ライフサイエンスコーパス: finger

1 G-1 are separable functions of the RAG-2 PHD finger.

2 imilar for flexion and extension of the same finger.

3 l and tangential forces applied by the index finger.

4 eye, chest, left ring finger, and right ring finger.

5 tic pressing or sliding contact of the index finger.

6 BCVA was counting fingers.

7 A-binding residue in the first of three zinc fingers.

8 hat the transcription factor GLI family zinc finger 1 (GLI1) mediates Sulf2 expression during HCC dev

9 he stem cell-expressed genes GLI family zinc finger 1 (Gli1) or achaete-scute homolog 1 (Ascl1).

10 likely because of repression of muscle RING finger 1 (MuRF1), a proatrophic FOXO1 target gene.

11 anscription factors, VASCULAR PLANT ONE-ZINC FINGER 1 (OsVOZ1) and OsVOZ2, and promotes their degrada

12 Vascular endothelial zinc finger 1 (VEZF1) plays important roles in endothelial li

13 to determine that variants of the TOP domain finger 1 motif destabilizes the channel structure and im

14 e transcription factor GLI1 (GLI family zinc finger 1) plays a key role in the development and progre

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

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

17 esults suggest an active role for GATA3 zinc finger 2 mutants in ER-alpha positive breast tumors.

18 y retrieval-associated increases in BLA zinc finger 268 (zif268) and activity regulated cytoskeletal-

19 ee distinct targeted mutations of A20's zinc finger 7 (ZF7) ubiquitin-binding motif uniformly develop

20 The Arabidopsis E3 ubiquitin ligases RING-H2 FINGER A3A (RHA3A) and RHA3B mediate the monoubiquitinat

21 that Arabidopsis (Arabidopsis thaliana) RING Finger ABA-Related1 (RFA1) and RFA4 E3 ubiquitin ligases

22 he role of the ventral PMC in preshaping the fingers according to the size of the target.

23 h 2 female macaque monkeys moved their index finger against a resisting motor to track an on-screen t

24 ZBTB7C encodes the Zinc Finger and BTB Domain Containing 7C, a transcriptional r

25 reference pulse oximeters (positioned at the finger and earlobe) was 2.8 beats/min for over 65% of th

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

27 primary functional module consisting of the finger and GRIP domains.

28 this study, we investigate the role of Zinc finger and SCAN domain containing 4 (ZSCAN4) in human he

29 d finger PPG feet, ear and toe PPG feet, and finger and toe PPG feet.

30 erns in monkeys were quite distinct for both fingers and directions, which is similar to what was fou

31 Eyes with presenting VA between counting fingers and hand motion at 1 foot were more likely to un

32 an allosteric pocket at the junction of the fingers and palm subdomains by displacing residue V603 i

33 sual acuity was 20/50 (range, 20/20-counting fingers) and the final median visual acuity was 20/40 (r

34 LF4, KLF6, PLZF (promyelocytic leukemia zinc finger), and KLF15, are induced in TG neurons early duri

35 dose at 4 sites: left eye, chest, left ring finger, and right ring finger.

36 This interaction restricts movements of the fingers, and RdRPs use a subtle conformational change wi

37 We uncover a phenomenon-crustal fingering-and demonstrate how it may control methane-gas

38 Previously, we identified a zinc-finger antiviral protein ZAP that is commonly downregula

39 The cellular antiviral protein ZAP (zinc finger antiviral protein) binds CpGs and inhibits HIV-1

40 Maximum finger aperture during reach was used as the feature to

41 atterns for flexion or extension of the same finger are highly similar.

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

43 5 and designed a variant MEX-5 in which both fingers are fully folded in the absence of RNA.

44 geometry are enriched in genomes where zinc fingers are prevalent and specificity transitions would

45 inding activity of the rapidly evolving zinc finger array of PRDM9 (PR domain zinc finger protein 9).

46 For this challenge we propose a finger artery non-invasive tono-oscillometric monitor (F

47 al basis, the commands that hold the arm and finger at a target location depend on the mathematical i

48 p NTPases such as an alternative to arginine-finger-based catalysis.

