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3 5

# 3 5

The American-Italian 3 5 competition is a commemoration for the arrival of American baseball to Italy. It is a pity that this competition never took place - because it would have been a success.

## NUMBER

A decimal number can be defined as a number whose whole number part and the fractional part are separated by a decimal point. (Source: www.cuemath.com

Step 2: Multiply both numerator and denominator by that number to convert it into its equivalent fraction. (Source: www.cuemath.com)www.cuemath.com))Step 1: Find a number that we can multiply by the denominator of the fraction to make it 10 or 100 or 1000 and so on. (Source:

This disambiguation page lists articles associated with the same number. (Source: en.wikipedia.org In this article, we'll show you exactly how to calculate 3/5 of 3 so you can work out the fraction of any number quickly and easily! Let's get to the math! (Source:visualfractions.com))

As you can see in this case, the numerator is higher than the denominator. What this means is that we can simplify the answer down to a mixed number, also known as a mixed fraction. (Source: visualfractions.com)

"What is 3/5 of 3?". VisualFractions.com, http://visualfractions.com/calculator/fraction-of-number/what-is-3-5-of-3/. Accessed 22 November, 2021. (Source: visualfractions.com Hopefully this tutorial has helped you to understand how to find the fraction of any whole number. You can now go give it a go with more numbers to practice your newfound fraction skills. (Source:visualfractions.com))

In this article, we'll show you exactly how to calculate 3/5 of 100 so you can work out the fraction of any number quickly and easily! Let's get to the math! (Source: visualfractions.com)What is 3/5 of 3?. VisualFractions.com. Retrieved from http://visualfractions.com/calculator/fraction-of-number/what-is-3-5-of-3/. (Source: visualfractions.com)

The calculator performs basic and advanced operations with fractions, expressions with fractions combined with integers, decimals, and mixed numbers. It also shows detailed step-by-step information about the fraction calculation procedure. Solve problems with two, three, or more fractions and numbers in one expression. (Source: www.hackmath.net In this case, our new fraction can actually be simplified down further. To do that, we need to find the greatest common factor of both numbers. (Source:visualfractions.com))

Decimals (decimal numbers) enter with a decimal point . and they are automatically converted to fractions - i.e. 1.45. (Source: www.hackmath.net The colon : and slash / is the symbol of division. Can be used to divide mixed numbers 1 2/3 : 4 3/8 or can be used for write complex fractions i.e. 1/2 : 1/3. (Source:www.hackmath.net))

The calculator performs basic and advanced operations with fractions, expressions with fractions combined with integers, decimals, and mixed numbers. It also shows detailed step-by-step information about the fraction calculation procedure. Solve problems with two, three, or more fractions and numbers in one expression. (Source: www.hackmath.net)

The colon : and slash / is the symbol of division. Can be used to divide mixed numbers 1 2/3 : 4 3/8 or can be used for write complex fractions i.e. 1/2 : 1/3. (Source: www.hackmath.net Decimals (decimal numbers) enter with a decimal point . and they are automatically converted to fractions - i.e. 1.45. (Source:www.hackmath.net))

www.calculator.net www.calculator.net))This process can be used for any number of fractions. Just multiply the numerators and denominators of each fraction in the problem by the product of the denominators of all the other fractions (not including its own respective denominator) in tIn mathematics, a fraction is a number that represents a part of a whole. It consists of a numerator and a denominator. The numerator represents the number of equal parts of a whole, while the denominator is the total number of parts that make up said whole. For example, in the fraction of (Source: he problem. (Source:

The process for dividing fractions is similar to that for multiplying fractions. In order to divide fractions, the fraction in the numerator is multiplied by the reciprocal of the fraction in the denominator. The reciprocal of a number a is simply (Source: www.calculator.net An alternative method for finding a common denominator is to determine the least common multiple (LCM) for the denominators, then add or subtract the numerators as one would an integer. Using the least common multiple can be more efficient and is more likely to result in a fraction in simplified form. In the example above, the denominators were 4, 6, and 2. The least common multiple is the first shared multiple of these three numbers. (Source:www.calculator.net))

, and so on. Simply determine what power of 10 the decimal extends to, use that power of 10 as the denominator, enter each number to the right of the decimal point as the numerator, and simplify. For example, looking at the number 0.1234, the number 4 is in the fourth decimal place, which constitutes 10 (Source: www.calculator.net)

