Sentences with phrase «h after»

Reminder e-mails were sent to participants who had not completed their assessment 1.5 h after the initial invitation was sent, followed by text messages and phone calls to those who had still not completed their assessment 1.5 h after the reminder had been sent.

Facilitators completed one form for each participating parent within 72 h after the first group session the parent attended.

The infant's exposure to SSRIs can be reduced by emptying the breasts of milk and discarding it («pump and dump») approximately 8 h to 9 h after the mother has taken the medication [67].

It has been identified that hmF2 increases systematically 1 — 3 h after the geomagnetic storm main phase onset (at the largest change of Dst) independently of the storm intensity (according to the Dst index) followed by an additional uplift in the nighttime sector.

A few of these tips and tricks are found below, written by our own Ben H after trying and retrying to (unsuccessfully) beat my score...

Marvel Studios returns to Comic - Con International: San Diego and Hall H after a skipping 2015, but with what news?

Peripheral venous blood samples were obtained before ingestion of each meal and every 20 min for 2 — 3 h after meal consumption.

Tissue protein turnover measurements were performed at the end of the 21 - d experiment in rats in either the postabsorptive state (PA), 4 i.e., after 12 h of the light period, or in the postprandial state (PP), i.e., 2 h after the ingestion of the high protein meal (pulse groups) or 2 h after the ingestion of the standard protein meal (spread groups).

Additionally, full - fat milk, skimmed milk, ORS, and orange juice BHIs were greater than that for still water at 3 and 4 h after drink consumption (P < 0.05).

Colonic fermentation and its effects may be long - lasting, as it has been observed to occur up to 13 h after the previous meal (73).

In summary, short - term studies (mostly single - meal studies) indicate reduced hunger and increased satiety 2 — 4 h after pulse consumption when meals were controlled for energy but not when controlled for available carbohydrate.

Under local anaesthesia (1 % Xylocaine) a resting biopsy from the vastus lateralis of one leg was obtained 3 h after commencement of the tracer infusion using a 5 - mm Bergstrom needle modified with suction, during the first trial only.

Cumulative urine output at 4 h after ingestion of cola, diet cola, hot tea, iced tea, coffee, lager, orange juice, sparkling water, and a sports drink were not different from the response to water ingestion.

In regard to the last one it's interesting to note that the reasons for Delayed Onset Muscle Soreness are still unclear and that it may well be a sign of your muscles rebuilding — and DOMS happen 12 to 48 h after a workout.

Postprandial increases in both blood glucose and blood insulin were significantly inhibited in subjects in the borderline group who took the test food in comparison with the placebo group (blood glucose: p < 0.05 and p < 0.01 at 1 and 1.5 h after ingestion respectively; insulin: p < 0.05, p < 0.01 and p < 0.05 at 1, 1.5, and 2 h after ingestion respectively).

The first moderate increase (more pronounced in Study 1) occurred ∼ 2 — 3 h after test meal consumption, followed by the major response observed at 5 h (after the lunch meal).

Blood glucose and insulin were measured before ingestion, and at 0.5, 1, 1.5, and 2 h after ingestion.

Serum concentration of the flavonoid epicatechin was shown to be highest 2 h after cocoa consumption (6, 17).

The supplement was on average taken 3.9 ± 0.2 h after cessation of exercise, allowing net muscle protein accretion during overnight sleep.

We found this to be the case, because a mixture of 6 g EAAs + 35 g glucose given immediately before exercise resulted in a greater stimulation of net muscle protein balance than when it was given either immediately or 1 h after exercise.

it's unfortunate that all of the rats used in the quoted study were killed as part of the experiment: «At different 175 time intervals 176 between 0, 0.5, 1, 2, 6 and 24 h after ingestion, the animal was euthanized with 177 Nembutal ® (100 mg / kg body weight of the animal) and 5 ml of blood specimens 178 were collected.»

Endothelial function assessed by flow - mediated vasodilation and plasma concentration of 8 - isoprostanes were measured at baseline and at 1 and 2 h after coffee intake.

Regions with significantly different cerebral blood flow 4 h after test meals (P ≤ 0.002).

