1 Of the 4,
we named 2 patterns "fruit, vegetables, and dairy" and "
2 into a structure with the same topology that
we name (
3 + 1) quadruplex assembly.
3 ariants in both serotypes 33A and 33F, which
we named 33X1 (DeltawciG) and 33X2 (DeltawciG DeltawcjE)
4 cumulated incomplete ribosomal subunits that
we named 45SYphC and 44.5SYsxC particles.
5 ts of a cell-directed adhesion system, which
we name a BM-LINKage (B-LINK), that connects adjacent ti
6 te, derived mutations on this lineage, which
we named A00.
7 a previously uncharacterized protein, which
we name Acm1 (APC/CCdh1 modulator 1).
8 This new gene, which
we name Adh-Twain, resulted from an Adh mRNA that retrot
9 cium-dependent, adipose-specific PLA(2) that
we named AdPLA (adipose-specific phospholipase A(2)).
10 l modifier of the AHR signaling pathway that
we named Ah-receptor associated protein 3 (ARA3).
11 we identify a BBSome-associated protein that
we name alphaTAT1, with a highly specific alpha-tubulin
12 n another homologue of ribonuclease A, which
we named Amphinase (Amph).
13 The first, which
we name Anbu, is sparsely distributed among cyanobacteri
14 es outside of politically relevant research,
we name and give broad descriptions to three questionabl
15 ewly identified site of vulnerability, which
we named antigenic site O.
16 ontrolled by a single biallelic locus, which
we name aphicarus (api), on the X chromosome.
17 vel azide-containing derivative of cisplatin
we named APPA, a cellular pre-extraction protocol and th
18 s these inferred dosage probabilities, which
we name as the dosage-TDT (dTDT).
19 d Tsr1 indicated that the new species, which
we named as A. tanneri, belongs to Aspergillus section C
20 Both proteins, which
we named AtRibF1 and AtRibF2, carry N-terminal extension
21 nannotated gene encoding a tetraspan protein
we named Atthog.
22 isplay of pooled tissue samples, a technique
we name averaged differential expression (ADE).
23 hanical nociception, we identify a gene that
we name balboa (also known as CG8546, ppk26).
24 We have now discovered a BBSome subunit that
we named BBIP10.
25 cteristics of a beta-barrel arrangement that
we named beta-barrel pore-forming Abeta42 oligomers (bet
26 us SJ1 with unusual structural features that
we named bicereucin.
27 ined by four transcriptional biomarkers that
we named BioAge (biological age), Alz (Alzheimer), Infla
28 This novel inhibitor, which
we named "
bislysine", resembles two lysine molecules lin
29 el Ig superfamily transmembrane protein that
we named Borderless (Bdl), as a novel regulator of neuri
30 mospecies 1 comprise a single species, which
we name Borrelia americana sp. nov.
31 ith a single quantitative trait locus, which
we named BOY NAMED SUE, and whose beneficial allele was
32 novel erp Operator 2-binding protein, which
we named BpaB.
33 This phase (which
we name C(3)) is predicted to be thermodynamically stabl
34 escribe here the identification of a protein
we named Caliban, which can directly interact with the H
35 we describe the identification of a compound
we named cambinol that inhibits NAD-dependent deacetylas
36 oth primary and secondary metabolites, which
we named canalization metabolite quantitative trait loci
37 sels through a newly discovered process that
we name "
canalogenesis." Functional inhibition of KDR (V
38 NT5E-2 encodes a shorter CD73 isoform
we named CD73S.
39 PDZ and three C-terminal LIM domains, which
we named chicken LMP-4.
40 tebrates have two Survivin paralogues, which
we name class A and B.
41 One sequence, which
we named Clus1, is not a known TF binding site.
42 This protein, which
we named coaggregation factor A (CafA), is one of 14 cel
43 ain single or multiple microorganisms, which
we named community-based culture collections (CBC).
44 ed previously unknown proteins including one
we named COPR1, for comodulator of PPAR and RXR.
45 e, we identified a transcriptional regulator
we name CosR for compatible solute regulator.
46 This emergent behavior, which
we named cosubstrate compensation (CSC), enables the ETC
47 a MarR family transcriptional regulator that
we named CouR.
