ライフサイエンスコーパス: similarit(y|ies) (to|with)

1 proteins on its surface that have structural similarities to a protein crucial for invasion of red bl

2 m Chryseobacterium meningosepticum, indicate similarities to a superfamily phosphate diesterase [Xant

3 The weed has morphological similarities to a wild relative of maize and has general

4 l structure for HopBA1 and found that it has similarity to a class of proteins that includes esterase

5 ndem repeat domain that shares high sequence similarity to a non-syntenic zebrafish analog, cat7l Def

6 y N-terminal domain that has high structural similarity to a recently discovered motif present in sev

7 ith an extended series of PAMs with chemical similarity to A-867744, TBS-516, and TQS suggests that a

8 e nonrepeat region, one of which shares some similarity with a carbohydrate binding module.

9 drug-target prediction based on topological similarity with a heterogeneous network, and may be read

10 , AAD3 shares the highest degree of sequence similarity with AAD2 and AAD4.

11 tide (IAPP), a peptide which shares sequence similarity with Abeta.

12 graded, displaying some superficial chemical similarities to abiotic meteoritic organic matter) are r

13 In spite of its structural similarity to acetylcholine, there are no other reports

14 genesis factor PGC-1alpha falling, and shows similarities to adapted Tibetan highlanders.

15 rough a disulfide bond, revealing structural similarities with ADP regulation in the human ACOT12 thi

16 As hiPSC-BAPs display similarities with adult-BAPs, it opens new opportunities

17 L-ORD shows striking phenotypic similarities to age-related macular degeneration (AMD),

18 tudy, ORF52 shares functional and structural similarities with alphaherpesvirus VP22, underscoring th

19 Finally, we demonstrate pathological similarities to Alzheimer's disease, such as altered Tau

20 The new species also displays some similarities with amynodontids in craniodental structure

21 , whereas the C-terminal domain has sequence similarity to an FMN-dependent family of nitroreductase

22 2092, 2061 and 2117 amino acids (93% average similarity to An. gambiae).

23 ess of this approach in detecting functional similarity with an average F-score: 0.85.

24 designing polymers which have no structural similarities to antifreeze proteins but reproduce the sa

25 MnxE and MnxF have no similarity to any characterized proteins.

26 an evolutionary isolate with no discernible similarity to any other human protein.

27 genase of S. thermoautotrophicus have little similarity to anything found in draft genome sequences,

28 f TGSQA expression, a tulip gene with a high similarity to Arabidopsis APETALA1 Gene Ontology enrichm

29 Cr-UVR8 shares sequence and structural similarity to Arabidopsis thaliana UVR8, has conserved t

30 ava whole-genome sequence and their sequence similarity with Arabidopsis TCPs.

31 ly secreted proteins shared highest sequence similarity with archaeal and fungal enzymes, which peak

32 base crAssphage genome showed no significant similarity to available protein sequences, precluding cl

33 omes with substantial structural and genetic similarity to bacteria.

34 roteins specific to Lh VLPs possess sequence similarities with bacterial secretion system proteins.

35 Because of its sequence similarity to Bax and Bak, Bok has long been considered

36 +) cells with close molecular and functional similarity to beta cells.

37 enetic cause, despite clinical and molecular similarity to bone morphogenetic protein receptor type 2

38 This new form has similarities to both the vetulicolians and vetulocystids

39 N1-Src is poorly understood and its high similarity to C-Src has made it difficult to delineate i

40 ia, of which 12% shared the highest sequence similarity with candidate phyla (10,11) .

41 to identify proteins in kinetoplastids with similarity to canonical outer kinetochore proteins, sugg

42 biquitin ligase RNF146 that shows phenotypic similarities to CCD.

43 Based on similarities with Cdk2 3D structure, the Cdk9 peptide cr

44 ted phosphoproteins with greatest functional similarity to CDK2 substrates, particularly proteins inv

45 ons in quality of life and survival and have similarities to certain malignancies.

46 ers as templates but these have low sequence similarity to CFTR and are not ion channels.