49 rns were distinct for movements of different fingers, but were quite similar for flexion and extensio

50 to electronic signals by interdigitated comb finger capacitors at each wing's end along with a capaci

51 niquely at 48 hpi and genes involved in zinc finger CCCH protein, glycosyltransferase, 1-aminocyclopr

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

53 and donor-labeled DNA, we visualized dynamic fingers closing in single Pol beta-DNA complexes upon ad

54 elated conformational change referred to as "fingers closing." Here, we applied single-molecule FRET

55 gether, while neurons that control different finger combinations may be more spatially separated.

56 OSTERIX, an OB-specific zinc finger-containing transcription factor is for the first

57 For prosthetic finger control, regression-based methods are typically u

58 PHF23, KDM5A and BPTF, suggests a common PHD finger-dependent mechanism that promotes leukemogenesis

59 res were scored for the presence of Dawson's fingers (DF) and juxtacortical lesions (JCL).

60 Long Chain Family Member 5 (ACSL5) and Zinc Finger DHHC-Type Containing 6 (ZDHHC6), was characterise

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

62 cription regulators with a well-defined zinc finger DNA-binding domain and there is evidence that the

63 This complex, comprised of the zinc finger DNA-binding protein PRDM9 and the SNF2 family chr

64 ZNF281 binds XRCC4 through its zinc-finger domain and facilitates its recruitment to damaged

65 The N-terminal zinc finger domain enhances HDA15HD dimerization and increase

66 e outer mitochondrial membrane with its RING finger domain facing the cytoplasm.

67 he amino acid residue Phe257, located in the finger domain of FMDV polymerase and conserved across FM

68 ingle point mutations in the human MDM2 RING finger domain prevent the interaction of MDM2 with the E

69 educed by MKRN3 mutations affecting the RING finger domain, and that these mutations compromised the

70 ytic SET domain and an intervening MYND zinc finger domain, as well as an extended C-terminal domain.

71 uitinase activity of MKRN3 required its RING finger domain, in order to repress the promoter activity

72 ubiquitin ligase ubiquitin-like PHD and RING finger domain-containing protein 1 (UHRF1) and its DNA m

73 iquitin-like with plant homeodomain and RING finger domains 1 (Uhrf1) is essential for maintenance of

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

75 highly conserved C-terminal DNA-binding zinc finger domains.

76 Zinc finger E-box binding homeobox 1 (Zeb1) has been demonstr

77 h CRISPR/Cas9-mediated depletion of the zinc finger E-box binding homeobox 1 (ZEB1) in claudin-low tu

78 RING-finger E3 ligases are instrumental in the regulation of

79 The GATA3 zinc fingers efficiently bind their target 5'-GAT-3' sequence

80 ing the effect of wrist posture on extrinsic finger EMG activity in able-bodied subjects, these resul

81 Located on chromosome 5A, B1 is a C2H2 zinc finger encoding gene with ethylene-responsive element bi

82 revious studies have suggested that the zinc-finger epithelial-mesenchymal transition transcription f

83 ng of how a single mutation in the KLF1 zinc finger exerts effects on erythroid physiology in CDA typ

84 inger muscles, while the EMG activity of all finger extensor muscles were modulated in a similar way

85 h the highest levels of activity observed in finger extensors when the wrist was extended.

86 thesis were detected at lower rates and zinc finger family transcripts were of poorer quality.

87 sive) characteristics of the organization of finger flexion and extension movements.

88 ted the population activity in M1 for single finger flexion and extension, using 7T functional magnet

89 tary coupling between shoulder abduction and finger flexion, most probably as a result of the low res

90 Similarly, finger flexors were most active when the wrist was flexe

91 For the finger flexors, EMG variations with wrist posture were m

92 tary coupling between the shoulder and wrist/finger flexors.

93 R toward M(2)AChR, suggesting that the three-finger fold is a promising scaffold for developing G pro

94 he existence of strong synergies stabilizing finger force.

95 ysis of the H3K4me3-binding sites of the PHD fingers from PHF23, KDM5A and BPTF, suggests a common PH

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

97 ruppel-associated box domain-containing zinc finger genes on chromosome 19, both of which are associa

98 one-dimensional decoding of the movement of finger groups and in an offline two-dimensional cursor-c

99 This analysis also revealed roles for zinc-finger homeobox domain and SOX2-interacting genes in OFC

100 integrates the grasp with lift forces of the fingers in a coordinated manner.

