1 Questionnaires and genital samples
were collected at 0 and 4 months.
2 Contrast computed tomography scans
were collected at 0, 2, 4, 8, and 12-week (termination)
3 Human milk samples
were collected at 0.5 mo (n = 159), 2 mo (n = 131), and
4 Blood
was collected at 1, 4, 12, 24, 36, and 48 weeks.
5 Tissue biopsies and blood
were collected at 1 to 2, 6 to 8, 24, and 48 hours post-
6 Transepidermal water loss (TEWL) measures
were collected at 12 months from a subset (n=150) of the
7 PDF data for nanocrystalline platinum (n-Pt)
were collected at 12.5 GPa with a single 5 s X-ray expos
8 Data
were collected at 14 demonstration project sites in 7 st
9 Data on maternal BMI
was collected at 15 weeks of gestation, and paternal BMI
10 and nutritional and environmental exposures
were collected at 15 weeks' gestation, birth, and 2, 6,
11 The blood samples had
been collected at 2 time points (median interval, 8.8 ye
12 Dust samples from living rooms
were collected at 2 months of age.
13 Maxillae
were collected at 2, 4, and 6 weeks for microcomputed to
14 Fractions
were collected at 20 min intervals (2 muL) before and af
15 on participant schooling and smoking history
were collected at 23-25 y of age.
16 Synovial fluid
was collected at 24, 96, and 144 h for cytology, cytokin
17 gs, including blood flow and sweep gas flow,
were collected at 24 hours after initiation of extracorp
18 Blood and liver
were collected at 24 hours after ischemia-reperfusion fo
19 r parent reports) for the first 10 y of life
was collected at 3-y, 5-y, and 9-y follow-up.
20 Fecal samples
were collected at 3 (n = 16, 12, and 14, respectively),
21 s from schools in Melbourne, Australia, data
were collected at 3 assessments between 2004 and 2012.
22 in optical coherence tomography volume scans
were collected at 3 clinical sites, in Belfast, Northern
23 Clinical signs and symptoms
were collected at 3 time points from hospitalized infant
24 mples and peripheral blood mononuclear cells
were collected at 3 timepoints (pretransplant, mo 6, mo
25 es for functional limitations and disability
were collected at 3, 6 and 12 months.
26 Serum samples
were collected at 3, 6, and 12 months after treatment in
27 amples from mice inoculated with RML scrapie
were collected at 30, 60, 90, 105, and 120 days post ino
28 A total of 77,969 cells
were collected at 35 distinct locations, from the nose t
29 In this study, water column samples
were collected at 39 sites in the nGOM, 21 of which were
30 Blood
was collected at 4, 12, and 24 wk to assess chemistry an
31 Blood
was collected at 4, 8, and 16 years, and sensitization e
32 nscriptome following VEEV infection, samples
were collected at 4, 8, and 16 h postinfection and RNA-S
33 Blood samples
were collected at 4, 8, and 16 years of age for analysis
34 Spleen samples
were collected at 40 days post injection (dpi), and sequ
35 efore and during the urine collection period
was collected at 5 time points for the mother using pros
36 Urine
was collected at 6, 12, and 18 weeks.
37 Available follow-up data on VA
were collected at 6 months post baseline, 5 years and 10
38 equencing was applied to saliva samples that
were collected at 6-mo intervals for 24 mo from a subset
39 Serum samples
were collected at 7, 14 and 21 day post infection (DPI)
40 ablish the true pig M. hyopneumoniae status)
were collected at 7- to 14-day intervals through 98 dpi.
41 Mother and infant blood
was collected at 8 wk postpartum.
