ライフサイエンスコーパス: transmembrane protein

1 le of the phospholipase A2 receptor (PLA2R1) transmembrane protein.

2 onal adhesion molecule A (JAM-A), an Ig fold transmembrane protein.

3 es a calcineurin-like metallophosphoesterase transmembrane protein.

4 ating repression of Smoothened, a seven-pass transmembrane protein.

5 preference for acetylating N termini of the transmembrane proteins.

6 membrane (silicalemma) via interactions with transmembrane proteins.

7 city of TMD interactions and the activity of transmembrane proteins.

8 e further research on alloherpesvirus virion transmembrane proteins.

9 tethering, and proper assembly of multi-pass transmembrane proteins.

10 large yet poorly understood family of seven-transmembrane proteins.

11 ical roles in the processing of secreted and transmembrane proteins.

12 e constituent proteins of gap junctions, are transmembrane proteins.

13 matrix proteins, transcription factors, and transmembrane proteins.

14 different, highly polymorphic genes encoding transmembrane proteins.

15 e.g., the ion translocation kinetics of the transmembrane proteins.

16 okines), extracellular matrix molecules, and transmembrane proteins.

17 ncluding cytosolic, membrane-associated, and transmembrane proteins.

18 improving detection of actively secreted and transmembrane proteins.

19 liable topology models for hundreds of human transmembrane proteins.

20 translational N-terminal acetylation of many transmembrane proteins.

21 ess than 2% of all determined structures are transmembrane proteins.

22 SHV-induced expression of interferon induced transmembrane protein 1 (IFITM1) to limit virus infectio

23 n SynDIG4 [also known as Prrt1 (proline-rich transmembrane protein 1)] has recently been identified a

24 eloping FTLD-TDP by increasing expression of Transmembrane Protein 106B (TMEM106B), a lysosomal prote

25 Transmembrane protein 107 (TMEM107) is localized in the

26 Here, we identify transmembrane protein 119 (Tmem119), a cell-surface prot

27 The transmembrane protein 16 (TMEM16) family of membrane pro

28 Transmembrane protein 16A (TMEM16A), also called anoctam

29 ABSTRACT: Transmembrane protein 16A (TMEM16A), also known as ANO1,

30 Gain-of-function mutations in transmembrane protein 173 (TMEM173) encoding stimulator

31 Transmembrane protein 175 (TMEM175), the lysosomal K(+)

32 o our knowledge, the first known function of transmembrane protein 178 (Tmem178), a PLCgamma2 downstr

33 Knockdown of transmembrane protein 184A (TMEM184A) confirmed its invo

34 rovide evidence that the protein isolated is transmembrane protein 184A (TMEM184A).

35 i homeostasis, we identified uncharacterized transmembrane protein 199 (TMEM199, previously called C1

36 we determined that fibronectin leucine-rich transmembrane protein 2 (FLRT2), a repulsive ligand of t

37 neuroligin-1 (Nlg1) and leucine-rich-repeat transmembrane protein 2 (LRRTM2) in a dual-colour config

38 Proline-rich transmembrane protein 2 (PRRT2) has been identified as t

39 Proline-Rich Transmembrane Protein 2 (PRRT2) has been shown to be a c

40 Here, we demonstrate the impact of transmembrane protein 2 (tmem2) on cell-matrix interacti

41 PRRT2 (proline-rich transmembrane protein 2 gene) has been identified as the

42 ntified mutations in the PRRT2 (proline-rich transmembrane protein 2) gene as the leading cause for a

43 Here, we describe how transmembrane protein 24 (TMEM24) helps coordinate these

44 The antiviral restriction factor IFN-induced transmembrane protein 3 (IFITM3) inhibits cell entry of

45 The interferon-induced transmembrane protein 3 (IFITM3) inhibits infection of m

46 Interferon-induced transmembrane protein 3 (IFITM3) is a cellular endosome-

47 Interferon-induced transmembrane protein 3 (IFITM3) restricts endocytic fus

48 , we show that endogenous interferon-induced transmembrane protein 3 is S-fatty acylated on three cys

49 We identified lysosomal-associated transmembrane protein 4B (LAPTM4B), which interacts with

50 Myomaker [Transmembrane protein 8c (TMEM8c)] is a muscle-specific

51 re, coexpression of the viral reticulon-like transmembrane protein A17 and the capsid-like scaffold p