48 ip of this second vertebrate CRH gene, which
we name CRH2, to CRH1 (previously known as CRH) and uroc
49 The three V. cholerae sRNAs, which
we name CsrB, CsrC and CsrD, act redundantly to control
50 These novel ORFs, which
we name cylc-1 and -2, share sequence homology with stat
51 One lncRNA, TCONS_00023265, which
we named DACOR1 (DNMT1-associated Colon Cancer Repressed
52 pe lectin of the NK cell receptor group that
we named DC, NK lectin group receptor-1 (DNGR-1).
53 The result is a representation
we name "
deep patient".
54 ratrylenes exhibit a crown conformation that
we named dendritic crown.
55 cted to a previously unknown ascaroside that
we named dhas#18, a dihydroxy derivative of the known as
56 lar leucine-rich repeat (LRR) domains, which
we named DMA-1 (dendrite-morphogenesis-abnormal), promot
57 possess member of the newly identified clade
we named DRB6.
58 second new and highly conserved DRB family (
we named DRB7) whose members possess a single dsRBM that
59 utant with aberrant leaf architecture, which
we named drooping leaf1 (drl1).
60 phila vesicular glutamate transporter, which
we name DVGLUT.
61 encodes a peptide of 34 amino acids and that
we named dwarf open reading frame (DWORF).
62 Two of the five encoded proteins, which
we named E. histolytica ILWEQ (EhILWEQ) and E. histolyti
63 This compound, which
we named EGA, also delays lysosomal targeting and degrad
64 erentiate into another type of colony, which
we name "
Endocrine/Acinar." These Endocrine/Acinar colon
65 r lesions in a hitherto uncharacterized gene
we named Enigma.
66 ases, autoimmunity and alopecia, a condition
we named enteropathy-lymphocytopenia-alopecia.
67 ve identified the key pEtN transferase which
we named EptAPa and characterized its strict activity on
68 In the second case, mutation of a gene
we name ethanol sensitive with low memory (elm), place m
69 One phenovariant, which
we named feeble, showed abrogation of both TLR-induced t
70 Here we present a new approach that
we name '
forensic genomics', combining field surveys, to
71 e from the same A. tumefaciens strain, which
we named Galactarolactone cycloisomerase (At Gci) (E.C.
72 ecedented two-dimensional polyphenylene that
we name graphenylene.
73 se that this GST belongs to a new class that
we name GSTFuA, for fungal specific GST class A.
74 titute a major nucleotide repair system that
we name guanine glycation repair.
75 : hEdc3, Rck/p54, and a protein in decapping
we name Hedls.
76 reductase required for this reduction, which
we named High Arsenic Content 1 (HAC1).
77 ch type of patterned network activity, which
we named "
hippocampal respiration rhythm" (HRR), also oc
78 tly human-tropic polyomavirus species, which
we name HPyV10.
79 and a unique transcriptional regulator that
we named HrtR.
80 ed trihelix transcription factor gene, which
we named HYPOXIA RESPONSE ATTENUATOR1 (HRA1), as highly
81 e formation of a new metastable phase, which
we name Ice 0.
82 genome-engineering platform in hPSCs, which
we named iCRISPR.
83 njugative element (ICE)-encoded DNase, which
we name IdeA, is necessary and sufficient for inhibiting
84 9(+)CD5(+)Thy-1(int)IgM(high)IgD(high)) that
we name "
initiator B cells." Analysis of BCR H chain gen
85 ected in a previously undefined region which
we named intermediate dorsomedial hypothalamus.
86 of iGluR-related genes in Drosophila, which
we name ionotropic receptors (IRs).
87 from the carboxylic to the keto group; thus,
we name it an ol structure.
88 rminal cleavage product of profibrillin, and
we name it Asprosin.
89 as a hypoxia-inducible lncRNA and therefore
we name it LncHIFCAR (long noncoding HIF-1alpha co-activ
90 that it is topoisomerase III, and therefore
we named it "NeqTop3." At high enzyme concentrations, Ne
91 protein is involved in mannan biosynthesis,
we named it 'mannan synthesis-related' (MSR).
92 expression and activity in cultured ECs, and
we named it androgen-dependent TFPI-regulating protein (
93 ndependent of caspase activation; therefore,
we named it caspase-independent mitotic death (CIMD).
94 e 5'-phosphate, and ATP as substrates; thus,
we named it PAPST1.
