Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jill O Fuss"'
Autor:
Eric Campeau, Victoria E Ruhl, Francis Rodier, Corey L Smith, Brittany L Rahmberg, Jill O Fuss, Judith Campisi, Paul Yaswen, Priscilla K Cooper, Paul D Kaufman
Publikováno v:
PLoS ONE, Vol 4, Iss 8, p e6529 (2009)
The ability to express or deplete proteins in living cells is crucial for the study of biological processes. Viral vectors are often useful to deliver DNA constructs to cells that are difficult to transfect by other methods. Lentiviruses have the add
Externí odkaz:
https://doaj.org/article/4f722a938c074f44af58f8c1f007f6a7
Autor:
Jill O Fuss, Priscilla K Cooper
Publikováno v:
PLoS Biology, Vol 4, Iss 6, p e203 (2006)
Externí odkaz:
https://doaj.org/article/7a3be525009d434aba2116570ec87354
Autor:
Sayo Kashiwagi, Isao Kuraoka, Yoshie Fujiwara, Kenichi Hitomi, Quen J. Cheng, Jill O. Fuss, David S. Shin, Chikahide Masutani, John A. Tainer, Fumio Hanaoka, Shigenori Iwai
Publikováno v:
Journal of Nucleic Acids, Vol 2010 (2010)
Human DNA polymerase η (HsPolη) plays an important role in translesion synthesis (TLS), which allows for replication past DNA damage such as UV-induced cis-syn cyclobutane pyrimidine dimers (CPDs). Here, we characterized ApPolη from the thermophil
Externí odkaz:
https://doaj.org/article/b1aa0d079d1b4a6eb756cdd3ce8515eb
Autor:
Steven Hahn, Olivia Luyties, Susan E. Tsutakawa, Jill O. Fuss, Chi Lin Tsai, James Fishburn, Jenna K. Rimel, Eric J. Tomko, Eric A. Galburt, Dylan J. Taatjes
Publikováno v:
J Mol Biol
Journal of molecular biology, vol 433, iss 14
Journal of molecular biology, vol 433, iss 14
The general transcription factor TFIIH contains three ATP-dependent catalytic activities. TFIIH functions in nucleotide excision repair primarily as a DNA helicase and in Pol II transcription initiation as a dsDNA translocase and protein kinase. Duri
Autor:
Justin P. Ishida, John A. Tainer, Chris Jeans, Jill O. Fuss, Scott D. Gradia, Miaw Sheue Tsai
Recombinant expression of large, multi-protein complexes is essential and often rate-limiting for determining structural, biophysical, and biochemical properties of DNA repair, replication, transcription, and other key cellular processes. Baculovirus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8baf7c5e39ec0639468debde35bb8e59
https://doi.org/10.1016/bs.mie.2017.03.008
https://doi.org/10.1016/bs.mie.2017.03.008
Autor:
Jill O. Fuss, John A. Tainer
Publikováno v:
DNA Repair. 10:697-713
Helicases must unwind DNA at the right place and time to maintain genomic integrity or gene expression. Biologically critical XPB and XPD helicases are key members of the human TFIIH complex; they anchor CAK kinase (cyclinH, MAT1, CDK7) to TFIIH and
Damaged bases in DNA are known to lead to errors in replication and transcription, compromising the integrity of the genome. We have proposed a model where repair proteins containing redox-active [4Fe-4S] clusters utilize DNA charge transport (CT) as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b330aef05f0d18ecf69ce9e1d2099fae
https://resolver.caltech.edu/CaltechAUTHORS:20120228-100512207
https://resolver.caltech.edu/CaltechAUTHORS:20120228-100512207
Using DNA-modified electrodes, we show DNA-mediated signaling by XPD, a helicase that contains a [4Fe-4S] cluster and is critical for nucleotide excision repair and transcription. The DNA-mediated redox signal resembles that of base excision repair p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc023545a20be71de15e0e95a25b0de
https://europepmc.org/articles/PMC3234108/
https://europepmc.org/articles/PMC3234108/
Autor:
John A. Tainer, Fumio Hanaoka, Quen J. Cheng, Kenichi Hitomi, Chikahide Masutani, David S. Shin, Jill O. Fuss, Isao Kuraoka, Yoshie Fujiwara, Shigenori Iwai, Sayo Kashiwagi
Publikováno v:
Journal of Nucleic Acids, Vol 2010 (2010)
Journal of Nucleic Acids
Journal of Nucleic Acids
Human DNA polymeraseη(HsPolη) plays an important role in translesion synthesis (TLS), which allows for replication past DNA damage such as UV-inducedcis-syncyclobutane pyrimidine dimers (CPDs). Here, we characterized ApPolηfrom the thermophilic wo
Autor:
Michal Hammel, Andrew S. Arvai, John A. Tainer, Jill O. Fuss, Victoria A. Roberts, Quen J. Cheng, Li Fan, Priscilla K. Cooper
SummaryMutations in XPD helicase, required for nucleotide excision repair (NER) as part of the transcription/repair complex TFIIH, cause three distinct phenotypes: cancer-prone xeroderma pigmentosum (XP), or aging disorders Cockayne syndrome (CS), an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59699533f1fa7d2ce27bf89ec74a99b7
https://europepmc.org/articles/PMC3055247/
https://europepmc.org/articles/PMC3055247/