ライフサイエンスコーパス: alternatively spliced

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

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

3 Numerous eukaryotic genes are alternatively spliced.

4 Nearly 50% of genes are alternatively spliced.

5 nctional classes determine whether a gene is alternatively spliced.

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

7 l exons have been identified and shown to be alternatively spliced.

8 Two viral mRNAs are alternatively spliced.

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

10 ur results indicate that the presence of the alternatively spliced 1/4 CTLA-4 isoform can further pro

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

12 CD45 is known to be alternatively spliced, a process that is partially regul

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

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

18 Previous work suggests that ced-4 can be alternatively spliced and that the splice variants funct

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

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

23 ved in blood that correlate with tics or are alternatively spliced are involved in the pathophysiolog

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

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

26 Eight human and six chicken novel alternatively spliced (AS) variants of telomerase revers

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

28 Arterial smooth muscle cell Ca(V)1.2 mRNA is alternatively spliced at exon 1 (e1), generating e1b or

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

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

31 Within the CNS, the zelda gene is alternatively spliced beginning at mid-embryogenesis int

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

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

34 Most human pre-mRNA transcripts are alternatively spliced, but the significance and fine-tun

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

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

37 into introns can lead to their activation as alternatively spliced cassette exons, an event called ex

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

39 associated with increased production of the alternatively spliced CD137 isoform, soluble CD137, whic

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

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

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

43 We found that CHCHD4 encodes 2 alternatively spliced, differentially expressed isoforms

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

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

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

47 In polarized epithelia, a low-abundance, alternatively spliced eight-exon isoform of CAR, CAR(Ex8

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

49 opment of the rod bipolar pathway, while the alternatively spliced exon 19 was not.

50 rientation, the repeat is located within the alternatively spliced exon 2A of junctophilin-3 (JPH3),

51 Serine 73 is encoded by the alternatively spliced exon 2B, which is preferentially s

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

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

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

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

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

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

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

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

60 sence or absence of three inserts encoded by alternatively spliced exons 2, 3, and 10 of the Tau gene

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

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

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

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

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

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

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

68 severe TS2) arise from missense mutations in alternatively spliced exons that cause the same G406R re

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

70 Characterization of the C terminus alternatively spliced exons using whole-cell patch clamp

71 d the transcript scanning method to identify alternatively spliced exons within the Ca(V)1.4 transcri

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

73 Among alternatively spliced exons, tissue-specific exons play

74 rt to define both the position and extent of alternatively spliced exons.

75 Cellular fibronectin that contains the alternatively spliced extra domain A (EIIIA) is up-regul

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

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

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

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

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

81 a soluble form of the receptor encoded by an alternatively spliced FcmuR transcript.

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

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

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

85 The alternatively spliced FN variant containing the extra do

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

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

88 helial abundance of soluble flt1 (sflt1), an alternatively spliced form of the VEGF receptor Flt1 enc

89 end, we documented the UPR by detecting the alternatively spliced form of the XBP1 protein as well a

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

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

92 MacroH2A1 is produced as one of two alternatively spliced forms, macroH2A1.1 and macroH2A1.2

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

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

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

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

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

98 tal genes, suggesting that a specific set of alternatively spliced genes may be regulated through DNA

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

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

101 Numerous alternatively spliced genes with varying temporal patter

102 In alternatively spliced genes, stress-related Gene Ontolog

103 For most alternatively spliced genes, the ratio of variants in po

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

105 , including transcription factors, contained alternatively spliced genes.

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

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

108 The mpz transcript was found to be alternatively spliced, giving rise to P0 isoforms with a

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

110 The alternatively spliced GRbeta isoform acts as dominant ne

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

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

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

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

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

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

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

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

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

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

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

122 DNMT3B is also highly alternatively spliced in a tissue- and disease-specific

123 lk is not only differentially methylated and alternatively spliced in Apis, but also seems to be regu

124 tely 147 genes, and 18% of these were either alternatively spliced in human tumors or involved in apo

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

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

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

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

129 of palmitoylated cysteine residues within an alternatively spliced insert in the C terminus of the la

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

131 his locus suggested it encoded a single gene alternatively spliced into two transcripts: a 555 amino

132 of the GFP coding sequence interrupted by an alternatively spliced intron of SCL33, we investigated w

133 Alternatively spliced introns are the ones that are usua

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

135 y to oligomerize differentiates GAC from its alternatively spliced isoform and the cycling of phospha

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

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

138 We have identified a novel alternatively spliced isoform of HsMCM9 that results in

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

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

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

142 Here, we report that the alternatively spliced isoform of RIL, denoted here as RI

143 Axonal SMN (a-SMN) is an alternatively spliced isoform of SMN1, generated by rete

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

145 Furthermore, evidence exists that an alternatively spliced isoform of TF also affects tumor g

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

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

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

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

150 s a large fraction of transcripts, including alternatively spliced isoforms and transcripts from rece

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

152 a single spliced isoform for hcTnT but three alternatively spliced isoforms for mcTnT.

