ライフサイエンスコーパス: zinc finger protein

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

2 defects in knock-out lines of KEG and a CCCH zinc finger protein.

3 transcription factor promyelocytic leukemia zinc finger protein.

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

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

6 ich it carries out redundantly with SLR-2, a zinc-finger protein.

7 rated the target search process of the Egr-1 zinc-finger protein.

8 of decoys on the search process of the Egr-1 zinc-finger protein.

9 tristetraprolin (TTP) family of CCCH tandem zinc finger proteins.

10 We fuse 223 yeast CRs to programmable zinc finger proteins.

11 346), a member of a new class of Cys-2-His-2 zinc finger proteins.

12 which encode EAR motif-containing C2H2-type zinc finger proteins.

13 d member of the Prdm family of PR/SET domain zinc finger proteins.

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

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

16 nsion and diversification of repressive C2H2 zinc finger proteins.

17 ese findings support a role for iron in some zinc-finger proteins.

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

19 omplex, Tramtrack, Bric-a-brac/Pox virus and Zinc finger) proteins.

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

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

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

23 report the identification of Myc-interacting Zinc finger protein 1 (Miz1) as a Smo and Gli2 binding p

24 the Caenorhabditis elegans ortholog of AF10, zinc finger protein 1 (ZFP-1).

25 Among these, the GATA-3 repressor zinc finger protein 1 (Zfpm1) emerged as a potential med

26 first Drosophila mutation in the gene Zpr1 (Zinc finger protein 1) by the inability of Zpr1-mutant t

27 NT The deletion of the Miz1 (Myc-interacting zinc finger protein 1) POZ (POxvirus and Zinc finger) do

28 in injured DRG through activation of myeloid zinc finger protein 1, a transcription factor that binds

29 S264G), which encodes CIZ1, Cip1-interacting zinc finger protein 1.

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

31 B cell transcription factors, Ikaros family zinc finger proteins 1 and 3 (IKZF1 and IKZF3).

32 or enhance the degradation of Ikaros family zinc finger proteins 1 and 3.

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

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

35 Myc interacting zinc finger protein-1 (Miz1) is a transcription factor k

36 erize the Cuz1 protein (Cdc48-associated UBL/zinc finger protein-1), encoded by a previously uncharac

37 Zinc finger protein 106 (ZFP106) has previously been ass

38 The RNA-binding Zinc-finger protein 106 (ZFP106) detected in both librar

39 tudy focused on one of the seven candidates, zinc finger protein 111 (Zfp111).

40 veral candidates, we identified mouse or rat zinc finger protein 111 (zfp111).

41 also known as Phf12 (plant homeodomain [PHD] zinc finger protein 12), is a member of the PHD zinc fin

42 The transcription factor Zinc finger protein 148 (Zfp148) was shown recently to m

43 lysis identifies allele-preferred binding of Zinc finger protein 148 (ZNF148) to rs36115365-C, furthe

44 Herein we show that zinc finger protein 157 (Zfp157) is required to establis

45 ination mutants, we identified a mutation in zinc finger protein 16-like (znf16l).

46 Here we show that the chromatin-associated zinc finger protein 217 (ZFP217) coordinates epigenetic

47 d a zinc finger transcription factor, ZNF24 (zinc finger protein 24), as a novel inhibitor of tumor a

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

49 ding protein, tristetraprolin (also known as zinc finger protein 36 (ZFP36)), which is itself up-regu

50 The zinc finger protein 36-like 2, Zfp36l2, has been implica

51 822013 on chromosome 10q21.2, located in the zinc finger protein 365 (ZNF365) gene, showed a consiste

52 ificant association of a polymorphism in the zinc finger protein 365 gene (ZNF365) with total IgE lev

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

54 ated kinase (c.791dup; p.Ser265ValfsX64) and zinc finger protein 408 (ZNF408) (c.1363C>T; p.His455Tyr

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

56 hare a common pool of progenitor cells, with Zinc finger protein 423 (Zfp423) as a key initiator of a

57 It has been recently discovered that zinc finger protein 423 (Zfp423) is an early actor in ad

58 Zinc finger protein 423 (Zfp423), a 30-zinc finger trans

59 male OB offspring had a higher expression of Zinc finger protein 423 (zfp423), a key transcription fa

60 gamma (PPARgamma) transcriptional activator zinc finger protein 423 (Zfp423), and this complex is di

61 induces DNA demethylation in the promoter of zinc finger protein 423, which renders progenitor cells

62 al. investigate the interaction of CXXC-type zinc finger protein 5 (CXXC5) with Dishevelled as one su

63 We recently identified zinc finger protein 521 (Zfp521) as a downstream target

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

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

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

67 , P = 3.6 x 10(-8)) on chromosome17p13.1 and zinc finger protein 676 (ZNF676; rs412658, P = 3.3 x 10(

68 10C>G (p.Pro937Arg) missense mutation in the zinc finger protein 687 gene (ZNF687).

