ライフサイエンスコーパス: alternatively spliced

1 Two viral mRNAs are alternatively spliced.

2 approximately 42% of multi-exonic genes were alternatively spliced.

3 ch gene by selecting exons classified as not alternatively spliced.

4 d genes; over 95% human multi-exon genes are alternatively spliced.

5 Numerous eukaryotic genes are alternatively spliced.

6 Nearly 50% of genes are alternatively spliced.

7 nctional classes determine whether a gene is alternatively spliced.

8 that 60.3% of honey bee multi-exon genes are alternatively spliced.

9 estimate that most human multiexon genes are alternatively spliced.

10 oxious stimulus-detecting TrpA1 channels are alternatively spliced.

11 (GGG-alpha(1C)), or (3) introduction of the alternatively spliced 25-amino acid exon 9* mimicking a

12 ng activities of full-length, truncated, and alternatively spliced 57kT forms of MCPyV large T antige

13 ICAM-1, an alternatively spliced adhesion molecule, is believed to

14 assessed the transforming properties of the alternatively spliced AE isoform AE9a (or alternative sp

15 However, the unique functions of various alternatively spliced amelogenins in enamel formation ar

16 One pre-mRNA that is alternatively spliced and linked to neurodegenerative di

17 ibing SR proteins as NXF1 adaptors that flag alternatively spliced and polyadenylated mRNA isoforms a

18 Additionally, we recovered both alternatively spliced and putative paralogous dsx transc

19 The immense majority of genes are alternatively spliced and there are many isoforms specif

20 The TP73 gene transcript is alternatively spliced and translated into the transcript

21 many introns are constitutively, rather than alternatively, spliced and therefore do not contribute t

22 Approximately 95% of human genes are alternatively spliced, and aberrant splicing events can

23 Most human transcripts are alternatively spliced, and many disease-causing mutation

24 The Zasp52 primary transcript is extensively alternatively spliced, and we describe its splicing patt

25 Over 95% of human genes are estimated to be alternatively spliced as a powerful means of producing f

26 Discovery of the sets of genes that are alternatively spliced as the fetal kidney mesenchyme dif

27 NAs in intronic regions, in the proximity of alternatively spliced (AS) exons and poly(A) sites.

28 ity of a SERS platform to monitor individual alternatively spliced (AS) variants and miRNA copies wit

29 minus because BBP (also known as 53BP2S), an alternatively spliced ASPP2 isoform lacking the N termin

30 Neurexins are extensively alternatively spliced at six canonical sites that regula

31 VEGF-A pre-mRNA is alternatively spliced at the terminal exon to produce tw

32 -Barr virus-infected epithelial cancers, the alternatively spliced BamHI A rightward transcripts (BAR

33 In the present study, an alternatively spliced beta4 subunit lacking the variable

34 To test this hypothesis, we used the alternatively spliced BRCA2 exon 12 (E12) as a model sys

35 merase is a key example of a protein that is alternatively spliced, but it is expressed at very low l

36 CLK1, CASP3, PPFIBP1, and TERT, validate as alternatively spliced by EWS-FLI1.

37 that il12rb1-the mouse homolog of IL12RB1-is alternatively spliced by leukocytes to produce a second

38 Alternatively spliced Cav1.2 Ca(2+) channels have been f

39 The alternatively spliced CD274-L2A transcript forms the maj

40 hancer region regulates the expression of an alternatively spliced CD33 isoform lacking exon2 (D2-CD3

41 Various proteins interact with the alternatively spliced channel C-terminus regulating gati

42 CircRNA abundance, and even which alternatively spliced circRNA isoforms are expressed, va

43 We identified three alternatively spliced ClC-3 isoforms, ClC-3a, ClC-3b, an

44 ere one such nanobody, NJB2, specific for an alternatively spliced domain of fibronectin expressed in

45 TCF7 and TCF-4/TCF7L2) use the C-clamp as an alternatively spliced domain to regulate cell-cycle prog

46 e active GC receptor alpha (GRalpha) and the alternatively spliced dominant negative regulator isofor

47 Alternatively spliced dPix isoforms that contain a speci

48 The large and alternatively-spliced ECRs of adhesion G protein-coupled

49 und specifically to its cognate antigen, the alternatively spliced EDA domain of fibronectin, and sel

50 t of ADCs based on an antibody targeting the alternatively spliced EDA of fibronectin coupled to one