A number that will divide evenly into both the numerator and denominator so it can be reduced, or (Source: www.calculatorsoup.com Convert improper fractions to mixed numbers in simplest form. This calculator also simplifies proper fractions by reducing to lowest terms and showing the work involved. (Source:www.calculatorsoup.com wThe numerator must be greater than the denominator, (an improper fraction), so it can be converted to a mixed number. (Source:ww.calculatorsoup.com wwWrite down the whole number result (Source:w.calculatorsoup.com))))

Example: Convert the improper fraction 16/3 to a mixed number. (Source: www.calculatorsoup.com Use the remainder as the new numerator over the denominator. This is the fraction part of the mixed number. (Source:www.calculatorsoup.com wThe whole number result is 5 (Source:ww.calculatorsoup.com)))

The remainder is 1. With 1 as the numerator and 3 as the denominator, the fraction part of the mixed number is 1/3. (Source: www.calculatorsoup.com The mixed number is 5 1/3. So 16/3 = 5 1/3. (Source:www.calculatorsoup.com wWhen possible this calculator first reduces an improper fraction to lowest terms before finding the mixed number form. (Source:ww.calculatorsoup.com)))

Example: Convert the improper fraction 45/10 to a mixed number. (Source: www.calculatorsoup.com)

The remainder is 1. With 1 as the numerator and 2 as the reduced denominator, the fraction part of the mixed number is 1/2. (Source: www.calculatorsoup.com The remainder is 1. With 1 as the numerator and 2 as the reduced denominator, the fraction part of the mixed number is 1/2. (Source:www.calculatorsoup.com w

For additional explanation of factoring numbers to find the greatest common factor (GCF) see the Greatest Common Factor Calculator. (Source: www.calculatorsoup.com)The mixed number 4 1/2. So 45/10 = 4 1/2. (Source:ww.calculatorsoup.com)))

To perform math operations on fractions before you simplify them try our Fractions Calculator. This calculator will also simplify improper fractions into mixed numbers. (Source: www.calculatorsoup.com If your improper fraction numbers are large you can use the Long Division with Remainders Calculator to find whole number and remainder values when simplifying fractions by hand. (Source:www.calculatorsoup.com))

What was remarkable about Laveran's discovery was that it was without precedent as no protozoan had previously been found inhabiting any kind of human blood cell. Unbeknown to Laveran or the Italian malariologists, however, the Russian physiologist, Vassily Danilewsky had been examining the blood of birds and reptiles in the Ukraine and had discovered a number of parasites including trypanosomes and others that he identified as 'pseudovacules'. Anyone who has studied blood parasites will immediately recognise his description of 'pseudovacuoles' as unstained malaria parasites. By 1885 Danilewsky had recognised the three most common genera of intraerythrocytic blood parasites of birds now known as Plasmodium, Haemoproteus and Leucocytozoon but, as he had published much of his work in Russian, it was not until his three volume book La Parasitologie Comparée du Sang had been published in French in 1889 that this information became widely available [20]. Thereafter there began searches for other malaria parasites in reptiles, birds and mammals and this was facilitated by the accidental discovery of a methylene blue-eosin stain by Dimitri Leonidovitch Romanowsky in 1891 [6]. Romanowsky's stains became popular at the beginning of the twentieth century and remain the basis of blood stains such as Leishman's, Giemsa's and Wright's to the present day. These stains colour the nucleus of the parasite red and the cytoplasm blue permitting their easy identification and are used not only for malaria parasites but also for trypanosomes, leishmanias and filarial worms. Romanowsky's discovery is one of the most significant technical advances in the history of parasitology. (Source: parasitesandvectors.biomedcentral.com)

The life cycle in humans, however, remained incompletely understood and nobody knew where the parasites developed during the first 10 days or so after infection during which they could not be seen in the blood. Grassi was the first to suggest that there must be some developmental stage in cells other than red blood cells, possibly white blood cells [25]. This theory was elaborated by Grassi and his colleagues from1893 and 1894 onwards but was later abandoned mainly due to too much reliance on a mistake by the influential German scientist Fritz Schaudinn who, in 1903, described the direct penetration of red blood cells by the infective sporozoites of P. vivax[43]. No one else was able to confirm these observations and the phenomenon is now referred to among malariologists unkindly as 'Schaudinn's fallacy'. Nevertheless Schaudinn's ideas were adopted by such authorities as Grassi and dominated scientific opinion for over forty years. Meanwhile evidence that there was a phase of multiplication preceding that in the blood was accumulating from another source, the avian malarias. MacCallum in 1898 had observed developmental stages of P. relictum in the liver and spleen of infected birds [30] and thereafter there were numerous somewhat inadequate descriptions of exoerythrocytic development of a number of avian malaria parasites [6, 44]. In 1937 Sydney James and Parr Tate conclusively demonstrated that in sporozoite-induced P. gallinaceum infections in chickens there was phase of multiplication between the injection of sporozoites and the appearance of parasites in the blood and that this occurred in cells of the reticuloendothelial system [45]. (Source: parasitesandvectors.biomedcentral.com)

