ライフサイエンスコーパス: clam

1 tors, and all 20 amino acids required by the clam.

2 ands from each KChIP1 form each shell of the clam.

3 ed surface and encloses one side of the beta-clam.

4 ts is opposite to the closed end of the beta-clam.

5 missible cell derived from a single original clam.

6 different as giant squid and microscopic pea clams.

7 hemocytes and adductor muscle from leukemic clams.

8 ar activity (E2-C) has also been observed in clams.

9 ic primary production in the form of lucinid clams.

10 uitinated proteins during heat stress in CWD clams.

11 a serious population decline of soft-shelled clams.

12 row forward scattering cone similar to giant clams.

13 phere-based assay for mussels, scallops, and clams.

14 as differentially expressed in intersex male clams.

15 chinoids, but not brachiopods and laternulid clams.

16 cellular symbiosis with insects and deep-sea clams.

17 uding corals, jellyfish, anemones, and giant clams.

18 The in vitro-expressed clam AHR exhibited sequence-specific interactions with a

19 ion analysis using either in vitro-expressed clam AHR or clam cytosolic proteins showed that this AHR

20 Phylogenetic analysis shows that the clam AHR sequence groups within the AHR subfamily of the

21 gen-binding hemoglobins from human, soy, and clam also trap HNO to form adducts which are stable over

22 in CTVT, DFTD, and as well as the soft-shell clam and Syrian hamster, can advance studies of tumor bi

23 elices located on opposite sides of the beta-clam and three flexible loops.

24 Clams and biofilm samples were also removed from the con

25 Clams and biofilms accumulated the most nanoparticles on

26 ed assays and confirmed its FRAP, ORAC, beta-CLAMS and PCL values to be 79.95 mumol AAE/g DW, 1544 mu

27 Our results suggest that clams and scallops are unlikely to acclimate to ocean ac

28 Methylmercury concentrations in clams and snails also declined with productivity, and co

29 Molluscs (snails, octopuses, clams and their relatives) have a great disparity of bod

30 seful for identification of the two kinds of clams and to assess their nutritional characteristics.

31 e cancers, and these affect dogs, soft-shell clams, and Tasmanian devils, respectively.

32 These clam archives can increase our understanding of the ther

33 her the increase in thermal tolerance in CWD clams are due to genetic adaptation and/or phenotypic pl

34 Filter feeders, like mussels and clams, are suitable bioindicators of environmental pollu

35 amelea gallina of indigenous origin, whereas clams breeding is supported almost entirely by the Tapes

36 The clam Calyptogena magnifica lives at abyssal depths in as

37 We show that the predicted cytochrome P450 ClaM catalyzes the dimerization of nataloe-emodin to cla

38 onoclonal antibodies raised against isolated clam centrosomes, we have identified a novel 135-kD cent

39 We present CLAM (CLIP-seq Analysis of Multi-mapped reads).

40 mples evaluated (mussels, scallops, oysters, clams, cockles) nor interference from other shellfish to

41 ta californiensis and an invasive freshwater clam Corbicula fluminea to reduce concentrations of the

42 sel Anodonta californiensis and the invasive clam Corbicula fluminea.

43 degrees C per day) were assessed in invasive clams Corbicula fluminea from two pristine populations a

44 using either in vitro-expressed clam AHR or clam cytosolic proteins showed that this AHR homologue b

45 Vesicomyid clams depend entirely on sulfur-oxidizing endosymbiotic

46 3-dependent mechanism may be involved in the clam disease.

47 0, which shares 61% amino acid identity with clam E2-C and can substitute for clam E2-C in vitro.

48 Dominant-negative clam E2-C and human UbcH10 proteins, created by altering

49 r, the molecular identity of Xenopus UBCx or clam E2-C has not been established.

50 entity with clam E2-C and can substitute for clam E2-C in vitro.

51 al structure of the cyclin-specific Ubc from clam, E2-C, determined at 2.0 A resolution.

52 In clam eggs, this process is catalyzed by a cyclin-selecti

53 following fertilization of echinoid and also clam eggs.

54 Future characterization of the ClaM enzyme should facilitate engineering the biosynthes

55 A 21-year strontium/calcium record of two clams from 9 degrees50'N on the East Pacific Rise captur

56 egrees C) lethal temperature thresholds than clams from the pristine areas.

57 Several species of the Asian clam genus Corbicula reproduce via androgenesis.

58 CWD clams had considerably higher (by ~8-12 degrees C) letha

59 Clams have long been a fisheries and aquaculture sector

60 nterface of mammalian Hbs or the contacts in clam Hb where the E and F helices form the interface.

