ライフサイエンスコーパス: be phenotyped

1 onal breeding to obtain mutant mice that can be phenotyped.

2 ion (BC1F2) segregating for the glossy trait was phenotyped.

3 f medical records was performed and patients were phenotyped according to the Montreal classification

4 Sixteen subjects with asthma were phenotyped according to their response to inhaled a

5 Patients with asthma were phenotyped and 80% had late-onset asthma, 50% had f

6 The skin-emigrated DCs were phenotyped and analyzed for T cell stimulatory capa

7 ing fluorescently labeled Ara h 1 or Ara h 2 were phenotyped and isolated by means of flow cytometric

8 The cells were phenotyped and polymerase chain reaction studies we

9 Spleen cells were phenotyped, and enzyme-linked immunospot assays for

10 All available relatives were phenotyped, and SLC2A1 was sequenced.

11 Adult rats have been phenotyped as high (HRs) or low (LRs) responders to

12 CD14+HLA-DR(-/lo) cells were phenotyped as CD11b+, CD33+, CD34+, arginase-I+, an

13 rmethrin exposure, 439 F(3) adult mosquitoes were phenotyped as knockdown resistant, knocked down/rec

14 Patients were phenotyped based on magnetic resonance imaging/angi

15 e up of 384 inbred lines from the Ames Panel was phenotyped by extracting root traits from images usi

16 ntigen presentation-related molecules by KCs was phenotyped by flow cytometry.

17 Study participants were phenotyped by an oral glucose tolerance test (OGTT)

18 Fifty-two family members were phenotyped by baseline QTc, QTc maximum on serial E

19 F2 and N2 progeny were phenotyped by evaluating histopathologic lesions in

20 Blood- and sputum-extracted progenitors were phenotyped by flow cytometry before and 24 hours af

21 mphocytes proliferating in 10-day cocultures were phenotyped by flow cytometry, studied for cytokine

22 e was harvested and cells in DPPIV+ colonies were phenotyped by immunofluorescence and histochemical

23 Eosinophils were phenotyped by multicolor flow cytometry in digested

24 Tr1 were phenotyped by multicolor flow cytometry, and suppre

25 eneration had fasting glucose <126 mg/dl and were phenotyped by oral and intravenous glucose toleranc

26 Cord blood was phenotyped for 26 different immune cell subsets, and

27 The F(2) population was phenotyped for growth and energy intake at weekly in

28 Baseline envelopes were phenotyped for 724 patients; 50% harbored R5 strain

29 Fruits were phenotyped for a broad range of metabolites, includ

30 ains collected over 3 years from 16 patients were phenotyped for antibiotic resistance and mutator st

31 Isolated peripheral blood mononuclear cells were phenotyped for CD14/CD16 receptor expression using

32 MDSCs were phenotyped for cell surface receptor expression and

33 Animals were phenotyped for cross-sectional atherosclerotic lesi

34 All 10 subjects were phenotyped for cytochrome P4501A2 (CYP1A2), N-acety

35 Rats were phenotyped for DMBA-induced mammary carcinomas and

36 SSD lines of the resulting MAGIC population were phenotyped for earliness and genotyped with the 9K

37 /6J (B6) x DBA/2J (D2) F2 intercross animals were phenotyped for ethanol response, and the phenotypic

38 b-PI3Kgamma(-/-) mice and control db/db mice were phenotyped for glucose homeostasis, insulin sensiti

39 nd CFU-megakaryocyte (CFU-Meg)-derived cells were phenotyped for messenger RNA expression and protein

40 Diverse rice genotypes were phenotyped for the above traits in S. asiatica- (Ta

41 A total of 1883 animals were phenotyped for the number of ribs and thoracolumbar

42 A panel of (NZB x SWR)F(2) hybrids were phenotyped (for renal disease, early mortality, and

43 n parents are unavailable, siblings need not be phenotyped if the disease is rare, but a loss of powe

44 of 466 diverse plant introduction accessions were phenotyped in multiple field and controlled environ

45 nce these lines have been genotyped they can be phenotyped multiple times, making it possible (as wel

46 density genotyping of the populations, which were phenotyped over 3 years in both short- and long-day

47 or traits related to these four trait groups was phenotyped to understand the interactions among trai

48 The rabbit retinal ganglion cell layer was phenotyped using intrinsic small molecule signals (a

49 Leukocytes were phenotyped using multicolor flow cytometry, and who

50 12-month-old infants were phenotyped using open oral food challenges.

51 r blinded to culture conditions, and tubules were phenotyped using specific markers.

52 Patients were phenotyped using the Montreal Disease Classificatio

53 F2 hybrids between these two strains were phenotyped using two-bottle tests involving a choic

54 expression, and peripheral-blood leukocytes were phenotyped with flow cytometry.