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Transversion
Molecular Biology and Applied Genetics
Increased Transversions in a Novel Mutator Colon Cancer Cell Line
CRISPR-Cas9 DNA Base-Editing and Prime-Editing
Oxidative Damage and Mutagenesis in Saccharomyces Cerevisiae: Genetic Studies of Pathways Affecting Replication Fidelity of 8-Oxoguanine
Mutation & Mutagenesis
Spontaneous and Induced Mutations to Rifampicin, Streptomycin
Botany Honours
(III)-Weight Matrices for Sequence Similarity Scoring
The Rate and Molecular Spectrum of Spontaneous Mutations in the GC-Rich Multichromosome Genome of Burkholderia Cenocepacia
Possible Cause of GWCCCWG Transversion Mutation by Guanine Oxidation Product, Imidazolone
The Transversion Pathway (Spontaneous Mutation/Acid Mutagenesis/Glycosidic Bond Migration) PAUL M
Aflatoxin B1 Induces the Transversion of G -- T in Codon 249 of the P53 Tumor Suppressor Gene in Human Hepatocytes FERNANDO AGUILAR, S
The Genetics of Heterotaxy Syndrome
Aguilar Aflatoxin B1 Induces the Transversion of G to T of P53 In
Rate of De Novo Mutations and the Importance of Father’S Age to Disease Risk
Types of Mutations (Table 15-1 on P. 464) II. Reverse Mutations
IGA 8/E Chapter 14
The Impact of the Transversion/Transition Ratio on the Optimal Genetic Code Graph Partition
Top View
Article in Press
Glossary of Biotechnology and Genetic Engineering 1
Interspecific Differences in Single Nucleotide Polymorphisms (Snps) and Indels in Expressed Sequence Tag Libraries of Oil Palm Elaeis Guineensis and E
Comprehensive Genetic Analysis of OEIS Complex Reveals No Evidence for a Recurrent Microdeletion Or Duplication Christopher N
Transition and Transversion Mutations Are Biased Towards GC in Transposons of Chilo Suppressalis (Lepidoptera: Pyralidae)
Segmental Duplications Promote Genomic Instability In
Positive Selection in Transcription Factor Genes
Crop Improvement a Glossary
Spontaneous and Photosensitization-Induced Mutations in Primary Mouse Cells Transitioning Through Senescence and Immortalization
Mutation, Repair, and Recombination 1
Genomic Analysis of Human Spinal Deformity and Characterization of a Zebrafish Disease Model Jillian Gwen Buchan Washington University in St
Single-Base Mutation
The Genetics of Intellectual Disability
TURNER-DISSERTATION-2014.Pdf
Generation, Repair and Replication of Guanine Oxidation Products Katsuhito Kino1*, Masayo Hirao-Suzuki2, Masayuki Morikawa3, Akane Sakaga1 and Hiroshi Miyazawa1
411-4 OUTLINE I. Spontaneous Mutation A. Single Base Pair Changes 1. Mutational "Fingerprinting" 2. Cytosine Deamina
Biol 3301: Genetics Exam #3 Practice Questions
Doyne Lecture Rhodopsin and Autosomal Dominant Retinitis Pigmentosa
Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
DNA Base Changes and Alkylation Following in Vivo Exposure
Models of DNA and Protein Change) a U/3 G U/3 U/3 U/3 U/3 C T U/3
Rare Deleterious Mutations of HNRNP Genes Result in Shared Neurodevelopmental Disorders Madelyn A
Determinants of Spontaneous Mutation in the Bacterium
Neurodevelopmental Disease Genes Implicated by De Novo Mutation and CNV Morbidity
(12) United States Patent (10) Patent No.: US 8,669,048 B2 Reijo Pera Et Al
How Does Human 8-Oxoguanine DNA Glycosylase 1 (OGG1) Find 8-Oxoguanine in the Genome?
Oxidative Nucleotide Damage: Consequences and Prevention
Estimation of the Mutagenic Potential of 8-Oxog in Nuclear Extracts of Mouse Cells Using the “Framed Mirror” Method
Glossary Genetics
Mutational Specificity of Depurination (Bacteriophage M13mp2/Transversion Mutagenesis/SOS Repair/Base Selection/Noncoding Lesion) THOMAS A