51 Finally, we identify shared networks of alternatively spliced exocytic genes from islets of rode

52 u mutations are located within or around the alternatively spliced exon 10, it is important that iPSC

53 Finally, exclusion of the alternatively spliced exon 23 of alpha(2)delta-2 is esse

54 h a MAPT probe that targets transcription of alternatively spliced exon 3 in frontal cortex (P=9.2 x

55 me (TS) is caused by a point mutation in the alternatively spliced exon 8A of the calcium channel Ca(

56 Expression of an alternatively spliced exon in CAPS leads to enhanced cat

57 -throughput mutagenesis data obtained for an alternatively spliced exon in the proto-oncogene RON and

58 e polymorphism (rs41283526) is located in an alternatively spliced exon of ANK3 and has a strong and

59 RNAs, we identified a novel, abundantly used alternatively spliced exon of Nrxn1alpha and Nrxn3alpha

60 ads to altered levels of H3K4 methylation in alternatively spliced exon regions, which is accompanied

61 n assays demonstrated that SRSF3 binds to an alternatively spliced exon uniquely included in p53beta

62 rate regions of the motor (central stalk, an alternatively spliced exon, and the globular tail).

63 inclusion level for an exon to be called an alternatively spliced exon.

64 rms and dicots, in particular, correspond to alternatively-spliced exonic sequences.

65 med U2AF35a and U2AF35b) that are encoded by alternatively spliced exons 3 and Ab, respectively.

66 Alternatively spliced exons also overlap more frequently

67 luding distinct features of branchpoints for alternatively spliced exons and a family of conserved se

68 ms motif analyses of RBPs in the vicinity of alternatively spliced exons and creates RNA maps that de

69 We identified 2 alternatively spliced exons embedded within a proline-ri

70 We also identified two alternatively spliced exons in the cytoplasmic tail, wit

71 NPF)-binding sites and near hnRNPF-regulated alternatively spliced exons in the human transcriptome.

72 so appears to regulate the inclusion of some alternatively spliced exons of cacophony.

73 It then identifies alternatively spliced exons that are supported by both e

74 ted that RBM25 regulates a large fraction of alternatively spliced exons throughout the human genome.

75 y transcripts but are focussed in and around alternatively spliced exons with intermediate inclusion

76 e further show that KDM5B is enriched nearby alternatively spliced exons, and depletion of KDM5B lead

77 ons frequently alter the inclusion levels of alternatively spliced exons, consistent with the concept

78 s (ESRP1 and ESRP2), flank many AR-regulated alternatively spliced exons.

79 The F8 antibody recognizes the alternatively spliced extra domain A of fibronectin, a m

80 The alternatively spliced extra domains A and B (EDA and EDB

81 ithin cellular fibronectin, specifically the alternatively spliced extra domains A and B, and the FnI

82 te its abundance, the function of the large, alternatively spliced extracellular domain of CD45 has r

83 aGPCRs have large alternatively spliced extracellular regions (ECRs) that

84 he A2440G mutation causes upregulation of an alternatively spliced F5 transcript that results in an i

85 Critical for these effects was both the alternatively spliced FGF14b N-terminus and direct inter

86 ich is associated with reduced levels of the alternatively spliced fibrinogen gamma' chain.

87 Yet, earlier studies have shown that the alternatively spliced, flip and flop variants of GluA1 A

88 The alternatively spliced FN variant containing the extra do

89 An alternatively spliced form of Brk (Alt Brk) which contai

90 we report that activated T cells produce an alternatively spliced form of gammac mRNA that results i

91 Of all the alternatively spliced forms of amelogenins, exon4 is mos

92 sistance in advanced PC is the generation of alternatively spliced forms of the AR termed AR variants

93 uplication there will be partitioning of the alternatively spliced forms such that the products of ea

94 II BMP receptor (BMPRII) is expressed as two alternatively spliced forms, a long and a short form (BM

95 essed and its transcripts consist of several alternatively spliced forms, including KDM2A and the sho

96 w that the MLV P50 protein, produced from an alternatively spliced gag RNA, interacts with the C term

97 precipitated with wild-type (gammaA/gammaA), alternatively-spliced (gamma'/gamma'), and alphaC-trunca

98 the splicing mechanism of EWS-FLI1, showing alternatively spliced gene patterns that significantly o

99 FXR1 is an alternatively spliced gene that encodes RNA binding prot

100 process of subfunctionalization, in which an alternatively spliced gene upon duplication divides dist

101 east cancer susceptibility gene, is a highly alternatively spliced gene.

