ライフサイエンスコーパス: sperm tail

1 inear Ca(2+) signaling nanodomains along the sperm tail.

2 and localized to the principal piece of the sperm tail.

3 head by the neck or the middle piece of the sperm tail.

4 cal association of these two proteins on the sperm tail.

5 and Ca(v)3.3 on the principal piece of human sperm tail.

6 C8 is confined to the principal piece of the sperm tail.

7 present in the plasma membrane of the entire sperm tail.

8 d specifically in the principal piece of the sperm tail.

9 isoforms were observed in the axoneme of the sperm tail.

10 by Slo3, a K(+) channel also present in the sperm tail.

11 atSper) Ca(2+)-selective ion channels in the sperm tail.

12 microtubules nucleated from centrosomes and sperm tails.

13 l mice presented with impaired fertility and sperm tail abnormalities.

14 compartmentalized signaling programs in the sperm tail and head; in the tail, GIV enhances PI3K Akt

15 ally localized to the principal piece of the sperm tail and is required for sperm cell hyperactivatio

16 vely in the plasma membrane of the mammalian sperm tail and it is essential for sperm motility.

17 arrangement of CatSper nanodomains along the sperm tail and regulates the pH and Ca(2+) sensitivity o

18 g males is characterised by abnormalities in sperm tails and reduced numbers in some sperm cysts, whe

19 ton channel Hv1 has been identified in human sperm tail, and the P2X2 ion channel has been identified

20 Giant sperm tails are the cellular equivalent of the peacock's

21 a splice-generated C-terminal extension of a sperm tail-associating protein mediates unanticipated ce

22 e two classes of singlet microtubules in the sperm tail axoneme, the central pair and the accessory m

23 fically the central pair microtubules in the sperm tail axoneme.

24 body, and beta 2 is utilized for the motile sperm tail axoneme.

25 ted spermatozoa requires Ca2+ entry into the sperm tail by an alkalinization-activated voltage-sensit

26 nel, and KSper (Slo3) are core regulators of sperm tail calcium entry and sperm hyperactivated motili

27 The Ca(2+)-dependent sperm tail curvature phenotypes, "fishhook", where abnor

28 initially identified as a major component of sperm tail cytoskeleton and later was suggested to be a

29 ially identified as a major component of the sperm tail cytoskeleton, and was later suggested to be l

30 amatic cell morphological changes going from sperm tail elongation and nuclear reshaping to cell memb

31 The electrophoretic mobility of sperm tail flagellar tubulins and tektins from an echino

32 The findings show that JAM-A is involved in sperm tail formation and is essential for normal motilit

33 such as vesicle transport and the beating of sperm tails; however, their mechanism of force generatio

34 he acrosomal vesicle and migrates toward the sperm tail in elongated spermatids.

35 tubulin doublets occur in most Stamp(tm/tm) sperm tails in conjunction with substantial reduction in

36 CA4 expression in the principle piece of the sperm tail is essential for hyperactivated motility and

37 Sperm tails or flagella are specialized cilia essential

38 cifically to the centriolar region where the sperm tail originates and to the perinuclear ring from w

39 f tyrosine and serine phosphorylation of the sperm tail proteins AKAP-3 and AKAP-4.

40 ctin cones that synchronously move along the sperm tails, removing inter-spermatid bridges and most o

41 We find that mice lacking the sperm tail-specific CATSPERdelta are infertile and their

42 lization to the principal piece of the human sperm tail suggest that CABYR may be involved in sperm m

43 ucture of the motility apparatus in Pmca4-/- sperm tails was normal, but an increased incidence of mi

44 Significant morphological alterations in sperm tails were observed in GP compared to GC.

45 t is localized to the principle piece of the sperm tail, which is also the location of the major Ca2+

46 ources assert that during fertilization, the sperm tail, with its mitochondria, gets excluded from th