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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 5) than that of full-sibling, non-transgenic channel catfish and hybrid catfish.
10    This approach may produce growth-enhanced channel catfish and increase productivity.
11 e of CRISPR/Cas9 HDR for gene integration in channel catfish and may contribute to the generation of
12                    This opsin, identified in channel catfish and termed parapinopsin, defines a new g
13              Most ribosomal protein mRNAs in channel catfish are highly similar to their mammalian co
14                              Most 40S RPs in channel catfish are highly similar to their orthologues
15                Peripheral waves (PWs) in the channel catfish are odorant-induced neural oscillations
16 s derived from peripheral blood cells of the channel catfish, as well as on lymphocyte-like cells, bu
17  role in the activation and proliferation of channel catfish B cells.
18 persistence study, LSU-E2 was able to invade channel catfish by the immersion route and persist in in
19 t the transcription of the Cec B promoter in channel catfish cells exhibited an inducible pattern and
20 termine the phenotypes of cytotoxic cells in channel catfish, clonal alloantigen-dependent leukocyte
21                       Outbred populations of channel catfish contained an average of eight alleles pe
22  15.80 and 24.06% larger than non-transgenic channel catfish control at 4 and 18 months of age, respe
23  americanus (opAFP-ccGH), and non-transgenic channel catfish control.
24 235 unique genes matched previously reported channel catfish ESTs while 847 (44.4%) ESTs representing
25      The hybrid catfish produced by crossing channel catfish females with blue catfish males exhibit
26 e form at a dose of 8x10(7) CFU/g and fed to channel catfish for 14 days before they were challenged
27  and substitute the preferred codon usage of channel catfish for the native sequences of the genes.
28       Microsatellite loci were identified in channel catfish gene sequences or random clones from a s
29             Functional categorization of the channel catfish genes indicated that the largest group w
30 fish genome, and opens ways for facilitating channel catfish genetic enhancement and functional genom
31                 A genetic linkage map of the channel catfish genome (N = 29) was constructed from two
32                 A genetic linkage map of the channel catfish genome (N=29) was constructed using EST-
33 9 is a highly efficient tool for editing the channel catfish genome, and opens ways for facilitating
34 ermaid and Merman elements exist per haploid channel catfish genome, respectively.
35  a cDNA that codes for a granzyme homologue, channel catfish granzyme-1 (CFGR-1), from nonspecific cy
36                         Ictalurus punctatus (channel catfish) granzyme cDNA encodes a protein with ap
37  catfish, channel catfish transgenic for the channel catfish growth hormone (ccGH) cDNA driven by the
38                   The X and Y chromosomes of channel catfish have the same gene contents.
39                     Ictalurid herpesvirus 1 (channel catfish herpesvirus [CCV]) is economically very
40                                              Channel catfish Ictalurus punctatus express two Ig isoty
41         The primary olfactory projections of channel catfish Ictalurus punctatus have been examined w
42 ella ictaluri, a host-restricted pathogen of channel catfish (Ictalurus punctatus) and the main patho
43 in gene into a targeted non-coding region of channel catfish (Ictalurus punctatus) chromosome 1 using
44 osome (BAC) contig-based physical map of the channel catfish (Ictalurus punctatus) genome was generat
45           The Ig heavy chain enhancer of the channel catfish (Ictalurus punctatus) has an unusual pos
46 cond cluster of H chain gene segments in the channel catfish (Ictalurus punctatus) has been determine
47        Previous molecular genetic studies on channel catfish (Ictalurus punctatus) have focused on li
48                      The alpha-actin gene of channel catfish (Ictalurus punctatus) was cloned and seq
49 les derived from external taste epithelia of channel catfish (Ictalurus punctatus) were incorporated
50 report multiple CK isoenzymes in the diploid channel catfish (Ictalurus punctatus) with one unusual c
51 ed 32 40S RP complementary DNAs (cDNAs) from channel catfish (Ictalurus punctatus), making them one o
52 t of all 47 60S ribosomal protein cDNAs from channel catfish (Ictalurus punctatus), of which 43 inclu
53  a high-quality reference genome sequence of channel catfish (Ictalurus punctatus), the major aquacul
54 eae family that causes enteric septicemia in channel catfish (Ictalurus punctatus).
