ライフサイエンスコーパス: channel catfish

1 965 Gb, approximately the genome size of the channel catfish.

2 istinct regions of the forebrain (FB) in the channel catfish.

3 related L5 cDNAs, L5a and L5b, were found in channel catfish.

4 6 and S27, for which two cDNAs were found in channel catfish.

5 fficiency of selective breeding programs for channel catfish.

6 ctional divergence of oocyte TFIIIA from the channel catfish.

7 have been identified in Ictalurus punctatus (channel catfish), a well characterized immunological mod

8 The channel catfish alpha-actin gene is associated with two

9 This approach may produce growth-enhanced channel catfish and increase productivity.

10 This opsin, identified in channel catfish and termed parapinopsin, defines a new g

11 Most ribosomal protein mRNAs in channel catfish are highly similar to their mammalian co

12 Most 40S RPs in channel catfish are highly similar to their orthologues

13 Peripheral waves (PWs) in the channel catfish are odorant-induced neural oscillations

14 s derived from peripheral blood cells of the channel catfish, as well as on lymphocyte-like cells, bu

15 role in the activation and proliferation of channel catfish B cells.

16 persistence study, LSU-E2 was able to invade channel catfish by the immersion route and persist in in

17 t the transcription of the Cec B promoter in channel catfish cells exhibited an inducible pattern and

18 termine the phenotypes of cytotoxic cells in channel catfish, clonal alloantigen-dependent leukocyte

19 Outbred populations of channel catfish contained an average of eight alleles pe

20 235 unique genes matched previously reported channel catfish ESTs while 847 (44.4%) ESTs representing

21 The hybrid catfish produced by crossing channel catfish females with blue catfish males exhibit

22 e form at a dose of 8x10(7) CFU/g and fed to channel catfish for 14 days before they were challenged

23 and substitute the preferred codon usage of channel catfish for the native sequences of the genes.

24 Microsatellite loci were identified in channel catfish gene sequences or random clones from a s

25 Functional categorization of the channel catfish genes indicated that the largest group w

26 fish genome, and opens ways for facilitating channel catfish genetic enhancement and functional genom

27 A genetic linkage map of the channel catfish genome (N = 29) was constructed from two

28 A genetic linkage map of the channel catfish genome (N=29) was constructed using EST-

29 9 is a highly efficient tool for editing the channel catfish genome, and opens ways for facilitating

30 ermaid and Merman elements exist per haploid channel catfish genome, respectively.

31 a cDNA that codes for a granzyme homologue, channel catfish granzyme-1 (CFGR-1), from nonspecific cy

32 Ictalurus punctatus (channel catfish) granzyme cDNA encodes a protein with ap

33 Ictalurid herpesvirus 1 (channel catfish herpesvirus [CCV]) is economically very

34 Channel catfish Ictalurus punctatus express two Ig isoty

35 The primary olfactory projections of channel catfish Ictalurus punctatus have been examined w

36 ella ictaluri, a host-restricted pathogen of channel catfish (Ictalurus punctatus) and the main patho

37 osome (BAC) contig-based physical map of the channel catfish (Ictalurus punctatus) genome was generat

38 The Ig heavy chain enhancer of the channel catfish (Ictalurus punctatus) has an unusual pos

39 cond cluster of H chain gene segments in the channel catfish (Ictalurus punctatus) has been determine

40 Previous molecular genetic studies on channel catfish (Ictalurus punctatus) have focused on li

41 The alpha-actin gene of channel catfish (Ictalurus punctatus) was cloned and seq

42 les derived from external taste epithelia of channel catfish (Ictalurus punctatus) were incorporated

43 report multiple CK isoenzymes in the diploid channel catfish (Ictalurus punctatus) with one unusual c

44 ed 32 40S RP complementary DNAs (cDNAs) from channel catfish (Ictalurus punctatus), making them one o

45 t of all 47 60S ribosomal protein cDNAs from channel catfish (Ictalurus punctatus), of which 43 inclu

46 a high-quality reference genome sequence of channel catfish (Ictalurus punctatus), the major aquacul

47 eae family that causes enteric septicemia in channel catfish (Ictalurus punctatus).

48 ermic vertebrate, has been identified in the channel catfish (Ictalurus punctatus).

49 A (cDNA) library made from the brain mRNA of channel catfish (Ictalurus punctatus).

50 cent protein (gfp) as a reporter in cells of channel catfish (Ictalurus punctatus).

51 Here we describe, from a teleost fish (the channel catfish, Ictalurus punctatus), a novel complex c

52 receptors were dissociated from the gills of channel catfish, Ictalurus punctatus, and cultured.

53 nal enhancer (Emu3') of the IgH locus of the channel catfish, Ictalurus punctatus, differs from enhan

54 Channel catfish, Ictalurus punctatus, leukocyte immune t

55 Cas9 was utilized to successfully target the channel catfish, Ictalurus punctatus, muscle suppressor

56 l enhancer (E(mu)3') of the IgH locus of the channel catfish, Ictalurus punctatus, shows strong B cel

57 tion experiments were carried out with naive channel catfish, Ictalurus punctatus, using immobilizing

58 In recent studies in channel catfish, Ictalurus punctatus, we identified 26 d

59 QHCl) and amino acids were identified in the channel catfish, Ictalurus punctatus.

60 tic spinal nerves, in fixed specimens of the channel catfish, Ictalurus punctatus.

61 nsive mortalities and economic losses to the channel catfish industry of the southeast United States.

62 Bacillus strains isolated from soil or channel catfish intestine were screened for their antago

63 Taste bud formation in channel catfish is first seen to occur in stage 39 embry

64 The lateral line system of the channel catfish is formed by mechanoreceptive neuromasts

65 Two genes encode the multiple forms of the channel catfish M-CK cDNAs.

66 identify differentially expressed genes from channel catfish macrophages, a cDNA library from LPS-sti

67 ts the cloning of partial cDNAs encoding the channel catfish orthologues of rhodopsin and the red con

68 nuclei of the secondary gustatory nucleus of channel catfish project to different diencephalic target

69 The channel catfish reference genome sequence, along with tw

70 -dependent T cell lines established from the channel catfish revealed distinctly different TCR beta r

71 Channel catfish skin collagens were typical type I colla

72 Channel catfish skin is a by-product from catfish fillet

73 The cathodic CK isoform existed only in the channel catfish stomach, ovary, and spleen, but not in a

74 4, L14, and L29 are significantly shorter in channel catfish than in mammals due to deletions in the

75 Channel catfish that were vaccinated with a single immer

76 oduce desirable genes from blue catfish into channel catfish through introgression, a genetic linkage

77 l studies indicating that taste responses of channel catfish to L-Arg are mediated by high-affinity r

78 t impart differential temporal regulation of channel catfish virus (CCV) genes, the transcriptional k

79 d that SalHV-1 shares at least 18 genes with channel catfish virus (CCV), a fish herpesvirus whose co

80 gous gynogenetic catfish were immunized with channel catfish virus (CCV)-infected MHC-matched clonal

81 transcripts from the terminal repeat of the channel catfish virus (CCV; also known as ictalurid herp

82 -1) and equine herpesvirus 1 (EHV-1), and of channel catfish virus, an evolutionarily remote herpesvi

83 ar DNA, derived from lymphocytes of juvenile channel catfish, was used to construct lambda libraries

84 As part of our transcriptome analysis of channel catfish, we have analyzed 1909 expressed sequenc

85 Escherichia coli, mammalian COS-7 cells, and channel catfish where it elicited antigen-specific immun