ライフサイエンスコーパス: zinc finger protein

1 gi apparatus-specific Asp-His-His-Cys (DHHC) 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 rated the target search process of the Egr-1 zinc-finger protein.

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

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

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

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

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

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

11 ck transcription factors (HSFs), and several zinc finger proteins.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 le nucleotide insertion in the gene encoding zinc finger protein 191 (Zfp191), which is a widely expr

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

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

41 related GTPase related family, M (IRGM) and zinc finger protein 300 (ZNF300), are associated with Cr

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

43 the bone morphogenetic protein 4 (BMP4) and zinc finger protein 36 C3H type-like 1 (ZFP36L1/TPP).

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

45 822013 on chromosome 10q21.2, located in the zinc finger protein 365 (ZNF365) gene, showed a consiste

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

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

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

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

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

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

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

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

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

55 Zinc finger protein 521 (Zfp521) antagonizes Runx2 in vi

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

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

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

59 ecently identified frequent mutations in the zinc finger protein 668 (ZNF668), the function of which

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

61 10C>G (p.Pro937Arg) missense mutation in the zinc finger protein 687 gene (ZNF687).

62 Reactivity toward zinc finger protein 688 and mitochondrial ribosomal prot

63 (5'-untranslated region variant of exon 2 of zinc finger protein 750 (ZNF750), and in an intron of TB

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

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

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

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

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

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

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

71 entify Tsh1 and found that it encodes a GATA zinc-finger protein, a close homolog of HANABA TARANU (H

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

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

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

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

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

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

78 suppressor RB1 and RBAK, encoding a C(2)H(2) zinc-finger protein and transcriptional binding partner

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

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

81 P568, a Kruppel-Associated-Box (KRAB) domain Zinc finger protein, and causes a unique set of extraemb

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

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

84 Several applications of such engineered zinc finger proteins are described here, including some

85 Here we report that the zinc finger protein Ars2 (arsenite-resistance protein 2;

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

106 ed via the Drosophila melanogaster CCCH-type zinc finger protein CG6694/dZC3H3 through both physical

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

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

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

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

111 Zinc finger proteins constitute the largest family of tr

112 Zif268 is a zinc-finger protein containing three Cys(2)-His(2)-type

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

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

115 The zinc finger protein CTCF has been invoked in establishin

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

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

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

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

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

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

122 -2 is an obligate binding partner of the BTB-zinc finger protein EOR-1 in Caenorhabditis elegans.

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

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

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

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

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

128 ulators include the cell-type-specific multi-zinc finger protein Friend of GATA-1 (FOG-1), the histon

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

130 The three-finger and four-finger zinc-finger protein fusions to the REL_DKK pair among th

131 ix-loop-helix proteins SCL/TAL1 and E47, the zinc finger protein GATA-1, and LIM-domain interacting p

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

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

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

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

136 and partial characterization of Kruppel-like zinc finger protein Glis3 mutant (Glis3(zf/zf)) mice.

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

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

139 The zinc finger protein growth factor independent-1 (Gfi1) i

140 EOR-1 BTB dimer, a region that, in other BTB-zinc finger proteins, has been proposed to interact with

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

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

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

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

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

146 CTCF is a highly conserved zinc finger protein implicated in diverse regulatory fun

147 strong homology to OSISAP1, an A20/AN1-type zinc finger protein implicated in stress tolerance in ri

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 ctors is important for understanding how BTB-zinc finger proteins influence transcription.

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

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

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

156 hat a binding site for the Sp1/KLF family of zinc-finger proteins is required for PRE activity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

179 ce energy transfer results indicate that the zinc finger protein (nucleocapsid) locally melts the TAR

180 The analysis revealed that the zinc finger protein of cerebellum (Zic) family member tr

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

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

183 dd paired (opa), a Drosophila homolog of the Zinc finger protein of the cerebellum (Zic) family of ma

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

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

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

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

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

189 ct, and that EOR-2 can bind to the human BTB-zinc finger protein PLZF.

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

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

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

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

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

195 f evidence suggest that the rapidly evolving zinc-finger protein PRDM9 binds to this motif and that s

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

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

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

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

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

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

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

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

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

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

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

207 Here, we report that the zinc-finger protein, SLR-2, is a master stress regulator

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

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

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

211 e third major heterochromatin component, the zinc-finger protein Su(var)3-7.

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

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

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

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

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

217 st Cth2 protein is a CX(8)CX(5)CX(3)H tandem zinc finger protein that binds AU-rich element (ARE)-con

218 ncodes an evolutionarily conserved Cys(3)His zinc finger protein that binds specifically to polyadeno

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

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

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

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

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

224 RDM16 (PR domain containing 16) is a 140 kDa zinc finger protein that robustly induces brown fat dete

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

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

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

228 the DNA-binding properties of two engineered zinc finger proteins that differ by a single amino acid.

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

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

231 anced by three factors: the Senseless (Sens) zinc finger protein, the Abdominal-A (Abd-A) Hox factor,

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

233 gence of CD4 and CD8 lineages, including the zinc finger proteins Thpok and Gata3, which are required

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

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

236 ZFNs are formed by fusing zinc-finger proteins to the nonspecific cleavage domain

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

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

239 virus replication, we tested three synthetic zinc finger protein transcription factors (ZF-TFs), each

240 otrophic factor-based therapy by engineering zinc finger protein transcription factors (ZFP TFs) that

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

242 Zinc finger protein tristetraprolin (TTP) modulates macr

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

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

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

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

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

248 NA-binding domains of two well-characterized zinc-finger proteins were similar to those described pre

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

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

251 onserved complex and the presence of a novel zinc finger protein with similarities to the mammalian t

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

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

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

255 Zic genes encode a conserved family of zinc finger proteins with essential functions in neural

256 ealed four putative response elements to the zinc-finger proteins WT1 (Wilms tumor suppressor 1) and

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

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

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

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

261 We show that the maternal zinc-finger protein Zelda (Zld) is absolutely required f

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

269 ranscriptional components, we identified the zinc-finger protein Zfp423 as a factor enriched in pread

270 mutants in the Kruppel-associated box (KRAB) zinc finger protein ZFP568, providing strong genetic evi

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

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

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

274 Here we identify the zinc finger protein ZFP809 as the recognition molecule t

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

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

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

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

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

280 ntify potential binding sites for engineered zinc finger proteins (ZFPs) in user-supplied DNA sequenc

281 himeric enzymes are based on custom-designed zinc finger proteins (ZFPs).

282 of beta-lactamase each linked to engineered zinc finger proteins (ZFPs).

283 Engineered zinc-finger proteins (ZFPs) are hybrid proteins develope

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

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

286 ation Factor A family, LDOC1-related family, Zinc Finger Protein ZIC, and GLI family) that show evide

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

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

289 eraction with an uncharacterized KRAB family zinc finger protein, ZIFCAT.

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

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

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

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

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

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

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

297 We report here the characterization of the zinc finger protein ZNF638 as a novel regulator of adipo

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

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.