42 or 640 nm), and the maximal emission signal
was collected at a shorter wavelength (i.e., higher ener
43 In the TRACK-TBI Pilot study, plasma
was collected at a single time point from 196 patients w
44 leeding events and antithrombotic medication
were collected at a median follow-up of 12 years (range
45 In this study, tree-core samples
were collected at a Superfund site to determine if the s
46 e, DeltaP, tidal volume, Cdyn, and PaO2/FIO2
were collected at acute respiratory distress syndrome on
47 Fecal samples
were collected at age 1 week, 1 month, and 1 year, and h
48 th, and 1 year, and hypopharyngeal aspirates
were collected at age 1 week, 1 month, and 3 months and
49 er-reported callous traits and brain imaging
were collected at age 10 years from participants of the
50 at age 4(+) years; samples from 293 children
were collected at age 3 to 15 months and 2 to 3 and 4(+)
51 Fecal samples
were collected at age 3 to 16 months, and the children w
52 Nasal swab samples
were collected at age 3, 6, 12, 18, 24, and 36 months an
53 Intestinal microbiome samples
were collected at age 3-6 months in children participati
54 sumed milk and serum samples of the children
were collected at age 4 years.
55 Samples
were collected at age 6 and 8 weeks of life.
56 Blood pressure measurements had
been collected at ages 36, 43, 53, 60-64, and 69 years.
57 Blood samples
were collected at ages 2, 4, 6, and 11 years, and serum-
58 MRI data
were collected at ages 8 and 10.
59 Mie scatter patterns
are collected at all photodiode angles for each of the i
60 Matched blood and semen samples
were collected at all visits, and all additional episode
61 Filter samples
were collected at an urban background site in the city c
62 l blood mononuclear cells (PBMCs) and plasma
were collected at and 2 time points after diagnosis.
63 tibodies at Srinagarind Hospital in Thailand
were collected at annual follow-up visits (median follow
64 Color fundus photographs
were collected at annual study visits and graded central
65 Color fundus photographs
were collected at annual study visits and graded central
66 Fundus photographs
were collected at annual study visits and graded central
67 tion was measured in spot-urine samples that
were collected at approximately 12, 20, and 35 wk of ges
68 early life and 12 adults (>/=18 years old),
were collected at autopsy in Jackson, Mississippi.
69 Between 5 and 12 metastatic sites
were collected at autopsy together with available primar
70 elected case-mix factors were recommended to
be collected at baseline to facilitate comparison of res
71 elected case-mix factors were recommended to
be collected at baseline.
72 Blood
was collected at baseline and at 3 and 4 wk.
73 Self-reported weight (previously validated)
was collected at baseline and updated every 2 y during t
74 Scalp hair
was collected at baseline and week 20 for measurement of
75 For each patient, a peripheral blood sample
was collected at baseline for the evaluation of CTCs and
76 Blood
was collected at baseline, 1, 3, 6, and 12 mo.
77 olled, crossover study, and peripheral blood
was collected at baseline, 2, 4, 6, and 24 hours post ad
78 Serum
was collected at baseline, after 24 and 72 hours, at 7 a
79 PA
was collected at baseline, and PA and neurocognitive dat
80 n lifestyle score components and confounders
was collected at baseline.
81 Plasma and urine
were collected at baseline (in a subset), the beginning
82 try, blood gases, cytokines, and blood cells
were collected at baseline (just before peritonitis indu
83 Plasma samples
were collected at baseline (n = 62).
84 Data
were collected at baseline (preintervention), at 60 days
85 Data
were collected at baseline (recruitment) with follow-up
86 Periodontal parameters and GCF
were collected at baseline (t0), 3 months after periodon
87 Laboratory data
were collected at baseline and 1 mo after (90)Y radioemb
88 CSF samples
were collected at baseline and 12 months after DMF.
89 Blood samples
were collected at baseline and 16 weeks, and analyzed fo
90 Efficacy outcomes regarding AD, PAR and PAA
were collected at baseline and 16 weeks.
91 Fecal samples
were collected at baseline and 16 weeks; bile acids were
92 ealthy individuals (controls); fecal samples
were collected at baseline and 2, 6, and 30 weeks after
93 urs after challenge, and bone marrow samples
were collected at baseline and 24 hours after challenge
94 Blood and subcutaneous (SUBQ) adipose tissue
were collected at baseline and 3 mo.
