ライフサイエンスコーパス: zinc finger

1 ng to GC bases as reported for the wild-type zinc finger.

2 a DNA-binding residue in the first of three zinc fingers.

3 cation, confirming a functional role for the zinc-fingers.

4 ted that the transcription factor GLI family zinc finger 1 (GLI1) mediates Sulf2 expression during HC

5 of the stem cell-expressed genes GLI family zinc finger 1 (Gli1) or achaete-scute homolog 1 (Ascl1).

6 ce transcription factors, VASCULAR PLANT ONE-ZINC FINGER 1 (OsVOZ1) and OsVOZ2, and promotes their de

7 ulation, which expresses the Teashirt family zinc finger 1 (Tshz1) and belongs to the direct pathway,

8 al transcription factor vascular endothelial zinc finger 1 (VEZF1) as a direct target of miR-483-3p.

9 Vascular endothelial zinc finger 1 (VEZF1) plays important roles in endotheli

10 ed for CTCF binding to its cognate DNA site: zinc finger 1 (ZF1) or zinc finger 10 (ZF10).

11 The transcription factor GLI1 (GLI family zinc finger 1) plays a key role in the development and p

12 stochemistry staining for Glis1 (GLIS family zinc finger 1) was conducted in developing heart of mice

13 e for the transcription factor MZF1 (myeloid zinc finger 1).

14 We have subsequently identified Tandem Zinc Finger 1, encoding a processing body localized RNA-

15 show that combined biallelic Cebpa and Gata2 zinc finger-1 (ZnF1) mutations cooperatively induce bili

16 its cognate DNA site: zinc finger 1 (ZF1) or zinc finger 10 (ZF10).

17 We found that zinc fingers 11-13 are necessary and sufficient for DNA

18 GLI family zinc finger 2 (GLI2) coordinates the Hh transcriptional

19 ese results suggest an active role for GATA3 zinc finger 2 mutants in ER-alpha positive breast tumors

20 memory retrieval-associated increases in BLA zinc finger 268 (zif268) and activity regulated cytoskel

21 that PCFU self-renewal requires GLIS family zinc finger 3 (GLIS3), a zinc-finger transcription facto

22 iginal alpha-helical segment in the Cys2His2 zinc finger 3 of transcription factor Egr1 (also known a

23 g three distinct targeted mutations of A20's zinc finger 7 (ZF7) ubiquitin-binding motif uniformly de

24 odule within KDM2A consisting of a CXXC type zinc finger, a PHD domain and a newly identified Heteroc

25 te that, in addition to binding DNA, PRDM9's zinc fingers also mediate its multimerization, and we sh

26 but coincided in upregulation of a DHHC-type zinc finger and an aspartyl protease gene, possible cand

27 ZBTB7C encodes the Zinc Finger and BTB Domain Containing 7C, a transcriptio

28 Zinc finger and BTB domain containing transcriptional re

29 n thermogenic gene activation and identified zinc finger and BTB domain-containing 7b (Zbtb7b) as a p

30 The ZZ-type zinc finger and EF-hand domain protein 1 (ZZEF1) is a mu

31 nsertion at the C-terminus of the C-terminal zinc finger and has no observable activity.

32 In this study, we investigate the role of Zinc finger and SCAN domain containing 4 (ZSCAN4) in hum

33 ly contacts U1 snRNA at the Sm site with its zinc finger and traps snRNP biogenesis intermediates in

34 e., KLF4, KLF6, PLZF (promyelocytic leukemia zinc finger), and KLF15, are induced in TG neurons early

35 The zinc finger antiviral protein (ZAP) binds regions of vir

36 The zinc finger antiviral protein (ZAP) depletes cytoplasmic

37 Here, we look into one such factor: zinc finger antiviral protein (ZAP) inhibits a variety o

38 Zinc finger antiviral protein (ZAP) is a powerful restri

39 The cellular antiviral protein ZAP (zinc finger antiviral protein) binds CpGs and inhibits H

40 en using small inhibitory RNAs revealed that zinc-finger antiviral protein (ZAP) inhibited virion pro

41 Previously, we identified a zinc-finger antiviral protein ZAP that is commonly downr

42 The MDMX acidic domain and zinc finger are necessary and sufficient for binding and

43 this geometry are enriched in genomes where zinc fingers are prevalent and specificity transitions w

44 DNA binding activity of the rapidly evolving zinc finger array of PRDM9 (PR domain zinc finger protei

45 iplets of otherwise adjacent fingers in each zinc-finger array.

