ライフサイエンスコーパス: be localized at

1 This regulatory element was localized at -246 to -233 base pairs upstream from t

2 t103 and the Rat1/Rai1 5' --> 3' exonuclease are localized at 3' ends of protein coding genes.

3 suggest that the most frequent region of LOH is localized at 3p24.3.

4 A functional cAMP response element (CRE) was localized at -48 in the CFTR promoter, and we have a

5 ional sensing by G protein-coupled receptors is localized at a discrete step in the signaling pathway

6 The m.7551A > G mutation is localized at a highly conserved nucleotide(A37), adja

7 The NGF target is localized at a postsynaptic site and involves a new T

8 plication were blocked; however, the Z-rings were localized at a subpolar region of the cell.

9 ing epitope-tagged Myo5p indicate that Myo5p is localized at actin patches.

10 mmunofluorescence analysis shows that PDZD11 is localized at adherens junctions in a PLEKHA7-dependen

11 Both cadherin complex components and L1CAM are localized at all sites of cell-cell contact during g

12 cell-conditioned medium, proliferating cells were localized at ampullae, where a binding receptor for

13 Dlg is localized at and required for the formation of both s

14 hird transcriptional unit, designated csk22, was localized at approximately 173 degrees on the chromo

15 we found that in interphase, Sec13 and Nup96 are localized at both sides of the NPC in addition to ot

16 major inhibitory receptors in the brain and are localized at both synaptic and extrasynaptic membran

17 GABA(A) receptors (GABA(A)-Rs) are localized at both synaptic and extrasynaptic sites,

18 ed obscurin, has been described and found to be localized at both the M-lines and Z-discs of striated

19 Moreover, a p95 partner protein has been localized at both focal adhesions and actin-cytoske

20 PDGF-A and -B chains have now been localized at both the mRNA and protein levels to th

21 OCT3 protein is localized at both basolateral (blood-facing) and apic

22 for3p-GFP is localized at both cell tips in an actin-dependent man

23 We show that SDCCAG8 is localized at both centrioles and interacts directly w

24 We show that Nasonia otd maternal mRNA is localized at both poles of the embryo, and resulting

25 ssed on both the mRNA and protein levels and is localized at both the apical and basolateral membrane

26 the capillary in that the TNF-alpha effects were localized at branch points, while the arachidonate

27 s a cell-cycle-related localization pattern, being localized at cell ends during interphase and formi

28 ly deposited RNA is present, and the protein is localized at cell membranes during cellularization.

29 Moreover, PSGAP is localized at cell periphery in fibroblasts in a pleck

30 Components of this complex are localized at centrosomes and spindle poles from inte

31 Furthermore, UVRAG was also found to be localized at centrosomes and physically associated wi

32 APC/C activator Fizzy-related (Fzr or Cdh1) is localized at centrosomes in animal cells.

33 taining also reveals that the SAPAP proteins are localized at cholinergic synapses, including neurona

34 PRODH is localized at chromosome 22q11 in a region deleted in

35 The CAPN14 gene is localized at chromosome 2p23.1-p21 and is most homolo

36 The LOT1 gene is localized at chromosome 6q24-25, a chromosomal region

37 des a protein with 276 amino acids; the gene is localized at chromosome 9q34.

38 The gene for PrLZ was localized at chromosome 8q21.1, a locus most frequen

39 w that two components of the insulin pathway are localized at CNS synapses, where they are components

40 that dynactin, the dynein-activator complex, is localized at cortical microtubule attachment sites an

41 TNFR2 was localized at cortical neurons including parvalbumin-

42 nd the dystrophin-glycoprotein complex (DGC) are localized at costameres and neuromuscular junctions

43 s of the planar cell polarity (PCP) pathway, are localized at developing glutamatergic synapses and i

44 molecules (CAM) neurofascin (NF) and Nr-CAM are localized at developing nodes of Ranvier in peripher

45 gap is smaller and because its HOMO and LUMO are localized at different stations (HOMO exclusively at

46 IPL, suggesting that the two alpha-subunits are localized at different synaptic sites.

47 PolC-GFP was localized at discrete intracellular positions, predo

48 binatorial alternative splicing pathways and is localized at diverse intracellular sites including th

49 lK from Bacillus subtilis (WalK(Bsu)), which is localized at division septa, immunofluorescence micro

50 ence microscopy, we have now shown that PBP1 is localized at division sites in vegetative cells of B.