55 ermic vertebrate, has been identified in the channel catfish (Ictalurus punctatus).
56 A (cDNA) library made from the brain mRNA of channel catfish (Ictalurus punctatus).
57 cent protein (gfp) as a reporter in cells of channel catfish (Ictalurus punctatus).
58   Here we describe, from a teleost fish (the channel catfish, Ictalurus punctatus), a novel complex c
59 receptors were dissociated from the gills of channel catfish, Ictalurus punctatus, and cultured.
60 nal enhancer (Emu3') of the IgH locus of the channel catfish, Ictalurus punctatus, differs from enhan
61                                              Channel catfish, Ictalurus punctatus, leukocyte immune t
62 Cas9 was utilized to successfully target the channel catfish, Ictalurus punctatus, muscle suppressor
63 l enhancer (E(mu)3') of the IgH locus of the channel catfish, Ictalurus punctatus, shows strong B cel
64 tion experiments were carried out with naive channel catfish, Ictalurus punctatus, using immobilizing
65                         In recent studies in channel catfish, Ictalurus punctatus, we identified 26 d
66 QHCl) and amino acids were identified in the channel catfish, Ictalurus punctatus.
67 tic spinal nerves, in fixed specimens of the channel catfish, Ictalurus punctatus.
68 hh genes in the developing dorsal fin of the channel catfish, Ictalurus punctatus.
69 nsive mortalities and economic losses to the channel catfish industry of the southeast United States.
70       Bacillus strains isolated from soil or channel catfish intestine were screened for their antago
71                       Taste bud formation in channel catfish is first seen to occur in stage 39 embry
72               The lateral line system of the channel catfish is formed by mechanoreceptive neuromasts
73   Two genes encode the multiple forms of the channel catfish M-CK cDNAs.
74 identify differentially expressed genes from channel catfish macrophages, a cDNA library from LPS-sti
75 ts the cloning of partial cDNAs encoding the channel catfish orthologues of rhodopsin and the red con
76 nuclei of the secondary gustatory nucleus of channel catfish project to different diencephalic target
77                                          The channel catfish reference genome sequence, along with tw
78 -dependent T cell lines established from the channel catfish revealed distinctly different TCR beta r
79                                              Channel catfish skin collagens were typical type I colla
80                                              Channel catfish skin is a by-product from catfish fillet
81  The cathodic CK isoform existed only in the channel catfish stomach, ovary, and spleen, but not in a
82 4, L14, and L29 are significantly shorter in channel catfish than in mammals due to deletions in the
83                                              Channel catfish that were vaccinated with a single immer
84 oduce desirable genes from blue catfish into channel catfish through introgression, a genetic linkage
85 l studies indicating that taste responses of channel catfish to L-Arg are mediated by high-affinity r
86 mance among the channel-blue hybrid catfish, channel catfish transgenic for the channel catfish growt
87 t impart differential temporal regulation of channel catfish virus (CCV) genes, the transcriptional k
88 d that SalHV-1 shares at least 18 genes with channel catfish virus (CCV), a fish herpesvirus whose co
89 gous gynogenetic catfish were immunized with channel catfish virus (CCV)-infected MHC-matched clonal
90  transcripts from the terminal repeat of the channel catfish virus (CCV; also known as ictalurid herp
91 -1) and equine herpesvirus 1 (EHV-1), and of channel catfish virus, an evolutionarily remote herpesvi
92 was 384.9% and their non-transgenic controls channel catfish was 352.6%.
93 percentage body weight gain of GH transgenic channel catfish was 559%, the channel-blue hybrid catfis
94    Condition factor of transgenic opAFP-ccGH channel catfish was higher (P < 0.05) than that of full-
95 ar DNA, derived from lymphocytes of juvenile channel catfish, was used to construct lambda libraries
96     As part of our transcriptome analysis of channel catfish, we have analyzed 1909 expressed sequenc
97               However, transgenic opAFP-ccGH channel catfish were 5.52 and 43.41% larger than channel
98 Escherichia coli, mammalian COS-7 cells, and channel catfish where it elicited antigen-specific immun