1 scular risk factors, and dietary composition
were collected at 0, 3, 6, and 12 months.
2 Blood
was collected at 1, 4, 12, 24, 36, and 48 weeks.
3 ek from day 12 to 1 mo of age, and specimens
were collected at 1 and 5 mo of age.
4 Tissue biopsies and blood
were collected at 1 to 2, 6 to 8, 24, and 48 hours post-
5 ng growth, graft outcomes and adverse events
were collected at 1 year (113 patients) and 2 years (106
6 e was administered yearly, and blood samples
were collected at 1, 2, 3, 5, 6, 7, 10, and 13 years of
7 Transepidermal water loss (TEWL) measures
were collected at 12 months from a subset (n=150) of the
8 PDF data for nanocrystalline platinum (n-Pt)
were collected at 12.5 GPa with a single 5 s X-ray expos
9 Data on maternal BMI
was collected at 15 weeks of gestation, and paternal BMI
10 Anterior and posterior planar images
were collected at 15 min, 1.5 h, 4 h, and 8 h.
11 Samples
were collected at 15 sites along the four streams.
12 and nutritional and environmental exposures
were collected at 15 weeks' gestation, birth, and 2, 6,
13 Milk samples from 25 mothers
were collected at 2 wk, 4 mo, and 9 mo postpartum for th
14 V13 at ages 2, 4, 6, and 12 months; NP swabs
were collected at 2, 4, 6, 7, 12, 13, 18, and 24 months,
15 Fractions
were collected at 20 min intervals (2 muL) before and af
16 Atrial tissue samples
were collected at 21 days for histological and molecular
17 on participant schooling and smoking history
were collected at 23-25 y of age.
18 Blood and liver
were collected at 24 hours after ischemia-reperfusion fo
19 s from schools in Melbourne, Australia, data
were collected at 3 assessments between 2004 and 2012.
20 Clinical signs and symptoms
were collected at 3 time points from hospitalized infant
21 es for functional limitations and disability
were collected at 3, 6 and 12 months.
22 Serum samples
were collected at 3, 6, and 12 months after treatment in
23 amples from mice inoculated with RML scrapie
were collected at 30, 60, 90, 105, and 120 days post ino
24 Gastric mucosa samples
were collected at 35, 50, or 80 weeks of age from mice t
25 In this study, water column samples
were collected at 39 sites in the nGOM, 21 of which were
26 Blood
was collected at 4, 8, and 16 years, and sensitization e
27 nscriptome following VEEV infection, samples
were collected at 4, 8, and 16 h postinfection and RNA-S
28 Blood samples
were collected at 4, 8, and 16 years of age for analysis
29 Spleen samples
were collected at 40 days post injection (dpi), and sequ
30 Fecal samples (n = 3,108)
were collected at 50 field sites, tested for species and
31 Urine
was collected at 6, 12, and 18 weeks.
32 Blood samples
were collected at 6 time points.
33 Tissues
were collected at 7, 11, 29, and 67 days after infusion,
34 Serum samples
were collected at 7, 14 and 21 day post infection (DPI)
35 Having partnered with seven OPOs, data
were collected at 70 hospitals with high donor potential
36 unction, airway inflammation, and remodeling
were collected at 72 h after injection or after 2 weeks
37 Mother and infant blood
was collected at 8 wk postpartum.
38 Fouled membrane samples
were collected at 8 h, and 1, 2, and 4 weeks on a lab-sc
39 Samples of DNA
were collected at 9 sites from different countries.
40 Subsequently, nanoliter eluate fractions
are collected at a rate of one fraction per second on a
41 ately categorize cluster residency when data
are collected at a site distant from households.