69 Reactivity toward zinc finger protein 688 and mitochondrial ribosomal prot

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

71 (5'-untranslated region variant of exon 2 of zinc finger protein 750 (ZNF750), and in an intron of TB

72 ory pathways, including STAT3, NFkappaB, and zinc finger protein 750 (ZNF750).

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

74 transcription factors (4.1-fold), including zinc-finger proteins (8.75-fold).

75 gle-nucleotide polymorphism rs1344706 in the zinc finger protein 804A gene (ZNF804A) shows genome-wid

76 e found that the transcript encoding ZFP871 (zinc finger protein 871; also called ZNF709 in humans) i

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

78 st, as well as in positive-regulatory domain zinc finger protein 9-knockout mice, suggesting that rec

79 ding sites of the positive-regulatory domain zinc finger protein 9.

80 PLZF (Promyelocytic Leukemia Zinc Finger protein), a member of the POK family of tran

81 astoma protein homolog LIN-35 and the LIN-13 zinc finger protein act in the same pathway as HPL-2 to

82 Here, we report that ZFP3, a nuclear C2H2 zinc finger protein, acts as a negative regulator of ABA

83 ces lactis Rtr1, which reveals a new type of zinc finger protein and does not have any close structur

84 attempt to identify recombination associated zinc finger proteins and motifs.

85 showed that FOXJ3 may regulate a network of zinc finger proteins and that FOXK1 binds to the promote

86 ZFNs resulted from basic research on zinc finger proteins and the FokI restriction enzyme (wh

87 n a synthetic guide RNA and DNA, outperforms zinc-finger proteins and transcription activator-like ef

88 Our analyses shows that zinc finger proteins (and their splice variants) can res

89 anogaster, yet only CTCF, a highly conserved zinc finger protein, and the transcription factor TFIIIC

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

91 By using zinc-finger proteins, AND, OR, and NOR logic gates were

92 We found that the majority of zinc-finger proteins assembled from these modules have f

93 ing sites for CCCTC-binding factor (CTCF), a zinc finger protein associated with mammalian insulator

94 ured the target search kinetics of the Egr-1 zinc-finger protein at various ionic strengths between 4

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

96 ssay of specific regions of a Salt-inducible Zinc Finger Protein (AtSZF1) transcript revealed distinc

97 A B-box zinc finger protein, B-BOX32 (BBX32), was identified as

98 arsenic exposure led to oxidation of certain zinc finger proteins based on arsenic interaction with z

99 nt, which was abolished by deficiency in the zinc-finger protein Bcl11b but restored by IL-25R overex

100 tristetraprolin (TTP) family of CCCH tandem zinc finger proteins bind to AU-rich regions in target m

101 nd homeodomain proteins) and ASEs (T-box and zinc finger proteins) bind directly to several sites on

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

103 own, and all the six associate with zinc and zinc finger proteins (both previously found critical in

104 cting useful models, especially for C(2)H(2) zinc finger proteins, but it remains a challenging probl

105 The recently discovered novel zinc-finger protein, called MCPIP (MCP-1-induced protein

106 ovide insights into the mechanism by which a zinc finger protein can recognize mCpG sites as well as

107 tristetraprolin (TTP) family of CCCH tandem zinc finger proteins can bind directly to AU-rich elemen

108 malian tristetraprolin family of CCCH tandem zinc finger proteins can bind to certain AU-rich element

109 yeast Dph3 (also known as KTI11), a CSL-type zinc finger protein, can bind iron and in the reduced st

110 er of a class of tandem (R/K)YKTELCX8CX5CX3H zinc finger proteins, can destabilize target mRNAs by fi

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

112 Here, we report that the cardiac para-zinc-finger protein CASZ1 is expressed in murine cardiom

113 he last year have identified the DNA-binding zinc-finger protein CCCTC-binding factor (CTCF) as a cru

114 is of one of these potential regulators, the zinc-finger protein Charlatan, was carried out.