61 s are complexed in the cytoplasm of leukemic clam hemocytes (and not in normal hemocytes).

62 Based on these data, we introduce leukemic clam hemocytes as novel and easily accessible, in vivo a

63 We show that leukemic clam hemocytes have an intact p53 pathway, and that main

64 In addition, treatment of leukemic clam hemocytes with MKT-077, a cationic inhibitor of mor

65 and truncated variant, 620-fold above normal clam hemocytes) of human mortalin, an Hsp70 family prote

66 In untreated leukemic clam hemocytes, p53 is complexed throughout the cytoplas

67 In leukemic clam hemocytes, wild-type p53 and mortalin proteins co-l

68 ts localization in the cytoplasm of leukemic clam hemocytes.

69 of p53, and results in apoptosis of leukemic clam hemocytes.

70 toplasm with overexpressed variants for both clam homologues (full-length variant, 1,200-fold and tru

71 These clams host chemoautotrophic bacterial symbionts in their

72 These estimates are conservative; removal by clams in Connecticut, oysters and clams in New York, and

73 removal by clams in Connecticut, oysters and clams in New York, and denitrification are not included.

74 Therefore, Asian hard clam is an excellent source of several nutrients, which

75 ic studies have proposed that the intertidal clam, Lasaea, is one of a few animal groups with asexual

76 The Antarctic clam Laternula elliptica lives almost permanently below

77 study used a tractable model, the Antarctic clam, Laternula elliptica, which can live for 36 years,

78 Soft shell clam leukemia provides excellent in vivo and in vitro mo

79 s suum and the other from the sulfide-fixing clam Lucina pectinata, are compared with respect to conf

80 egulation by human MDM2, suggesting that the clam may have an mdm2 homologue.

81 Further studies of these gene products in clams may reveal p53/p73-related molecular mechanisms th

82 The single cysteine (Cys 51) in isolated clam (Mercenaria) RLC was labeled with an indanedione sp

83 uding foot, mantle and viscera of Asian hard clam (Meretrix lusoria) harvested from the coast of Anda

84 congruent with the host genealogy, based on clam mitochondrial cytochrome oxidase subunit I and larg

85 Perutz proposed a version of the clam model in which the distal histidine swings out of t

86 formation generally consistent with the beta-clam motif described for members of the lipid-binding pr

87 onal fold that includes an antiparallel beta-clam motif.

88 ation of human L-FABP shows the typical beta-clam motif.

89 , mature cordgrass, juvenile northern quahog clam, mud snails, and grass shrimp.

90 In nature the soft shell clam Mya arenaria develops a fatal neoplasm that shares

91 th Atlantic, most prominently the soft shell clam Mya arenaria, are afflicted with an epidemic transm

92 p) S19 from a marine bivalve, the soft-shell clam (Mya arenaria), and we have examined its pattern of

93 utative p53 gene (Map53) from the soft-shell clam (Mya arenaria).

94 n tissues from normal and leukemic softshell clams (Mya arenaria).

95 opy number in neoplastic cells of soft-shell clams (Mya arenaria).

96 In nature, the soft shell clam, Mya arenaria, develops a fatal blood cancer in whi

97 AHR homologue was cloned from the soft-shell clam, Mya arenaria.

98 biquitination and destruction of cyclin B in clam oocyte extracts.

99 Surf clam oocytes are an attractive model to approach this pr

100 In the germinal vesicles of clam oocytes at prophase of meiosis I, p62 binds to the

101 Previously, we reported that in clam oocytes, cytoplasmic polyadenylation element-bindin

102 rt the purification and cloning of E2-C from clam oocytes.

103 ally to one another, thus exhibiting a "beta-clam" or "beta-sandwich" fold: beta-sheet 1 is comprised

104 Core sequence of the predicted clam p53 (Map53) and p73 (Map73) proteins is virtually i

105 Predicted sequences for human and clam p53 proteins exhibit conservation in key domains.

106 The levels of clam PABP are constant in early embryogenesis, although

107 tate-methanol extract of the venerid bivalve clam Paphia malabarica led to isolation of three unprece

108 d consisting of phytoplankton/filter feeding clam, periphyton/grazing snail, and leaves/shredding amp

109 1.2 (Chironomidae larvae), 107 +/- 4.5 (pea clams Pisidium sp.), 131 +/- 105 (three-spined stickleba

110 hark prey and, via a trophic cascade, caused clam populations to crash.

