ライフサイエンスコーパス: companion paper

1 new genes: Gpr65, Plzp, Toso, and Cd5l (in a companion paper).

2 ) and food as unconditional stimulus (US) [ (companion paper)].

3 brovascular risk factors is the subject of a companion paper.

4 chromatography (IC), which is discussed in a companion paper.

5 as based on studies described in a preceding companion paper.

6 article is part of a Special Issue entitled Companion Paper.

7 sional cellular microscopy, described in the companion paper.

8 ta-analysis papers are discussed in the next companion paper.

9 comparison of arms A and B is described in a companion paper.

10 mer's Disease Genetic Consortium (ADGC) in a companion paper.

11 comparison of arms A and C is described in a companion paper.

12 hes, EMG sites and motor units reported in a companion paper.

13 ctivity of KatG is addressed here and in our companion paper.

14 investigated and discussed in the following companion paper.

15 nd high-hroughput AMS measurement are in the companion paper.

16 e algorithms and parameters discussed in the companion paper.

17 for the preparation of AHA is presented in a companion paper.

18 of the DURS2 phenotype, as described in the companion paper.

19 n alternative route to AHA is presented in a companion paper.

20 of the selected sequences is described in a companion paper.

21 d in vitro, and the data are reported in the companion paper.

22 entatively identified as cytokeratin 18 in a companion paper.

23 ucture of wild-type HPPK as described in the companion paper.

24 ribution of ejecta blocks are discussed in a companion paper.

25 ies of the 'ponds' are discussed in a second companion paper.

26 and propriospinal input was examined in the companion paper.

27 g the forward and backward potential sweeps (companion paper 1), the semiempirical treatment here, wh

28 agenic activity results are presented in our companion paper.1 The results show that ELCR values for

29 tatistical analysis approach, presented in a companion paper (10.1021/acs.analchem.9b01325), to relia

30 in complex with both enzymes described in a companion paper, (34) provides a rationale for the obser

31 om Facebook, building on the analysis in our companion paper(7).

32 We have presented in a companion paper a suppressor-based electrodialytic buffe

33 re variation across genes and species in our companion paper, and here we explore variation within in

34 This outcome is evaluated further in a companion paper appearing later in this journal.

35 o be a source of confusion.Dual Perspectives Companion Paper: Are the Neural Correlates of Consciousn

36 In a companion paper both mutants are shown to be deficient i

37 Along with a companion paper by Livraghi et al., we argue that ivory,

38 A companion paper by McClintock, printed and bound back-to

39 In the companion paper by Ufimtsev and Levitt [Ufimtsev IS, Lev

40 Indeed, in a companion paper, Christopher Mahoney and colleagues perf

41 A companion paper comes to similar conclusions on the basi

42 Our companion paper describes the performance of the model f

43 A companion paper describes the thalamic connections of CM

44 The companion paper () describes two neurophysiological corr

45 A companion paper discusses several other utilitarian attr

46 based on traditional views.Dual Perspectives Companion Paper: Diverse Spatiotemporal Scales of Cholin

47 The companion paper (DOI: 10.1021/jm100060b) describes how t

48 Evidence is provided in a companion paper for an IL-7-associated molecular complex

49 anding of ACh in the brain.Dual Perspectives Companion Paper: Forebrain Cholinergic Signaling: Wired

50 In a companion paper from the same authors, the spine generic

51 A companion paper has brought forward an innovative approa

52 ype method for amino acids, developed in the companion paper in this issue of the Journal, are used.

53 A companion paper in this issue provides details on demogr

54 of aging-associated variables reported in a companion paper in this issue) and targeted replication

55 free and DNA-bound forms is presented in the companion paper in this issue.