102 Moreover, there are differences between alternatively spliced genes and genes with a single tran

103 pothesized that hPTMs regulate expression of alternatively spliced genes for specific processes durin

104 Notably, 69% of alternatively spliced genes have predicted alternative f

105 Differential expression analysis of the alternatively spliced genes in healthy and smut-infected

106 re used to identify differentially expressed alternatively spliced genes in ribeye muscle tissue betw

107 ify networks of differentially expressed and alternatively spliced genes resulting from haploinsuffic

108 More than 14% of alternatively spliced genes were associated with a T-DMR

109 Numerous alternatively spliced genes with varying temporal patter

110 ator, also induces changes in the pattern of alternatively spliced genes, many of which were lost whe

111 dary contributions of splicing (selection on alternatively spliced genes, splice junctions, and splic

112 In alternatively spliced genes, stress-related Gene Ontolog

113 y throughout development in 19% of the 2,285 alternatively spliced genes.

114 , including transcription factors, contained alternatively spliced genes.

115 ome sequencing has skyrocketed proportion of alternatively spliced genes; over 95% human multi-exon g

116 ier all require a heretofore uncharacterized alternatively spliced giant exon of ankyrin-G (AnkG).

117 The gene encoding U2AF35 (U2AF1) is alternatively spliced, giving rise to two isoforms U2AF3

118 nvertebrate chordate, and identified several alternatively spliced HIFalpha isoforms.

119 Expression of an alternatively spliced HMGCR transcript lacking exon 13,

120 In mammals, most multi-exon genes are alternatively spliced; however, few alternative transcri

121 the mechanisms controlling the expression of alternatively spliced HTLV-1 mRNAs and suggest a link be

122 ed the Rex dependence of the complete set of alternatively spliced HTLV-1 mRNAs.

123 we first report the cellular localization of alternatively spliced human MOCS1 proteins.

124 ation of novel protein isoforms derived from alternatively spliced ie3 transcripts prompted the const

125 ification of novel ie3 isoforms derived from alternatively spliced ie3 transcripts.

126 The DM epidermis expressed an alternatively spliced IL-15 mRNA isoform, IL-15DeltaE7,

127 identified approximately 190 genes that are alternatively spliced in a GSK-3-dependent manner, suppo

128 Most mammalian pre-mRNAs are alternatively spliced in a manner that alters the result

129 temperature range and FLM is transcribed and alternatively spliced in a temperature-dependent manner.

130 me diversity, with >/=94% of multiexon genes alternatively spliced in humans.

131 es CLTA and CLTB, and both gene products are alternatively spliced in neurons.

132 Importantly, the genes found to be alternatively spliced in response to glucocorticoid trea

133 owed that exon alpha in MEF2C was aberrantly alternatively spliced in RMS cells, with the ratio of al

134 identified a small subset of genes that were alternatively spliced in the spinal cord compared with c

135 p150(Glued) is alternatively spliced in vivo, with the full-length isof

136 Intriguingly, exitrons, alternatively spliced internal regions of protein-coding

137 e we show that Drosophila Nmnat (DmNmnat) is alternatively spliced into two mRNA variants, RA and RB,

138 Interestingly, aphid feeding induced alternatively spliced intron-retaining CCA1a/b transcrip

139 Alternatively spliced introns are the ones that are usua

140 cations within stable mRNAs tend to occur in alternatively spliced introns, suggesting they regulate

141 associated kinase 4 (IRAK4) was the dominant alternatively spliced isoform in MDS and AML and is char

142 dtype KLF6 (KLF6(WT) ) and its antagonistic, alternatively spliced isoform KLF6(SV1) in cultured HSCs

143 SMN2 primarily produces an alternatively spliced isoform lacking exon 7, which is c

144 Remarkably, a particular alternatively spliced isoform of GPR56 is selectively re

145 Overexpression of a specific, alternatively spliced isoform of Hdac7 lacking the N-ter

146 We previously identified a novel alternatively spliced isoform of human myeloid different

147 This ultimately increases the levels of an alternatively spliced isoform of integrin-alpha6 (ITGA6)

148 with increased expression of Kv11.1-3.1, an alternatively spliced isoform of Kv11.1, are correlated

149 ociated with the upregulation of p53beta, an alternatively spliced isoform of p53 that promotes p53-m

150 Here, we show that an alternatively spliced isoform of syntaphilin (SNPH), a c

151 orts ULBP1 expression by suppressing a novel alternatively spliced isoform of ULBP1 mRNA.

