Sentence examples for models of little from inspiring English sources

We consider the problem of identifiability in the recently developed carcinogenesis models of Little and Wright (Math Biosci 2003 183 111 134) and Little et al. (J Theoret Biol 2008 254 229 238).

[It should be noted that given extra information, for example on numbers and sizes of intermediate cell compartment clones, there is information on an additional parameter.] In this paper we consider the problem of identifiability in recently developed carcinogenesis models of Little and Wright [11] and Little et al. [12].

We consider applications to a recently developed class of cancer models of Little and Wright (Math Biosciences 183 (2003) 111 134) and Little et al. (J Theoret Biol 254 (2008) 229 238) that generalize a large number of other recently used quasi-biological cancer models.

However, as noted above, the generalized multistage models of Little [ 4], Little and Wright [ 5] and Little et al. [ 6] allow for modelling of a final stochastic-growth or stochastic birth-death process of tumour growth from the first malignant cell; in particular this last process could be used to model the "angiogenic switch".

The model of Little Matterhorn was created by the graphics group in Utah.

These results have obvious implications for the large number of other quasi-biological cancer models that are special cases of these models, in particular those of Armitage and Doll [13], the two-mutation model [10], the generalized multistage model of Little [14], and a recently developed cancer model of Nowak et al. [15] that incorporates genomic instability.

These models generalize a large number of other quasi-biological cancer models, in particular those of Armitage and Doll [13], the two-mutation model [10], the generalized multistage model of Little [14], and a recently developed cancer model of Nowak et al. [15] that incorporates genomic instability.

These models generalize a large number of other quasi-biological cancer models, in particular those of Armitage and Doll [21], the two-mutation model [17], the generalized multistage model of Little [22], and a recently developed cancer model of Nowak et al. [23] that incorporates genomic instability.

Given the estimate of y0, the model of Little et al. (2012)—implemented in a spreadsheet provided with their publication estimates partitioning within a room.

Because TPP is an SVOC (Weschler and Nazaroff 2008), we used the SVOC model of Little et al. (2012) to assess indoor exposure to TPP.

Dermal absorption from contact with dust or surface films was not included in the model of Little et al, (2012), and this is a potentially important limitation.