95 tein of unknown function lacking PPR motifs;
we named it RNA-editing factor interacting protein 1 (RI
96 Duo and Duet and its homology with Quattro,
we named it Solo.
97 que biochemistry and a stable genetic basis,
we named its novel capsule serotype 35D.
98 We named its protein product delangin.
99 , we identified a small drug-like molecule -
we named Kartogenin (KGN) - that greatly stimulates chon
100 BTB/POZ domain and six kelch repeats, which
we named kelch homolog 10 (KLHL10).
101 A pollen-specific protein
we named kinase partner protein (KPP) interacted with th
102 [1,4]oxazin-5-yl)-4-oxobutanoi c acid, which
we named kynoxazine.
103 new lipid droplet-associated proteins, which
we named LDAP1 and LDAP2.
104 Therefore,
we named linc1992 THRIL (TNFalpha and hnRNPL related imm
105 ogs, as well as a third related protein that
we named Liprin-gamma.
106 This lncRNA, which
we named lnc18q22.2 based on its chromosomal location, c
107 fy a novel lncRNA from the X chromosome that
we named lncRHOXF1 and which is abundantly expressed in
108 This RNA, which
we named lncRNA-CMPK2, was a spliced, polyadenylated nuc
109 e the identification of a novel LPCAT, which
we named LPCAT3.
110 The protein encoded by that gene, which
we named LsrS, is a membrane protein belonging to the CA
111 quences revealed three unique prophages that
we named M1T1.X, M1T1.Y, and M1T1.Z.
112 ously unknown isomer of maoecrystal V, which
we named maoecrystal ZG.
113 ceptor-like cytoplasmic kinase (RLCK), which
we named MARIS (MRI).
114 The prion state, which
we name [
MCA], was transmitted to the chromosomally enco
115 the implementation of a new technique, which
we name '
MicroED', that may have wide applicability in s
116 rd family of NKG2DL-like class I genes which
we named MILL (MHC class I-like located near the leukocy
117 (miR-1, miR-133, miR-208, and miR-499) that
we named miR combo.
118 hat HHV-6A encodes at least one miRNA, which
we named miR-U86.
119 This parasite, which
we name Mitosporidium daphniae gen. et sp. nov., possess
120 e, the 2-(methoxycarbonyl)ethenyl group that
we name MocVinyl) serve as protecting groups for the abo
121 ted action of two mutation mechanisms, which
we named Morgan and Sanger mechanisms.
122 Among them, we focused on a lncRNA that
we named MYC-induced long noncoding RNA (MINCR), showing
123 Here we show that Gm7325, which
we name myomerger, induces the fusion of myomaker-expres
124 e discovered a conserved micropeptide, which
we named myoregulin (MLN), encoded by a skeletal muscle-
125 In mice, these transcripts, which
we named myosin heavy-chain-associated RNA transcripts (
126 f the first alpha-N-methyltransferase, which
we named N-terminal RCC1 methyltransferase (NRMT).
127 ule with functional equivalence to NF, which
we name NemF.
128 e identified a novel class of protein, which
we named neuronal pentraxin with chromo domain (NPCD), a
129 roendocrine cells a cytoplasmic process that
we named neuropod.
130 , we discovered a novel nuclear protein that
we named NIAM (nuclear interactor of ARF and MDM2) for i
131 mutations in one gene in this region, which
we named NIPBL, in four sporadic and two familial cases
132 d that they carried mutations in a gene that
we named NO CATALASE ACTIVITY1 (NCA1).
133 rosophila maternal effect-lethal mutant that
we named ;
no poles' (nopo).
134 nterphase nodes and cytokinesis rings, which
we named Nod1.
135 ), Integration Host Factor, and an activator
we name Npa regulate pilE transcription.
136 We identified a novel gene, which
we named off-schedule (ofs), as being essential for this
137 In our scheme, that
we name Optical Pump Rectification Emission, a THz field
138 This procedure, which
we name optimized calibration (OC-LIBS), is a hybrid bet
139 rame (ORF) in the antisense orientation that
we named ORF0.
140 We name our method QOMA (Quasi-Optimal Multiple Alignmen
141 d another OxyR homolog in V. cholerae, which
we named OxyR2, and we renamed the previous OxyR OxyR1.
