U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 19

1.
Yeast Mer1 Mutants Display Reduced Levels of Meiotic Recombination
J. Engebrecht, G. S. Roeder
Genetics. 1989 Feb; 121(2): 237–247. doi: 10.1093/genetics/121.2.237
PMCID:
PMC1203613
SummaryPDF–1.0M
2.
MER1, a yeast gene required for chromosome pairing and genetic recombination, is induced in meiosis.
J Engebrecht, G S Roeder
Mol Cell Biol. 1990 May; 10(5): 2379–2389. doi: 10.1128/mcb.10.5.2379
PMCID:
PMC360586
SummaryPage BrowsePDF–2.6M
3.
A subset of Mer1p-dependent introns requires Bud13p for splicing activation and nuclear retention
Frederick W. Scherrer, Jr, Marc Spingola
RNA. 2006 Jul; 12(7): 1361–1372. doi: 10.1261/rna.2276806
PMCID:
PMC1484446
AbstractArticlePDF–642K
4.
Binding of a cell-type-specific RNA splicing factor to its target regulatory sequence.
K Nandabalan, G S Roeder
Mol Cell Biol. 1995 Apr; 15(4): 1953–1960. doi: 10.1128/mcb.15.4.1953
PMCID:
PMC230421
SummaryPDF–402K
5.
An essential role for trimethylguanosine RNA caps in Saccharomyces cerevisiae meiosis and their requirement for splicing of SAE3 and PCH2 meiotic pre-mRNAs
Zhicheng R. Qiu, Stewart Shuman, Beate Schwer
Nucleic Acids Res. 2011 Jul; 39(13): 5633–5646. Published online 2011 Mar 11. doi: 10.1093/nar/gkr083
PMCID:
PMC3141232
AbstractArticlePDF–5.5M
6.
Ama1p is a meiosis-specific regulator of the anaphase promoting complex/cyclosome in yeast
Katrina F. Cooper, Michael J. Mallory, Daniel B. Egeland, Michal Jarnik, Randy Strich
Proc Natl Acad Sci U S A. 2000 Dec 19; 97(26): 14548–14553. Published online 2000 Dec 12. doi: 10.1073/pnas.250351297
PMCID:
PMC18956
AbstractArticlePDF–292K
7.
The SR-protein Npl3 is an essential component of the meiotic splicing regulatory network in Saccharomyces cerevisiae
Rima Sandhu, Aniketa Sinha, Ben Montpetit
Nucleic Acids Res. 2021 Mar 18; 49(5): 2552–2568. Published online 2021 Feb 12. doi: 10.1093/nar/gkab071
PMCID:
PMC7969001
AbstractArticlePDF–5.8M
8.
Determinants of Nam8-dependent splicing of meiotic pre-mRNAs
Zhicheng R. Qiu, Beate Schwer, Stewart Shuman
Nucleic Acids Res. 2011 Apr; 39(8): 3427–3445. Published online 2011 Jan 5. doi: 10.1093/nar/gkq1328
PMCID:
PMC3082912
AbstractArticlePDF–13M
9.
Defining the Mer1 and Nam8 meiotic splicing regulons by cDNA rescue
Zhicheng R. Qiu, Beate Schwer, Stewart Shuman
RNA. 2011 Sep; 17(9): 1648–1654. doi: 10.1261/rna.2792011
PMCID:
PMC3162330
AbstractArticlePDF–395K
10.
Test of intron predictions reveals novel splice sites, alternatively spliced mRNAs and new introns in meiotically regulated genes of yeast
Carrie A. Davis, Leslie Grate, Marc Spingola, Manuel Ares Jr
Nucleic Acids Res. 2000 Apr 15; 28(8): 1700–1706. doi: 10.1093/nar/28.8.1700
PMCID:
PMC102823
AbstractArticlePDF–195K
11.
Snu56p Is Required for Mer1p-Activated Meiotic Splicing
Richard J. Balzer, Michael F. Henry
Mol Cell Biol. 2008 Apr; 28(8): 2497–2508. Published online 2008 Feb 11. doi: 10.1128/MCB.00405-07
PMCID:
PMC2293118
AbstractArticlePDF–522K
12.
Isolation of Mutants Defective in Early Steps of Meiotic Recombination in the Yeast Saccharomyces Cerevisiae
R. E. Malone, S. Bullard, M. Hermiston, R. Rieger, M. Cool, A. Galbraith
Genetics. 1991 May; 128(1): 79–88. doi: 10.1093/genetics/128.1.79
PMCID:
PMC1204456
SummaryPDF–927K
13.
Mer1p is a modular splicing factor whose function depends on the conserved U2 snRNP protein Snu17p
Marc Spingola, Javier Armisen, Manuel Ares, Jr
Nucleic Acids Res. 2004; 32(3): 1242–1250. Published online 2004 Feb 18. doi: 10.1093/nar/gkh281
Correction in:
Nucleic Acids Res. 2006; 34(5): 1667.