42 This will enable a much larger sample to
be collected at a fraction of the cost, facilitating fut
43 or 640 nm), and the maximal emission signal
was collected at a shorter wavelength (i.e., higher ener
44 In the TRACK-TBI Pilot study, plasma
was collected at a single time point from 196 patients w
45 Food and environmental specimens
were collected at a hospital (hospital A) where 6 patien
46 rains found in clinical fecal specimens that
were collected at a single hospital over an 18-year time
47 G1/G3/G4-P[8]-I1-C1-R1-A1-N1-T1-E1-H1) that
were collected at a single location in Washington, DC, d
48 In this study, tree-core samples
were collected at a Superfund site to determine if the s
49 Data
were collected at a wastewater treatment plant (WWTP) in
50 e, DeltaP, tidal volume, Cdyn, and PaO2/FIO2
were collected at acute respiratory distress syndrome on
51 Blood
was collected at admission and plasma CD133 and CD39 MP
52 Serum and blood cell samples
were collected at admission.
53 microbiological, and echocardiographic data
were collected at admission.
54 Fecal samples
were collected at age 1 week, 1 month, and 1 year, and h
55 th, and 1 year, and hypopharyngeal aspirates
were collected at age 1 week, 1 month, and 3 months and
56 Fecal samples
were collected at age 3 to 16 months, and the children w
57 Intestinal microbiome samples
were collected at age 3-6 months in children participati
58 sumed milk and serum samples of the children
were collected at age 4 years.
59 Samples
were collected at age 6 and 8 weeks of life.
60 Blood samples
were collected at ages 2, 4, 6, and 11 years, and serum-
61 MRI data
were collected at ages 8 and 10.
62 Mie scatter patterns
are collected at all photodiode angles for each of the i
63 cal, and post-bronchodilator spirometry data
were collected at an in-person study visit.
64 Filter samples
were collected at an urban background site in the city c
65 l blood mononuclear cells (PBMCs) and plasma
were collected at and 2 time points after diagnosis.
66 ntional absorption optics, provided the data
are collected at appropriate sample concentrations and t
67 tion was measured in spot-urine samples that
were collected at approximately 12, 20, and 35 wk of ges
68 cluding Nematodirus), as well as body weight
were collected at approximately 16, 20 and 24 weeks of a
69 early life and 12 adults (>/=18 years old),
were collected at autopsy in Jackson, Mississippi.
70 Between 5 and 12 metastatic sites
were collected at autopsy together with available primar
71 elected case-mix factors were recommended to
be collected at baseline to facilitate comparison of res
72 elected case-mix factors were recommended to
be collected at baseline.
73 Blood
was collected at baseline (visit 1) and 30 days after pr
74 Blood
was collected at baseline and at 3 and 4 wk.
75 Blood
was collected at baseline and at the midpoint and end of
76 Self-reported weight (previously validated)
was collected at baseline and updated every 2 y during t
77 Induced sputum
was collected at baseline before rhinovirus inoculation
78 For each patient, a peripheral blood sample
was collected at baseline for the evaluation of CTCs and
79 n lifestyle score components and confounders
was collected at baseline.
80 Plasma and urine
were collected at baseline (in a subset), the beginning
81 Liver biopsy specimens
were collected at baseline (n = 48) and 48 weeks (n = 34
82 Data
were collected at baseline (n=14 567) and after interven
83 Blood samples
were collected at baseline 2 h, 6 h and daily up to 10 d
84 Laboratory data
were collected at baseline and 1 mo after (90)Y radioemb
85 Blood samples
were collected at baseline and 16 weeks, and analyzed fo
86 Fecal samples
were collected at baseline and 16 weeks; bile acids were
87 urs after challenge, and bone marrow samples
were collected at baseline and 24 hours after challenge
88 vironmental factors (SES and social network)
were collected at baseline and 3-mo follow-up, together
89 nt-reported outcomes (PROs) and biospecimens
were collected at baseline and 4 and 9 months after enro
90 Clinical and standardized radiographic data
were collected at baseline and 6 months after treatment.
91 Colonoscopic biopsies
were collected at baseline and 6 months or when patients
92 Peripheral blood and sputum samples
were collected at baseline and 7 and 24 hours after chal
93 Data
were collected at baseline and 8 wk after therapy.
94 Diffusion imaging and clinical data
were collected at baseline and after 1 year.