95 vironmental factors (SES and social network)
were collected at baseline and 3-mo follow-up, together
96 nt-reported outcomes (PROs) and biospecimens
were collected at baseline and 4 and 9 months after enro
97 Clinical and standardized radiographic data
were collected at baseline and 6 months after treatment.
98 Colonoscopic biopsies
were collected at baseline and 6 months or when patients
99 Peripheral blood and sputum samples
were collected at baseline and 7 and 24 hours after chal
100 Data
were collected at baseline and 8 wk after therapy.
101 Diffusion imaging and clinical data
were collected at baseline and after 1 year.
102 Fecal samples
were collected at baseline and after 4 weeks and analyze
103 Biologic specimens and clinical parameters
were collected at baseline and after 8 weeks on aspirin.
104 jections (numbers, dates, and names of drug)
were collected at baseline and annual study visits and d
105 ngival biofilm and gingival crevicular fluid
were collected at baseline and at 1-, 3-, and 6 mo posto
106 , and psychological data and blood and feces
were collected at baseline and at 8 weeks and 3 months a
107 Blood samples
were collected at baseline and at an early time-point (2
108 grin) and 99 healthy controls; fecal samples
were collected at baseline and at weeks 2, 6, and 14.
109 Stool and blood samples
were collected at baseline and end of trial.
110 , anthropometric measures, and blood samples
were collected at baseline and endline.
111 Vaginal samples
were collected at baseline and every 6 months.
112 Data
were collected at baseline and immediately postintervent
113 cs, visual outcomes, OCT, and treatment data
were collected at baseline and months 1, 3, 6, and 12 af
114 Angina and QOL questionnaires
were collected at baseline and months 1, 6, and 12.
115 Study data
were collected at baseline and months 6, 12, and 18.
116 ken biweekly from baseline, and hair samples
were collected at baseline and postintervention.
117 e functional magnetic resonance imaging data
were collected at baseline and posttreatment to examine
118 Data
were collected at baseline and prospectively every 2 mon
119 nal partnerships and self-management ability
were collected at baseline and three months later.
120 went esophagogastroduodenoscopy and biopsies
were collected at baseline and week 16.
121 Ophthalmic data
were collected at baseline and yearly visits by means of
122 HRQoL data
were collected at baseline for 362 (88%) of 410 patients
123 heral blood mononuclear cells or whole blood
were collected at baseline from 425 participants and fro
124 Blood and stool
were collected at baseline, 1, 3, 6 and 12 months.
125 Salivary samples
were collected at baseline, 1-, 2-, 3-, 4-weeks and 3 mo
126 essing speed, and general cognitive function
were collected at baseline, 12-week, and 24-week.
127 etailed clinical data and sputum for culture
were collected at baseline, 2 months, and 5-6 months.
128 ocollagen type III N-terminal peptide (P3NP)
were collected at baseline, 24 and 48 weeks.
129 Rectal swabs
were collected at baseline, 36 months, and 48 months for
130 ECGs
were collected at baseline, after reperfusion, and analy
131 P and 32 patients with GAgP, and GCF samples
were collected at baseline, after the treatment, and dur
132 Plasma/sera
were collected at baseline, and 1, 3, 6 and 12 months af
133 Data
were collected at baseline, before WM, and after WM (wee
134 Cervicovaginal samples
were collected at baseline, crossover and exit for chara
135 Biobank samples
were collected at baseline, day 3 and day 9.
136 Blood and nasal scrapings
were collected at baseline, during reactions, and after
137 Data
were collected at baseline, immediately after completion
138 Clinical and biological parameters
were collected at baseline, including bioactive-adrenome
139 Fasted venepuncture samples
were collected at baseline, midline (week 5), and endlin
140 Serum cytokine concentrations
were collected at baseline, midpoint, and endpoint to as
141 Study data
were collected at baseline, months 6, 12, and 18.
142 mmunospot (IFN-gamma ELISPOT), blood samples
were collected at baseline, post-doses 2, 3, and 4.
143 Data
were collected at baseline, post-test (3 months after di
144 etric, body composition, and behavioral data
were collected at baseline, postintervention (6 months),
145 graphics, clinical data, and health literacy
were collected at baseline.