142 Here we identify a parasite protein, which
we name P. falciparum Merozoite Organizing Protein (PfMO
143 lly, we uncovered a new ompA promoter, which
we named P3, utilizing the GFP reporter system combined
144 We named PA2588 as CdpR (ClpAP-degradation and pathogeni
145 e Mexican frog Pachymedusa dacnicolor, which
we named pachymodulin.
146 The second enzyme, which
we named Pal, converts UDP-6-deoxy-D-GlcNAc-5,6-ene to U
147 ly unidentified green-sensitive opsin, which
we name parietopsin.
148 the first divergence in Neoaves, two groups
we named Passerea and Columbea, representing independent
149 eviously undetected, conserved domain, which
we named PATAN (after PatA N-terminus), and a potential
150 d by the uncharacterized gene YPL272C, which
we name Pbi1p (PstB2p-interacting 1).
151 The first enzyme, which
we named Pen, converts UDP-d-GlcNAc to an uncommon UDP-s
152 Loss-of-function of this gene - which
we named perdido (perd)-results in rounded, unattached m
153 ge reacting with the primers deployed, which
we named Phi8, was more frequent in VTEC O157 strains fr
154 e, we show that a p53-regulated lncRNA which
we named PINCR (p53-induced noncoding RNA), is induced
155 gene plu2096, coding for a novel lectin that
we named PllA.
156 s otherwise unstable bacterial siRNAs, which
we named pro-siRNAs for prokaryotic siRNAs.
157 ed features of a processed pseudogene, which
we named psi1Rac1, that could be detected by Southern bl
158 rogenitor domains within the thalamus, which
we name pTH-R and pTH-C, located caudal to the ZLI.
159 dentify a novel dsRNA-binding protein, which
we named R3D1-L, that forms a stable complex with Dicer-
160 he more potent of these two compounds, which
we named regacin, disrupts the DNA binding capacity of R
161 ptional elongation factor S-II domain, which
we named REPRESSOR OF VERNALIZATION1 (RVR1), represses V
162 nd functionally characterized a snaclec that
we named "
rhinocetin" from the venom of West African gab
163 genes encoding rhoptry neck proteins, which
we named RONs, demonstrated that toxofilin and Rab11 are
164 putative mycobacterial endopeptidase, which
we named Rpf-interacting protein A (RipA).
165 lerae RTX (repeats in toxin) toxin gene that
we named rtxA1.
166 For this reason
we named Rv0190/MT0200 RicR for regulated in copper repr
167 ng that a fourth transcription factor, which
we name Ryp4, is required for yeast-phase growth and gen
168 Divergent strains of this new virus, which
we named salivirus, were detected in 18 stool samples fr
169 dependent screens yielded ORF YDL139C, which
we named SCM3.
170 d LysR-type transcriptional regulator, which
we name ScmR (for secondary metabolite regulator), serve
171 reen yielded a mutant lacking all DRG, which
we named sensory deprived (sdp).
172 omologues of S. bongori sboK and sboC, which
we named seoC SboC and SeoC are homologues of EspJ from
173 tations in KCNJ10 cause this syndrome, which
we name SeSAME.
174 ously uncharacterized pancreatic factor that
we named Shirin.
175 Among those isolated was At5g24740, which
we named SHRUBBY (SHBY).
176 ur model into a MATLAB-based simulation tool
we named Simulation of Temperature Effects on ElectroPho
177 We have identified a novel isoform of Skp2
we named Skp2B, which differs from Skp2 only in the C-te
178 410-derived Sle2 susceptibility locus, which
we named Sle2c2.
179 aling a targeted mode of cell migration that
we named "
slithering," in which cells transiently lose e
180 sent in bacteria, protozoa and plants, which
we named "
SlRd2".
181 The evolved FP, which
we named small ultra-red FP (smURFP), covalently attache
182 The three proteins, which
we name Snd1, Snd2 and Snd3 (for SRP-independent targeti
183 germ-cell-specific transcription factor that
we named Sohlh1 (testis and ovary expressed basic helix-
184 M1 motif in gamma-TuCRs, a second motif that
we named Spc110/Pcp1 motif (SPM) is also important for M
185 ed DNA-binding protein and a nuclease, which
we named SsbP and NucP, respectively.
186 lting in an intimate quaternary complex that
we name SSCAP complex.
187 RNAs) induced by IL-6-activated STAT3, which
we named STAiRs.
188 acting protein from syncytial embryos, which
we named Stepping stone (Sstn).