152 esidue insert unique to the muscle-specific, alternatively spliced isoform of vinculin, termed metavi

153 n results in the induction of CD6Deltad3, an alternatively spliced isoform that lacks the ligand-bind

154 stent with subfunctionalization partitioning alternatively spliced isoforms among duplicate genes and

155 We found multiple alternatively spliced isoforms expressed from the Set lo

156 Production of these negatively acting alternatively spliced isoforms is induced by stimulation

157 basis of the relative abundance of multiple alternatively spliced isoforms mRNAs generated by the sa

158 species and the proteoforms translated from alternatively spliced isoforms of a gene actually execut

159 Alternatively spliced isoforms of CD44 containing variab

160 que neuroprotective role for neuron-specific alternatively spliced isoforms of endophilin-B1.

161 However, it remains unknown whether alternatively spliced isoforms of p53, known to modulate

162 There are multiple alternatively spliced isoforms of RUNX1.

163 Our findings suggest that the different alternatively spliced isoforms of SH2B1 perform differen

164 ed from HeLa cells for the quantification of alternatively spliced isoforms of the Fas gene, involved

165 Expression of neurexins in hundreds of alternatively spliced isoforms suggested that individual

166 musculus myosin-18A gene is expressed as two alternatively spliced isoforms, alpha and beta, with rep

167 NA-seq) data for predicting the functions of alternatively spliced isoforms, and we discuss their app

168 Neurexins, expressed in thousands of alternatively spliced isoforms, are central components o

169 The MYO1C gene produces three alternatively spliced isoforms, differing only in their

170 t to predict and differentiate functions for alternatively spliced isoforms, instead of genes, using

171 , AtRTD2-QUASI, for use in Quantification of Alternatively Spliced Isoforms, outperform other availab

172 Ser5 has five alternatively spliced isoforms, Ser5-001, -004, -005, -0

173 P-25 exists as two developmentally regulated alternatively spliced isoforms, SNAP-25a and SNAP-25b.

174 of TF-initiated coagulation produced in two alternatively spliced isoforms, TFPIalpha and TFPIbeta.

175 seq reads are often compatible with multiple alternatively spliced isoforms.

176 nscript level to differentiate functions for alternatively spliced isoforms.

177 Ser5 produces 5 alternatively spliced isoforms: Ser5-001 has 10 putative

178 enes have multiple alternative promoters and alternatively spliced isoforms; 6) NF-kappaB family gene

179 We found that the protein product of an alternatively spliced Junctin isoform is N-glycosylated

180 eridone caused greater in vitro block of the alternatively spliced Kv11.1-3.1 isoform than full-lengt

181 iggered nonsense-mediated decay (NMD) of the alternatively spliced LDLR mRNA.

182 a comprehensive database of miRNA targets in alternatively spliced linear and circRNAs (ASmiR) and a

183 closed conformation that is stabilized by an alternatively spliced linker and a conserved calcium-bin

184 findings suggest that studies on the role of alternatively spliced MBSs affecting transcript levels a

185 The S324Tfs*3 variant is located in an alternatively spliced micro-exon encoding six perfectly

186 trons, producing an average of three or more alternatively spliced mRNA isoforms.

187 -4 (sCTLA-4) protein isoform generated by an alternatively spliced mRNA of CTLA4 lacking transmembran

188 n eukaryotic cells to produce a multitude of alternatively spliced mRNA products during development a

189 ate that AtNSRs interact not only with their alternatively spliced mRNA targets but also with the ASC

190 tein level, corresponding to full-length and alternatively spliced mRNA transcripts, decreasing mRNA

191 cular, 3-AP-Me led to an upregulation of the alternatively spliced mRNA variant XBP1 (16-fold).

192 The data document translation of alternatively spliced mRNAs and expose ribosome associat

193 to any cohort of tissues expressing several alternatively spliced mRNAs generated by the same gene,

194 Isoforms are alternatively spliced mRNAs of genes.

195 ernal ribosomal entry, convert pseudo-mRNAs (alternatively spliced mRNAs with a PTC) into protein enc

196 eomics to better evaluate the translation of alternatively spliced mRNAs.