47 At the same time, distinct similarities with chiral supramolecular and biological s

48 share morphological, biochemical, or genetic similarities with classic necrosis, necroptosis, parthan

49 The data identify similarities with classical chemokine-receptor interacti

50 class-I aminoacyl-tRNA synthetases with high similarities to consensus amino acid sequences of human

51 High percent similarities to consensus subtype C Gag, p17, p24, and p

52 o exist filter sequences based on nucleotide similarity to contaminants and risk eliminating sequence

53 s arising at the same time suggest lifestyle similarity to crocodiles.

54 is of ergothioneine in EgtB shows structural similarities to cysteine dioxygenase which transfers two

55 Despite antigenic similarities with dengue viruses, structural studies hav

56 DFT2 bears no detectable cytogenetic similarity to DFT1 and carries a Y chromosome, which con

57 reening based on protein interaction profile similarity to discover new targets for molecules, includ

58 The mutations observed here share similarities with disease-causing, complex, large-scale

59 ontrast, DOCK5, which possesses the greatest similarity to DOCK1, remains sparingly studied.

60 domain in HgGLAND18 contains unique sequence similarity to domains of an immunosuppressive effector o

61 but lower levels in the mPFC; a pattern with similarities to dopamine dysbalance in schizophrenia.

62 Issues such as the similarity to downhill folding as well as the interpreta

63 from chemoinformatics (i.e., pharmacological similarity with drugs of known fetal effect) and empiric

64 ermore, the PHP-exonuclease shows a striking similarity to E. coli endonuclease IV, which provides cl

65 s and their siblings had more vocal sequence similarity with each other than with non-sibling infants

66 plant evolution and exhibits more functional similarity with eIF4G than with eIFiso4G1 during Omega-m

67 dynein arm assembly factors show structural similarities to either Tah1 or Pih1, the other two compo

68 erma genus and Xyl2 contained a protein with similarity to endo-1,4-beta-xylanase.

69 lity of cancer cell lines is affected by the similarity to endogenous tumour cells.

70 decarboxylase-dehydrogenase enzyme with high similarity to enzymes that form epoxyketones.

71 Leptospira licerasiae-which shares sequence similarity to eukaryotic CNG and HCN channels-in the pre

72 uble helical filaments that show exceptional similarity to eukaryotic F-actin.

73 hese effectors share structural and sequence similarity with eukaryotic proteins.

74 Exposure therapy bears similarity to extinction learning.

75 ences for attractive faces result from their similarity to facial prototypes, the categorical central

76 CAs display similarities with FAs but are established in an integrin

77 light contained few major proteins, one with similarity to ferritin.

78 Although FLNb shows high amino acid sequence similarity with FLNa, we reveal that only FLNa, but not

79 ark, sleep/wake and meal schedule, which has similarities to flying west or sleeping in the daytime a

80 matics predictions that suggested structural similarity to folliculin, the Birt-Hogg-Dube syndrome tu

81 ed by the upper and lower jaws, bearing some similarity to fossil traces interpreted as footprints.

82 ngle nanoparticle level, which reveal marked similarities to foundational principles of polymerizatio

83 ated mechanism of dissociation, which shares similarities with fragment types produced in electron de

84 hway in Catharanthus roseus showing distinct similarity to gamma-tocopherol C-methyltransferases was

85 es in the gymnosperm Pinus taeda shared some similarities with gbM genes in Amborella trichopoda.

86 Sequence similarity to genes characterized in previous studies id

87 for these traits in pigeonpea have sequence similarity to genes functionally characterized in other

88 Because of its structural similarity to glucose, genetic studies of 1,5-AG can del

89 which identified a parvovirus with a greater similarity to goose parvovirus (GPV) (97% protein homolo

90 -HLA-F bound to the inhibitory LIR1 revealed similarities to high-affinity recognition of the viral M

91 xhibit striking qualitative and quantitative similarities with histology (e.g., using Sholl analysis)

92 lade HD-Zip I TFs share significant sequence similarities with homologous genes from other plants, th

93 Our findings have similarities with how life-history strategies are struct

94 resource due to their incidence and striking similarities to human cancers, sharing similar clinical

95 Given the key similarities to human infection, a marmoset model of ZIK

96 c carcinomas with histological and molecular similarities with human disease.

97 These data combined with physiological similarities with human roseoloviruses collectively sugg

98 pecialization of platelets shares remarkable similarities with human-engineered unmanned aerial vehic

99 40-amino acid peptide showing high sequence similarity to human (93%), mouse (93%), and Xenopus (88%

100 lls with NOTCH overexpression, and molecular similarity to human tumors was observed, demonstrating t

101 s been shown to share a variety of metabolic similarities with humans.

