Results 211 to 220 of about 1,908,891 (267)

Genome-wide mutation spectra of canonical and atypical UV photoproducts in S. cerevisiae. [PDF]

Nucleic Acids Res
Laughery MF, Haueter JC, Patchett HN, Mieczkowski PA, Roberts SA, Wyrick JJ.   +5 more
europepmc   +1 more source

The dual axis of tumorigenesis: MAPK and PI3K/AKT pathways in papillary thyroid carcinoma. [PDF]

Oncoscience
Rathod G, Parmar P.
europepmc   +1 more source

Pathogenesis of nonfamilial somatotroph adenomas.

J Clin Endocrinol Metab
Ben-Shlomo A, Melmed S.
europepmc   +1 more source

Heterogeneity within AML with CEBPA mutations; only CEBPA double mutations, but not single CEBPA mutations are associated with favourable prognosis

British Journal of Cancer, 2009
CCAAT/enhancer binding protein alpha (CEBPA) mutations in AML are associated with favourable prognosis and are divided into N- and C-terminal mutations. The majority of AML patients have both types of mutations. We assessed the prognostic significance of
Thomas Pabst, Beatrice U Mueller, Pabst T   +2 more
exaly   +2 more sources

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Mutation systems

International Journal of Computer Mathematics, 2011
We propose mutation systems as a model of the evolution of a string subject to the effects of mutations and a fitness function. One fundamental question about such a system is whether knowing the rules for mutations and fitness, we can predict whether it is possible for one string to evolve into another.
Dana Angluin, James Aspnes, Raonne Barbosa Vargas   +2 more
openaire   +1 more source

Mutation and Mutation Screening

2013
Molecular techniques have created the opportunity for great advances in plant mutation genetics and the science of mutation breeding. The powerful targeted induced local lesions in genomes (TILLING) technique has introduced the possibility of reverse genetics-the ability to screen for mutations at the DNA level prior to assessing phenotype. Fundamental
Lee, L Slade, Till, Bradley J, Hill, H, Huynh, Owen A, Jankowicz-Cieslak, Joanna   +4 more
openaire   +3 more sources

Mutation Nomenclature

Current Protocols in Human Genetics, 2003
AbstractAs part of the Human Genome Variation Society (formerly known as the HUGO Mutation Database Initiative), a committee was formed to suggest standards for the description of sequence variants in DNA, RNA, and protein sequences. The committee proposed that the nomenclature should be unequivocal, precise, and short, and should prevent any possible ...
den Dunnen, J. T., Antonarakis, Stylianos   +1 more
openaire   +3 more sources