46 gnal amplifier in BCCs with implications for zinc finger-based signal transduction and therapeutics.

47 A canonical DNA-zinc finger binding model predicts that 3 of the variant

48 Variation in the gene encoding zinc finger binding protein 804A (ZNF804A) is associated

49 TAGGGAA-3') and encompasses a Myc-associated zinc finger-binding site that regulates KRAS transcripti

50 plex, Tramtrack, and Bric-abrac/poxvirus and zinc finger (BTB/POZ) transcription factor family and ma

51 ted uniquely at 48 hpi and genes involved in zinc finger CCCH protein, glycosyltransferase, 1-aminocy

52 ovel RNA-binding protein interactors ZC3H14 (zinc finger CCCH-type containing 14) and THOC1 (THO comp

53 is coselected with the U12 splicing factor, zinc finger CCCH-type, RNA binding motif, and Ser/Arg ri

54 onal change process, revealing that a unique zinc finger (CCCH) in VP2 acts as the major low pH senso

55 The highly conserved zinc finger CCCTC-binding factor (CTCF) regulates genomi

56 The zinc finger CCCTC-binding protein (CTCF) carries out man

57 m-resolution crystal structure of human CCHC zinc finger-containing protein ZCCHC4, a 28S rRNA-specif

58 OSTERIX, an OB-specific zinc finger-containing transcription factor is for the f

59 The highly basic second zinc finger contains a pocket that selectively accommoda

60 Specifically, the 4 zinc fingers create a basic patch on the hZAP RBD surfac

61 d polyadenosine RNA-binding protein, ZC3H14 (Zinc finger CysCysCysHis domain-containing protein 14),

62 etase Long Chain Family Member 5 (ACSL5) and Zinc Finger DHHC-Type Containing 6 (ZDHHC6), was charact

63 Here, we identified zinc finger DHHC-type containing 7 (DHHC7) protein as an

64 of 25 kDa) is mediated by a subset of Golgi zinc finger DHHC-type palmitoyltransferase (zDHHC) enzym

65 on SbMATE expression arise from a WRKY and a zinc finger-DHHC transcription factor (TF) that bind to

66 rm upregulates BTV mRNA translation, whereas zinc-finger disruption decreases viral mRNA translation,

67 transcription regulators with a well-defined zinc finger DNA-binding domain and there is evidence tha

68 This complex, comprised of the zinc finger DNA-binding protein PRDM9 and the SNF2 famil

69 and both its physical interaction to GR and zinc finger domain appear to be required for ZNF764 to r

70 The N-terminal zinc finger domain enhances HDA15HD dimerization and inc

71 DD8 trimer, specifically bound to the second zinc finger domain of PARP-1 and attenuated its activati

72 omodimers, or forming a heterodimer with the zinc finger domain of UNC-10/RIM (C2A/RIM).

73 PRMT3, we found that ZNF277 uses a C2H2-type zinc finger domain to recognize uS5.

74 of OsWRKY45 (OsWRKY45-DBD, i.e. the WRKY and zinc finger domain) in complex with a W-box DNA.

75 catalytic SET domain and an intervening MYND zinc finger domain, as well as an extended C-terminal do

76 glycoprotein, non-structural protein with a Zinc-Finger domain and a nucleoprotein.

77 a forms a two-site interaction with the GLI1 zinc-finger domain and acetylation site, stabilizing an

78 ZNF281 binds XRCC4 through its zinc-finger domain and facilitates its recruitment to da

79 (CBD) directly interacts with the N-terminal zinc-finger domain of CLAMP.

80 packed against N-terminal GRF-type and C2H2 zinc finger domains and a C-terminal CCHC domain, creati

81 transcription factors that contain conserved zinc finger domains involved in binding to target DNA se

82 Pra1, known to interact selectively with the zinc finger domains of Piccolo.

83 vivo and in vitro through their conserved C-zinc finger domains.

84 the highly conserved C-terminal DNA-binding zinc finger domains.

