Transcription factors tend to recognize short and often degenerate sequences, making it difficult to identify over-represented candidate binding sites using so-called ab initio motif-finding methods.
The above-mentioned studies with African children either did not look at all these variables at the same time or were cross sectional making it difficult to identify predictors of cognition over time [8], [9], [10], [11], [12], [13], [14], [15], [16].
The appearance of a forefoot push-off mechanism in the hominin lineage has been difficult to identify, partially because researchers disagree over the use of the external skeletal morphology to differentiate metatarsophalangeal joint functional differences in extant great apes and humans.
A steady and higher adsorption occurs in the region 2. The region 3 is difficult to identify because of its occurrence over a narrow range.
These forests are typically difficult to identify and monitor with satellite remote sensing techniques, yet may extend over considerable areas.
When metastases are closely spaced, or as the area of skeletal involvement overlaps over time, it becomes difficult to identify individual sites.
It is difficult to identify quality change trends or patterns across the whole sample, which usually consists of 100 to over 2000 tiles/panels.
Susceptibilities vary among individuals and over the course of a lifetime, making it difficult to identify a beneficial hormetic exposure at the population level.
The condition of these younger patients would presumably improve over time, and so their risk is more difficult to identify with this scale.
Thus it has generally proven difficult to identify the possible factors causing changes in woody vegetation structure, composition and cover over time [27], [36].