51 The direct interaction of CaM with DR5 is localized at DR5 death domain.

52 Actomyosin-rich purse strings are localized at each of the two leading edges of latera

53 Although previous work has shown that Erk is localized at endosomal compartments, no role for Erk

54 ANSPORT I (ESCRT-I) component ELCH (ELC) and is localized at ESCRT-I-positive late endosomes likely t

55 AMPA receptors are localized at excitatory synapses and are not found o

56 The EphB receptor tyrosine kinases are localized at excitatory synapses where they cluster

57 in the control of junction assembly and has been localized at extrajunctional sites in association w

58 The protein is localized at focal contacts in adherent erythroleukem

59 0-76% of connexin-36-immunolabeled particles were localized at focal sites on apposed plasma membrane

60 tem, but it is not known how these receptors are localized at GABA-dependent synapses.

61 We show that ErbB4 is localized at GABAergic terminals of the prefrontal co

62 Heterochromatin protein 1 (HP1) is localized at heterochromatin sites where it mediates

63 morphogenetic protein-4 (Bmp-4) transcripts are localized at high levels in the distal tips of the e

64 ymmetrically expressed in the myocardium and is localized at high levels on the basal side of the myo

65 ound that a portion of the active MAP kinase is localized at kinetochores, asters, and the midbody du

66 human katanin antibody and that this protein is localized, at least in part, to the basal body comple

67 on ultrastructural analysis showed that CD44 was localized at mature synapses in the adult brain.

68 GFP-FtsL was localized at mid-cell in vegetative cells and at the

69 at, like Cdc20, previously has been shown to be localized at mitotic spindle poles and is involved in

70 ron microscopy provide evidence that GABAARs are localized at MNTB axon terminals.

71 Ca(v)2.2 channels are localized at nerve terminals where they play a criti

72 AnkyrinGs of 270 and 480 kDa are localized at nodes of Ranvier and are candidates to

73 that phosphatidylinositol signaling pathways are localized at nuclear speckles.

74 And the spin-up electrons are localized at one edge, the spin-down holes localized

75 IcsA, which is localized at one pole of the bacterium, mediates acti

76 Proteins within these pathways are localized at opposite ends of the cell to generate t

77 Moreover, at metaphase, some ATRX is localized at or close to the ribosomal DNA (rDNA) arr

78 In addition, AP1M2 was localized at or near the trans-Golgi network.

79 ven proximal aphidicolin-induced breakpoints were localized at or near the end of a THE element.

80 logical analyses suggest that these proteins are localized at particular sites within the chromosome.

81 result is that electrochemical reactions can be localized at particular locations on the perimeter of

82 (SRIF) receptor subtype, the sst2A receptor, is localized at postsynaptic sites of the principal neur

83 rge proteins that contain two C2-domains and are localized at presynaptic active zones, where neurotr

84 co-culture system to show that P2X receptors are localized at presynaptic sites on DRG neurons; that

85 Immunoelectron microscopy shows that FMRP is localized at presynaptic terminals and in axons withi

86 SYD-2 protein is localized at presynaptic termini independently of the

87 We show that Mcm1 is localized at replication origins and plays an importa

88 The spins are localized at silicon step edges having the form of g

89 mmadelta T cells, but not alphabeta T cells, were localized at sites of DSS-induced epithelial cell d

90 ELG1 protein interacts with PCNAs that are localized at stalled replication forks.

91 ious studies have shown that the M2 receptor is localized at steady state to the apical domain in Mad

92 ed in nonsyndromic progressive hearing loss, is localized at stereocilia tips.

93 bsite -1, even though both Glu180 and Asp309 are localized at subsite 1.

94 The SAPAP proteins are localized at synapses in a manner consistent with mR

95 ine receptor (AChR) clustering in vitro, and are localized at synapses in vivo.

96 a prevailing assumption that beta1-integrins are localized at synapses, where they contribute to syna

97 Microscopic analysis confirmed that Gs alpha is localized at synapses both pre- and postsynaptically.

98 ted membrane protein) family of proteins and is localized at synapses.

99 tochondria were significantly more likely to be localized at synaptic sites.

100 omo- and heterodimers with TRF1; both dimers were localized at telomeres.

101 sion site by binding to its substrate, which is localized at that place.