85 Zinc finger E-box binding homeobox 1 (Zeb1) has been dem

86 s with CRISPR/Cas9-mediated depletion of the zinc finger E-box binding homeobox 1 (ZEB1) in claudin-l

87 to hypoxia because carbonic anhydrase IX and zinc finger E-box binding homeobox 1 (Zeb1) protein leve

88 Zinc finger E-box binding homeobox 1 (ZEB1), primarily s

89 transcription factors SRY-box 10 (SOX10) and zinc finger E-box binding homeobox 2 (ZEB2).

90 ZEB1 and ZEB2 are zinc-finger E homeobox-binding transcription factors bes

91 The GATA3 zinc fingers efficiently bind their target 5'-GAT-3' seq

92 Located on chromosome 5A, B1 is a C2H2 zinc finger encoding gene with ethylene-responsive eleme

93 Previous studies have suggested that the zinc-finger epithelial-mesenchymal transition transcript

94 tanding of how a single mutation in the KLF1 zinc finger exerts effects on erythroid physiology in CD

95 n synthesis were detected at lower rates and zinc finger family transcripts were of poorer quality.

96 ctor 6 (KLF6), a transcription factor of the zinc finger family, regulates lipid homeostasis in clear

97 a transcription factor from the Kruppel-like zinc finger family.

98 Very few other members of the zinc finger FYVE domain-containing family (zfyve) have d

99 mbryo polarity rests on a previously unnamed zinc finger gene (cucoid), or pangolin (dTcf), respectiv

100 4D imaging of pri-miR430 and zinc-finger-gene activities by a novel, native transcrip

101 in Kruppel-associated box domain-containing zinc finger genes on chromosome 19, both of which are as

102 n Sonic hedgehog (SHH) signaling, GLI family zinc finger (GLI)-mediated diverse gene transcription ou

103 Bcd1, an essential zinc finger HIT protein functionally conserved in eukary

104 Zinc finger HIT-type containing 1 (Znhit1) is an evoluti

105 This analysis also revealed roles for zinc-finger homeobox domain and SOX2-interacting genes i

106 of the TSHZ3 gene, encoding for the teashirt zinc-finger homeobox family member 3 (TSHZ3) transcripti

107 ein-RNA complex containing the N-terminal, 4-zinc finger human (h) ZAP RNA-binding domain (RBD) and a

108 lving the sixth PHD domain and its preceding zinc finger in MLL3 and MLL4 specifically recognizes an

109 )S double mutation, which disrupts both CCHC zinc fingers in the NC domain, does not abrogate Alix-me

110 The zinc-finger in ZBTB24 binds PARP1-associated poly(ADP-ri

111 dimerization of CESA6 through its N-terminal zinc finger is critical in defining its functional prope

112 The Cys2His2 zinc finger is the most common DNA-binding domain expand

113 needs to be functional, only one of the two zinc fingers is folded.

114 Two zinc-finger-like motifs are present in each NS1 monomer,

115 alysis provides evidence that the engineered zinc finger motif adopts a folded structure in which the

116 phosphates but involves interactions with a zinc finger motif in the Sin3-associated protein 30 (SAP

117 s stimulate HDAC activity and that the SAP30 zinc finger motif performs roles similar to that of the

118 could directly bind TOR mRNA via its tandem zinc finger motif to affect TOR mRNA stability.

119 Further analyses show that only three zinc finger motifs are essential for PAR recognition.

120 is NEIL3 C terminus has two highly conserved zinc finger motifs containing GRXF residues (designated

121 Disruption of the zinc finger motifs in GATA-1, such as produced by germli

122 an cells revealed that intact PIN domain and Zinc finger motifs in human hUTP23 are essential for 18S

123 arsenic interacts with the N- and C-terminal zinc finger motifs of GATA-1, causing zinc loss and inhi

124 onserved cysteine-rich motifs reminiscent of zinc finger motifs.

125 shift assays showed that wild-type, but not zinc-finger mutant ZFP36L1, bound to HIF1A 3'UTR and med

126 s define a temporal expression window of BTB-zinc finger nuclear protein, Mamo.

127 rat expressing the G551D variant obtained by zinc finger nuclease editing of a human complementary DN

128 The zinc finger nuclease method was used to establish rat li

129 n T1D, we targeted Ubash3a in NOD mice using zinc-finger nuclease mediated mutagenesis.