101 Visual acuity was reduced to counting fingers in the left eye with the neovascular membrane as

102 re, the spreading test exhibits formation of fingers in the moving interfaces, there appear swirls in

103 uble mutation, which disrupts both CCHC zinc fingers in the NC domain, does not abrogate Alix-mediate

104 e to a lack of understanding of how adjacent fingers influence each other's binding specificity.

105 ata included history of cricket-related hand/finger injury leading to > 4 weeks of reduced exercise,

106 phenomenon similar to Saffman-Taylor viscous-fingering instabilities, which occur at moving interface

107 ization of CESA6 through its N-terminal zinc finger is critical in defining its functional properties

108 himeric RAG-2 protein in which the mouse PHD finger is replaced by the corresponding domain from the

109 The Cys2His2 zinc finger is the most common DNA-binding domain expanding i

110 s to be functional, only one of the two zinc fingers is folded.

111 less glove that can reconfigure all types of finger joint movements and external presses simultaneous

112 ading to > 4 weeks of reduced exercise, hand/finger joint pain on most days of the last month, self-r

113 Matched venepuncture and finger lancet DBS samples were collected from n = 100 RA

114 Filopodia are finger-like actin-rich protrusions that extend from the

115 intricate stem cell niche boundary formed by finger-like extensions generates asymmetry in stem cell

116 Microridges form by accreting simple finger-like precursors.

117 migration mechanisms-'push-pull' (forming a finger-like protrusion, adhering to an ECM node, and pul

118 on the stability and activity of RLIM (RING finger LIM-domain-interacting protein, encoded by the RN

119 The conformation of the finger loop in betaarr1 is different from that adopted b

120 lated receptor residues and insertion of the finger loop of betaarr1 into the M2R seven-transmembrane

121 taarr1 is different from that adopted by the finger loop of visual arrestin when it couples to rhodop

122 idence of a novel surface at the base of the finger loop that dictates non-GPCR interactions specifyi

123 ovel surface on beta-arr1 at the base of the finger loop, at a site that is distinct from the recepto

124 g of another compound (NITD-640) ordered the fingers loop preceding the F motif, close to the RNA tem

125 formed with a betaarr1 mutant, in which the finger-loop, required to interact with the receptor core

126 tions for the same finger (or combination of fingers) may cluster closely together, while neurons tha

127 Finger millet (Eleusine coracana L.) is gaining populari

128 Proximate analysis of finger millet genotypes revealed moisture, total carbohy

129 Nutritional and phytochemical profiling of finger millet genotypes showed its potentiality to becom

130 nutritional and phytochemical profile of ten finger millet genotypes.

131 on treated plants against pink stem borer in finger millet plants.

132 zed ten different Si transporters genes from finger millet through transcriptome assembly.

133 nsition of several segments of the thumb and fingers modules and an inward motion of the fingers subd

134 IL3 C terminus has two highly conserved zinc finger motifs containing GRXF residues (designated as Zf

135 Disruption of the zinc finger motifs in GATA-1, such as produced by germline mu

136 ic interacts with the N- and C-terminal zinc finger motifs of GATA-1, causing zinc loss and inhibitio

137 ved cysteine-rich motifs reminiscent of zinc finger motifs.

138 in sensor decodes the complex motion of five finger motions in real-time, and the rapid situation lea

139 l selection of three channels to capture all finger motions with an accuracy of about 99% for seven c

140 mmary, the observation and quantification of fingers movement in human Pol beta reported here provide

141 associated with DNA binding and prechemistry fingers movement of human Pol beta.

142 odied subjects during unrestricted wrist and finger movements across the entire range of motion.

143 his gap, we measured the kinematics of right finger movements in 17 male and female human participant

144 sights into the general organization of fine finger movements in M1.SIGNIFICANCE STATEMENT The primar

145 (M1) is important for producing individuated finger movements.

146 motor cortex (M1) organized to control fine finger movements?

147 quantify the posture-dependence of extrinsic finger muscle activity using bipolar fine-wire electrode

148 activity changed by up to 70% in individual finger muscles for the same movement, with the highest l

149 -wire electrodes inserted into the extrinsic finger muscles of able-bodied subjects during unrestrict

150 cle lengths and moment arms of the extrinsic finger muscles that cross the wrist.

