ライフサイエンスコーパス: finger

1 at the cued finger while ignoring the other finger).

2 with the location of the identified arginine finger.

3 rical stimulation to the left or right index finger.

4 trimethylation through its plant homeodomain finger.

5 odule on the volar surface of his right ring finger.

6 ot patterns passing under their right middle finger.

7 le in determining the selectivity of the PHD fingers.

8 (95% CI, 15.4%-30.4%) for at least counting fingers.

9 1) compared with vertical movement and piano fingers.

10 rted fingers, the other half showing natural fingers.

11 that can result in flexible movements of the fingers.

12 ties (TUBEs) and the K29-selective Npl4 Zinc Finger 1 (NZF1) domain from the deubiquitinase TRABID to

13 omenon by which the E3 ligase mahogunin ring finger-1 (MGRN1) translocates to the nucleus in an age-d

14 ight a functional role for plant homeodomain finger 11 (PHF11) in 5' end resection at DNA double-stra

15 Here we report that PHF11 (plant homeodomain finger 11) encodes a previously unknown DDR factor invol

16 Double plant homeodomain finger 2 (DPF2) is a highly evolutionarily conserved mem

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

18 ore, increased levels of K63 and muscle RING finger 2 (MuRF2) protein could also be important enhance

19 A2 bases are recognized specifically by zinc finger 2 (ZF2) of CPSF-30 and the A4 and A5 bases by ZF3

20 time of recurrence and declined to counting fingers (20/25 to hand motion) at the most recent follow

21 BROMO domain adjacent to zinc finger 2B (BAZ2B) is a multidomain histone-binding prote

22 mportant TRPV3 region comprising an atypical finger 3 and oxygen-dependent hydroxylation site.

23 he HIV nucleocapsid p7 protein (NCp7-F2) and finger 3 of the Sp1 transcription factor (Sp1-F3).

24 ow that the noncanonical Polycomb group RING finger 3/5 (PCGF3/5)-PRC1 complex initiates recruitment

25 CCCH Zn fingers that bind to A-rich RNAs and fingers 5-7 are critical for these functions.

26 binding A11G RNA induces dimerization of Zn fingers 5-7 mediated by the novel spatial arrangement of

27 within KDM2A consisting of a CXXC type zinc finger, a PHD domain and a newly identified Heterochroma

28 al cortex commonly fail in identifying their fingers, a condition known as finger agnosia, yet are re

29 l motor neuron excitability (F-waves), index finger abduction force and electromyographic activity as

30 performing a power grip but not during index finger abduction or precision grip.

31 while performing a power grip but not index finger abduction or precision grip.

32 g different degrees of hand dexterity: index finger abduction, a precision grip, and a power grip.

33 es) in an intrinsic hand muscle during index finger abduction, precision grip and power grip.

34 grip compared with precision grip and index finger abduction, suggesting a cortical origin for these

35 grip compared with precision grip and index finger abduction.

36 in over the volar portion of his right fifth finger after a fall during a football match 3 days befor

37 performance on tasks commonly used to assess finger agnosia is modulated by changes in hand posture.

38 ntifying their fingers, a condition known as finger agnosia, yet are relatively unimpaired in sensati

39 at, in addition to binding DNA, PRDM9's zinc fingers also mediate its multimerization, and we show th

40 rmogenic gene activation and identified zinc finger and BTB domain-containing 7b (Zbtb7b) as a potent

41 The electrocardiogram and finger and ear photoplethysmograms were recorded simulta

42 ardless of the initial moisture state of the finger and of the normal force applied.

43 ators that replicate the motion of the index finger and thumb.

44 (ICD-9-CM code) of cellulitis and abscess of finger and toe (681.XX) and other cellulitis and abscess

45 The model predicted that GSCs drive invasive fingering and that GEC spontaneously form a network with

46 a conserved DNA-binding domain of three zinc fingers and a variable N-terminal domain responsible for

47 We previously identified Zhx2 (zinc fingers and homeoboxes 2) as a regulator of numerous liv

48 tact mechanics that take place between human fingers and smooth, impermeable surfaces.

49 ceding the ZF helix, conserved in two PRDM9a fingers and three PRDM9c fingers, permits adaptability t

50 d rubbing movement, vertical movement, piano fingers, and other.