102 Breaks in chromosome 18 are localized at the 3'-UTR of BCL2 gene or downstream a

103 yze the interconversion between SA and MeSA, are localized at the apical region of pollen tubes, indi

104 ZeExp1 and ZeExp3 mRNA are localized at the apical tip, whereas ZeExp2 mRNA is

105 proteins of Mycobacterium tuberculosis that are localized at the bacterial cell surface or secreted

106 lear matrix, indicating that these sequences are localized at the base of chromatin loops.

107 Because NHERF1 and -2 are localized at the BB, where they bind NHE3 as well as

108 teropentamers and their ligand binding sites are localized at the beta+ / alpha- interfaces.

109 y through interaction with EI and HPr, which are localized at the cell pole.

110 eria indicates that certain PE_PGRS proteins are localized at the cell surface of BCG and M. tubercul

111 on molecule and the Shaker potassium channel are localized at the Drosophila neuromuscular junction,

112 mechanical insulator whose zero-energy modes are localized at the edge.

113 ne H3 dimethylated at lysine 4 (di-Me H3-K4) are localized at the ends of the active DJ domains of bo

114 mRNA and its zipcode-binding protein, ZBP1, are localized at the growth cone and become asymmetrical

115 moesin family (ERM) of adapter proteins that are localized at the interface between the cell membrane

116 ly the existence of such states: states that are localized at the interface between two topologically

117 recursors, the three reversible redox events are localized at the iron centers distal from the NO lig

118 Mn(+2)-activatable receptors for ATX, which are localized at the leading edge of polarized cells.

119 trates UvrAB introduces changes in DNA which are localized at the lesion and are limited to 1-3 bp.

120 Within the structure, individual taxa are localized at the micron scale in ways suggestive of

121 the cell but exist as defined clusters that are localized at the mid-cell, or at the 1/4 and 3/4 cel

122 and dimethylated H3R8 (histone 3 arginine 8) are localized at the myogenin promoter in differentiatin

123 g mutant nesprin-1alpha, lamin A/C and SUN2, are localized at the nuclear membrane in this model.

124 Both are localized at the pilus tip, and HifE appears to medi

125 ry we show that endogenous Kir2.1 and Kir2.2 are localized at the plasma membrane and T-tubules in ro

126 apparent proportions of DHE and filipin that are localized at the plasma membrane.

127 g cells in Ae. aegypti and Anopheles gambiae are localized at the posterior part of the posterior mid

128 s receptors, ErbB receptor tyrosine kinases, are localized at the postjunctional membrane presumably

129 The eigenstates with the smallest spacing are localized at the saddle point.

130 usively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars.

131 le-specific ankyrin isoforms, ankB and ankG, are localized at the subsarcolemma level, at which they

132 r the interior whereas for D < 4 nm the ions are localized at the surface, but with much less tendenc

133 ess to CCL21 and CCL19 than do FO cells, and are localized at the T/B cell border in spleen.

134 tron superatoms, where the 8 shell electrons are localized at the two icosahedral halves of the metal

135 rB operon, virB1 and virB2, are predicted to be localized at the bacterial surface, where they could

136 e protein, CheW, into complexes that tend to be localized at the cell poles.

137 ith confocal microscopy, we found ratAurA to be localized at the centrosome in normal and neoplastic

138 Moreover, a fraction of Crm1 was found to be localized at the centrosomes.

139 GfsA was found to be localized at the Golgi apparatus based on cellular fr

140 ucleotide sugars and is demonstrated here to be localized at the Golgi apparatus.

141 In solution, the conantokins appear to be localized at the headgroup of vesicles and do not ins

142 Neutron diffraction studies showed VP1 to be localized at the hydrophobic core of model palmitoylo

143 se2 where palmitoylation occurs was found to be localized at the inner leaflet of the plasma membrane

144 e junctional SR, a small number of RyR2s can be localized at the middle of the sarcomere and in the z

145 acetylcholinesterase (A(12)-AChE) appears to be localized at the neuromuscular junction in associatio

146 Additionally, c-di-GMP was found to be localized at the outer boundary of mature colonies in

147 ed to have a membrane-spanning domain and to be localized at the plasma membrane.

148 juxtanuclear compartment and also appears to be localized at the plasma membrane.

149 ansduction channel of hair cells, thought to be localized at the tips of their stereocilia.