151 EMG activity of all the recorded finger muscles were significantly different (p < 0.05, A

152 wrist posture were most prominent for index finger muscles, while the EMG activity of all finger ext

153 A RING finger mutant RLIM is resistant to LANA-mediated degrada

154 t assays showed that wild-type, but not zinc-finger mutant ZFP36L1, bound to HIF1A 3'UTR and mediated

155 at can be easily observed cutaneously at the finger nailfold.

156 xpressing the G551D variant obtained by zinc finger nuclease editing of a human complementary DNA sup

157 , we targeted Ubash3a in NOD mice using zinc-finger nuclease mediated mutagenesis.

158 irst with meganucleases and followed by zinc finger nucleases, transcriptional activator-like effecto

159 reported history of physician-diagnosed hand/finger OA.

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

161 ing disulfiram that directly targets the PHD finger of PHF23 (PHF23PHD).

162 The structure of the second zinc finger of SALL4 in complex with pomalidomide, cereblon a

163 in the functions of the C-tail and sigma3.2 finger of the bacterial factor suggest mechanistic conve

164 enes that include homologs of mammalian Zinc finger of the cerebellum and Purkinje cell protein 4 Dro

165 Our data support a critical role for the PHD fingers of NUP98-PHF23, and related NUP98-KDM5A and NUP9

166 ormed by the helix of the GDF9 chain and the fingers of the BMP15 chain.

167 ikely through replacing zinc within the zinc fingers of the critical transcription factor GATA-1.

168 ity was 20/100 in the right eye and counting fingers on the left.

169 Finger-operated reservoirs and valves capable of fully-r

170 Eleven of 15 patients retained count fingers or better vision, and all were considered diseas

171 d all the patients showed a BCVA of counting fingers or less.

172 In the tetrapod limb, the digits (fingers or toes) are the elements most subject to morpho

173 hile 31.2% had poor visual outcomes of count fingers or worse.

174 o different movement directions for the same finger (or combination of fingers) may cluster closely t

175 determined by (1) measuring (a) ECG and ear, finger, or toe PPG waveforms or (b) two of these PPG wav

176 uperior to other cPTTs including the popular finger PAT as a marker of changes in BP and systolic BP

177 ortical cells in monkeys responding to index finger perturbations.

178 Finger positions are perceived during both point-by-poin

179 nfirmed that speckle-type pox virus and zinc finger (POZ) protein (SPOP) functions as a substrate ada

180 , R-wave and toe PPG foot (toe PAT), ear and finger PPG feet, ear and toe PPG feet, and finger and to

181 the ECG R-wave and ear PPG foot, R-wave and finger PPG foot [finger pulse arrival time (PAT)], R-wav

182 ts, together with reference ECG and arterial finger PPG signals for validation.

183 ses were negatively correlated with arterial finger PPG.

184 gzhou, China), using two drops of blood from finger prick samples.

185 at the device can detect N-acetylasparate in finger-prick blood samples from patients with TBI, and t

186 le promise for addressing the limitations of finger-prick blood testing toward tracking glucose trend

187 the development and validation of a at-home finger-prick dried blood spot collection kit and an anal

188 thermore, we demonstrated the feasibility of finger-prick sampling for Ab detection against SARS-CoV-

189 test in capillary blood samples collected by finger-prick was noninferior to venous blood collected i

190 of acetaminophen (paracetamol) in plasma and finger-prick whole blood was fabricated.

191 e intervention arm were provided with 2 free finger-prick-based HIVST kits at enrollment and could re

192 ioning of small delicate objects (the "thick fingers" problem), and can be applied to mechanically re

193 hat control flexion or extension of the same finger produce distinct outputs, but interact tightly wi

194 The Kruppel-associated box zinc finger protein (KRAB-ZFP) family diversified in mammals.

195 effects and identify a cluster of KRAB zinc finger protein (KZFP) genes that modifies VM-IAPs in tra

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

197 CIP1-interacting zinc finger protein 1 (CIZ1) is a nuclear matrix associated p

198 expressed MYC and MIZ1 (MYC-interacting zinc-finger protein 1 [ZBTB17]).

