Mutations can involve large sections of DNA becoming duplicated, usually through genetic recombination.

Mutations can involve large sections of DNA becoming duplicated, usually through genetic recombination.

Mutations that deactivate p53 in cancer usually occur in the DBD.

Mutations are permanent, transmissible changes to the genetic material ( usually DNA or RNA ) of a cell.

Mutations can involve large sections of DNA becoming duplicated, usually through genetic recombination.

Mutations are permanent, transmissible changes to the genetic material ( usually DNA or RNA ) of a cell.

Mutations that cause the altered codon to produce an amino acid with similar functionality ( i. e. a mutation producing leucine instead of isoleucine ) are often also classified as silent ; if the properties of the amino acid are conserved, this mutation does not usually significantly affect protein function.

* IARC TP53 Somatic Mutations database maintained at IARC, Lyon, by Magali Olivier

Koolhaas's next landmark publications were a product of his position as professor at Harvard University, in the design school's " Project on the City "; firstly the 720-page Mutations, followed by The Harvard Design School Guide to Shopping ( 2002 ) and The Great Leap Forward ( 2002 ).

Suddenly, evolutionary theorists could answer the charge that spontaneous random mutations should result overwhelmingly in deleterious changes to a fragile, monolithic genome: Mutations in homeobox regulation could safely — yet dramatically — alter morphology at a high level, without damaging coding for specific organs or tissues.

Mutations in some homeotic genes can often be lethal and the cycle of life will end at embryogenesis.

COUM's earliest public events were impromptu musical gigs performed at various pubs around Hull ; titles for these events included Thee Fabulous Mutations, Space Between the Violins, Dead Violins and Degradation and Clockwork Hot Spoiled Acid Test.

* Beck's " High Five ( Rock the Catskills )" on the album Odelay ( 1996 ), starting at 2: 10 and finishing at 2: 30 ; and on " Tropicalia " from the album Mutations ( 1998 ) played by Smokey Hormel

Mutations in the Notch 3 gene ( on the short arm of chromosome 19 ) cause an abnormal accumulation of Notch 3 at the cytoplasmic membrane of vascular smooth-muscle cells both in cerebral and extracerebral vessels, seen as granular osmiophilic deposits on electron microscopy.

Mutations in the fukutin gene, located at human chromosome 9q31, are the cause of FCMD.

Mutations at many steps in the pathway towards the restriction point can result in cancerous growth of cells.

He wrote seven songs with the band-" Ill in the Head " and " Forward to Death ", both of which appear on the band's debut album Fresh Fruit for Rotting Vegetables ; " Short Songs ", " Gaslight ", and " Straight A's ", which appear on the live album Live at the Deaf Club ; " Mutations of Today ", which appears on The 1978 Demos ; and " Religious Vomit ", which appears on the EP In God We Trust, Inc ..

Mutations in these photo receptors and their signal transduction components lead to seedling development that is at odds with light conditions, for example seedlings that show photomorphogenesis when grown in the dark.

Mutations in nsP2 that produce noncytopathic viruses or a temperature sensitive phenotypes cluster at the P2 / P3 interface region.

In 1998, Beck released the album Mutations on the Geffen label, which led to a series of lawsuits between Beck, Bong Load and Geffen which were settled in 1999.

Alfredo de Palchi's Addictive Aversions is a series of erotic poems divided into three sections, Moments, Movements and Mutations, but it is more than merely erotic love which concerns the poet.

# REDIRECT Fallout ( series )# Mutations and their causes

Mutations are considered the driving force of evolution, where less favorable ( or deleterious ) mutations are removed from the gene pool by natural selection, while more favorable ( or beneficial ) ones tend to accumulate.

Mutations can have an impact on the phenotype of an organism, especially if they occur within the protein coding sequence of a gene.

Mutations are characterized as either β < sup > o </ sup > or β thalassemia major if they prevent any formation of β chains, the most severe form of β thalassemia.

Mutations are the ultimate source of genetic variation because they alter the order of bases in the nucleotides of DNA.

Mutations in two regulatory genes of white grapes turn off production of anthocyanins which are responsible for the color of purple grapes.

Mutations are changes in the DNA sequence of a cell's genome and are caused by radiation, viruses, transposons and mutagenic chemicals, as well as errors that occur during meiosis or DNA replication.

Mutations are caused by radiation, viruses, transposons and mutagenic chemicals, as well as errors that occur during meiosis or DNA replication.

Mutations in transpeptidases that lead to reduced interactions with an antibiotic are a significant source of emerging antibiotic resistance.

Mutations are an important force driving evolution.

Mutations that affect insulin-like signaling in worms, flies, and the growth hormone / IGF1 axis in mice are associated with extended lifespan.

Mutations leading to the loss of function of a gene are much more common than mutations that produce a new, fully functional gene.

Mutations in the tafazzin gene ( TAZ, also called G4. 5 ) are closely associated with

Mutations periodically occur within the Y chromosome and these mutations are passed on to males in subsequent generations.

Mutations of the genes VHL, RET, NF1 ( Gene 17 Neurofibromatosis type 1 ), SDHB and SDHD are all known to cause familial pheochromocytoma / extra-adrenal paraganglioma.

Mutations are likely to be rare and most mutations are neutral or deleterious, but in some instances the new alleles can be favored by natural selection.

Mutations in the Ras family of proto-oncogenes ( comprising H-Ras, N-Ras and K-Ras ) are very common, being found in 20 % to 30 % of all human tumours.

Mutations in this gene are rare.

Mutations affecting repressor are said to be recessive to wild type ( and that wild type is dominant ), and this is explained by the fact that repressor is a small protein which can diffuse in the cell.

Mutations within the desmosome are the main cause of Arrhythmogenic right ventricular cardiomyopathy ( ARVC ).

Mutations of the WT1 gene on chromosome 11 p 13 are observed in approximately 20 % of Wilms ' tumors .< ref > At least half of the Wilms ' tumors with mutations in WT1 also carry mutations in CTNNB1, the gene encoding the proto-oncogene beta-catenin.