102 Similarity to humans has motivated research into nonhuma

103 icate the dynamics of liquid water have more similarities to ice than previously thought.

104 rson's correlation analysis, and peak height similarity to identify ion adducts, duplicate peak repor

105 ument is made that the former has electronic similarities to indole.

106 to widespread human exposure, and structural similarities with known endocrine disruptors, concerns h

107 ule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure-a

108 cterial fucose-specific lectins that have no similarity to known bacterial fucose-binding proteins, b

109 Many of the ASF virus genes lack similarity to known genes and have not been characterize

110 potential colibactin binding site and shares similarity to known hydrolases.

111 d because both Izumo1 and Juno lack sequence similarity to known membrane fusogens.

112 x-bladed beta-propeller fold bearing limited similarity to known paramyxoviral attachment glycoprotei

113 virus (ASFV) genome do not have significant similarity to known proteins and have not been studied e

114 d similarity and 3D pharmacophoric and shape similarity to known selective tau aggregate binders iden

115 n additional 8 ORFans (non-host RNAs with no similarity to known sequences).

116 newest NHEJ factor, which shares structural similarity with known NHEJ factors-XRCC4 and XLF.

117 Despite close similarities with late-onset Alzheimer's disease, indivi

118 This condition has similarities to living "hook-and-pull" digging mammals a

119 in the Vi antigen biosynthesis locus shares similarity with LpxL, an acyltransferase from lipid A bi

120 ls and showed transcriptional and phenotypic similarities to lymphoid Tfh cells, and hence representi

121 We identified cells with morphological similarities to M1 and M2 cells described previously in

122 The structure of this domain revealed high similarity to mammalian deubiquitinases with a unique al

123 ke gene in lampreys exhibits higher sequence similarity with mammalian BAFF than APRIL.

124 Rapid embryogenesis, together with genetic similarities with mammals, and the desire to reduce mamm

125 tistical method to quantify a CRM's sequence similarity to many different training sets of CRMs, and

126 responses in mammalian cells and surprising similarities with mechanisms in yeast that deal with DSB

127 Similarity with memory athlete connectivity patterns pre

128 H1/17 cells have gene signatures with marked similarity to mouse pathogenic TH17 cells.

129 Of note, these sequences bear no similarity to mucin 1 except that they also contain a pa

130 IDH1 mice showed many molecular and clinical similarities to muIDH1 human gliomas, including a 100-fo

131 demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from div

132 lass 27 myosin, TgMyoF, which has structural similarity to myosin V, the prototypical cargo transport

133 els of cellular complexity and physiological similarity to native organ systems.

134 Individuals with 22q11DS share overarching similarities with ND individuals in psychosis symptoms a

135 tion patterns, time of emergence and genetic similarity to Near Eastern populations are highly sugges

136 Emphasizing the similarity with Nef, we show that S2 is myristoylated, a

137 not NKT2 and NKT17 cells, had transcriptome similarity to NK cells and were also similar to other IF

138 Many, but not all, of these changes share similarities to normal older animals.

139 disorder with clinical and histopathological similarity to OB, represents the leading cause of long-t

140 interference that bears striking conceptual similarity to oligoadenylate signalling in mammalian inn

141 arranged on a hexagonal grid based on their similarity to one another in the original genomic space

142 coelacanths) does tetherin exhibit sequence similarity to one potential sister gene.

143 axonomic units showed the strongest sequence similarity to Ophiocordyceps, Verticillium, Pseudallesch

144 teraction and its structural and fingerprint similarities to other compounds belonging to the differe

145 odel for cell walls in general, as it shares similarities with other cell wall proteomes while also c

146 sease burden profiles differed; India showed similarities with other developing countries (around 50%

147 Some of these features share similarities with other LCD-related neurodegenerative di

148 aucoma is a chronic disease that shares many similarities with other neurodegenerative disorders of t

149 It has similarities with other viral proteins through which DNA

150 udomonas FliD exhibits unexpected structural similarity to other flagellar proteins at the domain lev

151 9,174-nt-long genome showed limited sequence similarity to other known viruses.

152 , over 90% of which has significant sequence similarity to other legumes.