199 protein complex with prohibitin and the ring finger protein 2 (RNF2).

200 uitin-specific peptidase 22 (Usp22) and ring finger protein 20 (Rnf20).

201 ajor stimulator of puberty, and makorin RING finger protein 3 (MKRN3) as an inhibitory signal that pr

202 Herein, Zinc finger protein 367 (ZNF367) was identified as a potentia

203 duced expression 1 (REX1; also known as zinc finger protein 42), to be selectively down-regulated in

204 forced expression of the testis-specific PHD finger protein 7 (PHF7) disrupts oogenesis, leading to e

205 Here, we show that zinc-finger protein 750 (ZNF750) opposes the migration and in

206 cal processes and diseases revealed that PHD finger protein 8 (PHF8, KDM7B) was significantly associa

207 g zinc finger array of PRDM9 (PR domain zinc finger protein 9).

208 F274, a Kruppel-associated box-A-domain zinc finger protein capable of recruiting epigenetic machiner

209 dent kinase 7 (CDK7), Cyclin H, and the RING-finger protein MAT1 form the heterotrimeric CDK-activati

210 ARS2 (arsenite-resistance protein 2), a zinc finger protein that is essential for early mammalian dev

211 awn inhibition in wheat, encodes a C2H2 zinc finger protein with EAR motifs which putatively function

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

213 Here, we identify a novel role for the zinc-finger protein ZNF281 in participating in the ordered re

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

215 We report that zinc finger protein ZPR1 binds to RNA polymerase II, interact

216 ene encoding a putative DNA binding with one finger protein, controls the stem solidness trait in whe

217 Here we report a cortex-specific PHD finger protein, Phf21b, which is highly expressed in the

218 In addition, we identify the KRAB zinc finger protein, ZNF446, and its associated tripartite mo

219 signaling and repression of the muscle ring-finger protein-1 (MURF1)-mediated ubiquitylation of pero

220 ches on two large, independent Cys2His2 zinc finger protein-DNA interaction datasets. We demonstrate

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

222 me activation, implying that other KRAB-zinc finger proteins (KZNFs) recruit KAP1 prior to blastocyst

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

224 ly of ubiquitously expressed human C2H2 zinc finger proteins comprised of ZFX, ZFY and ZNF711.

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

226 as genes coding for aminotransferases, zinc finger proteins, and several uncharacterized proteins.

227 duce three epigenome-editing platforms: zinc-finger proteins, transcriptional activator-like effector

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

229 nd ear PPG foot, R-wave and finger PPG foot [finger pulse arrival time (PAT)], R-wave and toe PPG foo

230 in ligases, members of the RING between RING fingers (RBR)-type RSL1/RFA family, are key regulators o

231 ion of the two through the known Zn-cysteine finger redox trap effect.

232 Through in vitro engineering of MT7 finger regions that was guided by the structure, we have

233 association was found between force and full finger reperfusion time (beta = -0.033 +/- 0.016; 95% CI

234 Finger temperature was associated with full finger reperfusion time (beta = -0.18 +/- 0.041; 95% CI,

235 me and clinician capillary refill time (full finger reperfusion time 1.14 s longer).

236 Correlation coefficient between full finger reperfusion time and clinician capillary refill t

237 showed a consistent difference between full finger reperfusion time and clinician capillary refill t

238 ild had 10 measurements, including five full finger reperfusion time and five clinician capillary ref

239 s should focus on the clinical value of full finger reperfusion time as a monitoring device for hemod

240 Full finger reperfusion time demonstrated good reproducibilit

241 producibility and validity of the novel full finger reperfusion time measurement using clinicians' vi

242 Full finger reperfusion time was 1.14 seconds longer than cap

243 Intraclass correlation coefficient of full finger reperfusion time within each patient was 0.76 (95

244 aveform analysis exists, referred to as full finger reperfusion time.