146 Demographic data and medical history
were collected at baseline.
147 , FIB-4, clinical, and biochemical variables
were collected at baseline.
148 Subgingival plaque samples
were collected at baseline; 0.5, 1, and 3 months followi
149 DBS
are collected at birth for the child.
150 Placentas and lung tissue
were collected at birth for morphometric and Western blo
151 Biopsies
were collected at both endoscopies for PGE2 quantificati
152 mptoms, polyp size, and clinical indications
were collected at colonoscopy.
153 Visceral adipose tissue (VAT)
was collected at d17.5 of pregnancy for analysis.
154 PBMCs from ELGAN/ELBW neonates
were collected at day 14, day 28, and postmenstrual week
155 a on sociodemographics, feeding, and illness
were collected at defined intervals.
156 dities, demographic characteristics, and QoL
were collected at diagnosis and 12 and 24 mo after diagn
157 Oral rinse samples
were collected at diagnosis and after treatment (9, 12,
158 Additionally, 12-lead ECGs
were collected at diagnosis, before initiation of mexile
159 0 EIS spectra of commercial Li-ion batteries
are collected at different states of health, states of c
160 etabolic profiling of plant leaves that have
been collected at different time points during the growi
161 /kg, i.p. every 12 h) or saline-treated mice
was collected at different time points and tested ex viv
162 -stage heart failure and tissue samples that
were collected at different disease stages from desmogle
163 First, crystals of both compounds
were collected at different electrodes under the influen
164 Blood and urine
were collected at different intervals and analysed by LC
165 Cardoon (Cynara cardunculus L.) bracts
were collected at different maturation stages to investi
166 Pancreata
were collected at different stages of tumor development
167 Such curves
were collected at different temperatures, thereby provid
168 Feces
were collected at different time points after infection
169 Blood samples
were collected at different time points and analyzed for
170 Colon tissues
were collected at different time points during colitis d
171 Liver tissues
were collected at different timepoints during developmen
172 Digesta
were collected at different times, in the different comp
173 Neonatal data
were collected at discharge, and sociodemographic inform
174 Serum
was collected at each visit for ELISA measurement of ant
175 hroughout the study, and a spot urine sample
was collected at each visit.At baseline, 8 participants
176 s for total and specific IgE of the children
were collected at each follow-up visit.
177 ontrolled transient elastography (VCTE) data
were collected at each site.
178 oint was assessment of adverse events, which
were collected at each visit and for 28 days after the l
179 Adverse event data
were collected at each visit and included an assessment
180 Electrophysiological recordings
were collected at each visit from both the cortical and
181 Samples
were collected at eight time points to monitor rates and
182 Fecal samples
were collected at enrollment and at 7, 28, and 56 days a
183 Stools
were collected at enrollment and, for cases, after a 5-m
184 Respiratory swabs
were collected at enrollment to identify and quantify ba
185 Respiratory swabs
were collected at enrollment to identify and quantify ba
186 Data
were collected at enrollment, each trimester, birth, and
187 Risk factor data
were collected at enrolment and during follow-up.
188 Data on development of infection
were collected at evaluations performed at screening, ba
189 lk consumption was measured and milk samples
were collected at every feed.
190 Magnetic resonance images
were collected at five time-points in 24 male and female
191 Plasma
was collected at four time points: preoperative, postane
192 RS), stay green trait (SGT), and NDVI values
were collected at four environments (2016, 2017, and 201
193 Stormwater samples
were collected at four locations in the lower San Diego
194 A total of 590 faecal samples
were collected at four roosting sites in the USA and cul
195 Plasma and placental samples
were collected at GD120 (control n = 8, MNR n = 9), GD14
196 red to clean water after 10 days, and larvae
were collected at hatch.
197 Conversely, monthly case data
are collected at health facilities but suffer from biase
198 , mid-IR emissivity image cubes of paintings
were collected at high collection rates with a low-noise
199 Anal self-swabs
were collected at inclusion and every 6 months thereafte
200 Blood samples and fecal samples
were collected at intervals and analyzed by LC-MS.