95 Fecal samples
were collected at baseline and after 4 weeks and analyze
96 Fasting blood samples
were collected at baseline and after 6 wk of the interve
97 l impression cytology and tear fluid samples
were collected at baseline and after an 8-week treatment
98 Duodenal biopsies
were collected at baseline and after gluten challenge.
99 Measures
were collected at baseline and after intervention by ass
100 Data
were collected at baseline and after treatment (1 week a
101 child emotional and behavioral outcome data
were collected at baseline and at 2, 6, and 12 months po
102 Blood samples
were collected at baseline and at an early time-point (2
103 Demographic and clinical variables
were collected at baseline and at follow-up and analyzed
104 and gingival crevicular fluid (GCF) samples
were collected at baseline and at follow-up visits.
105 Detailed data on clinical phenotype
were collected at baseline and at regular clinic reviews
106 Breath samples
were collected at baseline and during isotopic plateaus.
107 , anthropometric measures, and blood samples
were collected at baseline and endline.
108 tifocal visual evoked potential (mfVEP) data
were collected at baseline and every 6 to 8 weeks until
109 ss data related to bundle element compliance
were collected at baseline and monthly during the interv
110 Angina and QOL questionnaires
were collected at baseline and months 1, 6, and 12.
111 Data
were collected at baseline and prospectively every 2 mon
112 and average days on mechanical ventilation)
were collected at baseline and quarterly during the inte
113 nal partnerships and self-management ability
were collected at baseline and three months later.
114 In addition, samples of blood and GCF
were collected at baseline and week 8.
115 Ophthalmic data
were collected at baseline and yearly visits by means of
116 HRQoL data
were collected at baseline for 362 (88%) of 410 patients
117 heral blood mononuclear cells or whole blood
were collected at baseline from 425 participants and fro
118 Data
were collected at baseline from September 1, 2007, throu
119 onal magnetic resonance imaging (fMRI) scans
were collected at baseline prior to treatment and at 3-m
120 ng smoking and body mass index measurements,
were collected at baseline using questionnaires.
121 Blood and stool
were collected at baseline, 1, 3, 6 and 12 months.
122 etailed clinical data and sputum for culture
were collected at baseline, 2 months, and 5-6 months.
123 Data
were collected at baseline, 2 wks after the intervention
124 Self-report measures
were collected at baseline, 4 months, and 12 months.
125 The interviews from the parent study
were collected at baseline, 6 months, and 12 months post
126 ECGs
were collected at baseline, after reperfusion, and analy
127 P and 32 patients with GAgP, and GCF samples
were collected at baseline, after the treatment, and dur
128 Blood samples
were collected at baseline, at 6 wk, and after the inter
129 Data
were collected at baseline, before WM, and after WM (wee
130 Measures
were collected at baseline, completion of the interventi
131 Blood and nasal scrapings
were collected at baseline, during reactions, and after
132 Outcome measures
were collected at baseline, each treatment session, post
133 aliva samples per day for 3 consecutive days
were collected at baseline, end of treatment, and 1, 3,
134 Serum cytokine concentrations
were collected at baseline, midpoint, and endpoint to as
135 mmunospot (IFN-gamma ELISPOT), blood samples
were collected at baseline, post-doses 2, 3, and 4.
136 Data
were collected at baseline, post-test (3 months after di
137 etric, body composition, and behavioral data
were collected at baseline, postintervention (6 months),
138 graphics, clinical data, and health literacy
were collected at baseline.
139 Blood and tumor tissue samples
were collected at baseline.
140 osocial status, and clinical characteristics
were collected at baseline.
141 plaque and gingival crevicular fluid samples
were collected at baseline; after 7, 14, and 21 days of
142 Data
were collected at:
baseline, end of intervention and thr
143 Cord blood samples
were collected at birth and analyzed for 25(OH)D levels
144 Biopsies
were collected at both endoscopies for PGE2 quantificati
145 em/Behavior Activation System questionnaire)
were collected at both time points.
146 er biopsy samples from 43 HCV+ LT recipients
were collected at clinical HCVrec time and at 3 years po
147 a on sociodemographics, feeding, and illness
were collected at defined intervals.
