ライフサイエンスコーパス: Malpighian tubule

1 expected complexity in the physiology of the Malpighian tubule.

2 results in the absence of stem cells in the Malpighian tubules.

3 tis, larval male gonads, adult intestine and Malpighian tubules.

4 e basal surfaces of the digestive system and Malpighian tubules.

5 tanding of the development and physiology of Malpighian tubules.

6 the corpus allatum (CA), gastric cecum, and malpighian tubules.

7 ead, ovaries, gut, cuticle plus fat body and malpighian tubules.

8 ses in tissues such as the gut, trachea, and malpighian tubules.

9 increase the rate of fluid secretion by the malpighian tubules.

10 heral nervous systems, and the ureter of the Malpighian tubules.

11 h same manner as they alter the shape of the Malpighian tubules.

12 constrictions and for the elongation of the Malpighian tubules.

13 cell types, including the posterior hindgut, Malpighian tubules, anal plate, garland cells, and a sub

14 amily, perform osmolyte transport within the Malpighian tubule and hindgut.

15 preventing osmolyte accumulation within the Malpighian tubule and hindgut.

16 phila causes lethal abnormalities in muscle, Malpighian tubule and trachea formation.

17 , composed of the kidneys in mammals and the Malpighian tubules and hindgut in insects, can increase

18 ulate fluid secretion from the renal organs (Malpighian tubules) and hindgut contractions by activati

19 heral tissues such as the epidermis, midgut, Malpighian tubules, and fat body, i.e., tissues known to

20 ed in the nervous tissue of the synganglion, Malpighian tubules, and muscle.

21 developing midgut endoderm, the hindgut and Malpighian tubules, and the epidermis and central nervou

22 ted that several differentiated cells in the malpighian tubules arise from these stem cells.

23 as of various tubules (e.g., nephric ducts, Malpighian tubules), as it is driven by cell rearrangeme

24 NO-stimulated fluid secretion in Drosophila Malpighian tubules, both when applied in the form of a N

25 e invaginating posterior midgut, evaginating Malpighian tubule buds, elongating hindgut, invaginating

26 Specifically, wal affects evagination of the Malpighian tubule buds, fas and thr affect bud extension

27 Ultrastructural examination of larval Malpighian tubule cells depleted for NS1 showed a loss o

28 showing highly abundant expression in adult Malpighian tubules, ClC-c, did not impact depolarization

29 s of ALAT1 or ALAT2 in fat body, thorax, and Malpighian tubules compared with dsRNA firefly luciferas

30 Further analysis of the role of cv-c in the Malpighian tubules demonstrates that its activity is req

31 In Diptera, Malpighian tubules derive from ectodermal cells that eva

32 genes, into a genetic pathway that controls Malpighian tubule development.

33 In Drosophila, the renal (Malpighian) tubule displays the highest per-cell transpo

34 cv-c activity, tubulogenesis in the renal or Malpighian tubules fails and they collapse into a cyst-l

35 adult eye, larval salivary glands and larval Malpighian tubules for each of three different chromosom

36 cules in the salivary glands, midgut, ovary, Malpighian tubules, haemolymph and the tick cell line IR

37 Cells of Chironomus salivary glands and Malpighian tubules have junctions of the "septate" kind.

38 gans such as the mammalian kidney and insect Malpighian tubule/hindgut requires a region of hypertoni

39 epolarize the transepithelial voltage of the malpighian tubule in concentrations of less than 10(-9)

40 The kidneys in vertebrates and the malpighian tubules in Drosophila accomplish these functi

41 The Drosophila Malpighian tubule is a model system for studying genetic

42 a stable boundary between midgut and hindgut/Malpighian tubules is not established during early embry

43 gh byn is not expressed in the midgut or the Malpighian tubules, it is required for the formation of

44 the endodermal midgut and ectodermal hindgut/Malpighian tubules, maintain populations of dividing ste

45 nd one novel gene, walrus (wal), that affect Malpighian tubule morphogenesis.

46 The Malpighian tubules (MT), of chill susceptible Drosophila

47 Mas-DH by incubating it in vitro with larval Malpighian tubules (Mt), the target organ of the hormone

48 Malpighian tubules mutant for raw or rib are wider and s

49 ic bud and metanephric mesoderm, whereas the malpighian tubules of Drosophila develop from the hindgu

50 ts expression was high in the integument and Malpighian tubules of last instar larvae and adults.

51 rease cAMP production and fluid secretion in Malpighian tubules of several insect species.

52 hat strongly inhibits fluid secretion by the Malpighian tubules of this insect.

53 nhibits a Kir channel cloned from the renal (Malpighian) tubules of Aedes aegypti (AeKir1).

54 ost abundantly expressed in the adult renal (Malpighian) tubule rather than in neuronal tissues.

55 r, some secretory epithelia (choroid plexus, Malpighian tubule, rectal gland, etc.) have "backwards"

56 origin of stem cells found in the excretory Malpighian tubules ('renal stem cells') has not been est

57 itzi, and that it is distributed in ovaries, malpighian tubules, salivary glands and midguts of the t

58 ce fluid secretion or depolarizations in the malpighian tubules suggest that there may be more than o

59 is the only endogenous insect ADF acting on Malpighian tubules to be sequenced, and the first coleop

60 cently, multipotent stem cells in Drosophila malpighian tubules were identified, and it was demonstra

61 Expression is high in gut, ovaries, and Malpighian tubules where immunofluorescence microscopy r

62 tected in clock-containing tissues including Malpighian tubules, where it mediates both light-depende