130 developed a novel Bace1(-/-) rat line using zinc-finger nuclease technology and compared Bace1(-/-)

131 Using zinc-finger nuclease technology to engineer an integrati

132 an approach for improving the specificity of zinc finger nucleases (ZFNs) that engineers the FokI cat

133 iew, we introduce the three central methods, zinc finger nucleases (ZFNs), transcription activator-li

134 ccurring nucleases, including meganucleases, zinc finger nucleases, and transcription activator-like

135 ry and development of DNA-editing nucleases (Zinc Finger Nucleases, TALENs, CRISPR/Cas systems) has g

136 go, first with meganucleases and followed by zinc finger nucleases, transcriptional activator-like ef

137 to enable such high-precision targeting with zinc-finger nucleases (ZFNs), we have developed an expan

138 genome editing proteins, Cre recombinase and zinc-finger nucleases, under conditions in which (-30)GF

139 The CDA mutation is in the second zinc finger of KLF1 at a position functionally involved

140 strate how a missense mutation in the second zinc finger of Kruppel-like factor-1 (KLF1) leads to deg

141 The structure of the second zinc finger of SALL4 in complex with pomalidomide, cereb

142 rol genes that include homologs of mammalian Zinc finger of the cerebellum and Purkinje cell protein

143 sis likely through replacing zinc within the zinc fingers of the critical transcription factor GATA-1

144 5 causal missense variants in or near IKZF5 zinc fingers, of which 2 occurred de novo and 3 co-segre

145 estored by C-terminal fusion with ETO's NHR4 zinc-finger or the repressor domain 3 of N-CoR, while ot

146 tors, and express the promyelocytic leukemia zinc finger (PLZF) transcription factor that distinguish

147 transcription factor Promyelocytic Leukemia Zinc Finger (PLZF).

148 ve confirmed that speckle-type pox virus and zinc finger (POZ) protein (SPOP) functions as a substrat

149 The Kruppel-associated box zinc finger protein (KRAB-ZFP) family diversified in mam

150 the rapidly evolving Kruppel-associated box-zinc finger protein (KRAB-ZFP) family linked primarily t

151 these effects and identify a cluster of KRAB zinc finger protein (KZFP) genes that modifies VM-IAPs i

152 the Kruppel-associated box (KRAB)-containing zinc finger protein (KZFP) ZFP57 protects select ICRs fr

153 ked to recruitment of the monocytic leukemia zinc finger protein (MOZ) histone acetyltransferase to t

154 SET1 methyltransferase activity is the CxxC zinc finger protein 1 (Cfp1).

155 CIP1-interacting zinc finger protein 1 (CIZ1) is a nuclear matrix associa

156 The nuclear matrix protein Cip1-interacting zinc finger protein 1 (CIZ1) promotes DNA replication in

157 In this study, we identify the conserved zinc finger protein 277 (ZNF277) as a new uS5-associated

158 Herein, Zinc finger protein 367 (ZNF367) was identified as a pot

159 r, reduced expression 1 (REX1; also known as zinc finger protein 42), to be selectively down-regulate

160 We identify zinc finger protein 568 (ZFP568), a member of the rapidl

161 Zinc finger protein 57 (ZFP57) is critical for maintenan

162 We studied the Zinc Finger Protein 598 (ZNF598) using PAR-CLIP and reve

163 ion of parkin interacting substrate protein (zinc finger protein 746) and aminoacyl tRNA synthetase c

164 olving zinc finger array of PRDM9 (PR domain zinc finger protein 9).

165 tor for male-specific lethal [MSL] proteins) zinc finger protein binds these GA repeat motifs, increa

166 ut ZNF274, a Kruppel-associated box-A-domain zinc finger protein capable of recruiting epigenetic mac

167 mage sites, allowing identification of ZPET (zinc finger protein proximal to RAD eighteen)/ZNF280C as

168 The CFP1 CXXC zinc finger protein targets the SET1/COMPASS complex to

169 that ARS2 (arsenite-resistance protein 2), a zinc finger protein that is essential for early mammalia

170 important for brain function, we engineered zinc finger protein transcription factors (ZFP-TFs) to t

171 for awn inhibition in wheat, encodes a C2H2 zinc finger protein with EAR motifs which putatively fun

172 Here, we show that the zinc finger protein ZBED2 is aberrantly expressed in PDA

173 Here, we demonstrate that the zinc finger protein Zbtb20 is required for DNL.

174 d a distinct complex containing Mtr4 and the zinc finger protein ZFC3H1.