150 AR has been localized at the sites of tissue damage, and inhibi

151 mmunoprecipitation assays indicated that BAD is localized at the 12-O-tetradecanoylphorbol-13-acetate

152 the anterior segmentation gene bicoid (bcd) is localized at the anterior pole of the Drosophila egg

153 EGL-26 is localized at the apical edge of the vulE cell.

154 Nf2 is localized at the apical region of NPCs.

155 Interestingly, the Au plasmon resonance is localized at the Au/vacuum interface, rather than pre

156 The Shaker-type K channel Kv1.1 is localized at the axon arborization preceding the term

157 teins form a complex called the BBSome which is localized at the basal body or ciliary axoneme and re

158 We also found that Dlg5 is localized at the basal body, where it associates with

159 of these phenotypes, endogenous Cby protein is localized at the base of cilia.

160 We report that Sept7 is localized at the base of dendritic protrusions and at

161 sicles at the presynaptic active zone, which is localized at the base of the ribbon.

162 In this paper, we show that Dlg1 is localized at the basolateral cell cortex during mitos

163 es uptake of conjugated bile acids (BAs) and is localized at the basolateral membrane of hepatocytes.

164 The epidermal growth factor receptor (EGFR) is localized at the basolateral membrane of most epithel

165 Here, we have shown that Mct8 is localized at the basolateral membrane of thyrocytes a

166 pithelia, the TGFbeta type II receptor (T2R) is localized at the basolateral membranes.

167 e and porcine eyes indicated that bestrophin is localized at the basolateral plasma membrane of RPE c

168 r, termed the isthmic organizer (IsO), which is localized at the boundary between them.

169 er, charge resonance vanishes and the cation is localized at the bridge center (the mixed valence pro

170 The Chk1-interacting region of CK2beta is localized at the C-terminus and the complex between C

171 mes occur at the replication terminus, which is localized at the cell center.

172 RGS-7 is localized at the cell cortex, and its effects require

173 We found that Bud5 is localized at the cell division site and the presumpti

174 Both of these methods revealed that DnaA is localized at the cell membrane, further suggesting th

175 In resting cells, most of the eNOS is localized at the cell membrane.

176 nd cultured neuroendocrine PC12 cells, Glut3 is localized at the cell surface and, also, in a distinc

177 y glycosylated CD39 has apyrase activity and is localized at the cell surface.

178 A C-terminal Pro-Cys motif is localized at the center of the tetramer and forms rev

179 Green fluorescent protein-C-terminal Plk is localized at the centrosome and the midbody of transf

180 ds are necessary for activity; and (e) BARD1 is localized at the centrosome throughout the cell cycle

181 The peptide with intermediate affinity (RP2) is localized at the ciliary transition zone as a gate ke

182 Fak protein is localized at the cortex of notochord cells and at the

183 sites for the guanosine triphosphatase Ran, is localized at the cytoplasmic periphery of the nuclear

184 Because iPLA2gamma is localized at the endoplasmic reticulum (ER), this stu

185 with two predicted transmembrane helices and is localized at the endoplasmic reticulum.

186 For the tryptic peptides, fragmentation is localized at the ends of the peptides suggesting that

187 GBA2 is localized at the ER and Golgi, which puts GBA2 in a k

188 ve-cell imaging analyses revealed that ORP3a is localized at the ER, and that binding to this organel

189 Dasm1 is localized at the excitatory synapses.

190 In swarmer cells, a short form of PodJ is localized at the flagellated pole.

191 that the RAD50-interacting protein, RINT-1, is localized at the Golgi apparatus and the centrosome i

192 ed-coil protein, also known as giantin, that is localized at the Golgi membrane.

193 Additionally, PITPbeta is localized at the Golgi, and EGF stimulation resulted

194 subunit interaction domain, NAB(HERG), that is localized at the hydrophilic cytoplasmic N terminus a

195 tein Np65, encoded by the Neuroplastin gene, is localized at the IHC presynaptic region.

196 nfocal microscopy analysis showed that IL-15 is localized at the immunologic synapse of LCs and naive

197 Because activated ERK is localized at the immunological synapse, we investigat

198 itochondrial membrane (OMM), while 3betaHSD2 is localized at the inner mitochondrial space (IMS), whe

199 The peptide is localized at the interface between membrane and solve

200 crystal structure of PKCbeta showed that it is localized at the interface between the C2 and catalyt

201 cts: (i) contactin-associated protein-2 that is localized at the juxtaparanodes in myelinated axons;

202 h is phosphorylated on tyrosine residue 342, is localized at the membrane.