51 ing small inhibitory RNAs revealed that zinc-finger antiviral protein (ZAP) inhibited virion producti

52 intermediate state where the SecA two-helix finger appears to play a role in both templating the sub

53 ll, the common input shared across different fingers are found to be at low to moderate levels, in co

54 ere-associated protein: TZAP (telomeric zinc finger-associated protein).

55 ) visual acuity was 20/70 (20/20 to counting fingers at 1 foot) at time of recurrence and declined to

56 trovirus, identified in the germline of long-fingered bats (Miniopteridae).

57 2 as the actual number of fingers between the fingers named.

58 icipants estimate the number of unstimulated fingers between two touched fingers or a localization ta

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

60 AA-3') and encompasses a Myc-associated zinc finger-binding site that regulates KRAS transcription.

61 oscopic approaches to show that the Set3 PHD finger binds di- and trimethylated states of H3K4 with c

62 a monomers occludes the active site arginine finger, blocking its access to DnaA.

63 Individuals provided a finger-blood sample to assess malaria infection by micro

64 a dual inhibitor of the bromodomain and PHD finger (BRPF) family member BRPF2 and the TATA box bindi

65 The C2H2 zinc finger (C2H2-ZF) is the most numerous protein domain in

66 alin2 S339 to leucine, which can cause Fifth Finger Camptodactyly, a human genetic disease, completel

67 s tended to be higher as compared with other finger combinations.

68 The bromodomain and plant homeodomain finger-containing (BRPF) family are scaffolding proteins

69 The BRPF (bromodomain and PHD finger-containing) family are scaffolding proteins impor

70 yadenosine RNA-binding protein, ZC3H14 (Zinc finger CysCysCysHis domain-containing protein 14), that

71 p understand the working principle and guide finger design, revealing amplification when the cavity m

72 on of proteins is primarily mediated by zinc finger DHHC domain-containing palmitoyltransferases (ZDH

73 l acyltransferase enzymes, a group of Zn(2+)-finger DHHC-domain-containing proteins (ZDHHC).

74 CCCTC-binding factor (CTCF) is an 11 zinc finger DNA-binding domain protein that regulates gene ex

75 5 gene-targeting strategy: a Dlg4/PSD95 zinc finger DNA-binding domain was engineered and fused to ef

76 SEE FINGER DOI101093/AWW312 FOR A SCIENTIFIC COMMENTARY ON T

77 The fast recruitment is mediated by the zinc finger domain and poly (ADP-ribose) (PAR).

78 both its physical interaction to GR and zinc finger domain appear to be required for ZNF764 to regula

79 e specificity of the mutant recombinant zinc finger domain by performing biophysical measurements of

80 of over 100 previously uncharacterised zinc finger domain containing genes, located on the long arm

81 ion, whereas deletion of its C-terminal zinc-finger domain diminished this effect.

82 al structure of the tandem plant homeodomain finger domain of human DPF2 at 1.6-A resolution.

83 hows that the binding specificity of the PHD-finger domain of VIN3 plays a role in mediating a proper

84 ration in the binding specificity of the PHD-finger domain of VIN3 results in a hypervernalization re

85 hly conserved amino acid residue in the zinc finger domain of ZNHIT3.

86 VIN3 encodes a PHD-finger domain that binds to modified histones in vitro.

87 neous-backbone foldamers that mimic the zinc finger domain, a ubiquitous and biologically important m

88 nts with two mutated ankyrin repeat and zinc-finger domain-containing 1 (ANKZF1) alleles (homozygous

89 ified a transcriptional repressor, GATA zinc finger domain-containing 2B (GATAD2B), that interacted s

90 due within a novel viral integrase-like zinc finger domain.

91 nning membrane protein with a cytosolic RING finger domain.

92 ions (R674G and Q697R) of amino acids in the fingers domain that coordinate the incoming dNTP.

93 inc finger protein 1) POZ (POxvirus and Zinc finger) domain in Schwann cells causes a neuropathy.

94 In addition to zinc finger domains in CPSF30, we identify using quantitative

95 cription factors that contain conserved zinc finger domains involved in binding to target DNA sequenc

96 iddle of the DH that is composed of the zinc finger domains of both hexamers.

