpighian tubules for each of three different chromosom
37 a stable boundary between midgut and hindgut/Malpighian tubules is not established during early embry
39 ic bud and metanephric mesoderm, whereas the malpighian tubules of Drosophila develop from the hindgu
40 ts expression was high in the integument and Malpighian tubules of last instar larvae and adults.
43 ce fluid secretion or depolarizations in the malpighian tubules suggest that there may be more than o
44 is the only endogenous insect ADF acting on Malpighian tubules to be sequenced, and the first coleop
45 cently, multipotent stem cells in Drosophila malpighian tubules were identified, and it was demonstra
47 ulate fluid secretion from the renal organs (Malpighian tubules) and hindgut contractions by activati
48 as of various tubules (e.g., nephric ducts, Malpighian tubules), as it is driven by cell rearrangeme
49 cell types, including the posterior hindgut, Malpighian tubules, anal plate, garland cells, and a sub
50 heral tissues such as the epidermis, midgut, Malpighian tubules, and fat body, i.e., tissues known to
52 developing midgut endoderm, the hindgut and Malpighian tubules, and the epidermis and central nervou
53 NO-stimulated fluid secretion in Drosophila Malpighian tubules, both when applied in the form of a N
54 showing highly abundant expression in adult Malpighian tubules, ClC-c, did not impact depolarization
55 cules in the salivary glands, midgut, ovary, Malpighian tubules, haemolymph and the tick cell line IR
56 gh byn is not expressed in the midgut or the Malpighian tubules, it is required for the formation of
57 the endodermal midgut and ectodermal hindgut/Malpighian tubules, maintain populations of dividing ste
58 itzi, and that it is distributed in ovaries, malpighian tubules, salivary glands and midguts of the t
59 tected in clock-containing tissues including Malpighian tubules, where it mediates both light-depende
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