Sentence examples for consistent with a sequence from inspiring English sources

These results are consistent with a sequence of events whereby an effect on the formation of neurofibrillary tangles accounts for the association of the ZNF224 allele with cognitive function.

This ancestral sequence was consistent with a sequence inferred using the Dnapars program from the Phylip package (ver. 3.66; J. Felsenstein, U. Washington).

This is consistent with a ClustlW2 [31] sequence alignment between PrgI and Bcl-xL that resulted in a low 14.3% sequence similarity, which falls below the twilight zone of sequence similarity [32].

The guiding rule reveals that the semimetallic and semiconducting variation is consistent with a peculiar sequence with a period of 3 for odd and even indices differently.

A preliminary analysis of the trajectory of emerging bipolar disorder based on the Canadian Flourish high-risk offspring cohort was consistent with a progressive sequence of psychopathology over development (see Fig. 1 reproduced with permission (Duffy 2014).

Members of the same enzymatic family, such as SpPgdA from S. pneumoniae (PDB ID 2c1g [6]) and PdaA from B. subtilis (PDB ID 1w17 [9]) are structurally less similar, consistent with a lower sequence identity.

In eba175, codons 388/390 KP are always present with particular alleles at flanking polymorphisms, consistent with a recent sequence analysis in which an indel at codons 401 402 (IS/–) was in complete LD with 336 D, 388/390 KP, and 403-5 ENK in Thailand [33], but not in a Kenyan [33] or Nigerian [34] population.

DOI: http://dx.doi.org/10.7554/eLife.07999.011 The MK R pathway is consistent with a reaction sequence proposed by Bae and Paik (1997), who reported that zymosterol was preferred over lanosterol as a substrate for C-24-reduction in rat liver microsomes.

Temporal investigation of these models is often consistent with a linear sequence in which the disease causing insult leads to synaptic dysfunction and loss that precedes eventual neuronal cell loss, although alternative pathways to neuronal loss may also operate.

Analysis of 'orphan' scaffolds not incorporated into the main chromosomal assembly identified another 14 orphan scaffolds larger than 100 kb showing high hit/kb values comparable to scaffold 7. Of these, scaffold 35 (27 hit/kb) is covered by high-density reads only on 30% of its length, consistent with a bad sequence join.

Positions in wild-type and tdp-1 ok803 tdp-1 ok803th a disamplescy betwith the genomic sequence andiscrepancyence consistent with A-to-I editing (A-G and C-T transitions) were identified.