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1 e (CKD) and its progression remains controversial, and most studies have been limited by a lack of direct glomerular filt

2 However, these studies have been limited by a lack of in vitro models of thr

3 Previous studies have been limited by a weak interaction between Drp1

4 Previous studies have been limited by convenience sampling, short foll

5 predictive value of wound outcomes, and culture-independent studies have been limited by cross-sectional design and small

6 esults of previous studies have been inconsistent, and many studies have been limited by inadequate data on outcomes and

7 ant generally have indicated no differences; however, these studies have been limited by inclusion of either a small numb

8 sis may be dominated by a small number of clones, but these studies have been limited by insensitive detection methods, l

9 potential cause of adverse pregnancy outcomes, but previous studies have been limited by low exposures and small study si

10 able, attempts to identify the alleles involved in previous studies have been limited by relatively small sample sizes.

11 Prior studies have been limited by reliance on simple target detect

12 However, the above studies have been limited by small cohorts of diabetic patien

13 rmed with outdated technology and methods, and previous PET studies have been limited by small sample sizes and incomplet

14 Although preclinical studies have been limited by the absence of anti-CD20 reagent

15 Unfortunately, these studies have been limited by the absence of direct experiment

16 Further studies have been limited by the difficulty in expressing fun

17 Previous biomarker studies have been limited by the extent of tissue analyzed, s

18 These structural studies have been limited by the fact that only endogenous Ta

19 re attractive targets for antiviral therapy, but functional studies have been limited by the lack of genetically tractabl

20 ed in a host of physiological processes, current functional studies have been limited by the lack of molecular markers sp

21 enoma samples has not been examined in detail, and previous studies have been limited by the lack of specific antibodies.

22 the viral population structure and phenotype, experimental studies have been limited by the relatively poor resolution o

23 disorders (FASD) has revealed structural abnormalities, but studies have been limited by the use of cross-sectional desig

24 otypes and expression profiles, although comparisons across studies have been limited by the use of different protocols.

25 tive changes in the alloimmune response over time, but such studies have been limited by uncertainties in the conventiona

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