201 TA muscles
were collected at intervals over the 36 h of exercise re
202 AC meeting attendance data
were collected at intervention facilities prospectively
203 Plasma samples
were collected at L1, L2, and 1 day after LT (postoperat
204 ic, clinical, radiological, and genetic data
were collected at Massachusetts General Hospital (Boston
205 Specimens
were collected at monthly interval (months 1-6 and month
206 In rat tissues, which could
be collected at multiple time points after osteotomy, th
207 rse during initial and repeat KPro placement
were collected at multiple centers across the country.
208 ng sensitization, wheeze, asthma, and eczema
were collected at multiple follow-ups up to age 18 years
209 lasma and peripheral blood mononuclear cells
were collected at multiple time points, and comprehensiv
210 Rumen epithelial tissues
were collected at necropsy at 17 weeks of age.
211 Liver and rumen epithelial tissues
were collected at necropsy at 17 weeks of age.
212 Sediment samples
were collected at nine sampling sites within Admiralty B
213 Samples
were collected at patient enrollment and not during acut
214 administrated to subjects and blood samples
were collected at predetermined time points.
215 Blood and urine samples
were collected at predetermined times.
216 Blood
was collected at preinjury baseline and within 6 hours (
217 Blood samples
were collected at presentation, and IL-1beta and sST2 le
218 A 3-day continence record
was collected at recruitment and every 4 weeks up until
219 surements, blood samples, and lifestyle data
were collected at recruitment.
220 Blood samples and urine
were collected at regular intervals to determine (68)Ga-
221 Blood and muscle biopsy samples
were collected at rest and after exercise during primed
222 al and internal jugular venous blood samples
were collected at rest and coupled with volumetric measu
223 The data
are collected at room temperature.
224 Serum samples
were collected at routine clinic visits from 50 pediatri
225 Blood samples
were collected at routine clinical appointment visits, c
226 rements (only for patients with F4 fibrosis)
were collected at screening and at weeks 48 and 96.
227 Blood
was collected at selected time points.
228 OF
was collected at several time points in a placebo-contro
229 Data
were collected at specialist centers on patients diagnos
230 asma, echocardiograms, and clinical outcomes
were collected at standardized intervals in breast cance
231 In Barcelona, samples of fine PM
were collected at street level at sites with variable tr
232 ding demographic and clinical information to
be collected at study enrollment, important aspects rela
233 Serial plasma samples
were collected at study baseline prior to mesenchymal st
234 BM aspirates and blood samples
were collected at surgery, or in local anesthesia in non
235 Beta spectra
were collected at temperatures up to 100 degrees C with
236 Twenty-five samples
were collected at ten sites via riverbed access through
237 Fruit
are collected at the mature green stage then stored and
238 induces particle movement, and the particles
are collected at the surface of one of the two electrode
239 Simultaneously, a redox signal
is collected at the CFE due to the release of internaliz
240 Subgingival biofilm
was collected at the deepest site of each sextant, and b
241 Since the information on the CCT
was collected at the end of the study, we do not know th
242 f-reported nonadherence to tamoxifen therapy
was collected at the same time through semistructured in
243 Patient demographic and clinical information
was collected at the time of screening.
244 we and 20 samples of goat colostrum and milk
were collected at the 1st, 2nd, 3rd, 4th, 5th and 15th d
245 Non-fasting blood samples
were collected at the ages of 1, 1.5, 2, 3, and 4 years
246 Blood samples
were collected at the ages of 1, 2, 3, 5, 6, 7, 10, and
247 Data
were collected at the annual Twins Days Festival in Twin
248 mains of a small bear (Protarctos abstrusus)
were collected at the Beaver Pond fossil site in the Hig
249 vitamin B-12, and phospholipid fatty acids,
were collected at the beginning and end of the feeding p
250 inidia chinensis) (Gold3, Gold9 and Hort16A)
were collected at the commercial harvesting time, and ph
251 Data for this observational case study
were collected at the Department of Ophthalmology, Unive
252 Cardiac tissues
were collected at the end of e-cigarette exposure for pa
253 Fasting plasma samples
were collected at the end of each intervention diet.