115 Here, we report that the CDKN1-interacting zinc finger protein CIZ1 is critical for localization of

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

117 emonstrate that a previously uncharacterized zinc finger protein, CLAMP (chromatin-linked adaptor for

118 K, which phosphorylates threonine 173 of the zinc finger protein CNBP in response to Hedgehog activat

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

120 Zinc finger proteins constitute the largest family of tr

121 of a family of RNA-binding, CCCH-containing zinc-finger proteins control TNF expression through its

122 f this highly choreographed process with the zinc finger protein CTCF and with cohesin, a protein com

123 The zinc finger protein CTCF has been invoked in establishin

124 The role of the zinc finger protein CTCF in organizing the genome within

125 that chromatin neighbourhoods, formed by the zinc-finger protein CTCF, can sequester enhancers and th

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

127 suggest an evolutionary shift in C-terminal zinc finger proteins during fungal evolution, transformi

128 Our current study of the zinc-finger protein Egr-1 (also known as Zif268) and its

129 chains upon protein-DNA association for the zinc-finger protein Egr-1.

130 e transcription factor Miz1 (Myc-interacting zinc finger protein; encoded by Zbtb17) in mouse Schwann

131 We show here that the zinc finger protein Evi1 increases in preadipocytes at t

132 CIZ1 is a p21(Cip1/Waf1) -interacting zinc finger protein expressed in brain and involved in D

133 zinc finger GATA-type transcription factors ZINC FINGER PROTEIN EXPRESSED IN INFLORESCENCE MERISTEM

134 response factor, heat shock factor, MYB and zinc-finger protein expressed in inflorescence meristem

135 C (JmjC) domain and belongs to the C(2)H(2) zinc-finger protein family.

136 ned using a P16 promoter-specific engineered zinc finger protein fused with the catalytic domain of d

137 ments), microsatellite loci, X- and Y-linked zinc-finger protein gene (ZFX and ZFY) sequences, and wh

138 rts the epigenetic silencing of Kruppel-type zinc finger protein genes on chromosome 19q13 in orophar

139 an interferon (IFN) gene, a chemokine gene, zinc finger protein genes, nuclear factors, and histones

140 ted with genes belonging to the Kruppel-type zinc finger protein genes.

141 led that DHHC2 or DHHC3 (Golgi-specific DHHC zinc finger protein (GODZ)) self-associate when expresse

142 toylation by both Golgi-associated DHHC-type zinc finger protein (GODZ; also known as DHHC3) and its

143 Replication initiator 1 (Repin1) is a zinc finger protein highly expressed in liver and adipos

144 Kruppel-like factor 4 (KLF4) is a zinc finger protein highly expressed in the gut and skin

145 Notch induces the expression of zinc finger protein Hindsight and suppresses homeodomain

146 gi apparatus-specific Asp-His-His-Cys (DHHC) zinc finger protein; (ii) a GODZ dominant-negative mutan

147 The zinc-finger protein Ikaros is a key player in T-cell dev

148 Kaiso, a bifunctional Cys(2)His(2) zinc finger protein implicated in tumor-cell proliferati

149 cleotide binding motifs for all Cys(2)His(2) zinc finger proteins in Drosophila pseudoobscura and ide

150 have studied the translocation of the Egr-1 zinc-finger protein in the target DNA association proces

151 encoding a homolog of the Teashirt family of zinc-finger proteins in the planarian Schmidtea mediterr

152 ted with molecular processes/other proteins, zinc finger protein, intracellular/extracellular enzymes

153 The NET (nocA, Nlz, elB, TLP-1) subfamily of zinc finger proteins is an important mediator during dev

154 the target association process for the Egr-1 zinc-finger protein is the one involving intersegment tr

155 Zfp423/OAZ, a multi-zinc finger protein, is proposed to participate in neuro

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

157 Analysis of zinc finger proteins isolated from arsenic-exposed cells

158 The plant homeodomain zinc finger protein Jade-1 can act as an E3 ubiquitin li

159 nucleic acid binding protein (CNBP/ZNF9), a zinc-finger protein known to bind single-stranded G-rich

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

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

162 P809, a member of the Kruppel-associated box zinc finger protein (KRAB-ZFP) family, initiates the sil

163 bited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes.

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

165 Kruppel-associated box zinc finger proteins (KRAB-ZFPs) are a huge family of ve

166 Over 400 Kruppel-associated box zinc finger proteins (KRAB-ZFPs) are encoded in mammalia

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

168 as an essential corepressor for KRAB family zinc finger proteins (KRAB-ZNF).

169 Kruppel-associated box zinc-finger proteins (KRAB-ZFPs) make up the largest fam

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

171 em cell lineage that a spermatocyte-specific zinc finger protein, Kumgang (Kmg), working with the chr

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

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

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

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

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

177 se SEK-1, which functions in parallel to the zinc-finger protein LIN-29 to promote cellular demise.

