126 related articles for article (PubMed ID: 3791426)
1. Bivalent orientation and behavior in crane-fly spermatocytes recovering from cold exposure.
Janicke MA; LaFountain JR
Cell Motil Cytoskeleton; 1986; 6(5):492-501. PubMed ID: 3791426
[TBL] [Abstract][Full Text] [Related]
2. Malorientation in half-bivalents at anaphase: analysis of autosomal laggards in untreated, cold-treated, and cold-recovering crane fly spermatocytes.
Janicke MA; LaFountain JR
J Cell Biol; 1984 Mar; 98(3):859-69. PubMed ID: 6699088
[TBL] [Abstract][Full Text] [Related]
3. Malorientation in half-bivalents at anaphase in crane fly spermatocytes following Colcemid treatment.
LaFountain JR
Chromosoma; 1985; 91(5):337-46. PubMed ID: 3996101
[TBL] [Abstract][Full Text] [Related]
4. Centromeric dots in crane-fly spermatocytes: meiotic maturation and malorientation.
Janicke MA; LaFountain JR
Chromosoma; 1989 Nov; 98(5):358-67. PubMed ID: 2612294
[TBL] [Abstract][Full Text] [Related]
5. Malorientation and abnormal segregation of chromosomes during recovery from colcemid and nocodazole.
Ladrach KS; LaFountain JR
Cell Motil Cytoskeleton; 1986; 6(4):419-27. PubMed ID: 3757073
[TBL] [Abstract][Full Text] [Related]
6. Maloriented bivalents have metaphase positions at the spindle equator with more kinetochore microtubules to one pole than to the other.
LaFountain JR; Oldenbourg R
Mol Biol Cell; 2004 Dec; 15(12):5346-55. PubMed ID: 15385630
[TBL] [Abstract][Full Text] [Related]
7. Kinetochore microtubules in crane-fly spermatocytes: untreated, 2 degrees C-treated, and 6 degrees C-grown spindles.
Scarcello LA; Janicke MA; LaFountain JR
Cell Motil Cytoskeleton; 1986; 6(4):428-38. PubMed ID: 3757074
[TBL] [Abstract][Full Text] [Related]
8. Ultraviolet microbeam irradiations of epithelial and spermatocyte spindles suggest that forces act on the kinetochore fibre and are not generated by its disassembly.
Spurck T; Forer A; Pickett-Heaps J
Cell Motil Cytoskeleton; 1997; 36(2):136-48. PubMed ID: 9015202
[TBL] [Abstract][Full Text] [Related]
9. Effects of nanomolar taxol on crane-fly spermatocyte spindles indicate that acetylation of kinetochore microtubules can be used as a marker of poleward tubulin flux.
Wilson PJ; Forer A
Cell Motil Cytoskeleton; 1997; 37(1):20-32. PubMed ID: 9142436
[TBL] [Abstract][Full Text] [Related]
10. Effects of ultraviolet-microbeam irradiation of kinetochores in crane-fly spermatocytes.
Ilagan AB; Forer A
Cell Motil Cytoskeleton; 1997; 36(3):266-75. PubMed ID: 9067622
[TBL] [Abstract][Full Text] [Related]
11. Chromosome segregation in crane-fly spermatocytes: cold treatment and cold recovery induce anaphase lag.
Janicke MA; LaFountain JR
Chromosoma; 1982; 85(5):619-31. PubMed ID: 7128280
[TBL] [Abstract][Full Text] [Related]
12. Chromosome malorientations after meiosis II arrest cause nondisjunction.
Janicke MA; Lasko L; Oldenbourg R; LaFountain JR
Mol Biol Cell; 2007 May; 18(5):1645-56. PubMed ID: 17314397
[TBL] [Abstract][Full Text] [Related]
13. Direct visualization of microtubule flux during metaphase and anaphase in crane-fly spermatocytes.
LaFountain JR; Cohan CS; Siegel AJ; LaFountain DJ
Mol Biol Cell; 2004 Dec; 15(12):5724-32. PubMed ID: 15469981
[TBL] [Abstract][Full Text] [Related]
14. Behaviour of meiotic univalents during metaphase I: natural variants and computer simulations.
Peters GB
Cytobios; 1985; 43(172-173):179-98. PubMed ID: 4075845
[TBL] [Abstract][Full Text] [Related]
15. Coordinated movements between autosomal half-bivalents in crane-fly spermatocytes: evidence that 'stop' signals are sent between partner half-bivalents.
Yin B; Forer A
J Cell Sci; 1996 Jan; 109 ( Pt 1)():155-63. PubMed ID: 8834800
[TBL] [Abstract][Full Text] [Related]
16. Colchicine promotes a change in chromosome structure without loss of sister chromatid cohesion in prometaphase I-arrested bivalents.
RodrÃguez EM; Parra MT; Rufas JS; Suja JA
Chromosoma; 2001 Dec; 110(7):478-86. PubMed ID: 11862455
[TBL] [Abstract][Full Text] [Related]
17. Nonrandom chromosome segregation in male meiosis of a sciarid fly: elimination of paternal chromosomes in first division is mediated by non-kinetochore microtubules.
Fuge H
Cell Motil Cytoskeleton; 1997; 36(1):84-94. PubMed ID: 8986380
[TBL] [Abstract][Full Text] [Related]
18. Traction force on a kinetochore at metaphase acts as a linear function of kinetochore fiber length.
Hays TS; Wise D; Salmon ED
J Cell Biol; 1982 May; 93(2):374-89. PubMed ID: 7096444
[TBL] [Abstract][Full Text] [Related]
19. Myosin localization during meiosis I of crane-fly spermatocytes gives indications about its role in division.
Silverman-Gavrila RV; Forer A
Cell Motil Cytoskeleton; 2003 Jun; 55(2):97-113. PubMed ID: 12740871
[TBL] [Abstract][Full Text] [Related]
20. Chromosomes selectively detach at one pole and quickly move towards the opposite pole when kinetochore microtubules are depolymerized in Mesostoma ehrenbergii spermatocytes.
Fegaras E; Forer A
Protoplasma; 2018 Jul; 255(4):1205-1224. PubMed ID: 29468300
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]