197 We found that 1) the induction of the alternatively spliced MyD88 form is due to alternative p

198 AnkG's alternatively spliced N terminus selectively gates acces

199 We report here the identification of six alternatively spliced Orf50 transcripts that are generat

200 t- and shoot-specific differential ratios of alternatively spliced OsPCS2a and OsPCS2b transcript exp

201 yza sativa) cultivar, the OsPCS2 produces an alternatively spliced OsPCS2b transcript that bears the

202 to interact with and alter the expression of alternatively spliced p53 isoforms in order to regulate

203 the 90-kDa band as the protein ZASP (Z-band alternatively spliced PDZ motif protein), a minor compon

204 ent up-regulation of alpha-actinin-2, z-band alternatively spliced PDZ-motif and myotilin at the Z-li

205 Z-disc-associated, alternatively spliced, PDZ motif-containing protein (ZAS

206 The murine melanopsin gene is indeed alternatively spliced, producing two distinct isoforms,

207 cing donor site than does WT and produces an alternatively spliced product of LMNA called progerin, w

208 ed action of which creates a distribution of alternatively spliced products in a given cell type.

209 The alternatively spliced products of LMNA, lamin C and prel

210 atabase from RNA-Seq may produce a subset of alternatively spliced protein isoform candidates that ha

211 o provide insights into the functions of the alternatively spliced protein isoforms and provide high-

212 ication of miRNA target sites located in the alternatively spliced region of linear and circular RNAs

213 the TEN2 barrel at a site far away from the alternatively spliced region.

214 Insertion of a short alternatively-spliced region within TENs abolishes the T

215 we identified miRNA target sites located in alternatively spliced regions of the linear and circular

216 exon skipping preferentially affects shorter alternatively spliced regions with weaker BPs.

217 eosome positioning pattern compared to other alternatively spliced regions.

218 s most of the SMN2-derived transcripts to be alternatively spliced resulting in a truncated and unsta

219 The ATXN3 gene is alternatively spliced, resulting in protein isoforms tha

220 most dicot plants, the SYP13II transcript is alternatively spliced, resulting in two isoforms, SYP13I

221 Here, we show that P50, generated from an alternatively spliced RNA encoded in gag, counteracts AP

222 rising from identical precursor transcripts, alternatively spliced RNAs can have dramatically differe

223 Strikingly, not all of the alternatively spliced RNAs examined were sensitive to Pt

224 uses, it does encode proteins generated from alternatively spliced RNAs.

225 We generated knockin mice in which alternatively spliced sequence #4 (SS4) of neuexin-3 is

226 of Nrxn1alpha and Nrxn3alpha (referred to as alternatively spliced sequence 6) that encodes a 9-resid

227 We also identified a novel, alternatively spliced Set-beta transcript lacking the nu

228 Of the four known alternatively spliced SH2B1 isoforms, SH2B1beta and SH2B

229 Our study indicates that the alternatively spliced short isoform of human MD-2 could

230 Importantly, alternatively spliced short isoforms of SON are markedly

231 rane (7TM) receptors, the MOR gene codes for alternatively spliced six-transmembrane (6TM) isoforms,

232 This ZASP region is alternatively spliced so that each isoform has unique ac

233 pite previous reports in the mouse model, no alternatively spliced, soluble form of Tim-3 was observe

234 show here that hypoxia specifically induces alternatively spliced species encoding for truncated for

235 We find evidence of an alternatively spliced spidroin, a spidroin expressed onl

236 y pathway of 1 nt intron shift, involving an alternatively spliced stwintron intermediate is proposed

237 he internal introns at the DNA level from an alternatively spliced stwintron.

238 licing depends on transformer, which is also alternatively spliced such that functional Tra is only p

239 ranscriptome analysis, and we identified the alternatively spliced TAg transcripts for RacPyV.

240 They also reveal a propensity of the alternatively spliced TAK1 isoform TAK1DeltaE12 to cause

241 t is currently not known whether the soluble alternatively spliced TF form (asTF) is expressed in BrC

242 riments to define unique functions for these alternatively spliced TFPI isoforms.

243 ally methylated genes were more likely to be alternatively spliced than not differentially methylated

244 ogous transcript of Aspergillus niger can be alternatively spliced; the exon downstream the stwintron

245 Alternatively spliced tissue factor (asTF) is a novel is

246 irus genome encode mRNA transcripts that are alternatively spliced to express two different viral pro

247 a A virus encodes an mRNA transcript that is alternatively spliced to express two viral proteins, the

248 e (JNK) kinase MAP kinase kinase 7 (MKK7) is alternatively spliced to favor an isoform that lacks exo

249 one receptor alpha gene (THRA) transcript is alternatively spliced to generate either thyroid hormone

250 plicing regulator in the nucleus, it is also alternatively spliced to produce cytoplasmic isoforms.