178 ght-inducible transcription using engineered zinc finger proteins (LITEZ), uses two light-inducible d

179 In this study we identify RING zinc finger protein Makorin 1 (MKRN1), a bona fide RNA-b

180 ed on protein arrays included Myc-associated zinc finger protein (MAZI) and ankyrin repeat motif.

181 ere, we report the identification of a small zinc finger protein, methylene blue sensitivity (MBS), t

182 This MEX-3 patterning requires the CCCH zinc-finger protein MEX-5, the RNA Recognition Motif pro

183 The transcription factor zinc-finger protein Miz1 represses TNF-alpha-induced JNK

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

185 tage-specific deletion of monocytic leukemia zinc finger protein (MOZ), a histone acetyltransferase,

186 A second pathway stabilizes a large set of zinc finger protein mRNAs, potentially through reduced l

187 AOXI transcription is regulated by the zinc finger protein Mxr1p (methanol expression regulator

188 Human ZIC1 (zinc finger protein of cerebellum 1), one of five homolo

189 ZNF469, encoding a zinc finger protein of hitherto undefined function, has

190 The Zinc-finger protein of the cerebellum 2 (Zic2) is one of

191 f the trimetallic compounds with DNA and the zinc-finger protein PARP-1 indicate that they exert anti

192 These included the gene encoding the zinc finger protein Phf6.

193 The C2H2 zinc-finger protein Pita binds to several BX-C boundarie

194 ies (ROS) on redox-sensitive targets such as zinc finger proteins plays a critical role in redox sign

195 scriptional repressor promyelocytic leukemia zinc finger protein (PLZF) at the rs12101261 site.

196 transcription factor promyelocytic leukemia zinc finger protein (PLZF).

197 ide glp-1 regulation by the CCCH-type tandem zinc finger protein POS-1 and the STAR-domain protein GL

198 In humans and mice, the Cys(2)His(2) zinc finger protein PRDM9 binds to a DNA sequence motif

199 ocations are predominantly determined by the zinc finger protein PRDM9, which binds to DNA in hotspot

200 ZNHIT3 encodes a nuclear zinc finger protein previously implicated in transcripti

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

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

203 prising the Mtr4-like protein, Mtl1, and the zinc-finger protein, Red1.

204 MORF [MOZ (monocytic leukemia zinc-finger protein)-related factor] and MOZ are catalyt

205 First, the ZFP354C zinc finger protein repressed basal and Sp1-induced acti

206 (H2)F1 is an octa-zinc finger protein required for mRNP-gRNP docking, pre-

207 We show that fusion to two designed zinc finger proteins rescued the Int(-) phenotype.

208 g domains with custom-designed Cys(2)-His(2) zinc-finger proteins results in the creation of engineer

209 ex Php2-Php3-Php5 and the CCAAT-box, and the zinc-finger protein Rst2 and its Oligo-C motif.

210 ression profiling, we identified a rice RING zinc-finger protein (RZFP), OsRZFP34, whose gene express

211 Mice lacking the large zinc finger protein Schnurri-3 (Shn3) display increased

212 ressor complex, which involves multiple KRAB zinc finger proteins, shields neuronal genomes from exce

213 tion (EMT) by reducing the expression of the zinc-finger protein SLUG.

214 ent study was to analyze in vivo the role of zinc finger protein SNAI1 (SNAI1) on renal fibrosis.

215 Here, we provide evidence that the zinc-finger protein Sp8 plays a supplementary role to Pa

216 essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional facto

217 This includes engineered zinc finger proteins, TALEs/TALENs, and the CRISPR/Cas9

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

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

220 PARIS is a KRAB and zinc finger protein that accumulates in models of parkin

221 a methanol- and biotin starvation-inducible zinc finger protein that acts as a negative regulator of

222 und that expression of Osr2, which encodes a zinc finger protein that antagonizes Msx1-mediated activ

223 FOG-2 is a multi-zinc finger protein that binds the transcriptional activ

224 Yin Yang 1 (YY1) is a zinc finger protein that functions as a transcriptional

225 Aebp2 encodes an evolutionarily conserved zinc finger protein that has not been well studied so fa

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

227 somi-1 encodes a zinc finger protein that localizes to nuclear foci and b

228 Methanol expression regulator 1 (Mxr1p) is a zinc finger protein that regulates the expression of gen

229 and synapsis by phosphorylating a family of zinc finger proteins that bind to specialized regions on

230 is the prototype of a family of CCCH tandem zinc finger proteins that can bind to AU-rich elements i

231 tristetraprolin (TTP) family of CCCH tandem zinc finger proteins that can bind to transcripts contai

232 C2H2 zinc finger proteins that do not bind arsenic were not o

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

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

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

236 tumor necrosis factor (TNF)-alpha-inducible zinc finger protein thought to limit NF-kappaB-mediated

237 Here we identify the uncharacterized zinc finger protein Tmc1 as a dynamically regulated stre

238 phage gamma HNHE and subsequently fused to a zinc finger protein to generate a chimeric NEase with a

239 , present in hundreds of vertebrate-specific zinc finger proteins, to assess the effect of its bindin

240 signaling activation and upregulation of the zinc-finger protein Tramtrack69 (Ttk69).