175 Here, we report the specific binding of zinc finger protein ZNF768 to the sequence motif GCTGTGT

176 We report that zinc finger protein ZPR1 binds to RNA polymerase II, int

177 The zinc finger protein ZPR1 interacts with SMN.

178 high colocalization of HMGNs and of REX1, a zinc finger protein, at promoters and enhancers.

179 Zfp189, which encodes a previously unstudied zinc finger protein, is the highest-ranked key driver ge

180 In this study, we identified a zinc finger protein, ZFP161 that functions as a replicat

181 In addition, we identify the KRAB zinc finger protein, ZNF446, and its associated triparti

182 c-Myc-interacting zinc finger protein-1 (Miz-1) is a poly-Cys2His2 zinc fi

183 pproaches on two large, independent Cys2His2 zinc finger protein-DNA interaction datasets. We demonst

184 by lowering mutant-Htt (mHtt) levels with a zinc finger protein.

185 gi apparatus-specific Asp-His-His-Cys (DHHC) zinc finger protein.

186 tion factor-binding motif for ZNF263, a C2H2 zinc finger protein.

187 ls coexpressed MYC and MIZ1 (MYC-interacting zinc-finger protein 1 [ZBTB17]).

188 Here, we show that zinc-finger protein 750 (ZNF750) opposes the migration a

189 rolin (TTP), encoded by the Zfp36 gene, is a zinc-finger protein that regulates RNA stability primari

190 Here, we identify a novel role for the zinc-finger protein ZNF281 in participating in the order

191 iated genes EPHA7, DCC netrin-1 receptor and zinc-finger protein ZNF479.

192 ing RNA AC099552.4 (p = 1.2 x 10(-7)), and a zinc-finger protein ZNF655 (gene-based p = 5.0 x 10(-6))

193 osophila Doublefault (Dbf) protein as a C2H2 zinc-finger protein, primarily expressed in testes, that

194 aternally expressed, TRIM28-interacting KRAB zinc-finger protein: ZFP708.

195 KRAB domain-containing zinc finger proteins (KRAB-ZFPs) and KRAB-associated pro

196 tetrapods, the Kruppel-associated box domain zinc finger proteins (KRAB-ZFPs), binds to specific EREs

197 hat Kruppel-associated box (KRAB)-containing zinc finger proteins (KZFPs) control the timely and plei

198 -genome activation, implying that other KRAB-zinc finger proteins (KZNFs) recruit KAP1 prior to blast

199 To accomplish this task, we designed zinc finger proteins (ZFPs) targeting within -300 bps of

200 our known CRBN neo-substrates [Ikaros family zinc finger proteins 1 (IKZF1) and 3 (IKZF3), casein kin

201 te Boundary Complex (LBC), that contains the zinc finger proteins CLAMP and GAF.

202 family of ubiquitously expressed human C2H2 zinc finger proteins comprised of ZFX, ZFY and ZNF711.

203 Viral expression of zinc finger proteins targeting histone acetylation to th

204 well as genes coding for aminotransferases, zinc finger proteins, and several uncharacterized protei

205 largely due to extensive divergence in C2H2 zinc finger proteins.

206 nsion and diversification of repressive C2H2 zinc finger proteins.

207 the large, but under-studied family of C2H2 zinc finger proteins.

208 EERV (Snerv) 1 and 2, Kruppel-associated box zinc-finger proteins (KRAB-ZFPs) that repressed NEERV by

209 For brain development, primate-specific KRAB zinc-finger proteins (KZNFs) are specifically up-regulat

210 domain to the amino terminus of one or both zinc-finger proteins (ZFPs) in the ZFN dimer, as well as

211 ology approach, we identify a new network of zinc-finger proteins that are expressed in one class of

212 myelodysplastic syndrome 1 (MDS)/EVI encode zinc-finger proteins that have been recognized as import

213 ese include DNA-targeting techniques such as zinc-finger proteins, transcription activator-like effec

214 introduce three epigenome-editing platforms: zinc-finger proteins, transcriptional activator-like eff

215 ing IRF8 and members of the Ikaros family of zinc-finger proteins.