148 inistered to tumor-bearing mice, and samples
were collected at defined times during pulse and chase p
149 2008, a total of 671 marine sediment samples
were collected at depths from 5 to 2012 m throughout the
150 dities, demographic characteristics, and QoL
were collected at diagnosis and 12 and 24 mo after diagn
151 Oral rinse samples
were collected at diagnosis and after treatment (9, 12,
152 Data on 1345 subjects
were collected at diagnosis and at 28 days, 6, 12, and 2
153 etabolic profiling of plant leaves that have
been collected at different time points during the growi
154 /kg, i.p. every 12 h) or saline-treated mice
was collected at different time points and tested ex viv
155 -stage heart failure and tissue samples that
were collected at different disease stages from desmogle
156 First, crystals of both compounds
were collected at different electrodes under the influen
157 Blood and urine
were collected at different intervals and analysed by LC
158 Slags samples
were collected at different sites throughout various cit
159 S. Daniele hams
were collected at different stages during dry-curing and
160 Colon tissues
were collected at different time points during colitis d
161 Liver tissues
were collected at different timepoints during developmen
162 al, mid-jejunal effluents and plasma samples
were collected at different times during 7h after meal i
163 Digesta
were collected at different times, in the different comp
164 Neonatal data
were collected at discharge, and sociodemographic inform
165 r dosing, vaginal biopsy and luminal samples
were collected at discrete locations in 8 subjects.
166 hroughout the study, and a spot urine sample
was collected at each visit.At baseline, 8 participants
167 s for total and specific IgE of the children
were collected at each follow-up visit.
168 Blood spots
were collected at each observation and assayed for CRP l
169 Bloodspots
were collected at each observation and assayed for CRP l
170 At least 5 pairs of samples
were collected at each of 7 time points (1 day, 3 days,
171 Counterregulatory hormone levels
were collected at each of these glycemic levels and rCBF
172 hr black carbon, and 96-hr nitrogen dioxide)
were collected at each school for 16 weeks.
173 oint was assessment of adverse events, which
were collected at each visit and for 28 days after the l
174 Adverse event data
were collected at each visit and included an assessment
175 Samples
were collected at eight time points to monitor rates and
176 Demographic and lifestyle information
was collected at enrollment; disease, treatment, and out
177 Stools
were collected at enrollment and, for cases, after a 5-m
178 Data
were collected at enrollment, each trimester, birth, and
179 Data on development of infection
were collected at evaluations performed at screening, ba
180 Plasma
was collected at four time points: preoperative, postane
181 A total of 590 faecal samples
were collected at four roosting sites in the USA and cul
182 Placenta and umbilical blood
were collected at GD 165.
183 , mid-IR emissivity image cubes of paintings
were collected at high collection rates with a low-noise
184 Number of nevi
was collected at inclusion.
185 etes, alcohol abuse, HIV, or HBV coinfection
were collected at inclusion.
186 TA muscles
were collected at intervals over the 36 h of exercise re
187 Data
were collected at kindergartens and parish centers by fa
188 Plasma samples
were collected at L1, L2, and 1 day after LT (postoperat
189 also more common in individuals for whom DNA
was collected at least 1 year before diagnosis with leuk
190 ic, clinical, radiological, and genetic data
were collected at Massachusetts General Hospital (Boston
191 imensional distributions in (99m)Tc activity
were collected at millimeter-resolution using decay-corr
192 Specimens
were collected at monthly interval (months 1-6 and month
193 ution is more difficult to defend if samples
are collected at multiple locations in the farm-to-table
194 In rat tissues, which could
be collected at multiple time points after osteotomy, th
195 Blood
was collected at multiple time points.
196 rse during initial and repeat KPro placement
were collected at multiple centers across the country.
197 The ONTT data
were collected at multiple centers in the United States.