111 netic tree; Figure 1); Bivalvia (mussels and clams), protected by shells and practically immobile; an

112 aggregation of polyglutamine, a mutant beta-clam protein, and protein L, we determined parameter val

113 egation of a slow-folding mutant of the beta-clam protein, cellular retinoic acid-binding protein I (

114 Clam proteins have either a short (Map53) or long (Map73

115 lams Venerupis philippinarum, and littleneck clams Protothaca staminea, Enteroctopus dofleini solved

116 CLAM provides a useful tool to discover novel protein-RN

117 CLAM recovered a large number of novel RNA regulatory si

118 Examination of hemolymph of diseased clams revealed high levels of reverse transcriptase acti

119 Globally, the Manila clam (Ruditapes philippinarum) stands as the second most

120 uced by bacteria harbored in soft tissues of clams (Ruditapes philippinarum), collected in high Hg po

121 Just one clam sample showed the presence of oxytetracycline at a

122 idelines, and applied it to 50 mussel and 50 clam samples derived from various Food and Agricultural

123 the dimeric hemoglobin (HbI) from the blood clam Scapharca inaequivalvis is mediated primarily by te

124 ing in the dimeric hemoglobin from the blood clam Scapharca inaequivalvis results primarily from tert

125 The complex reveals a clam-shaped dimeric assembly.

126 three beta-strands on the bottom half of the clam shell and the establishment of the native hydrogen

127 These sugars are known to crystallize in a clam shell conformation.

128 s B-G, mostly located on the top half of the clam shell structure, propagate from this hydrophobic co

129 inding mode essentially within the same beta-clam shell structure.

130 ding protein family, members of which have a clam shell type of motif formed by two five-stranded bet

131 e) domain and a large helical domain form a "clam shell" that buries the GDP molecule.

132 protein activation may involve "opening the clam shell" to facilitate GDP dissociation.

133 stin-2 results also suggest that there is no clam shell-like closure of the N- and C-domains and that

134 We find that, although barrel and clam-shell drops have different shapes, these conditions

135 nstance, it is unclear under what conditions clam-shell drops would move from the tip towards the roo

136 circular dichroism, to demonstrate that the clam-shell model is correct.

137 vironment, water drops with either barrel or clam-shell shapes are capable of self-running on conical

138 ly unchanged, contrary to expectations of a "clam-shell" model.

139 model of adsorption that involves an unusual clam-shell-like unhinging of the protein at an interface

140 thic suspension feeder Rangia cuneata (wedge clam) showed seasonal avoidance of toxin ingestion due t

141 ment, sea grass, microbes, biofilms, snails, clams, shrimp and fish.

142 ceans are represented by fairy, tadpole, and clam shrimps (Anostraca, Notostraca, Laevicaudata, Spini

143 up or crown-group Anostraca, Notostraca, and clam shrimps or Cladoceromorpha [8-10], which differ mor

144 analyzed the MSTN gene (Sc-MSTN) from razor clam (Sinonovacula constricta).

145 ABP in the early developmental stages of the clam Spisula solidissima.

146 library of RNAs extracted from isolated surf clam (Spisula solidissima) centrosomes, we describe a gr

147 solated centrosomes from oocytes of the surf clam, Spisula solidissima, and purified from them a uniq

148 cently been confirmed in oocytes of the surf clam, Spisula solidissima.

149 ation, is present in each oocyte of the surf clam, Spisula solidissima.

150 e for the future molecular breeding of razor clam strains.

151 ighlighted the important role of the lucinid clam symbiosis in maintaining the health and productivit

152 forward-scattering behavior of the Tridacnid clam system are reported, which presents the first geome

153 omyidae (Bivalvia: Mollusca) are a family of clams that form symbioses with chemosynthetic gamma-prot

154 heir native range, in the case of the Manila clam this has not resulted in new invasion waves in the

155 cid-binding protein (I-FABP) exhibits a beta-clam topology comprised of two five-stranded antiparalle

156 domain is not a required element of the beta-clam topology of I-FABP.

157 netic structure with the reported history of clam transfers across continents, and no evidence of rel

158 prisms, propellers, 2-solenoid, super-roll, clam, trefoil and box are not widely distributed and wer

159 CLAM uses an expectation-maximization algorithm to assig

160 , freshwater mussels (Unionoida), and marine clams (Veneroida) is the only known exception to the gen

161 en prey of mussels Mytilus trossulus, Manila clams Venerupis philippinarum, and littleneck clams Prot

162 duals representing eight species of deep-sea clams (Vesicomyidae) were examined for variation consist

163 High thermal tolerance of CWD clams was associated with overexpression of heat shock p

164 To demonstrate the utility of CLAM, we applied it to a wide range of public CLIP-seq/R

165 % of annual inputs, which would be higher if clams were included.

166 Buk2 folds like an open-shelled clam, with each of the two domains representing one of t