153 f Ara h 15 was determined that displays high similarity to other seed-derived oleosins.

154 ture and immature ZIKV have demonstrated its similarity with other known flaviviruses such as dengue

155 part of the spiralian organizer and suggest similarity with other metazoan organizers.

156 MnxG shares sequence similarity with other, structurally characterized MCOs.

157 ions) are discussed on the basis of observed similarities with our studied terrestrial chemistry.

158 share a surprising degree of transcriptional similarity with pancreatic beta cells, and expression of

159 and glucosylsphingosine, demonstrating their similarity to patients with Gaucher disease.

160 a sulfated peptide named RaxX, which shares similarity to peptides in the PSY (plant peptide contain

161 value-based decisions, explain the apparent similarity to perceptual decisions, and predict conditio

162 errhenate, an anion of great physicochemical similarity to pertechnetate, both having uses in nuclear

163 ositional role for Hofstenia muscle and this similarity with planarians suggests mesodermal muscle or

164 n the GREENC and CANTATA databases indicated similarity with plant long non-coding RNAs (lncRNAs) inv

165 1OHI3M) and that IGMT5, a gene with moderate similarity to previously characterized IGMTs, encodes th

166 oducts being published today bear structural similarity to previously published compounds, and that t

167 vated abundance of a cyanomyophage with high similarity to previously sequenced isolates known to inf

168 epidemic (Makona) shares significant genetic similarity with previously identified variants (Kikwit a

169 ic characteristics of these cells, and their similarities to primary islet alpha and beta cells, are

170 NpL2 cells have physiological similarities to primary neurons, representing a novel an

171 Thy1(+)LSK cells share significant molecular similarities with primary CD34(+) cells from PMF patient

172 and bulk expression profiling revealed their similarity to primary ALL cells isolated from pediatric

173 ides cluster products, reporting of sequence similarity to proteins encoded in experimentally charact

174 CelTOS is unknown because it lacks sequence similarity to proteins of known function.

175 lete and partial genomes showing no sequence similarities to public databases.

176 subphenotypes or if Cpc-PH shares molecular similarities to pulmonary arterial hypertension (PAH).

177 Cpc-PH bears similarities to pulmonary arterial hypertension.

178 ggering a signaling cascade that shares some similarities to responses to well-known elicitors such a

179 The transcription profiles reveal extensive similarity to retrograde signaling initiated by partial

180 larity to S. halichoeri CCUG 48324(T), 97.9% similarity to S. canis ATCC 43496(T), and 97.8% similari

181 rRNA gene sequencing analysis revealed 98.6% similarity to S. halichoeri CCUG 48324(T), 97.9% similar

182 ilarity to S. canis ATCC 43496(T), and 97.8% similarity to S. ictaluri ATCC BAA-1300(T).

183 protein with two cysteine residues and weak similarity to secreted proteins of other fungi.

184 vironments containing organisms with limited similarity to sequenced genomes, are needed.

185 cles by thermolysis, due to their structural similarities with silica materials.

186 mphipathic helix and exhibits 42% amino acid similarity with SM N100.

187 The method has formal similarities to so-called partially balanced incomplete

188 lly occurring neurodegenerative disease with similarities to some forms of amyotrophic lateral sclero

189 te its remarkable architectural and sequence similarities to spider silk fibroins, indicating that AS

190 ies a novel immunodeficiency with phenotypic similarities to STAT3 hyper-IgE syndrome caused by loss

191 distal to the imatinib binding pocket, show similarities to structural transitions involved in kinas

192 first recognized behavioral addiction, with similarities to substance use disorders but without the

193 a Plasmodium berghei protein with structural similarities to subtilisin-like proteins.

194 ared 98.6%, and 98.5% 16S rRNA gene sequence similarities to Sulfurospirillum multivorans.

195 icate that, although SynDIG4 shares sequence similarity with SynDIG1, it might act through a unique m

196 otic GVHD has clinical and histopathological similarities with systemic sclerosis, an autoimmune dise

197 The enzyme exhibits striking biochemical similarity to TaqII.

198 e being most pronounced for stimuli with low similarity to targets (p = 0.006).