198 r stream reaches were evaluated, and samples
were collected at multiple sites during summer and sprin
199 Plasma samples
were collected at multiple time points and used for the
200 lasma and peripheral blood mononuclear cells
were collected at multiple time points, and comprehensiv
201 Sediment samples
were collected at nine sampling sites within Admiralty B
202 Information
was collected at participants' homes through structured
203 The aerosol produced by the ultrasonic unit
was collected at patient's chest area, doctor's chest ar
204 Samples
were collected at patient enrollment and not during acut
205 In this study, retinas
were collected at postnatal (P) days P5-30, 90, 180, and
206 administrated to subjects and blood samples
were collected at predetermined time points.
207 Blood and urine samples
were collected at predetermined times.
208 swab specimens, and/or whole stool specimens
were collected at presentation, and serum was collected
209 eactive protein and faecal calprotectin will
be collected at recruitment and 3 months, and patient ex
210 surements, blood samples, and lifestyle data
were collected at recruitment.
211 Blood samples and urine
were collected at regular intervals to determine (68)Ga-
212 data including medical and family histories
were collected at research laboratories at Boston Childr
213 Nasal swabs
were collected at respiratory illness onset and every 7-
214 Blood and muscle biopsy samples
were collected at rest and after exercise during primed
215 The data
are collected at room temperature.
216 Serum samples
were collected at routine clinic visits from 50 pediatri
217 Blood samples
were collected at routine clinical appointment visits, c
218 Hereditary angioedema attack history
was collected at screening.
219 riodontal parameters and unstimulated saliva
were collected at screening, baseline, and each week dur
220 Blood
was collected at selected time points.
221 After DRB removal, cells
are collected at several time points, and tagged RNA is
222 The data underlying this relationship
were collected at sites with varying proportions of foli
223 Data
were collected at specialist centers on patients diagnos
224 asma, echocardiograms, and clinical outcomes
were collected at standardized intervals in breast cance
225 The cells
were collected at stationary phase and examined by Raman
226 In Barcelona, samples of fine PM
were collected at street level at sites with variable tr
227 ding demographic and clinical information to
be collected at study enrollment, important aspects rela
228 BM aspirates and blood samples
were collected at surgery, or in local anesthesia in non
229 ubcutaneous abdominal adipose tissue samples
were collected at surgical intervention.
230 A verbal review of systems also
was collected at that time.
231 induces particle movement, and the particles
are collected at the surface of one of the two electrode
232 The electrons
are collected at the UME, and the current-versus-time da
233 between week 5 and the end of month 7, feces
was collected at the ages of 5 weeks (n = 571), 13 weeks
234 climate dynamics available worldwide, which
was collected at the Hubbard Brook Experimental Forest i
235 Plasma
was collected at the time of bronchoscopy and analyzed f
236 A small amount of vitreous sample
was collected at the time of explant.
237 we and 20 samples of goat colostrum and milk
were collected at the 1st, 2nd, 3rd, 4th, 5th and 15th d
238 Non-fasting blood samples
were collected at the ages of 1, 1.5, 2, 3, and 4 years
239 Blood samples
were collected at the ages of 1, 2, 3, 5, 6, 7, 10, and
240 Data
were collected at the annual Twins Days Festival in Twin
241 Standardized spirometry data
were collected at the baseline examination.
242 Their blood and urine samples
were collected at the baseline, 1-, 3- and 6-months duri
243 uced gingivitis study, and gingival biopsies
were collected at the baseline, induction, and resolutio
244 mains of a small bear (Protarctos abstrusus)
were collected at the Beaver Pond fossil site in the Hig
245 vitamin B-12, and phospholipid fatty acids,
were collected at the beginning and end of the feeding p
246 inidia chinensis) (Gold3, Gold9 and Hort16A)
were collected at the commercial harvesting time, and ph
247 Data for this observational case study
were collected at the Department of Ophthalmology, Unive
248 Fasting blood samples
were collected at the end of each intervention arm.
249 Fasting plasma samples
were collected at the end of each intervention diet.
250 Fasting blood samples
were collected at the end of each sodium intervention.