PMCID:
PMC373413
AbstractArticlePDF–228K
14.
Integration of a splicing regulatory network within the meiotic gene expression program of Saccharomyces cerevisiae
Elizabeth M. Munding, A. Haller Igel, Lily Shiue, Kristel M. Dorighi, Lisa R. Treviño, Manuel Ares, Jr
Genes Dev. 2010 Dec 1; 24(23): 2693–2704. doi: 10.1101/gad.1977410
PMCID:
PMC2994042
AbstractArticlePDF–895K
15.
A Protein Interaction Map of the Mitotic Spindle
Jonathan Wong, Yuko Nakajima, Stefan Westermann, Ching Shang, Jung-seog Kang, Crystal Goodner, Pantea Houshmand, Stanley Fields, Clarence S.M. Chan, David Drubin, Georjana Barnes, Tony Hazbun
Mol Biol Cell. 2007 Oct; 18(10): 3800–3809. doi: 10.1091/mbc.E07-06-0536
PMCID:
PMC1995735
AbstractArticlePDF–796K
16.
An inter‐species protein–protein interaction network across vast evolutionary distance
Quan Zhong, Samuel J Pevzner, Tong Hao, Yang Wang, Roberto Mosca, Jörg Menche, Mikko Taipale, Murat Taşan, Changyu Fan, Xinping Yang, Patrick Haley, Ryan R Murray, Flora Mer, Fana Gebreab, Stanley Tam, Andrew MacWilliams, Amélie Dricot, Patrick Reichert, Balaji Santhanam, Lila Ghamsari, Michael A Calderwood, Thomas Rolland, Benoit Charloteaux, Susan Lindquist, Albert‐László Barabási, David E Hill, Patrick Aloy, Michael E Cusick, Yu Xia, Frederick P Roth, Marc Vidal
Mol Syst Biol. 2016 Apr; 12(4): 865. Published online 2016 Apr 23. doi: 10.15252/msb.20156484
PMCID:
PMC4848758
AbstractArticlePDF–2.1M
17.
A systematic proximity ligation approach to studying protein‐substrate specificity identifies the substrate spectrum of the Ssh1 translocon
Nir Cohen, Naama Aviram, Maya Schuldiner
EMBO J. 2023 Jun; 42(11): e113385. Published online 2023 Apr 19. doi: 10.15252/embj.2022113385
PMCID:
PMC10233368
AbstractArticlePDF–1.2M
18.
A global interaction network maps a wiring diagram of cellular function
Michael Costanzo, Benjamin VanderSluis, Elizabeth N. Koch, Anastasia Baryshnikova, Carles Pons, Guihong Tan, Wen Wang, Matej Usaj, Julia Hanchard, Susan D. Lee, Vicent Pelechano, Erin B. Styles, Maximilian Billmann, Jolanda van Leeuwen, Nydia van Dyk, Zhen-Yuan Lin, Elena Kuzmin, Justin Nelson, Jeff S. Piotrowski, Tharan Srikumar, Sondra Bahr, Yiqun Chen, Raamesh Deshpande, Christoph F. Kurat, Sheena C. Li, Zhijian Li, Mojca Mattiazzi Usaj, Hiroki Okada, Natasha Pascoe, Bryan-Joseph San Luis, Sara Sharifpoor, Emira Shuteriqi, Scott W. Simpkins, Jamie Snider, Harsha Garadi Suresh, Yizhao Tan, Hongwei Zhu, Noel Malod-Dognin, Vuk Janjic, Natasa Przulj, Olga G. Troyanskaya, Igor Stagljar, Tian Xia, Yoshikazu Ohya, Anne-Claude Gingras, Brian Raught, Michael Boutros, Lars M. Steinmetz, Claire L. Moore, Adam P. Rosebrock, Amy A. Caudy, Chad L. Myers, Brenda Andrews, Charles Boone
Science. Author manuscript; available in PMC 2017 Oct 30.
Published in final edited form as: Science. 2016 Sep 23; 353(6306): aaf1420. doi: 10.1126/science.aaf1420
PMCID:
PMC5661885
AbstractArticlePDF–2.6M
19.
New data and collaborations at the Saccharomyces Genome Database: updated reference genome, alleles, and the Alliance of Genome Resources
Stacia R Engel, Edith D Wong, Robert S Nash, Suzi Aleksander, Micheal Alexander, Eric Douglass, Kalpana Karra, Stuart R Miyasato, Matt Simison, Marek S Skrzypek, Shuai Weng, J Michael Cherry
Genetics. 2022 Apr; 220(4): iyab224. Published online 2021 Dec 13. doi: 10.1093/genetics/iyab224
PMCID:
PMC9209811
AbstractArticlePDF–818K

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center