203 We show that activated RhoA is localized at the mitotic cell cortex, and Rho-associa

204 eorganization contribution to DeltaDeltaH(U) is localized at the mutation site, in contrast to enviro

205 The formation of this ordered phase is localized at the nanometre scale; with increasing wat

206 Id3 is localized at the neural plate border during gastrulat

207 c-myc is localized at the neural plate border prior to the exp

208 oscopy showed that a portion of Sindbis nsP3 is localized at the nuclear envelope, suggesting a possi

209 GFP-cPLA(2) is localized at the nuclear membrane of stably transfect

210 AtNUP160 protein is localized at the nuclear rim, and poly(A)-mRNA in sit

211 Melt is localized at the onset of rapid ice flow in the large

212 the sensing zone of conical-shaped nanopores is localized at the orifice, the translocation of nanopa

213 Electron microscopy showed that Tom22 is localized at the outer mitochondrial membrane (OMM),

214 The catalytic activity is localized at the perimeter of the Au nanoparticles wh

215 sibility experiments showed that the protein is localized at the periplasmic side of the outer membra

216 ndependent evidence demonstrate that CYBASC1 is localized at the plant tonoplast (TO).

217 In striatal medium spiny neurons, PDE10A is localized at the plasma membrane and in dendritic spi

218 ly overexpressing TSPAN9 to show that TSPAN9 is localized at the plasma membrane and in early and lat

219 ls showed that the majority of hCtr1 protein is localized at the plasma membrane and no significant i

220 psis thaliana FLA4 we show that this protein is localized at the plasma membrane as well as in endoso

221 maging of live cells to demonstrate that Gag is localized at the plasma membrane in a striking puncta

222 ubset of small DRG sensory neurons, where it is localized at the plasma membrane of the soma, axon in

223 This receptor is localized at the plasma membrane, as well as in intra

224 that TgMTP1::green fluorescent protein (GFP) is localized at the plasma membrane, suggesting that TgM

225 Consistent with such functions, SHK1 is localized at the plasma membrane/cortex, and we show

226 nce protein fusions, we determined that ParC is localized at the poles of the bacteria in rapidly gro

227 at the NF-kappaB inducing IKK kinase complex is localized at the postsynaptic density (PSD) and activ

228 We show that Bud2p is localized at the presumptive bud site in G(1) cells i

229 urthermore, we find that vertebrate CK1gamma is localized at the primary cilium to promote Smo phosph

230 The mBD-3 gene is localized at the proximal portion of chromosome 8, th

231 Sap1 is localized at the replication origin ori2004 and this

232 We further show that in mouse alpha-catulin is localized at the sarcolemma and neuromuscular junctio

233 ercellular communication, and show that SepJ is localized at the septa.

234 t the product of this gene, the Dlg protein, is localized at the septate junctions between epithelial

235 ions for 2 indicate that the cationic charge is localized at the silicon center and depict a LUMO wit

236 ating that the effect of the phosphate group is localized at the ssDNA gap.

237 of an intermediate where the second electron is localized at the superoxo adsorption site.

238 a newly identified hair bundle protein that is localized at the tips of stereocilia of both cochlear

239 VAC7 encodes a novel 128-kDa protein that is localized at the vacuole membrane.

240 Thin protein is localized at the Z-disk in muscle, but l(2)tn mutants

241 In addition, Fun30 was localized at the 5' and 3' ends of genes and within

242 p-ERK was localized at the apical cell surface of bronchiolar

243 Immunostaining revealed that TM14 was localized at the apical pericellular regions of preo

244 In contrast to PSMA/NAALAD1, NAALADL2 was localized at the basal cell surface where it promote

245 The PPI/PI immunodominant epitope LALEGSLQK was localized at the C-peptide/A-chain junction.

246 is PGA59-gLUC fusion (referred to as gLUC59) was localized at the C. albicans cell surface, allowing

247 Confocal imaging revealed that BSEP-YFP was localized at the canalicular membrane and in tubulo-

248 uorescence microscopy demonstrated that VASP was localized at the cell cortex in round cells and redi

249 ocal immunomicroscopy revealed that cyclin E was localized at the centrosome.

