Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Tamara Goldfarb"'
Autor:
Shashikant Pujar, Jane Loveland, Alex Astashyn, Ruth Bennett, Andrew Berry, Eric Cox, Claire Davidson, Olga Ermolaeva, Catherine Farrell, Reham Fatima, Tamara Goldfarb, Jose Gonzalez, Diana Haddad, Matthew Hardy, Toby Hunt, John Jackson, Vinita Joardar, Michael Kay, Vamsi Kodali, Kelly McGarvey, Jonathan Mudge, Michael Murphy, Sanjida Rangwala, Françoise Thibaud-Nissen, Anjana Vatsan, Wallin Craig, Webb David, Adam Frankish, Fiona Cunningham, Terence Murphy
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100586- (2023)
Externí odkaz:
https://doaj.org/article/1cc1dd2a36124b0c942893b13ce0b29d
Autor:
Tamara Goldfarb, Michael Lichten
Publikováno v:
PLoS Biology, Vol 8, Iss 10, p e1000520 (2010)
Recombination between homologous chromosomes of different parental origin (homologs) is necessary for their accurate segregation during meiosis. It has been suggested that meiotic inter-homolog recombination is promoted by a barrier to inter-sister-c
Externí odkaz:
https://doaj.org/article/0c09380a1985438594dbdf334eafaa2b
Autor:
Joannella Morales, Shashikant Pujar, Jane E. Loveland, Alex Astashyn, Ruth Bennett, Andrew Berry, Eric Cox, Claire Davidson, Olga Ermolaeva, Catherine M. Farrell, Reham Fatima, Laurent Gil, Tamara Goldfarb, Jose M. Gonzalez, Diana Haddad, Matthew Hardy, Toby Hunt, John Jackson, Vinita S. Joardar, Michael Kay, Vamsi K. Kodali, Kelly M. McGarvey, Aoife McMahon, Jonathan M. Mudge, Daniel N. Murphy, Michael R. Murphy, Bhanu Rajput, Sanjida H. Rangwala, Lillian D. Riddick, Françoise Thibaud-Nissen, Glen Threadgold, Anjana R. Vatsan, Craig Wallin, David Webb, Paul Flicek, Ewan Birney, Kim D. Pruitt, Adam Frankish, Fiona Cunningham, Terence D. Murphy
Publikováno v:
Nature. 604:310-315
Comprehensive genome annotation is essential to understand the impact of clinically relevant variants. However, the absence of a standard for clinical reporting and browser display complicates the process of consistent interpretation and reporting. T
Autor:
Catherine M. Farrell, Tamara Goldfarb, Sanjida H. Rangwala, Alexander Astashyn, Olga D. Ermolaeva, Vichet Hem, Kenneth S. Katz, Vamsi K. Kodali, Frank Ludwig, Craig L. Wallin, Kim D. Pruitt, Terence D. Murphy
Publikováno v:
Genome Research. 32:175-188
Eukaryotic genomes contain many nongenic elements that function in gene regulation, chromosome organization, recombination, repair, or replication, and mutation of those elements can affect genome function and cause disease. Although numerous epigeno
Autor:
Claire Davidson, Jonathan M. Mudge, Marie-Marthe Suner, Vamsi K. Kodali, Ruth L. Seal, Ruth Bennett, Shashikant Pujar, Fergal J. Martin, Carol J. Bult, M. Kay, Catherine M. Farrell, Nuala A. O'Leary, Craig Wallin, Carlos García Girón, Andrew Berry, If Barnes, Tamara Goldfarb, Adam Frankish, Kelly M. McGarvey, Bronwen Aken, Kim D. Pruitt, Mark Diekhans, Sophia Zhu, Terence Murphy, Michael R. Murphy, Elspeth A. Bruford, Monica S. McAndrews, John D. Jackson, Lillian D. Riddick, Bhanu Rajput, David Webb, Sanjida H. Rangwala, Eric Cox, Jose Manuel Gonzalez, Jane E. Loveland, Toby Hunt, Vinita Joardar
Publikováno v:
Nucleic Acids Research
The Consensus Coding Sequence (CCDS) project provides a dataset of protein-coding regions that are identically annotated on the human and mouse reference genome assembly in genome annotations produced independently by NCBI and the Ensembl group at EM
Autor:
Barbara Robbertse, Patrick Masterson, Jinna Choi, Sanjida H. Rangwala, Vyacheslav Brover, Olga Blinkova, Stacy Ciufo, Kim D. Pruitt, Conrad L. Schoch, Daniel H. Haft, Kelly M. McGarvey, Richard McVeigh, Raymond E. Tully, Bhanu Rajput, Alexander Astashyn, Vinita Joardar, Wratko Hlavina, Vamsi K. Kodali, Kathleen O'Neill, Danso Ako-adjei, Hanzhen Sun, Craig Wallin, Mathew W. Wright, Michael DiCuccio, Daniel Rausch, Catherine M. Farrell, Susan S. Storz, Avi Kimchi, Terence Murphy, Tripti Gupta, Eneida L. Hatcher, Donna Maglott, Shashikant Pujar, Brian Smith-White, David Webb, Nuala A. O'Leary, Wenjun Li, Michael R. Murphy, Igor Tolstoy, Françoise Thibaud-Nissen, Diana Haddad, Olga Ermolaeva, Azat Badretdin, Andrei Shkeda, Lillian D. Riddick, Tatiana Tatusova, Wendy Wu, Melissa J. Landrum, Vyacheslav Chetvernin, Tamara Goldfarb, Anjana R. Vatsan, Paul Kitts, J. Rodney Brister, Yiming Bao, Eric Cox
Publikováno v:
Nucleic Acids Research
The RefSeq project at the National Center for Biotechnology Information (NCBI) maintains and curates a publicly available database of annotated genomic, transcript, and protein sequence records (http://www.ncbi.nlm.nih.gov/refseq/). The RefSeq projec
Publikováno v:
Genetics. 179:1807-1821
Efficient repair of DNA double-strand breaks (DSBs) requires the coordination of checkpoint signaling and enzymatic repair functions. To study these processes during gene conversion at a single chromosomal break, we monitored mating-type switching in
Autor:
Tamara Goldfarb, Shaked Afik, Shany Doron, Rotem Sorek, Yoav Charpak-Amikam, Eyal Weinstock, Gal Ofir, Ofir Cohen, Hila Sberro
Publikováno v:
The EMBO journal. 34(2)
The perpetual arms race between bacteria and phage has resulted in the evolution of efficient resistance systems that protect bacteria from phage infection. Such systems, which include the CRISPR-Cas and restriction-modification systems, have proven
Autor:
Eric Alani, Tamara Goldfarb
Publikováno v:
Genetics. 169:563-574
The Saccharomyces cerevisiae mismatch repair (MMR) protein MSH6 and the SGS1 helicase were recently shown to play similarly important roles in preventing recombination between divergent DNA sequences in a single-strand annealing (SSA) assay. In contr
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 101(25)
Recombination between moderately divergent DNA sequences is impaired compared with identical sequences. In yeast, an HO endonuclease-induced double-strand break can be repaired by single-strand annealing (SSA) between flanking homologous sequences. A