245 We demonstrate that unique BMP15 finger residues at this site (Arg(301), Gly(304), His(30

246 o)RORgammat(lo) (promyelocytic leukemia zinc finger, retinoic acid-related orphan receptor gT) iNKT1

247 ZFP36L1 is a tandem zinc-finger RNA-binding protein that recognizes conserved ade

248 hile it is known that shared and unique zinc finger sequences in CTCF and CTCFL enable CTCFL to bind

249 We found that the pinky finger subdomain is a major regulator of initiation and

250 fingers modules and an inward motion of the fingers subdomain-especially the O helix-to engage the p

251 The thumb, palm, and fingers subdomains of POL form an extensive interface wi

252 The potential of nuclease-deficient zinc fingers, TALEs or CRISPR fusion systems to treat these d

253 -2.3 +/- 0.21 to -2.4 +/- 0.37; P = .39), or finger tapping (from -2.3 +/- 1.20 to -2.7 +/- 1.40; P =

254 ed verb generation, sentence completion, and finger tapping functional MRI tasks were retrospectively

255 Furthermore, we found that finger tapping preceded by both imagined and executed mo

256 sing the Fugl-Meyer Assessment and the index finger tapping test.

257 port that, whereas executed movements (i.e., finger tapping) evoked neural responses in both the supe

258 t tasks of word-reading, pattern-viewing and finger-tapping.

259 Finger temperature was associated with full finger reper

260 Finally, we reveal that the N, C, and zinc finger terminal domains play unique roles in targeting e

261 nsferase Ehmt1 and stabilization of the zinc finger TF Zic2 at enhancers and promoters.

262 omain of MEX-5 contains an unstructured zinc finger that folds upon binding of its RNA target.

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

264 0.016; 95% CI, -0.065 to -0.0016; p = 0.04), finger thickness (beta = -0.20 +/- 0.089; 95% CI, -0.37

265 ncrease in motor torque rapidly returned the finger to its starting position (lever velocity >200 deg

266 and the path of allostery from the RAG-2 PHD finger to RAG-1, here we employed phylogenetic substitut

267 the fingertip of their dominant hand's index finger to rub or tap three textured surfaces (smooth fla

268 tes to the nucleus and interacts with a zinc finger transcription factor (FgZC1), also required for s

269 identified the constitutively expressed zinc finger transcription factor (TF) Zfp281 as a bidirection

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

271 mask a mutual requirement for Hivep3, a zinc finger transcription factor and adapter protein.

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

273 Odd-paired (Opa), a zinc-finger transcription factor expressed at cellularization

274 ythropoiesis is highly regulated by the zinc finger transcription factor GATA-1.

275 Here, we show that the zinc-finger transcription factor GLI1, a terminal effector of

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

277 -specifically spliced and encodes a BTB zinc-finger transcription factor proposed to be a master regu

278 interaction with the sequence-specific zinc-finger transcription factor ZNF143 and activates the exp

279 A highly conserved zinc finger transcription factor, Motif 1 Binding Protein (M1

280 t, POPOVICH (POP), which encodes a C2H2 zinc-finger transcription factor.

281 Ikaros zinc finger transcription factors are important regulators of

282 hin signalling system; a high number of zinc finger transcription factors; and novel factors that pre

283 /SET domain-containing (PRDM) family of zinc finger transcriptional regulators play diverse developme

284 Gfi1 is a zinc-finger transcriptional repressor that plays an important

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

286 nly two predicted genes, including C2H2 zinc finger transcriptional repressor TraesCS5A02G542800 upre

287 ratio is presented, in which interdigitated finger-type two-dimensional graphene electrodes are intr

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

289 essing with intermediate phalanges; only one finger was instructed to produce force at a time.

290 ontrolled bandgap behaviors and soft robotic fingers which can measure electrocardiogram from humans

291 Flexion and extension of the same finger, which never co-occur, should therefore be associ

292 s controlling opposite movements of the same finger, while producing distinct outputs, may cluster to

293 stent with locomotor power-grasping with the fingers, while that of the thumb is consistent with huma

294 meric CESA5 by replacing its N-terminal zinc finger with its CESA6 counterpart to investigate the con

295 tterns for flexion and extension of the same finger would appear very similar.

296 ier ring is structurally divided into a zinc finger (ZF) sub-ring followed by the oligosaccharide/oli

297 erozygous variants affecting the fourth zinc finger (ZF4) of Wilms' tumor 1 (WT1) (p.Ser478Thrfs*17,

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

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

300 rt mediated by a new type of monovalent zinc finger (ZnF).