250 RhoA was localized at the cleavage furrow or at the necks of

251 hat in the presence of B-lineage cells, CD28 was localized at the contact interface between B cell pr

252 fate-polyacrylamide gel electrophoresis, and was localized at the cytoplasm and plasma membrane.

253 green fluorescent fusion protein (DRP1C-GFP) was localized at the division plane in dividing cells an

254 en fluorescent protein--CalS1 fusion protein was localized at the growing cell plate, that expression

255 Reaction product in photoreceptor cells was localized at the inner/outer segment junction and in

256 apfp-1 was localized at the interface between stiff byssus and

257 C4d in PTC was localized at the interface of endothelium and baseme

258 Human, or Homo sapiens, MAD2 (hsMAD2) was localized at the kinetochore after chromosome conden

259 se C were at the apical membrane, E-cadherin was localized at the lateral membrane, and beta-catenin

260 lized EGF exhibited higher pPLCgamma1, which was localized at the leading edge.

261 in-dependent protein phosphatase calcineurin was localized at the light microscopic level in the rat

262 hoxyphenol and p-hydroquinone, respectively) was localized at the main heme access channel.

263 Necl-5 was localized at the membrane of midlobular and centrilo

264 PvGAMA was localized at the microneme in the mature schizont-st

265 When the UASG was localized at the nucleosomal pseudodyad, relative oc

266 Interestingly, NOX5 was localized at the outer membrane of the mitochondria

267 ulture demonstrated that phosphorylated sst2 was localized at the plasma membrane after 10 seconds of

268 o wild type occludin, its Y398A/Y402A mutant was localized at the plasma membrane and cell-cell conta

269 ectron microscopy revealed that polycystin-1 was localized at the plasma membrane and sarcoplasmic re

270 ana leaves, SYMRK-yellow fluorescent protein was localized at the plasma membrane, and interaction wi

271 rescence studies showed that alpha1D protein was localized at the plasma membrane, in cytosol and cel

272 fluorescence analysis demonstrated that FFHA was localized at the plasma membrane, whereas GFP was pr

273 whereas FGF-2 in normal corneal endothelium was localized at the plasma membrane.

274 ivIVA, which is required for an ovoid shape, was localized at the poles and septum of pneumococcal ch

275 scence in situ hybridization, the mBD-1 gene was localized at the proximal portion of chromosome 8, t

276 ulation site, and the central common pathway was localized at the region between the intersections of

277 pproximately 700 s(-1) mM(-1), respectively) was localized at the same exposed Trp-164 responsible fo

278 ed fibers expressing NFATc-GFP, fluorescence was localized at the sarcomeric z-lines and absent from

279 laudin-1 expressing Can 10 clones, Claudin-1 was localized at the TJ and paracellular permeability wa

280 tions suggest that the DA storage impairment was localized at the VMAT2 protein itself.

281 MYPN was localized at the Z-line in control skeletal muscles

282 evealed that most Mkc7p and Yap3p activities were localized at the cell surface.

283 The exogenous connexins were localized at the cell surfaces in junctional macula

284 rs after antigen challenge, immune complexes were localized at the ciliary body and iris of receptor-

285 Exogenous LM as well as peptide F-9 were localized at the epithelial-mesenchymal interface o

286 In all nuclei, m2 receptors were localized at the membrane of motoneuronal perikarya

287 Initially, osteoclasts were localized at the periosteum next to the synovial me

288 n of the infected immune cell population and were localized at the periphery of parasite plaques.

289 Both HA-TRHR and HA-K338STOP were localized at the plasma membrane of untreated cells

290 None of the RGS proteins examined were localized at the plasma membrane.

291 reover, the majority of infected tumor cells were localized at the tumor margin.

292 ally insertions or deletions (1-142 bp) that were localized at the ZFN cleavage site and likely deriv

293 sites of tumor growth, but abundant NK cells were localized at these sites.

294 Major differences are localized at two regions: residues 29-31 and residue

295 these results suggest that the core of PHF6 is localized at VYK, and the interaction between small a

296 ORFs, is seen exclusively in the nucleus and is localized at Xic.

297 edly, the gene encoding this protein, FANCB, is localized at Xp22.31 and subject to X-chromosome inac

298 at glycerol-3-phosphate dehydrogenase (GPDH) is localized at Z-discs and M-lines.