97 To assess the effect of zinc finger E box-binding homeobox 1 transcription factor (ZE

98 Induced by the EMT, zinc finger E-box binding homeobox 1 (ZEB1) binds and silence

99 transition (EMT) through activation of zinc finger E-box binding homeobox 1 (ZEB1) sensitized tumor

100 Mechanistically, we find that the ZEB1 (zinc finger E-box binding homeobox 1) transcription factor ac

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

102 Elevated expression of the Zinc finger E-box binding homeobox transcription factor-2 (ZE

103 ZEB1 is a zinc finger E-box binding transcription factor known for part

104 We identify SIAH2, a RING finger E3 ubiquitin ligase associated with the cellular

105 osphoproteomics, we have identified the RING finger E3 ubiquitin ligase RNF157 as a target at the int

106 mune cell interactions and a cluster of zinc finger-encoding genes associated with KMT2A rearrangemen

107 a programmable stimulator, and the resultant finger flexion joint angles were recorded using a motion

108 Here we co-crystallized the six-finger fragment ZF8-13 of PRDM9c, in complex with an oli

109 ional regulators such as Myc-associated zinc finger from accessing their binding sites on the KRAS pr

110 The process by which human fingers gives rise to stable contacts with smooth, hard

111 Piano fingers had the highest failure rate (36.5%).

112 For instance, a pointing finger held still for an extended period of time could a

113 of ZF11 with two other fingers, yielding 14 fingers in PRDM9c.

114 llowing for studies of phenomena such as the fingering instability or wound healing.

115 heory that grasping with the thumb and index finger is based on a combination of two goal-directed si

116 The finger is conserved in all algal septin sequences, sugge

117 tin cytoskeleton and report the existence of finger-like actin-based protrusions at fusion sites in v

118 Macrophage filopodia, finger-like membrane protrusions, were first implicated

119 The fabricated membranes exhibited finger-like pore morphologies and varying pore sizes.

120 nding surface, suggests a feature called the finger loop as a key region of the activation sensor.

121 hand control in humans with SCI during gross finger manipulations and suggest that this contribution

122 nal excitability during gross more than fine finger manipulations are largely cortical in origin and

123 present during power grip compared with fine finger manipulations are largely cortical in origin and

124 Drought transcriptome analysis of finger millet (Eleusine coracana) by cDNA subtraction id

125 The wheat finger millet (WFM) flour blend displayed up to 30.7% hi

126 Wheat and finger millet flour (two cultivars) were blended in the

127 ansferring genes from far related crops like finger millet.

128 if the invading fluid wets the beads while a fingered morphology is found for non-wetting invading fl

129 JMJ27 is a nuclear protein containing a zinc-finger motif and a catalytic JmjC domain with conserved

130 affect a single conserved residue in a zinc finger motif crucial for DNA binding and are deleterious

131 lencer for Thpok, and requires the last zinc-finger motif in Bcl11b protein, which by contrast is dis

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

133 lls revealed that intact PIN domain and Zinc finger motifs in human hUTP23 are essential for 18S rRNA

134 The individual finger motions averaged across the three joints were ana

135 an movements, including pulse monitoring and finger motions.

136 nsor is demonstrated to be able to recognize finger movement, hand gestures, acoustic vibrations, and

137 o suppress but not to execute upcoming rapid finger movements, which is probably related to impaired

138 ntribute to hand motor tasks involving gross finger movements.

139 y acquired through training on a sequence of finger movements.

140 ion is less pronounced during fine dexterous finger movements.

141 ion is less pronounced during fine dexterous finger movements.SIGNIFICANCE STATEMENT It has been long

142 m electromyographic activity in an intrinsic finger muscle during three motor tasks requiring differe

143 cospinal tract contributes to the control of finger muscles during precision and power grip.

144 were further identified in vivo in urine and finger nail samples, this suggests that in vitro assays

145 estigated by LC/ESI-Orbitrap-MS in urine and finger nails collected from a Norwegian cohort.

146 Finger nails may be a useful noninvasive matrix for huma

147 abolites had detection frequencies (% DF) in finger nails ranging from 46 to 95%.

148 V6 was identified for the first time in finger nails, suggesting that this matrix may also indic

149 detected in urine (97% DF) and identified in finger nails, while no DPHP metabolites were detected in

150 dary metabolites was higher in urine than in finger nails; the opposite was observed for the primary

151 as the actual number of fingers between the fingers named.