153 ver, a complete characterization of PTMs and alternatively spliced isoforms in cTnT present in vivo i

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

155 Alternatively spliced isoforms of CD44 containing variab

156 ach to comprehensively characterize PTMs and alternatively spliced isoforms of cTnT purified from hea

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

158 ound that MKs regulate the expression of two alternatively spliced isoforms of Pyk2 in OBs, which may

159 There are multiple alternatively spliced isoforms of RUNX1.

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

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

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

163 base machine learner and other species with alternatively spliced isoforms, and shifts the current g

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

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

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

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

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

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

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

171 nscript level to differentiate functions for alternatively spliced isoforms.

172 cytoplasmic protein expressed as a family of alternatively spliced isoforms.

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

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

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

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

177 the four isomer cDNAs that we prepared from alternatively spliced KDM2A transcripts, only one stimul

178 The four alternatively spliced kiss1rb mRNAs encoded 4 truncated

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

180 were more conserved across mammals than the alternatively spliced large exons.

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

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

183 ads to a change in the relative abundance of alternatively spliced messages.

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

185 -4 (sCTLA-4) protein isoform generated by an alternatively spliced mRNA of CTLA4 lacking transmembran

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

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

188 High-throughput genome-wide studies of alternatively spliced mRNA transcripts have become incre

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

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

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

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

193 AnkG's alternatively spliced N terminus selectively gates acces

194 very rates, we estimate that at least 25% of alternatively spliced NAGNAGs undergo tissue-specific re

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

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

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

198 ing that some of these PTC mutations--if not alternatively spliced out of the transcript--have neutra

199 LIM domain-binding protein 3-encoding Z-band alternatively spliced PDZ motif gene (ZASP) in a patient

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

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

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

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

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

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

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

207 Lamins A and C, alternatively spliced products of the LMNA gene, are key

208 e pyruvate kinase isoforms PKM1 and PKM2 are alternatively spliced products of the PKM2 gene.

209 in that is included in some of the predicted alternatively spliced products.

210 Alternatively spliced proteins belonging to the neuregul

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

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

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

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

215 We found that all three alternatively spliced segments modulated Tau aggregation

216 To determine the contribution of alternatively spliced segments to Tau aggregation propen

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

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

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

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

221 Importantly, alternatively spliced short isoforms of SON are markedly

222 nt with the role of histone modifications at alternatively spliced sites.

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

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

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

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

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

228 We perform similar experiments on alternatively spliced SRA isoforms to assess their struc

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

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

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

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

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

234 y, we identified mutations in a 75 base pair alternatively spliced TGFbetaRII exon, exon 1a that prod

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

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

237 RET is alternatively spliced to encode multiple isoforms that d

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

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

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

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

242 The MeCP2 gene is alternatively spliced to generate two proteins with diff

243 The "E tail" isoforms of TCFs are alternatively spliced to include a second DNA binding do

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

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

246 VEGF is alternatively spliced to produce numerous isoforms that

247 A proportion of MDM4 transcripts are alternatively spliced to produce protein products that a

248 brafish genome was found to contain a single alternatively-spliced tor1 gene, derived from a common a

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

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

251 nd that the IVS7 + 2T > G allele produces an alternatively spliced transcript lacking exons 4-7, enco

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

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

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

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

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

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

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

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

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

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

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

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

264 A survey of alternatively spliced transcripts found that, in the rgh

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

266 Alternatively spliced transcripts lacking exon 7 sequenc

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

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

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

270 ing novel loci, and by identifying candidate alternatively spliced transcripts that are differentiall

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

272 The ability of alternatively spliced transcripts to encode different pr

273 Evidence for additional alternatively spliced transcripts was obtained from de n

274 Alternatively spliced transcripts were regulated differe

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

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

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

278 ing the differential effects of a variant on alternatively spliced transcripts, as well as the diffic

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

280 tworks revealed the potential interaction of alternatively spliced transcripts.

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

282 licing in clock genes and dynamic changes in alternatively spliced transcripts.

283 identified 20,766 genes and 67,453 of their alternatively spliced transcripts.

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

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

286 recently uncovered the existence of a novel alternatively spliced, truncated GLI1 (tGLI1) that has a

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

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

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

290 ific primer pair is required to amplify each alternatively spliced variant individually.

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

292 uble fms-like tyrosine kinase 1 (sFlt-1), an alternatively spliced variant of the vascular endothelia

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

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

295 Alternatively spliced variants of several oncogenes and

296 NA, we cloned full-length cDNAs encoding two alternatively spliced variants of ssTnT.

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

298 distinguish the expression levels among the alternatively spliced variants.

299 ture of the genomic region that gave rise to alternatively spliced YAP1 transcripts in different meta

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