It subsequently increased and reached a peak of 774 ± 132 μmol / L (774 ± 132 μEq / L) at 45 min after dinner, declined until 3 h after dinner, and then increased again.

The glucagon response was not significantly different for the first 2 h after breakfast and lunch.

Bacterial CFUs were quantified in cell - free culture media at 4 h after infection.

(E) Intracellular (internalized) and extracellular bacteria (cell - free culture media) were quantified at 1 h after ex vivo infection of alveolar macrophages with an MOI of 20.

At 1 h after the final exposure, mice were anesthetized with isofluorane and infected with 1x105 CFU of S. pneumoniae via intranasal instillation [15].

For isolation of nuclei, embryos were collected overnight (0 — 16 h after egg laying [AEL]-RRB- onto apple juice agar plates and dechorionated in 25 % bleach for 5 min.

Blood was collected from the tail vein of mice (N = 5) either within 1 h of the final exposure or 24 h after exposure.

NSCs transfected with anti-HER2 antibody were used 24 h after transfection, the time - point that correlated with peak antibody expression.

Tiny colonies were formed 24 h after plating (Fig. 1A) and typical undifferentiated hESC morphology was observed 2 — 3 days after passage (Fig. 1B).

Approximately 48 h after injection, oocytes were stripped of their vitelline membrane and paired overnight in agar wells.

The filtered sample was allowed to settle for 72 h after which ten microscope slides were prepared.

(B) Neurite length of GDF5 - treated (200 ng / ml daily for 72 h) SH - SY5Y cells at 72 h. (C — F) p - Smad1 / 5 levels as determined by (C, D) Western blots or (E, F) immunocytochemistry in SH - SY5Y cells 24 h after transfection with control miRNA or miR - 181a inhibitor.

The increase in the p53 activity in the HepG2 cells was also time course - dependent and reached a plateau at 12 h after treatment with 10 nM ActD.

At the right, the counting of HUVEC migration into the «wounded» area at 8 and 24 h after «wounding» is depicted.

Briefly, ovaries were collected from abattoir and transported to our laboratory within 4 h after slaughter.

The luciferase activity was measured 36 h after transfection.

Photographs were taken on untreated (control) and 75 µM kahweol - treated HUVEC cells at 0, 8 and 24 h after «wounding».

Using the G - TRACE method [25], which allows us to identify both lineage - traced expression (marked with green fluorescent protein [GFP]-RRB- and live Gal4 (marked with DsRed), we found that C7 Gal4 expressed Gal4 strongly in the fat body and salivary glands at 24 h after L3 ecdysis (AL3E)(S1A Fig).

The p53 activity in the 293 and 293T cells increased from 12 through 24 h after treatment with 10 nM ActD (Fig. 2).

We found that the majority of the internalized Abeta in microaggregates was undegraded 72 h after uptake, whereas 70 - 80 % of internalized acetylated low density lipoprotein or alpha2 - macroglobulin was degraded and released from cells in trichloroacetic acid - soluble form after 4 h.

Cumulus - free immature oocytes from consenting ICSI patients were obtained 6 — 8 h after oocyte retrieval and transferred to the research laboratory.

L - arginine was administered (intra-peritoneal) at fed condition and the animals were sacrificed 48 h after treatment [19].

Treatment with 20 µM concentration of either U0126, LY294002 or SP600125 alone did not show significant increase in cell death at 48 h after drug treatment compared to control and sham group (data not shown).

Supernatants were collected 24 and 48 h after transfection.

HUVEC were selected with 0.35 μg ml − 1 and BP with 0.7 μg ml − 1 puromycin 24 h after infection for an additional 72 h at 37 °C.

We have considered the possibility that radiation could directly result in more apoptosis in the thymus of p21 - null mice; however, quantitation of sub -(G0 / G1) thymocytes after acute irradiation (10 Gy; and analysis 3 h after irradiation) has not supported this idea (data not shown).

Significantly more microspheres accumulated in tumours grown in Tie2PEKO mice 24 h after sphere injection (Fig. 6f — h).