152 loped a novel Bace1(-/-) rat line using zinc-finger nuclease technology and compared Bace1(-/-) mice

153 Here we develop a zinc-finger nuclease translocation reporter and screen for fa

154 ochondrial DNA (mtDNA) damage and after zinc finger nuclease-mediated gene mutation correction, mtDNA

155 ains (including wild-type CC-125) using zinc-finger nucleases (ZFNs), genetically encoded CRISPR/asso

156 tor-like effector nucleases (TALENs) or zinc-finger nucleases (ZFNs).

157 In addition, we used Zinc finger nucleases to generate isogenic SHANK3 knockout hu

158 We used zinc finger nucleases to induce stable expression of human im

159 the non-coding region of the CCHC-type zinc finger nucleic acid-binding protein (CNBP) gene.

160 Judged finger numerosity was analysed, in Exp.

161 This is the first report of an arginine finger observed in a septin and suggests that CrSEPT may

162 We show that the second PHD finger of CHD4 initiates recruitment to the nucleosome,

163 e how a missense mutation in the second zinc finger of Kruppel-like factor-1 (KLF1) leads to degenera

164 The plant homeodomain (PHD) finger of Set3 binds methylated lysine 4 of histone H3 i

165 entical to the prototype sequence (the third finger of specificity factor 1) and enhanced thermodynam

166 es not make sequence-specific contacts, each finger of ZF3-7 contacts three bases of the 15-bp consen

167 membrane was integrated over array of micro fingers of gold based sensor chip using double side tape

168 oove, which specifically recognizes the zinc fingers of JKD.

169 nants of methyllysine recognition by the PHD fingers of Set3 and its orthologs.

170 A pair of readers, the PHD fingers of the protein CHD4, has been shown to bivalentl

171 of unstimulated fingers between two touched fingers or a localization task in which participants jud

172 at emits light from regions touched by human fingers (or painted upon using a mixture of oil and wate

173 atients who have not undergone AHSCT, namely finger pad inflammation, palmar violaceous papules, and

174 The synthetic gold finger peptides were derived from the C-terminus of the

175 erved in two PRDM9a fingers and three PRDM9c fingers, permits adaptability to variations from a C:G b

176 Blood pressure (finger photoplethysmography), heart rate (electrocardiog

177 scription factor promyelocytic leukemia zinc finger (PLZF) seemed to control the ROS levels.

178 scription factor promyelocytic leukemia zinc finger (PLZF), as well as expression of intracellular si

179 e involved when the same participants used a finger press to make semantic association decisions on t

180 Finger-prick blood samples from consenting individuals o

181 Matched urine and finger-prick blood samples from participants >/=2 years

182 Using 100 microl finger-prick blood samples, the Cepheid Xpert HIV-1 Vira

183 including a simple microcentrifugation step, finger-prick PoC testing was a quick and accurate approa

184 y of an off-label protocol using whole blood finger-prick samples tested with and without a simple th

185 ated by the novel spatial arrangement of the fingers promoting each RNA chain binding two protein cha

186 rapidly evolving Kruppel-associated box-zinc finger protein (KRAB-ZFP) family linked primarily to sil

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

188 proteins of the Polycomb complex is the Ring finger protein 1 (RING1).

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

190 e deletion of the Miz1 (Myc-interacting zinc finger protein 1) POZ (POxvirus and Zinc finger) domain

191 The RNA-binding Zinc-finger protein 106 (ZFP106) detected in both libraries w

192 We identify RING finger protein 113A (RNF113A) as the E3 ligase responsib

193 identifies allele-preferred binding of Zinc finger protein 148 (ZNF148) to rs36115365-C, further sup

194 nocatmin 6; chromosome 15), and Rnf220 (Ring finger protein 220; chromosome 4) were considered candid

195 We also found that the ring finger protein 41 (RNF41) as an E3 ligase ubiquitinated

196 nvestigate the interaction of CXXC-type zinc finger protein 5 (CXXC5) with Dishevelled as one such ne

197 We identify zinc finger protein 568 (ZFP568), a member of the rapidly evo

198 We studied the Zinc Finger Protein 598 (ZNF598) using PAR-CLIP and revealed

199 scribe the function of the plant homeodomain finger protein 6 (PHF6) in leukemia and define its role

200 or male-specific lethal [MSL] proteins) zinc finger protein binds these GA repeat motifs, increases c

201 e, we report that the CDKN1-interacting zinc finger protein CIZ1 is critical for localization of Xist

202 The zinc finger protein CTCF has been invoked in establishing bou

203 chromatin neighbourhoods, formed by the zinc-finger protein CTCF, can sequester enhancers and their t

204 The C2H2 zinc-finger protein Pita binds to several BX-C boundaries, in

205 ZNHIT3 encodes a nuclear zinc finger protein previously implicated in transcriptional

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

207 istinct complex containing Mtr4 and the zinc finger protein ZFC3H1.