216 orted genome-wide significant locus: ZRANB3 (Zinc Finger RANBP2-Type Containing 3, lead SNP p = 2.831

217 e different tuning mechanisms of a synthetic zinc-finger repressor library, whose affinity and cooper

218 LZF(lo)RORgammat(lo) (promyelocytic leukemia zinc finger, retinoic acid-related orphan receptor gT) i

219 ZFP36L1 is a tandem zinc-finger RNA-binding protein that recognizes conserve

220 We also found that promyelocytic leukemia zinc finger seemed to play a role in regulating NKT cell

221 PR-domain-containing proteins (PRDMs) are zinc-finger sequence-specific chromatin factors that hav

222 While it is known that shared and unique zinc finger sequences in CTCF and CTCFL enable CTCFL to

223 The potential of nuclease-deficient zinc fingers, TALEs or CRISPR fusion systems to treat th

224 Finally, we reveal that the N, C, and zinc finger terminal domains play unique roles in target

225 yltransferase Ehmt1 and stabilization of the zinc finger TF Zic2 at enhancers and promoters.

226 ly comprises 44 activating and 12 inhibitory zinc-finger TFs and 83 cognate promoters, combined in a

227 TZF domain of MEX-5 contains an unstructured zinc finger that folds upon binding of its RNA target.

228 EIL3 contains two tandem C-terminal GRF-type zinc fingers that are absent in the other NEIL paralogs.

229 nteractions through mutations of 2 of its 11 zinc fingers that are not required for CTCF binding to i

230 al DNA-binding domain (DBD) containing three zinc fingers, the automodification domain (A), and the C

231 slocates to the nucleus and interacts with a zinc finger transcription factor (FgZC1), also required

232 and identified the constitutively expressed zinc finger transcription factor (TF) Zfp281 as a bidire

233 The Arabidopsis thaliana zinc finger transcription factor (ZF-TF), S-nitrosothiol

234 er unmask a mutual requirement for Hivep3, a zinc finger transcription factor and adapter protein.

235 Here, we show that the zinc finger transcription factor CASZ1 up-regulates MYOD

236 Here, we identify the zinc finger transcription factor EGR1 as a negative regu

237 al erythropoiesis is highly regulated by the zinc finger transcription factor GATA-1.

238 The zinc finger transcription factor gata3 regulates inner e

239 tion between Drosophila FOXO (dFOXO) and the zinc finger transcription factor Kruppel homolog 1 (Kr-h

240 gene 3 (Peg3), an imprinted gene encoding a zinc finger transcription factor postulated to function

241 Here, we have identified the C. elegans zinc finger transcription factor PQM-1 as a regulator of

242 GATA2, a zinc finger transcription factor predominantly expressed

243 caused by loss-of-function mutations in the zinc finger transcription factor THAP1.

244 GATA3 is a dual-zinc finger transcription factor that regulates gene exp

245 EGR1 is an early growth response zinc finger transcription factor with broad actions, inc

246 A highly conserved zinc finger transcription factor, Motif 1 Binding Protei

247 mechanism through which STAT3 and the Ikaros zinc finger transcription factors Aiolos and Ikaros coop

248 Ikaros zinc finger transcription factors are important regulato

249 The Myt1 family of zinc finger transcription factors contributes to fibrobl

250 and negatively regulates Snai1 and ZEB1, two zinc finger transcription factors that lead to increased

251 r 1-3 (GLIS1-3), a subfamily of Kruppel-like zinc finger transcription factors, function as key regul

252 es respectively, and tend to be regulated by zinc finger transcription factors.

253 otrophin signalling system; a high number of zinc finger transcription factors; and novel factors tha

254 The promyelocytic leukemia zinc-finger transcription factor (PLZF) is essential for

255 (NuRD) complex binding are required for the zinc-finger transcription factor CASZ1 to function as a

256 Odd-paired (Opa), a zinc-finger transcription factor expressed at cellulariz

257 Here, we show that the zinc-finger transcription factor GLI1, a terminal effect

258 equires GLIS family zinc finger 3 (GLIS3), a zinc-finger transcription factor important in pancreas d

259 utoregulatory, cis-acting motif in the che-1 zinc-finger transcription factor locus, a terminal selec

260 udy, we identified the pepper homolog of the zinc-finger transcription factor LOL1 (LSD ONE LIKE1; Cc

261 s sex-specifically spliced and encodes a BTB zinc-finger transcription factor proposed to be a master

262 Here, we report that the zinc-finger transcription factor Slug is highly expresse

263 homeodomain transcription factor Cut and the zinc-finger transcription factor Tramtrack-69 (Ttk69).