By the late 1930s there was no doubt that in all the avian malaria parasites studied there was a phase of multiplication in various nucleated cells before (and after) parasites appeared in the blood and over the next decade the complete life cycles of a number of avian Plasmodium and Haemoproteus species, differing only in detail particularly relating to the types of cells involved which varied from species to species, had been worked out. What happened in primates was not so clear and during the 1930s and 1940s there were sporadic reports of parasites in the tissues, particularly in the brain and nervous system, of animals infected with primate and bat malarias. After the end of the Second World War in 1945 malaria research throughout the world intensified and a number of workers became convinced that that there must be an exoerythrocytic stage in the life cycle of the primate malarias but what form this took was not known. This question was not resolved until 1947 when Henry Shortt and Cyril Garnham, working in London, showed that a phase of division in the liver preceded the development of parasites in the blood [46]. The crucial clues came from studies on Hepatocystis kochi, another parasite of monkeys first identified by Laveran as Haemamoeba kochi. Hepatocystis spp. are related to malaria parasites but do not have an erythrocytic stage in their life cycles so these parasites must have only an exoerythrocytic stage which in H. kochi is in the parenchyma cells of the liver [47]. This suggested to Shortt, Garnham and their colleagues that the liver might be the place to look for the elusive exoerythrocytic stages of primate malaria parasites and selected P. cynomolgi in rhesus monkeys for their investigations. Previous attempts by other workers had failed to find any liver forms so Shortt and Garnham decided to use 500 infected A. maculipennis atroparvus, a massive dose of sporozoites, and found exoerythrocytic stages seven days later [48]. Shortly afterwards Shortt, Garnham and their co-workers found exoerythrocytic forms of P. vivax in human volunteers [49] and subsequently in volunteers infected with P. falciparum in 1949 [50] and P. ovale in 1954 [51]. In the meantime the same team had also demonstrated exoerythrocytic stages of P. inui, a quartan form of primate malaria. The exoerythrocytic stages of P. malariae were more elusive and it was not until 1960 that Robert (Bill) Bray demonstrated their presence in experimentally infected chimpanzees [52]. The story of the discovery of the exoerythrocytic forms of malaria parasites until 1957 is told in some detail by Bray [44] and updated until 1966 by Garnham [6]. (Source: parasitesandvectors.biomedcentral.com)

It has already been noted that malaria-like parasites are commonly found in birds, mammals and reptiles and studies on many of these have contributed to our overall understanding of human malaria. Malaria-like parasites belonging to the genus Hepatocystis in non-human primates were first recognised by Laveran in1899 but true malaria parasites, Plasmodium spp., were not identified with certainty until 1907 with the independent discoveries of P. cynomolgi, P. inui, and P. pitheci in monkeys imported into Germany from Java [6]. Throughout the 1920s and 1930s there were increasing numbers of reports of new species from wild-caught primates including P. knowlesi in 1932 [6, 54]. During the 1960s, there were occasional reports of accidental infections with P cynomolgi, P. inui and P. knowlesi in humans suggesting that some primates might act as reservoirs for human malaria but it appeared that the chances of such naturally acquired infections were very remote. However it is now known that humans are at risk from infection with P. knowlesi, a malaria parasite with a 24 hour erythrocytic cycle, in Southeast Asia where its natural hosts are macaque and leaf monkeys. Until 1971 there had only been two authenticated cases of naturally acquired human infections with P. knowlesi both in peninsular Malaysia. No other cases were recorded until 2004 when a focus of human infections was identified in Sarawak, Malaysian Borneo [55]. Since then there have been several hundred reports of human infections in the region and there is now overwhelming evidence that P. knowlesi is a zoonosis involving macaque (Macaca spp.) and leaf (Presbytis spp.) monkeys as reservoir hosts with mosquitoes belonging to the Leucosphyrus group of Anopheles mosquitoes as the vectors in Malaysia and elsewhere in Southeast Asia [56]. Retrospective examination of blood films and the application of the polymerase chain reaction (PCR) and other molecular techniques have revealed that a number of malaria cases previously attributed to P. malariae in Malaysia were misidentified and that they were in all probability due to P. knowlesi[57]. (Source: parasitesandvectors.biomedcentral.com)

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