56 xperiments complement those presented in the companion paper in which binding and protonation of CH3-

57 Two companion papers in this Series specify policy actions a

58 lyse new data, presented in more detail in a companion paper, in which BrdU/IdU cell-labelling experi

59 ations for its utilization.Dual Perspectives Companion Paper: Integrating CRISPR Engineering and hiPS

60 matic studies reported in this article and a companion paper of theoretical calculations of the nanog

61 Co-authors may also want to consult our companion paper on ten simple rules for leading a many-a

62 ng therapies in the future.Dual Perspectives Companion Paper: Parkinson's Disease Is Not Simply a Pri

63 As reported in a companion paper (Piperno DR, et al., in this issue of PN

64 A companion paper presents a detailed study of how labware

65 ence that Slit is the midline Robo ligand; a companion paper presents biochemical evidence that Slit

66 This is the second of two companion papers proposing priority problems for researc

67 The companion paper provided evidence that patch-controlled

68 detergent or chaotropic conditions, but our companion paper provides strong evidence to the contrary

69 ut the etiopathology of PD.Dual Perspectives Companion Paper: Prying into the Prion Hypothesis for Pa

70 This work is accompanied by a companion paper (Pt.2/2).

71 lation of gene expression was described in a companion paper published in this journal, using flux-ba

72 A companion paper, Renson et al. 2025 (AJE, kwaf169) provi

73 (Companion papers report on the plasma, magnetic field, p

74 f our genetic humanization approach, and the companion paper reports that the humoral immune systems

75 promising research avenues.Dual Perspectives Companion Paper: Should a Few Null Findings Falsify Pref

76 and an antibody-stabilized active structure (companion paper) shows how binding events at both the ex

77 progress in drug discovery.Dual Perspectives Companion Paper: Studying Human Neurodevelopment and Dis

78 er results, some of which are presented in a companion paper, suggest that DspA acts as a global regu

79 een GluR6Q and GluR2Q(flip), reported in the companion paper, suggests that at a glutamate concentrat

80 urinary signals that can be quantified by a companion paper test.

81 We showed in the companion paper that a member of the cadherin family (ze

82 We show in the companion paper that the free membrane shape of lipid bi

83 p and a YAC-based physical map reported in a companion paper, the fundamental maps required for mouse

84 In a companion paper, the method is applied to data from the

85 In two companion papers, the model developed herein has been ap

86 consistent with bioaccumulation results in a companion paper (this issue) observed for amphipods.

87 consistent with bioaccumulation results in a companion paper (this issue) using a microbial bioreport

88 In a companion paper (this issue), we reported that repeated

89 chimeric mice with deletion of Tssk1 and 2 (companion paper) this centriolar kinase/substrate pair i

90 and the gp32 monomer-binding results of the companion paper to propose a detailed model for how gp32

91 In the companion paper to this work, we described development o

92 In this issue of Genes & Development, two companion papers (Trakala and colleagues [pp.

93 A companion paper uses pre-explosion images to rule out lu

94 A further companion paper was published in Human Molecular Genetic

95 In the companion paper we apply a model extension to investigat

96 In a companion paper we demonstrate that the C-rich strand of

97 In our companion paper we developed a 3D human atrial myocyte m

98 ms." Their contributions are summarized in a companion paper we have written to introduce the Special

99 In the companion paper we reported that Bacillus subtilis requi

100 In a companion paper we use growth data from lake trout (Salv

101 In these two companion papers we introduce a new approach to the anal

102 As we describe in the companion paper, we attempted to make mice that more eff

103 In a companion paper, we demonstrate that mutations at a diff

104 In an accompanying companion paper, we demonstrate the applicability of our

105 In the companion paper, we demonstrate the utility of F(n)()Ys

106 In a companion paper, we found that the evolutionary emergenc

107 In a companion paper, we identified a novel CK2 site adjacent

108 In a companion paper, we provided indirect evidence that cell

109 In a companion paper, we reported a data integration methodol

110 In a companion paper, we reported that the goldfish oculomoto

111 In a companion paper, we show that spontaneous release from t

112 In a companion paper, we show that these defects can be mimic

113 In a companion paper, we study the contributions of linker hi

114 In the companion paper, we used the virtual space (VS) techniqu

115 In this first of two companion papers, we analyze the natural sources of lumi

116 In these two companion papers, we introduce a new approach to the ana

117 In two companion papers, we present a list of problems nominate

118 ysical properties (with the exception of the companion paper where Tapia et al. demonstrate a direct