189 e, sequence-divergent D4 subgenotypes, which
we named subgenotypes D4.1 and D4.2.
190 anum-induced loss of apical dominance, which
we named SUPPRESSOR OF APICAL DOMINANCE1 (SAD1).
191 pentatricopeptide repeat (PPR) protein that
we named SUPPRESSOR OF VARIEGATION7 (SVR7).
192 This gene that
we named syncytin-Mar1 is distinct from all seven Syncyt
193 We identified one such gene, which
we named "
syncytin-Mab1," that has all the characteristi
194 Finally, we show that this gene, which
we named "
Syncytin-Rum1," is conserved among 16 represen
195 This gene, which
we named "
syncytin-Ten1," is conserved among Tenrecidae,
196 One such protein, which
we name T4P secretin-associated protein (TsaP), was iden
197 , confirming the location of this QTL, which
we named tb2r1, on chr.4.
198 modification via alkylation chemistry, which
we name the ALiPHAT strategy (augmented limits of detect
199 scriptional repressor of the suf operon, and
we name the gene sufR.
200 onfined to an anterior narrow segment, which
we name the hindgut proliferation zone (HPZ).
201 how that the C-terminus of mature FHA, which
we name the MCD, mediates adherence to epithelial and ma
202 echanism and chip-based system design, which
we name the microthermophotovoltaic (muTPV) generator.
203 eir similarities in sequences and functions,
we name the ponli and crb2b enhancers collectively rainb
204 We name the protein CAPC, cytokeratin-associated protein
205 racterized glycoprotein outermost layer that
we name the spore crust.
206 We name the tool CRISPR-ERA, for clustered regularly int
207 lecular packing of eight TPRs as a fold that
we name the TPR eddy.
208 ogically identified a novel cell type, which
we named the "ovoidal cell", that receives the convergen
209 related to Royal Family Tudor domains, which
we named the CryptoTudor domain.
210 Cdc42 via a nonconventional GEF module that
we named the CZH2 domain.
211 Thus,
we named the enzyme PUB synthase (PUBS).
212 We named the four lacrimal clones the delta, epsilon, ze
213 ated that a region of facial ectoderm, which
we named the frontonasal ectodermal zone (FEZ), regulate
214 According to the visual and behavioral data,
we named the head-lifting feeding as 'tread-water feedin
215 iation with a previously unknown domain that
we named the host integration motif (HIM).
216 ained an evolutionarily conserved motif that
we named the low zinc activation (LZA) element that was
217 Based on this sequence homology,
we named the molecule mouse cytosolic phospholipase A2ga
218 We named the new enzyme MACase (Macaca Acidic Chitinase)
219 c properties and phylogenetic relationships,
we named the new families OCP2 and OCPx to distinguish t
220 We named the new strain Sclerotinia sclerotiorum hypovir
221 We named the novel peptide "allatotropin-related peptide
222 We named the NRPS product 'equibactin' and genes of this
223 We named the orthologous proteins PvPHIST/CVC-81(95) and
224 Therefore,
we named the peptide vasoconstriction-inhibiting factor
225 We named the product of the yccD gene CbpM for "CbpA mod
226 We named the protein sialostatin L because of its inhibi
227 Consequently,
we named the protein taperin.
228 that of ClpP, but has a unique motif, which
we named the R-motif, forming a beta turn located near t
229 luded disruption of a ribosome-bound complex
we named the Ribosome Quality Control Complex (RQC) comp
230 Based on the observed morphological defects,
we named the two chromatin remodelers MINUSCULE 1 and 2.
231 n (UBL) that exists only in IKKbeta and that
we named the UBL-like domain (ULD).
232 We name them "t-stumps," to distinguish them from the we
233 in the rat were obtained for A, C and E, and
we named them "expression genes 1, 2 and 3, respectively
234 Because they are induced by JA
we named them JASMONATE-INDUCED OXYGENASES (JOXs).
235 IN TARGETING TO STARCH (PTST) protein; thus,
we named them PTST2 and PTST3.
236 Based on the core size,
we named them Xiao ( approximately 30 kb) and DA ( appro
237 We name these families the Ac and Buster families after
238 We name these genes LvHirz and LvIna, respectively.
239 We name these lncRNAs half-STAU1-binding site RNAs (1/2-
240 (T6SS) translocation apparatus; accordingly,
we name these proteins type VI lipase effectors.