199 The T. musculi KHC1 homolog showed high similarity with TbKHC1.

200 The modulation by serotonin has qualitative similarities with that for a decrease in stimulus contra

201 The gut microbiota of Atlantic salmon showed similarities with that of mammals.

202 mponent (270-450 ms) was found, which showed similarities with that of prior studies on auditory and

203 obic oxidation of aldehydes shares important similarities with that one of the recently revisited ben

204 ident in the zebrafish gut mucosa, in marked similarity to that found in the intestine of mammals.

205 The behavior of T c bears similarity to that of a regular 3D population imbalanced

206 of canthaxanthin oxidation bears significant similarity to that of beta-carotene.

207 n alpha1A/betaIII microtubules shows overall similarity to that of heterogeneous brain microtubules,

208 etermined, shows a high degree of structural similarity to that of human ADS lyase.

209 he stepwise mechanism of the reduction shows similarities to the Birch reduction known from organic c

210 A protein with similarities to the Ca(2+)/ calmodulin dependent protein

211 Arabidopsis (Arabidopsis thaliana) that has similarities to the cysteine-rich zinc-binding domain of

212 atio of 31 +/- 9 and demonstrated structural similarities to the gray matter distribution on conventi

213 This reaction has similarities to the H2 + H2(+) mechanism leading to form

214 Similarities to the hairpin ribozyme cleavage loop activ

215 otype of indeterminate PALF shares important similarities to the hyperinflammatory state characterist

216 ion on cellular stress and reveal functional similarities to the mammalian system.

217 P surface and spike-tip protein, p40, reveal similarities to the needle-tip invasin proteins SipD and

218 The NS5 structure has striking similarities to the NS5 protein of the related Japanese

219 The mechanism obtained has large similarities to the one suggested by spectroscopy, with

220 These findings have striking similarities to the pathological abnormalities reported

221 We find striking similarities to the unrelated Chlamydiales, suggesting c

222 Together, WarA and WarB have structural similarities with the bifunctional Escherichia coli lipo

223 m tens of thousands of 12-ns stimuli and the similarities with the conventional stimulation prove VGS

224 tive analyses reveal sequence and structural similarities with the distant Acidobacteria LexA protein

225 d epidermal cells of hornworts show striking similarities with the earliest plant fossils.

226 ceptor that shares structural and functional similarities with the family of atypical chemokine recep

227 fied pathway suggests intriguing mechanistic similarities with the initial mitochondrial-mediated ste

228 ce: Inflammatory pathways of psoriasis share similarities with the mechanisms identified in atheroscl

229 sordered H2 molecules, and shows topological similarities with the mineral quartz.

230 newly identified shear-NO oscillator shares similarities with the well-known Van der Pol oscillator,

231 signature of the pseudogap that bears close similarity to the analogous studies of the pseudogap in

232 xpected outcome given their close structural similarity to the antiandrogenic drug nilutamide.

233 pts a 6-bladed beta-propeller structure with similarity to the classic sialidase fold, but it has no

234 ea directly track the gradient of perceptual similarity to the conditioned stimulus in healthy indivi

235 rsion model coupled with PCA-LDA showed high similarity to the designed microbiota structure, with no

236 ably, the pyridine synthases show structural similarity to the elimination domain of lanthipeptide de

237 ed apelin receptor, despite lack of sequence similarity to the established ligand apelin.

238 ized peptidomimetics that bear no structural similarity to the established TLR4 ligand, lipopolysacch

239 Based on their geomorphic similarity to the features observed in our laboratory ex

240 intestinal organoids (HIOs) with remarkably similarity to the fetal intestine in cellular compositio

241 We then re-rank genes by their similarity to the given gene set, based on a second rand

242 high sequence (48% identity) and structural similarity to the GRE-type glycerol dehydratase from Clo

243 portion of the active site shows structural similarity to the GTP-binding site of MoaA, suggesting t

244 of a four-alpha-helix bundle with structural similarity to the high mobility group box, a domain that

245 Additionally, we observed similarity to the human phenotype of short stature and s

246 This enzyme shows a strong structural similarity to the human phosphatases of regenerating liv

247 psis, no predicted proteins with significant similarity to the known ADPR cyclases have been reported

248 was an unfolded, compact monomer with little similarity to the native structure.

249 ore accurate incidence maps showing a closer similarity to the observed incidence distribution, and p

250 l proteins that have no and distant sequence similarity to the ones used for training, receptively.