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

242 developed DNA-targeting platforms, including zinc finger proteins, transcription activator-like effec

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

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

245 Zinc finger protein tristetraprolin (TTP) modulates macr

246 The zinc-finger protein tristetraprolin (TTP) binds to AU-ri

247 ology of neurons through a metazoan-specific zinc finger protein, Unkempt.

248 Genes encoding two zinc finger proteins, Vasa, a LIM domain protein, Sox an

249 with "TAGteam" sequence motifs bound by the zinc finger protein Vielfaltig, also known as Zelda, a r

250 s, where the gene of MOZ (monocytic leukemia zinc finger protein) was first identified as a recurrent

251 ription factor, PLZF (promyelocytic leukemia zinc finger protein), which mediates conditioned protect

252 longs to the tristetraprolin (TTP) family of zinc-finger proteins, which bind to mRNAs containing AU-

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

254 Our results defined the function of a new zinc finger protein with specific function in oligodendr

255 Poly(ADP-ribose) polymerase-1 (PARP-1) is a zinc finger protein with well documented involvement in

256 s (KLFs) constitute a subfamily of C2H2-type zinc finger proteins with distinct cell-type expression

257 We identify another zinc finger protein, Yin Yang 1 (YY1), at the base of lo

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

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

260 Here we show that the zinc-finger protein ZBTB20 regulates TRP channels expres

261 transcriptional repression, mediated by the zinc-finger protein Zeb2 (also known as Sip1), is essent

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

263 rent classes of KAP1 target genes, including zinc finger protein (ZFP) and imprinted genes.

264 Viral-mediated delivery of engineered zinc finger proteins (ZFP) targeted histone H3 lysine 9/

265 matically compared four different engineered zinc finger proteins (ZFP), four transcription activator

266 Here, we identify the zinc finger protein Zfp106 as a specific GGGGCC RNA repe

267 Here we show that the nuclear zinc finger protein ZFP106 is highly enriched in skeleta

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

269 , that harbors a hypomorphic mutation in the zinc finger protein Zfp335.

270 The Kruppel-like zinc finger protein ZFP57 acts as a factor necessary for

271 the factors involved in this selection, the zinc-finger protein Zfp57 can be regarded as an imprint-

272 These include the conserved small zinc finger protein Zfp706 and the RNA binding protein P

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

274 complex bound to DNA by the ES cell-specific zinc-finger protein ZFP809.

275 Further analyses of the zinc finger protein Zfp871 and BTB/POZ domain transcript

276 Cys(2)-His(2) zinc finger proteins (ZFPs) are the largest family of tr

277 Cys2-His2 zinc finger proteins (ZFPs) are the largest group of tra

278 rategy to test repression of mutant HTT with zinc finger proteins (ZFPs) in an HD model.

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

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

281 e DNA-binding domains (DBDs) with engineered zinc-finger proteins (ZFPs).

282 rgeted specifically to Fosb using engineered zinc-finger proteins (ZFPs).

283 Here we show that a zinc finger protein, ZIC2, a key regulator for central n

284 arly genes (IEGs), protooncogene, c-Fos, and zinc finger protein, Zif268, after monocular inactivatio

285 scopy and edgetic mutations that the bitopic zinc-finger protein ZitP implements specialized developm

286 the ENCODE project, we demonstrate that the zinc-finger protein ZNF143 preferentially occupies ancho

287 The Kruppel-like zinc finger protein ZNF217 is a candidate oncogene in br

288 ntification of a SCAN domain-containing C2H2 zinc finger protein, ZNF24, that represses the transcrip

289 Here, we report that the zinc-finger protein ZNF274, in association with the hist

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

291 Here, we identify and characterize a nuclear zinc finger protein, ZNF335/NIF-1, as a causative gene f

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

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

294 The evolutionary conserved zinc finger protein ZNF503/Zeppo2 (zinc finger elbow-rel

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

296 The C2H2-type zinc finger protein ZNF764 acts as an enhancer for sever

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

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

299 The zinc finger protein ZPR1 interacts with SMN.

300 st and one gene that could modify SMA is the Zinc Finger Protein (ZPR1) gene.