208 Here, we identify the zinc finger protein Zfp106 as a specific GGGGCC RNA repeat-bi

209 ex bound to DNA by the ES cell-specific zinc-finger protein ZFP809.

210 Further analyses of the zinc finger protein Zfp871 and BTB/POZ domain transcription f

211 biochemistry approaches we identified the Zn-finger protein ZNF326, as a novel interaction partner an

212 The C2H2-type zinc finger protein ZNF764 acts as an enhancer for several st

213 The zinc finger protein ZPR1 interacts with SMN.

214 ll lineage that a spermatocyte-specific zinc finger protein, Kumgang (Kmg), working with the chromati

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

216 Here we show that a zinc finger protein, ZIC2, a key regulator for central nervou

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

218 coys on the search process of the Egr-1 zinc-finger protein.

219 paratus-specific Asp-His-His-Cys (DHHC) zinc finger protein.

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

221 paratus-specific Asp-His-His-Cys (DHHC) zinc finger protein; (ii) a GODZ dominant-negative mutant and

222 Kruppel-associated box zinc-finger proteins (KRAB-ZFPs) make up the largest family o

223 ally compared four different engineered zinc finger proteins (ZFP), four transcription activator-like

224 nown CRBN neo-substrates [Ikaros family zinc finger proteins 1 (IKZF1) and 3 (IKZF3), casein kinase 1

225 odysplastic syndrome 1 (MDS)/EVI encode zinc-finger proteins that have been recognized as important o

226 r complex, which involves multiple KRAB zinc finger proteins, shields neuronal genomes from excess CT

227 mutational analysis reveals a trans-arginine finger, R158, indispensable for ATP hydrolysis; (iii) th

228 ture, but also cluster within the N-terminal Finger region, indicating the presence of an activator i

229 -domain-containing proteins (PRDMs) are zinc-finger sequence-specific chromatin factors that have ess

230 Finger skin necrosis and histologic signs of severe chro

231 itioned their hand in two postures, with the fingers splayed (Apart posture) or pressed together (Tog

232 f ubiquitin, E1-like, E2-like and small-RING finger (srfp) protein components in the Aigarchaeota and

233 Small-volume blood samples were collected by finger stick at twice-weekly intervals and tested with t

234 rate, quantitative assessment of 25(OH)D3 in finger-stick blood.

235 Plasma and finger-stick capillary whole-blood samples were collecte

236 t HCV Viral Load assay with venepuncture and finger-stick capillary whole-blood samples.

237 st for HCV RNA detection by venepuncture and finger-stick collection with the Abbott RealTime HCV Vir

238 or HCV RNA detection in samples collected by finger-stick was 95.5% (95% CI 84.5-99.4) and specificit

239 -PKA pathway that inactivates conserved zinc finger stress-resistance transcription factors to sensit

240 e immediately adjacent to the SecA two-helix finger subdomain before channel entry.

241 to the body of lateral ventricles, Dawson's fingers, T1 hypointense lesions (multiple sclerosis), fl

242 Patients interrupted finger tapping (paced by a metronome) in response to a s

243 coherence between the middle and ring-little fingers tended to be higher as compared with other finge

244 odular structure that includes seven CCCH Zn fingers that bind to A-rich RNAs and fingers 5-7 are cri

245 ges of hands, half of them showing distorted fingers, the other half showing natural fingers.

246 ally human behavior, which involves moving a finger through space to direct an addressee towards a de

247 both repair methods, touch thresholds at the finger tips recovered to 81 +/- 3% and tactile gnosis on

248 th participants feeling and estimating their finger to be longer after the rising pitch condition.