251 ower replicative ability as well as a higher similarity to the population consensus (in this case HIV

252 rtical topography, individual stability, and similarity to the primate AR organization link ARC1 to t

253 We identified two factors with limited similarity to the Rap sporulation proteins of other spor

254 rmed on the model results demonstrating good similarity to the real data.

255 ost all eubacteria and plants, with sequence similarity to the RecA strand exchange protein and a rol

256 limited by the fact that only sequences with similarity to the reference genome are examined.

257 hybrid-like structure containing regions of similarity to the structures of BoNT/A1 and BoNT/F5.

258 This complex shows surprising similarity to the tandem dsRBDs from an adenosine-to-ino

259 spectra of driver genes in cancer show high similarity to the tissue-specific ASC mutation spectra,

260 gh expression of epithelial cell markers and similarity to the transcriptome for intrapulmonary airwa

261 n hair cells by negative pressure, with some similarity to the transduction current, persists in TMC

262 ion corresponded to increased neural pattern similarity with the average pattern associated with that

263 encoded by Fsd2, that has extensive sequence similarity with the C-terminus of myospryn.

264 y, an internal region of Mcc shares sequence similarity with the central domain of the prion protein,

265 otein of HAdV-C5 contains a region of strong similarity with the clip region of the known portal prot

266 CSF and IL-2, without sharing any structural similarity with the cytokine receptors.

267 They also show similarity with the earlier Iron-Age genome, suggesting

268 Phylogenetic analysis demonstrated high similarity with the ELO of Tribolium castaneum and Droso

269 era of a snail AChBP, which has 71% sequence similarity with the extracellular ligand-binding domain

270 gent H5N6 viruses, which share high sequence similarity with the human isolate A/Guangzhou/39715/2014

271 been proposed that reconcile the Earth-Moon similarity with the inferred heterogeneous nature of Ear

272 lity, resident species with a high catabolic similarity with the invader efficiently reduced the inva

273 is a dynamical phase transition that shares similarity with the plastic depinning transition occurri

274 icantly shorter and share almost no sequence similarity with the S. cerevisiae homolog.

275 ts is assessed by comparing the kernel-based similarity with the similarity in the trait using a scor

276 rphological mosaic with differences from and similarities to their western contemporaries.

277 ngal dockerin and scaffoldin domains have no similarity to their bacterial counterparts, yet several

278 , but surprisingly, they exhibit no sequence similarity with their RSV equivalents.

279 alogs, but the toxin does not share sequence similarity with these nucleases and lacks the characteri

280 hibit remarkable morphological and molecular similarities to those in mammals.

281 me of ccr1 ProSNBE:CCR1 still exhibited many similarities to those of ccr1 mutants, regardless of the

282 These fungal biofilms share many similarities with those of bacteria, including the prese

283 files in diabetic versus healthy dogs shared similarities with those reported in human T1D (e.g., alt

284 hat the protein shares intriguing structural similarity to ToxA from the wheat pathogen Pyrenophora t

285 lative to untreated rat liver shows striking similarity with toxicant-exposed cells in vivo, indicati

286 uring the postictal phase that show striking similarity to transient hypoxic/ischemic attacks.

287 Domain A, which exhibits structural similarity to tRNA, appears to be an essential core of t

288 Sequence similarities with tropomyosin and myosin from mollusks w

289 ions during singing correlated with acoustic similarity to tutor syllables, suggesting a process of o

290 ons of Izumo1 display significant structural similarities to two proteins expressed by the invasive s

291 B1 exhibits a remarkable degree of similarity to vaccinia virus-related kinases (VRKs), a f

292 protoplasmic networks also show a degree of similarity to vehicular transport networks.

293 d contigs with predicted amino acid sequence similarities to viruses in the nonredundant protein data

294 nce of chords is predicted by their relative similarity to voiced speech sounds.

295 RIFMO shares moderate sequence similarity with well characterized flavoprotein monooxyg

296 conformers has surprisingly high structural similarity with wild-type Abeta42.

297 Xyl1 contained three proteins with similarity to xylanase family 10, 62 and anarabinofurano

298 y domains with high amino acid compositional similarity to yeast prion domains.

299 the Y in all species examined, yet sequence similarity to YG2 is not detectable in the genome of a m

300 ls a double-wing structure indicating strong similarities with ZrZn2 and UGe2.