ライフサイエンスコーパス: we generated

1 n the basis of 15 clinical and demographic characteristics, we generated 1:1 pairs of alemtuzumab-rabbit antithymocyte gl

2 alysis of 88 CTCs isolated from 13 patients (training set), we generated a CNA-based classifier that we validated in 18 a

3 Cancer Genome Atlas (TCGA) expression data in CRC, whereby we generated a core regulatory network consisting of 58 signi

4 ne the lineage contribution of the Nkx2.5+ cardiomyoblasts, we generated a doxycycline suppressible Cre transgenic mouse

5 To determine the biological function of FDXR, we generated a Fdxr-deficient mouse model and found that loss

6 To better understand the function of PR3 in vivo, we generated a human PR3 transgenic mouse (hPR3Tg).

7 ether this phenomenon plays a role in disease pathogenesis, we generated a knock-in mouse model with NB disruption mediat

8 Using label-free ToF-SIMS imaging mass spectrometry, we generated a map of small molecules differentially expresse

9 In order to study the function of Mig-6 in P4 resistance, we generated a mouse model in which we specifically ablated M

10 In this study, we generated a new Tg(mrc1a:egfp)(y251) transgenic zebrafish

11 Here, we generated a novel mouse model (eAA) with the erythroid-spe

12 To investigate the effects of ARHGAP29 in vivo, we generated a novel murine allele by inserting a point mutat

13 We generated a novel mutant mouse (Dclre1c(leaky)) that devel

14 ajor isoforms of dysbindin-1, (A, B, and C) remain unknown, we generated a novel mutant mouse, dys-1A(-/-), with selectiv

15 nes are required to enable EGF receptor-mediated signaling, we generated a series of EGF receptors that contained only on

16 Using conditional cell reprogramming, we generated a stable cell culture of an extremely rare and a

17 To facilitate the VLP platform, we generated a stable cell line expressing high levels of ZIK

18 Using reverse genetics, we generated a ToV-PLP knockout recombinant virus.

19 We generated a uniquely large resource of gene expression dat

20 METHODS AND We generated cardiomyocyte-specific Cas9 mice and demonstrate

21 Therefore, we generated Cnr2-floxed mice that were crossed with DAT-Cre

22 In this study, we generated complete mitogenomes from the adder's tongue fer

23 We generated data for all gene copies (homeologs, paralogs, a

24 We generated distinct sets of rules for each age group to cap

25 Here, we generated echovirus 11 (E11) with resistance to chlorine d

26 in development and, in particular, neocortical development, we generated forebrain-specific Foxp1 conditional knockout mi

27 ssect how the microbiota contributes to tumor distribution, we generated germ-free (GF) Apc(Min/+) and Apc(Min/+) ;Il10(-

28 Using CRISPR/Cas9, we generated HID-1 KO rat neuroendocrine cells, and we show t

29 We generated Huh7 cell lines which ectopically express wild-t

30 n results from genetic variation or non-genetic mechanisms, we generated human iPSCs from monozygotic twins to investigat

31 We generated iPSC-derived cardiomyocytes from patients presen

32 ANCI is also involved in these FANCD2-dependent mechanisms, we generated isogenic FANCI-, FANCD2- and FANCI:FANCD2 double

33 t the physiological relevance of noncanonical TR signaling, we generated knockin mice with a mutation in the TR DNA-bindi

34 matically study the expression and function of H1 subtypes, we generated knockin mouse lines in which endogenous H1 subty

35 In this study, we generated metatranscriptomic libraries from actively growi

36 e of hepatocyte NAD levels from any systemic effects of NR, we generated mice overexpressing nicotinamide phosphoribosylt

37 To examine its role in endothelial cell (EC) biology, we generated mice with catalytic inactivation of one SHIP2 al

38 To test the role of Gank in degradation of CUGBP1, we generated mice with liver-specific deletion of Gank.

39 In this study, we generated Nf123aIN/23aIN mice, in which the splicing signa

40 When p53-compromised NCCs were transformed with N-Myc, we generated primitive neuroectodermal tumors with divergent

41 injecting mouse PSCs into Pdx-1-deficient rat blastocysts, we generated rat-sized pancreata composed of mouse-PSC-derive

42 In the present study, we generated recombinant versions of two highly conserved Lei

43 To address this deficit, we generated samples of a wild-type GPCR (A2AR) that are deut

44 To further address this issue, we generated Sco1hrt/hrt and Sco1stm/stm mice in which Sco1 w

45 Using the DEKK format, we generated the bispecific antibody MCLA-128, targeting huma

46 ected the organellar genomes of photosynthetic green algae, we generated the complete plastid genome (plastome) and mitoc

47 ic coiled-coil bundle and an Fc-binding Protein A fragment, we generated the Hex nanocarrier that is efficiently internal

48 To better understand the secoiridoid biosynthesis pathway, we generated transcriptome sequences from the root, leaf, ste

49 he functional and biochemical consequences of this variant, we generated transgenic zebrafish models expressing wild-type

50 In this study, we generated Zwitch, a Cre-dependent invertible gene-trap cas