Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Mutación frameshift")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 426

  • Page / 18
Export

Selection :

  • and

Singular DYT6 Phenotypes in Association with New THAP1 Frameshift MutationsBLANCHARD, Arnaud; ROUBERTIE, Agathe; BURBAUD, Pierre et al.Movement disorders. 2011, Vol 26, Num 9, pp 1775-1777, issn 0885-3185, 3 p.Article

Both microsatellite length and sequence context determine frameshift mutation rates in defective DNA mismatch repairCHUNG, Heekyung; LOPEZ, Claudia G; HOLMSTROM, Joy et al.Human molecular genetics (Print). 2010, Vol 19, Num 13, pp 2638-2647, issn 0964-6906, 10 p.Article

Frameshift mutagenesis in bacteriophage T7PIERCE, J. C; MASKER, W.Mutation research. Mutation research letters. 1992, Vol 281, Num 2, pp 81-87, issn 0165-7992Article

A homozygous frameshift mutation in the mouse Fig gene facilitates enhanced percutaneous allergen primingFALLON, Padraic G; SASAKI, Takashi; SUNDBERG, John P et al.Nature genetics. 2009, Vol 41, Num 5, pp 602-608, issn 1061-4036, 7 p.Article

Dentin phosphoprotein frameshift mutations in hereditary dentin disorders and their variation patterns in normal human populationSONG, Y. L; WANG, C. N; FAN, M. W et al.Journal of medical genetics. 2008, Vol 45, Num 7, pp 457-464, issn 0022-2593, 8 p.Article

Ultraviolet-induced dimerization of non-adjacent pyrimidines: a potential mechanism for the targeted -1 frameshift mutationNGUYEN, H. T; MINTON, K. W.Journal of molecular biology. 1988, Vol 200, Num 4, pp 681-693, issn 0022-2836Article

Entropies of coding and noncoding sequences of DNA and proteinsLAUC, G; ILLIC, I; HEFFER-LAUC, M et al.Biophysical chemistry. 1992, Vol 42, Num 1, pp 7-11, issn 0301-4622Article

Molecular basis of argininemia : identification of two discrete frame-shift deletions in the liver-type arginase geneHARAGUCHI, Y; APARICIO R., J. M; TAKIGUCHI, M et al.The Journal of clinical investigation. 1990, Vol 86, Num 1, pp 347-350, issn 0021-9738Article

Leftward ribsome frameshifting at a Hungry codonGALLANT, J. A; LINDSLEY, D.Journal of molecular biology. 1992, Vol 223, Num 1, pp 31-40, issn 0022-2836Article

Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop cordon and lipoprotein lipase deficiencyHENDERSON, H. E; DEVLIN, R; PETERSON, J et al.Molecular biology & medicine. 1990, Vol 7, Num 6, pp 511-517, issn 0735-1313, 7 p.Article

Duck hepatitis B virus can tolerate insertion, deletion, and partial frameshift mutation in the distal pre-S regionJI-SU LI; COVA, L; BUCKLAND, R et al.Journal of virology. 1989, Vol 63, Num 11, pp 4965-4968, issn 0022-538XArticle

A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathyWETERMAN, Marian A. J; SORRENTINO, Vincenzo; ZELCER, Noam et al.Human molecular genetics (Print). 2012, Vol 21, Num 2, pp 358-370, issn 0964-6906, 13 p.Article

A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian familyLEVRAT, Emmanuel; ABOUKHAMIS, Imad; DE MOERLOOSE, Philippe et al.Blood coagulation & fibrinolysis. 2011, Vol 22, Num 2, pp 148-150, issn 0957-5235, 3 p.Article

Correlation of Nonsense and Frameshift Mutations With Severity of Retinal Abnormalities in Neurofibromatosis 2FEUCHT, Matthias; KLUWE, Lan; MAUTNER, Victor-Felix et al.Archives of ophthalmology (1960). 2008, Vol 126, Num 10, pp 1376-1380, issn 0003-9950, 5 p.Article

MECANISME DE LA MUTAGENESE «FRAMESHIFT» INDUITE = MECHANISM OF INDUCED FRAMESHIFT MUTAGENESISLobo Napolitano, Rita; Fuchs, Robert P. P.1997, 224 p.Thesis

Effects of the umuDC, mucAB, and samAB operons on the mutational specificity of chemical mutagenesis in Escherichia coli. I: Frameshift mutagenesisWATANABE, M; NOHMI, T; OHTA, T et al.Mutation research. DNA repair. 1994, Vol 314, Num 1, pp 27-37, issn 0921-8777Article

Four new mutations in the apolipoprotein B gene causing hypobetalipoproteinemia, including two different frameshift mutations that yield truncated apolipoprotein B proteins of identical lengthYOUNG, S. G; PULLINGER, C. R; MALLOY, M. J et al.Journal of lipid research. 1993, Vol 34, Num 3, pp 501-507, issn 0022-2275Article

Impaired secretion of the elongated mutant of protein C (protein C-Nagoya) : molecular and cellular basis for hereditary protein C deficiencyYAMAMOTO, K; TANIMOTO, M; EMI, N et al.The Journal of clinical investigation. 1992, Vol 90, Num 6, pp 2439-2446, issn 0021-9738Article

Spontaneous and 9-aminoacridine-induced frameshift mutagenesis : second-site frameshift mutation within the N-terminal region of the lacI gene of Escherichia coliGORDON, A. J. E; HALLIDAY, J. A; HORSFALL, M. J et al.MGG. Molecular & general genetics. 1991, Vol 227, Num 1, pp 160-164, issn 0026-8925, 5 p.Article

Internal initiation and frameshifitng in infectious bursal disease sequence expressed in Escherichia coliMACREADIE, I. G; AZAD, A. A.Virology (New York, NY). 1991, Vol 184, Num 2, pp 773-776, issn 0042-6822Article

Frameshift mutagenesis in Escherichia coli by reversible DNA intercalators: sequence specificityRENE, B; AUCLAIR, C; FUCHS, R. P. P et al.Mutation research. 1988, Vol 202, Num 1, pp 35-43, issn 0027-5107Article

Detection of frame-shifts within homopolymeric DNA tracts using the amplification refractory mutation system (ARMS)GRAACK, H.-R; KRESS, H.BioTechniques. 1999, Vol 27, Num 4, pp 662-666, issn 0736-6205Article

Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runsFOSTER, P. L; TRIMARCHI, J. M.Science (Washington, D.C.). 1994, Vol 265, Num 5170, pp 407-409, issn 0036-8075Article

Base substitutions, frameshifts, and small deletions constitute ionizing radiation-induced point mutations in mammalian cellsGROSOVSKY, A. J; DE BOER, J. G; DE JONG, P. J et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 1, pp 185-188, issn 0027-8424Article

Mutants of translational components that alter reading frame by two steps forward or one step backFALAHEE, M. B; WEISS, R. B; O'CONNOR, M et al.The Journal of biological chemistry (Print). 1988, Vol 263, Num 34, pp 18099-18103, issn 0021-9258Article

  • Page / 18