Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Christine B. Anderson"'
Autor:
Ulrich Schweizer, Sandra Seeher, Michael T. Howard, Dolph L. Hatfield, Christine B. Anderson, Michael Doengi, Bradley A. Carlson, Noelia Fradejas-Villar
Publikováno v:
Nucleic Acids Research
Dual-assignment of codons as termination and elongation codons is used to expand the genetic code. In mammals, UGA can be reassigned to selenocysteine during translation of selenoproteins by a mechanism involving a 3΄ untranslated region (UTR) selen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b4d416ab845e835d4c554a069fc7009
https://doi.org/10.1093/nar/gkw1255
https://doi.org/10.1093/nar/gkw1255
Autor:
Michael T. Howard, Dolph L. Hatfield, Christine B. Anderson, Harold E. Seifried, Bradley A. Carlson, Petra A. Tsuji
Publikováno v:
Nutrients
Nutrients; Volume 7; Issue 8; Pages: 6529-6549
Nutrients, Vol 7, Iss 8, Pp 6529-6549 (2015)
Volume 7
Issue 8
Pages 6529-6549
Nutrients; Volume 7; Issue 8; Pages: 6529-6549
Nutrients, Vol 7, Iss 8, Pp 6529-6549 (2015)
Volume 7
Issue 8
Pages 6529-6549
Selenium is an essential element that is required to support a number of cellular functions and biochemical pathways. The objective of this study was to examine the effects of reduced dietary selenium levels on gene expression to assess changes in ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21557e41515a838a6775b7c08b36ce42
http://europepmc.org/articles/PMC4555136
http://europepmc.org/articles/PMC4555136
Autor:
Carsten G. Bönnemann, Richard S. Finkel, Mark B. Bromberg, Katherine D. Mathews, John W. Day, Kevin M. Flanigan, Andrew von Niederhausern, Julaine Florence, Jerry R. Mendell, Diane M. Dunn, Craig M. McDonald, Jacinda B. Sampson, Kathryn J. Swoboda, Anne M. Connolly, Michael T. Howard, Payam Soltanzadeh, Robert B. Weiss, Laura E. Taylor, Brenda Wong, Christine B. Anderson, Alan Pestronk
Publikováno v:
Human Mutation. 32:299-308
Nonsense mutations are usually predicted to function as null alleles due to premature termination of protein translation. However, nonsense mutations in the DMD gene, encoding the dystrophin protein, have been associated with both the severe Duchenne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a71b754c30a2baabbb87c3a56b6c192
https://doi.org/10.1002/humu.21426
https://doi.org/10.1002/humu.21426
Autor:
Christine B. Anderson, Julie F. Smart
Publikováno v:
Journal of Applied Rehabilitation Counseling. 41:3-10
Throughout the transition and vocational rehabilitation process those who are Culturally Linguistically Diverse (CLD), or identify as belonging to a racial and ethnic minority group, experience limited achievement in the following areas: high school
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e5c5fe73df2715c523c791f0333c6f3
https://doi.org/10.1891/0047-2220.41.4.3
https://doi.org/10.1891/0047-2220.41.4.3
Autor:
Michael T. Howard, Nikolay Grigorenko, Alex R. Khomutov, Jouko Vepsäläinen, Juhani Jänne, Christine B. Anderson, Tuomo A. Keinänen, Mervi T. Hyvönen, Leena Alhonen
Publikováno v:
Biochemical Journal. 422:321-328
The natural polyamines are ubiquitous multifunctional organic cations which play important roles in regulating cellular proliferation and survival. Here we present a novel approach to investigating polyamine functions by using optical isomers of MeSp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee831506647353de6a3da7d28190fb5b
https://doi.org/10.1042/bj20090737
https://doi.org/10.1042/bj20090737
Autor:
Steve D. Wilton, Olga L. Gurvich, Christine B. Anderson, Kevin M. Flanigan, Thérèse M. F. Tuohy, Michael T. Howard, Richard S. Finkel, Robert B. Weiss, Livija Medne
Publikováno v:
Annals of Neurology. 63:81-89
Objective The degenerative muscle diseases Duchenne (DMD) and Becker muscular dystrophy result from mutations in the DMD gene, which encodes the dystrophin protein. Recent improvements in mutational analysis techniques have resulted in the increasing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbbdfa9a820183fb1cf47b3758560367
https://doi.org/10.1002/ana.21290
https://doi.org/10.1002/ana.21290
Publikováno v:
RNA. 13:912-920
Selenocysteine insertion during decoding of eukaryotic selenoprotein mRNA requires several trans-acting factors and a cis-acting selenocysteine insertion sequence (SECIS) usually located in the 3′ UTR. A second cis-acting selenocysteine codon redef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::411e6f20d3baedf7bf338eb05569a15e
https://doi.org/10.1261/rna.473907
https://doi.org/10.1261/rna.473907
Publikováno v:
Nucleic Acids Research
Programmed ribosomal frameshifting provides a mechanism to decode information located in two overlapping reading frames by diverting a proportion of translating ribosomes into a second open reading frame (ORF). The result is the production of two pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d6629ea8b8803098b50b01834d626a8
Autor:
N Malik, Michael T. Howard, J. L A Voskuil, Christine B. Anderson, Richard J. Gibbons, John F. Atkins
Publikováno v:
Journal of Medical Genetics. 41:951-956
Nonsense mutations located in the 5′ end of the coding sequence of a gene are commonly considered to be null alleles. Not only do such mutations result in the production of a truncated and usually inactive protein product, but premature stop codon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6fb44d6de7c12f0acfd510bf15d26e0
https://doi.org/10.1136/jmg.2004.020248
https://doi.org/10.1136/jmg.2004.020248
Publikováno v:
Journal of Molecular Biology
The expression of eukaryotic antizyme genes requires +1 translational frameshifting. The frameshift in decoding most vertebrate antizyme mRNAs is stimulated by an RNA pseudoknot 3' of the frameshift site. Although the frameshifting event itself is co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed850270c0be8284ab2c0faa53a70b83
http://europepmc.org/articles/PMC7125782
http://europepmc.org/articles/PMC7125782