251 Esrp1 itself is also alternatively spliced to produce multiple protein isofor

252 VEGF is alternatively spliced to produce numerous isoforms that

253 binding results in a reduction of a specific alternatively spliced transcript expressed from the earl

254 human ATXN3 disease gene, expression of this alternatively spliced transcript is also enhanced.

255 identification and functional analysis of an alternatively spliced transcript of human AQP4, AQP4-Del

256 In addition, an alternatively spliced transcript variant of Ptgds missin

257 of 40,064 genes, 65,167 transcripts, 31,909 alternatively spliced transcript variants and 2,367 non-

258 gene that causes increased expression of an alternatively spliced transcript, which encodes a previo

259 RT-PCR validation, we found that a subset of alternatively spliced transcripts and 5'-extended mRNAs

260 erlapping changes in coding genes, including alternatively spliced transcripts and noncoding RNAs.

261 F followed by RNA sequence analysis, several alternatively spliced transcripts are significantly chan

262 r both traits, some differentially expressed alternatively spliced transcripts belonged to myosin and

263 er genes, in this way reducing the number of alternatively spliced transcripts duplicate genes produc

264 ased access to changes in RNA expression and alternatively spliced transcripts during human cortical

265 of highly expressed genes and the number of alternatively spliced transcripts expressed per gene, an

266 of highly expressed genes and the number of alternatively spliced transcripts expressed per gene, wh

267 we cloned full-length open reading frames of alternatively spliced transcripts for a large number of

268 splice sites were the most frequently found alternatively spliced transcripts for REA and IF content

269 A total of 166 alternatively spliced transcripts from 125 genes were si

270 or animals selected on their IF content, 269 alternatively spliced transcripts from 219 genes were di

271 t- and shoot-specific differential ratios of alternatively spliced transcripts in indica rice under C

272 We observed that the alternatively spliced transcripts of a subset of these g

273 wo protein isoforms are generated from three alternatively spliced transcripts of C9orf72; a long for

274 Finally, reduced expression and alternatively spliced transcripts of DvABCB1 were identi

275 the cell types that express more variants of alternatively spliced transcripts per gene are those tha

276 stage is characterised by a specific set of alternatively spliced transcripts that code for proteins

277 by the effector TH2 lineage consists of four alternatively spliced transcripts that regulate the expr

278 The ability of alternatively spliced transcripts to encode different pr

279 Alternatively spliced transcripts were regulated differe

280 nging because BDNF is generated by multiple, alternatively spliced transcripts with different 5'- and

281 Given that human IRF5 exists as multiple alternatively spliced transcripts with distinct function

282 ribe a revised protein annotation policy for alternatively spliced transcripts with more divergent pr

283 OCIATED1 (CCA1) splice variants, among other alternatively spliced transcripts, which is exacerbated

284 tworks revealed the potential interaction of alternatively spliced transcripts.

285 xon drives IRES activity in a diverse set of alternatively spliced transcripts.

286 pain through effects mediated in part by the alternatively spliced truncated isoform of the BDNF rece

287 acquired vemurafenib resistance caused by an alternatively spliced, truncated BRAF(V600E) that promot

288 We have also characterized a novel alternatively spliced, truncated isoform of human Musash

289 n-level analyses classified > 1,000 mRNAs as alternatively spliced under hypoxia and uncovered a uniq

290 The Ta7ANPR1 locus is alternatively spliced under pathogen inoculated conditio

291 differentially expressed and differentially alternatively spliced upon Fe deficiency, indicating a c

292 Giant ankyrin-B (ankB) is a neurospecific alternatively spliced variant of ANK2, a high-confidence

293 igomeric size, which may be influenced by an alternatively spliced variant of CL-K1.

294 ade urothelial carcinoma cell lines, whereas alternatively spliced variants and transcribed pseudogen

295 We previously cloned and characterised alternatively spliced variants of ADAM15 that differ in

296 tifying interactions between brain-expressed alternatively spliced variants of ASD risk factors.

297 Akt3 is expressed as two alternatively spliced variants, one of which lacks the k

298 1 and 294 genes differentially expressed and alternatively spliced with age, as well as 529 genes wit

299 conserved lysine-rich domain encoded by the alternatively spliced Zfp318 exon 10 abolished IgD expre

300 The strongest alternatively spliced ZMAT3 target was CD44, a cell adhe