249 Bromodomain PHD finger transcription factor (BPTF) is the largest subuni

250 c reprogramming, we discovered that the zinc finger transcription factor 281 (ZNF281) potently stimul

251 D) complex binding are required for the zinc-finger transcription factor CASZ1 to function as a neuro

252 Here, we identify the zinc finger transcription factor EGR1 as a negative regulator

253 Here, we identify a zinc-finger transcription factor Hindsight (Hnt) as the first

254 Kruppel-like factor 4 (KLF4, GKLF) is a zinc-finger transcription factor involved in a large variety

255 The Zfp423/ZNF423 gene encodes a 30-zinc-finger transcription factor involved in key developmenta

256 between Drosophila FOXO (dFOXO) and the zinc finger transcription factor Kruppel homolog 1 (Kr-h1), o

257 3 (Peg3), an imprinted gene encoding a zinc finger transcription factor postulated to function as a

258 osterix (osx; sp7) encodes a zinc-finger transcription factor that controls osteoblast dif

259 Here we establish the zinc finger transcription factor Tshz1 as a marker of ITCs du

260 FICANCE STATEMENT We show here that the zinc finger transcription factor Tshz1 is expressed during de

261 EGR1 is an early growth response zinc finger transcription factor with broad actions, includin

262 Yin and yang 1 (YY1) is a well-known zinc-finger transcription factor with crucial roles in normal

263 We show that Combgap (Cg), a zinc-finger transcription factor, antagonizes Eya-So function

264 ke factor 15 (KLF15), a kidney-enriched zinc finger transcription factor, is required for restoring p

265 rt the functional characterization of a zinc finger transcription factor, OsGATA12, whose overexpress

266 is study, we have identified the Ikaros zinc finger transcription factors Aiolos and Ikaros as novel

267 nism through which STAT3 and the Ikaros zinc finger transcription factors Aiolos and Ikaros cooperate

268 o proteins comprising the ZEB family of zinc finger transcription factors, ZEB1 and ZEB2, execute EMT

269 sly demonstrated that expression of the zinc finger transcriptional repressor Blimp1/PRDM1 is essenti

270 anscriptional targets recognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an essent

271 binding affinity for Klumpfuss (Klu), a zinc finger transcriptional repressor that regulates ss expre

272 nd RNA interference targeting mRNA, and zinc finger transcriptional repressors and CRISPR-Cas9 method

273 virally delivered RNA interference and zinc finger transcriptional repressors in advanced testing in

274 a symptom cluster including memory loss and finger tremor (OR 14, 95% CI: 3.5, 57).

275 er observe that restoration of Nrdp1, a RING finger type E3 ubiquitin ligase whose suppression in GBM

276 at, together with its ubiquitin-binding zinc finger (UBZ) domain, helps recruit FAN1 to ubiquitylated

277 tion) the iS1 at rest and during tonic index finger voluntary activity.

278 cortex (iS1) to sensory gating during index finger voluntary activity.

279 d to suppress but not to execute rapid index finger voluntary contractions in individuals with SCI co

280 At physical examination, the injured finger was swollen and purple.

281 litude during attention compared to when the finger was unattended.

282 We demonstrate a skinlike finger-wearable driver for a light-emitting diode.

283 Across blocks, the fingers were placed in three levels of splay.

284 ts were greater when non-adjacent stimulated fingers were positioned far apart compared to when they

285 ased judgments in both orientations when the fingers were splayed.

286 n task in which participants judge which two fingers were stimulated.

287 reas judgements were unaltered when adjacent fingers were stimulated.

288 proved to 20/150 from a baseline of counting fingers, whereas the frozen group improved to 20/400 fro

289 l is the creation of high aspect-ratio metal fingers which provide an optically narrow and low resist

290 ehavioral goal ("detect" stimuli at the cued finger while ignoring the other finger).

291 and a disulfide-stabilized C-terminal "index finger," yet how these binding events trigger receptor a

292 F9 and by replacement of ZF11 with two other fingers, yielding 14 fingers in PRDM9c.

293 Polydactyl zinc finger (ZF) proteins have prominent roles in gene regula

294 uence-specific DNA binding via its C2H2 zinc finger (ZF) tandem array, which is highly polymorphic wi

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

296 ariant, PRDM9 allele A (PRDM9a), contains 13 fingers (ZF1-13).

297 (CTCF), containing a tandem array of 11 zinc fingers (ZFs), modulates the three-dimensional organizat

298 ules: full-length DNA binding proteins, zinc fingers (ZFs), transcription activator-like effector (TA

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

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