241 We named these isoforms "pre-P" by analogy to the pre-C
242 are unrelated to the SAG proteins, and thus
we named these proteins SAG-unrelated surface antigens (
243 ix elements and their original architecture,
we named these structures "linear invadosomes." Interest
244 We name this approach the 'distance to resistance'.
245 In the current study,
we name this cell the "distal Dab1-immunoreactive cell."
246 We name this domain patch assembly domain (PA; residues
247 We name this highly diverse clade the cryptomycota in an
248 We name this interface PCI1 and the previously known nuc
249 We name this motif the NEET fold.
250 We name this new approach the "inverse armed-disarmed" s
251 We name this novel phenomenon splicing-regulated miRNA.
252 We name this order Combresomycetales and note that it pl
253 We name this peptide the "ybbR tag," because part of its
254 phase at low pressures and similar enthalpy (
we name this phase Ih-C(0)).
255 We name this protein Atg36 as its absence blocks pexopha
256 We name this region the phalanx-forming region (PFR), an
257 artial rotation of the gamma subunit; hence,
we name this step k(gamma).
258 We name this superfamily Fusexins: fusion proteins essen
259 We name this technique Inhibition of Synapses with CALI
260 We name this theory density-matrix functional embedding
261 We named this assignment system the gene signature-MELD
262 We named this combination the Gal4 technique for real-ti
263 We named this disinhibition-dementia-parkinsonism-amyotr
264 We named this enzyme P. trichocarpa hydroxyacid/fatty al
265 We named this enzyme SNIP (for snRNA incomplete 3' proce
266 We named this gene IRREGULAR TRICHOME BRANCH1 (ITB1).
267 We named this gene POLYGALACTURONASE INVOLVED IN EXPANSI
268 We named this genetic locus the commensal colonization f
269 We named this mechanism the ETI-Mediating and PTI-Inhibi
270 We named this network Reference Gene Association (RGA) n
271 We named this ORF paratox, determined its allelic distri
272 Therefore,
we named this PAI as Locus of Adhesion and Autoaggregati
273 We named this polyprotein PETs (for polyprotein of EF-Ts
274 Because of its mixed phenotype,
we named this population vascular leukocytes (VLCs).
275 We named this protease SepM for streptococcal extracellu
276 Therefore,
we named this protein Cox interacting (Coi) 1.
277 We named this protein IFN-gamma-inducible SCGB (IIS), be
278 We named this secreted fragment Vasculostatin as it inhi
279 We named this set of rules qMotor because it enables sen
280 We named this subdomain the "A-loop" (aromatic residue i
281 We named this type-C self-association to distinguish it
282 phoesterase domain-containing protein, which
we named "
trafficking of Emp24p/Erv25p-dependent cargo d
283 This phenomenon, which
we named "
TRAIN" (for "transcription of repeats activate
284 under the above described stimulation, which
we named transcranial individual neurodynamics stimulati
285 ed from protein-coding gene promoters, which
we name transcriptional start site miRNAs (TSS-miRNAs).
286 r through gap junction channels, a technique
we named Trojan-local activation of molecular fluorescen
287 ed was a new strain of simian rotavirus that
we named TUCH (for Tulane University and Cincinnati Chil
288 We name two additional new species, Pliosaurus carpenter
289 xial, and a previously undescribed mechanism
we named unipolar.
290 Hand2-associated long non-coding RNA, which
we named upperhand (Uph), is required to maintain the su
291 og and demonstrated that one of these, which
we named "
urumin," is virucidal for H1 hemagglutinin-bea
292 on studies revealed that this complex, which
we named VAIT (respiratory syncytial virus-activated inh
293 Two adaptor proteins are included that
we named VIT [VH1-interacting tetratricopeptide repeat (
294 One effector, which
we named VopX (A33_1663), is conserved only in V. choler
295 We focused on one such transcript that
we name VqmR.
296 g04490, a previously unannotated gene, which
we named VTE5.
297 econd-order somatosensory interneurons, that
we named Wave, whose activation in anterior and posterio
298 CG31665, which
we name weary (wry), has structural similarities to memb
299 n an operon with a small coiled-coil protein
we named ZauP.
300 entified two prominent neoblast classes that
we named zeta (zeta) and sigma (sigma).