264 Accumulating evidence indicates that the zinc-finger transcription factor ZEB1 is predominantly e

265 otein interaction with the sequence-specific zinc-finger transcription factor ZNF143 and activates th

266 , we demonstrate that SlBBX20, a B-box (BBX) zinc-finger transcription factor, is a positive regulato

267 threonine protein kinase, and a Kruppel-type zinc-finger transcription factor, respectively.

268 Here, we show that ztf-11 (Zinc-finger Transcription Factor-11), the sole Caenorhab

269 opment, POPOVICH (POP), which encodes a C2H2 zinc-finger transcription factor.

270 he PR/SET domain-containing (PRDM) family of zinc finger transcriptional regulators play diverse deve

271 eviously demonstrated that expression of the zinc finger transcriptional repressor Blimp1/PRDM1 is es

272 y, transcriptional targets recognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an e

273 ing only two predicted genes, including C2H2 zinc finger transcriptional repressor TraesCS5A02G542800

274 des and RNA interference targeting mRNA, and zinc finger transcriptional repressors and CRISPR-Cas9 m

275 Gfi1 is a zinc-finger transcriptional repressor that plays an impo

276 The SUPERMAN (SUP) gene encodes a C2H2 zinc-finger transcriptional repressor that regulates the

277 of target mRNAs, mediated through its tandem zinc finger (TZF) domain, TTP promotes the deadenylation

278 CCCH-type tandem zinc finger (TZF) domains are found in many RNA-binding

279 12 ubiquitin specific proteases featuring a zinc finger ubiquitin-binding domain (ZnF-UBD).

280 h substitutions that reduced the affinity of zinc fingers, we developed ZFNs specific for the TRAC lo

281 a chimeric CESA5 by replacing its N-terminal zinc finger with its CESA6 counterpart to investigate th

282 capsid proteins, a pH-sensing histidine of a zinc finger within the receptor-binding VP2 protein, and

283 vious studies suggested that the RanBP2-type Zinc Finger (ZF) domain is a suitable scaffold to invest

284 ps for the best characterized members of the zinc finger (ZF) family of MBPs in propagating DNA methy

285 Polydactyl zinc finger (ZF) proteins have prominent roles in gene r

286 ne family of proteins modified by H(2) S are zinc finger (ZF) proteins, which contain multiple zinc-c

287 e N-tier ring is structurally divided into a zinc finger (ZF) sub-ring followed by the oligosaccharid

288 finger protein-1 (Miz-1) is a poly-Cys2His2 zinc finger (ZF) transcriptional regulator of many cell

289 rotein oligomerization, such as a C(2) H(2) -zinc finger (ZF), and a leucine zipper (LZ), whose roles

290 Evidence suggests that the CXXC type zinc finger (ZF-CXXC) protein 5 (CXXC5) is a critical re

291 n Arabidopsis when tethered to an artificial zinc finger (ZF-RdDM).

292 h heterozygous variants affecting the fourth zinc finger (ZF4) of Wilms' tumor 1 (WT1) (p.Ser478Thrfs

293 ata revealed that the last four of the eight zinc fingers (ZFs) (i.e. ZF5-8) in ZBTB24 confer specifi

294 Gag or Gag mutants carrying deletions in NC zinc fingers (ZFs) or a nonmyristoylated version of Gag.

295 ctor (CTCF), containing a tandem array of 11 zinc fingers (ZFs), modulates the three-dimensional orga

296 The CPSF30 subunit contains five CCCH zinc fingers (ZFs), with ZF2-ZF3 being required for the

297 ormed by Zn(II) displacement from the parent zinc fingers (ZFs).

298 trate and further show that ZFP91 harbours a zinc finger (ZnF) motif, related to the IKZF1/3 ZnF, cri

299 in part mediated by a new type of monovalent zinc finger (ZnF).

300 combination is mediated by the fast-evolving zinc-finger (ZnF) domain of gene PRDM9.