Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Jocelyn E. Krebs"'
Autor:
Nealia CM House, Erica J Polleys, Ishtiaque Quasem, Marjorie De la Rosa Mejia, Cailin E Joyce, Oliver Takacsi-Nagy, Jocelyn E Krebs, Stephen M Fuchs, Catherine H Freudenreich
Publikováno v:
eLife, Vol 8 (2019)
CAG/CTG trinuncleotide repeats are fragile sequences that when expanded form DNA secondary structures and cause human disease. We evaluated CAG/CTG repeat stability and repair outcomes in histone H2 mutants in S. cerevisiae. Although the two copies o
Externí odkaz:
https://doaj.org/article/9a8483e0f83b486799cefa574f9e9f22
Extensively reorganized and revised with the latest data from this rapidly changing field, Lewin's Essential GENES, Third Edition, provides students with a comprehensive overview of molecular biology and molecular genetics.
Autor:
Nealia C.M. House, Ishtiaque Quasem, Cailin E. Joyce, Stephen M. Fuchs, Marjorie De la Rosa Mejia, Catherine H. Freudenreich, Jocelyn E. Krebs, Oliver Takacsi-Nagy, Erica J Polleys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9acd2dc561cdc003bc7b572ba4ade450
https://doi.org/10.7554/elife.53362.sa2
https://doi.org/10.7554/elife.53362.sa2
Autor:
Nealia Cm, House, Erica J, Polleys, Ishtiaque, Quasem, Marjorie, De la Rosa Mejia, Cailin E, Joyce, Oliver, Takacsi-Nagy, Jocelyn E, Krebs, Stephen M, Fuchs, Catherine H, Freudenreich
Publikováno v:
eLife
CAG/CTG trinuncleotide repeats are fragile sequences that when expanded form DNA secondary structures and cause human disease. We evaluated CAG/CTG repeat stability and repair outcomes in histone H2 mutants in S. cerevisiae. Although the two copies o
Autor:
Ryan B. Hayman, Erica J Polleys, Stephen M. Fuchs, Nealia C.M. House, Catherine H. Freudenreich, Jocelyn E. Krebs, Oliver Takacsi-Nagy, Ishtiaque Quasem, Cailin E. Joyce
DNA are sites of genomic instability. Long CAG/CTG repeats form hairpin structures, are fragile, and can expand during DNA repair. The chromatin response to DNA damage can influence repair fidelity, but the knowledge of chromatin modifications involv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d396bd80c518bbb0d58daa64a82479a
https://doi.org/10.1101/331413
https://doi.org/10.1101/331413
Now in its twelfth edition, Lewin's GENES continues to lead with new information and cutting-edge developments, covering gene structure, sequencing, organization, and expression. Leading scientists provide revisions and updates in their individual fi
Autor:
William Harbour, Sreepurna MalakarS. Malakar, Oya Yazgan, Chris Barnett, Amanda Fitzgerald, Hui Ching Kuo, Jonathan J. Henry, Trevor Thomas, Jocelyn E. Krebs
Publikováno v:
Mechanisms of Development. 129(9-12):324-338
Williams Syndrome Transcription Factor (WSTF) is one of ∼25 haplodeficient genes in patients with the complex developmental disorder Williams Syndrome (WS). WS results in visual/spatial processing defects, cognitive impairment, unique behavioral ph
Autor:
Jocelyn E. Krebs, Chris Barnett
Publikováno v:
Biochemistry and Cell Biology. 89:12-23
Williams syndrome transcription factor (WSTF) has emerged as an incredibly versatile nuclear protein. WSTF and the ATP-dependent chromatin remodeling complexes in which it exists, WINAC, WICH, and B-WICH, have been studied in a variety of organisms.
Publikováno v:
Biochemistry and Cell Biology. 87:767-779
There are a number of well-characterized and fundamental roles for noncoding RNAs (ncRNAs) in gene regulation in all kingdoms of life. ncRNAs, such as ribosomal RNAs, transfer RNAs, small nuclear RNAs, small nucleolar RNAs, and small interfering RNAs
Publikováno v:
Biochemistry and Cell Biology. 87:243-253
DNA damage from endogenous and exogenous sources occurs throughout the cell cycle. In response to this damage, cells have developed a series of biochemical responses that allow them to recover from DNA damage and prevent mutations from being passed o