254 Fasting plasma samples
were collected at the end of each period and analyzed us
255 Fasting blood samples
were collected at the end of each sodium intervention.
256 Tissue samples
were collected at the end of each study for immunoblotti
257 biopsy (TLSB) and cervical biopsy specimens
were collected at the end of the daily sampling period.
258 Functional and surgical outcome data
were collected at the latest available time point betwee
259 degrees retinal field centered at the fovea
were collected at the Moran Eye Center, Salt Lake City,
260 Drug costs
were collected at the National Database of Health Prices
261 Demographic, clinical, and genetic data
were collected at the National Institute of Mental Healt
262 Organization guideline phases of the switch
were collected at the national-level and in each of the
263 Hospitalization data
were collected at the pediatric ward of the National Hos
264 mation brine, and synthetic NaCl+CaCl2 brine
were collected at the pressures from 100 to 200 bar, tem
265 te, respiratory rate, and oxygen saturation)
were collected at the same time points.
266 Respiratory samples positive for InfA that
were collected at the same wards within 7 days were chos
267 Fecal samples
were collected at the start and end of the study, the fe
268 ith ESI-MS, laser-induced fluorescent images
were collected at the Taylor cone of the electrospray in
269 n Guidelines), and predefined risk variables
were collected at the time of enrollment to enable progn
270 The predictors included in each model
were collected at the time of ICU admission (early predi
271 Pulmonary hemodynamic variables
were collected at the time of PoPH diagnosis, at last ev
272 Nasal wash (NW) samples
were collected at the time of recruitment.
273 etwork predicted future severity scores that
were collected at the time of recurrence of psychotic de
274 bolic balance, and the tibia and final blood
were collected at the time of sacrifice.
275 Data on 15 comorbidities
were collected at the time of transplantation.
276 Human samples
were collected at the University of Utah between June 20
277 Crabs
were collected at the wreck location and 4 nmi north and
278 from the coronary sinus and the femoral vein
were collected at those time points and then analyzed fo
279 The air samples have
been collected at three sites according to urban functio
280 Data
was collected at three time points: (1) baseline (time 0
281 Rumen fluid
was collected at three timepoints on three days relative
282 Three 24-h sweat samples
were collected at three different days from each subject
283 Aerosol samples
were collected at three sites located in the Mediterrane
284 h aerodynamic diameters between 0.056-18 mum
were collected at three sites: (i) an active smelter ope
285 skeletal muscle tissue and plasma specimens
were collected at three time intervals at rest, postexer
286 hort of 29 pregnant women, from whom samples
were collected at three time points during pregnancy and
287 nical information and maternal serum samples
were collected at three time points during pregnancy: 11
288 Rectal swabs
were collected at time of acute diarrhea and 14 days lat
289 ecimens of five benthic invertebrate species
were collected at two distinct locations near Rothera re
290 Northern pike (Esox lucius)
were collected at two locations in 2011 near Montreal Is
291 These fossils
were collected at two sites in Germany, Neumark-Nord and
292 Ambient high volume PM2.5 air samples
were collected at two sites in the Pacific Northwest: (1
293 four commercial cultivars from North America
were collected at two sizes (3-5 and>7cm).
294 study during which anal self-swabs and serum
were collected at up to 5 bi-annual visits.
295 y measurement, small samples of venous blood
were collected at various time points after injection.
296 C-matched clonal T cells (G14D-CCV), and PBL
were collected at various times after immunization for f
297 y function measure, and adherence estimates)
were collected at visits and entered into the ACET Progr
298 g omeprazole, twice daily) and fecal samples
were collected at week 8.
299 Two endoscopic biopsy samples
were collected at weeks 0, 8, and 44 from the ileum, spl
300 Serum and livers
were collected at zeitgeber time 2, 6, 10, 14, 18, and 2