251 tion fine-structure (XAFS) spectra of Br-Ash
were collected at the Hg L(III)-edge, Br K-edge and S K-
252 pective case series, 202 BAL fluid specimens
were collected at the Johns Hopkins Hospital between Aug
253 The two samples (Coastal and Marine DOM)
were collected at the mouth of the Ogeechee River and in
254 Drug costs
were collected at the National Database of Health Prices
255 Organization guideline phases of the switch
were collected at the national-level and in each of the
256 were receiving antiretroviral therapy (ART),
were collected at the Nsambya Hospital in Kampala, Ugand
257 mation brine, and synthetic NaCl+CaCl2 brine
were collected at the pressures from 100 to 200 bar, tem
258 Home settled dust samples
were collected at the same time points for quantificatio
259 others (n = 107) and their infants (n = 108)
were collected at the same time points for the measureme
260 te, respiratory rate, and oxygen saturation)
were collected at the same time points.
261 iscontinuation was more likely when cultures
were collected at the start of therapy (adjusted OR 1.68
262 Clinical data
were collected at the time of diagnosis of ERM and at th
263 n Guidelines), and predefined risk variables
were collected at the time of enrollment to enable progn
264 Pulmonary hemodynamic variables
were collected at the time of PoPH diagnosis, at last ev
265 Nasal wash (NW) samples
were collected at the time of recruitment.
266 ction episodes, and postoperative medication
were collected at the time of surgery and 1, 2, and 5 ye
267 Data
were collected at the time of surgery and at 1, 2, and 5
268 Blood and sinus tissue explants
were collected at the time of surgery from control subje
269 Human samples
were collected at the University of Utah between June 20
270 Crabs
were collected at the wreck location and 4 nmi north and
271 Air samples
were collected at the Zeppelin observatory in the remote
272 polymorphisms related to choline metabolism
were collected at their first prenatal visit.
273 from the coronary sinus and the femoral vein
were collected at those time points and then analyzed fo
274 The air samples have
been collected at three sites according to urban functio
275 Data
was collected at three time points: (1) baseline (time 0
276 Three 24-h sweat samples
were collected at three different days from each subject
277 A total of 796 pharyngeal swabs
were collected at three separate clinical centers.
278 Aerosol samples
were collected at three sites located in the Mediterrane
279 h aerodynamic diameters between 0.056-18 mum
were collected at three sites: (i) an active smelter ope
280 hort of 29 pregnant women, from whom samples
were collected at three time points during pregnancy and
281 Data
were collected at three waves: baseline, 6 and 12 months
282 l, sociodemographic, and behavioral measures
were collected at three- to six-month intervals from a b
283 Rectal swabs
were collected at time of acute diarrhea and 14 days lat
284 house gas flux that results when corn stover
is collected at two different rates from corn-soybean an
285 Three indigenous fruits
were collected at two conservation areas in Kanchanaburi
286 Northern pike (Esox lucius)
were collected at two locations in 2011 near Montreal Is
287 Measurements
were collected at two locations, one directly over and t
288 nisotropy measures of white matter integrity
were collected at two sites as a part of the Bipolar-Sch
289 These fossils
were collected at two sites in Germany, Neumark-Nord and
290 Daily PM2.5 and PM10 samples
were collected at two sites in Houston over a 2-week per
291 Ambient high volume PM2.5 air samples
were collected at two sites in the Pacific Northwest: (1
292 four commercial cultivars from North America
were collected at two sizes (3-5 and>7cm).
293 on was affected by weathering, field samples
were collected at various intervals up to two years afte
294 Liver specimens
were collected at various timepoints after injection and
295 C-matched clonal T cells (G14D-CCV), and PBL
were collected at various times after immunization for f
296 g omeprazole, twice daily) and fecal samples
were collected at week 8.
297 and fine (PM2.5) particulate matter samples
were collected at weekly intervals with both bacterial a
298 articipated in ACT-1 or ACT-2; efficacy data
were collected at weeks 8, 30, and 54 (for ACT-1 only).
299 Recalled GWG and breastfeeding behavior
were collected at years 7 and 10.
300 Serum and livers
were collected at zeitgeber time 2, 6, 10, 14, 18, and 2