52 Outer segment transmembrane protein accumulation in Nphp5(-/-) endopla

53 h high resolution structure determination of transmembrane proteins, additional methods, including co

54 GPCR, Gpr175 (also known as Tpra1 or Tpra40: transmembrane protein, adipocyte associated 1 or of 40 k

55 highly induced upon UV treatment, encoding a transmembrane protein and a membrane-bound VirB4/HerA ho

56 nown as the (pro)renin receptor, is a type 1 transmembrane protein and an accessory subunit of the va

57 or activator inhibitor-1 (HAI-1) is a type I transmembrane protein and inhibitor of several serine pr

58 on and identified nectin-4 (PVRL4), a type I transmembrane protein and member of a family of related

59 to blockade by antiviral interferon-induced transmembrane proteins and neutralizing antibody KZ52.

60 tion to PTPRG, CNTNs associate with multiple transmembrane proteins and signal inside the cell via ci

61 fic inside-out signal transfer along cleaved transmembrane proteins and suggest that substrate dimeri

62 e propose that AP-3 and AP-1 directly select transmembrane proteins and target them to axon and dendr

63 eases are involved in ectodomain cleavage of transmembrane proteins, and ADAM17 is known to cleave Ne

64 us and mainly catalyze the Nt-acetylation of transmembrane proteins, and it also harbors lysine N(eps

65 a secreted protein that interacts with ADAM transmembrane proteins, and its mutations are linked to

66 Single-pass transmembrane proteins are an important class of recepto

67 hat mDA progenitors isolated on the basis of transmembrane proteins are capable of extensive, functio

68 ABSTRACT: Small transmembrane proteins are important for regulation of c

69 Many single-transmembrane proteins are sequentially cleaved by ectod

70 Transmembrane proteins are sorted from endosomes to avoi

71 Integral transmembrane proteins assume a beta-barrel structure, a

72 sented here enables studies of reconstituted transmembrane proteins at the nanomolar level.

73 t determination of extracellular segments of transmembrane proteins based on the identification of su

74 P2) encodes for CASPR2, a multidomain single transmembrane protein belonging to the neurexin superfam

75 he lipid- and protein-facing residues in the transmembrane protein beta-signal motif depend on the na

76 , which may lead to altered function of many transmembrane proteins beyond the intended targets.

77 This transmembrane protein binds to the transmembrane domain

78 e presence of IgE autoantibodies against the transmembrane protein BP antigen 2 (BP180, type XVII col

79 R as the Vgamma9Vdelta2 T cell Ag-presenting transmembrane protein butyrophilin 3A1, providing inform

80 ous work from our lab has shown that a small transmembrane protein called sarcospan (SSPN) can enhanc

81 process in all photosynthetic organisms is a transmembrane protein called the reaction center.

82 inclusion, which is enriched with bacterial transmembrane proteins called Incs.

83 ings demonstrate that the intrinsic shape of transmembrane proteins can determine their cellular loca

84 n requires clathrin adaptors that link it to transmembrane protein cargo.

85 l-type amino acid transporter 1 (LAT1) is a transmembrane protein carrying bulky and neutral amino a

86 SRC associated with, and phosphorylated, the transmembrane protein CBP/PAG at Tyr-317, resulting in C

87 SIRPalpha ligation by a broadly expressed transmembrane protein, CD47, results in phosphorylation

88 The transmembrane protein CD83, expressed on APCs, B cells,

89 ed junctional localization of the structural transmembrane protein claudin-18.

90 synthase proteins in this large multisubunit transmembrane protein complex and the number of cellulos

91 (CcO) or complex IV (EC 1.9.3.1) is a large transmembrane protein complex that serves as the last en

92 ll membrane by direct binding to actin and a transmembrane protein complex.

93 et-endothelial cell adhesion molecule-1 is a transmembrane protein connecting adjacent endothelial ce

94 ese principles, we analyzed 26-residue model transmembrane proteins consisting exclusively of leucine

95 e provide functional evidence showing that a transmembrane protein, Cornichon-1 (CNIH), acts as a car

96 The 93-residue transmembrane protein CrgA in Mycobacterium tuberculosis

97 function of STING (TMEM173), an ER-resident transmembrane protein critical for cytoplasmic DNA sensi

98 The transmembrane protein Crumbs (Crb) functions in apical p

99 ivating the SWH pathway independently of the transmembrane protein Crumbs and bypassing the negative

100 olding protein Stardust (Sdt) stabilizes the transmembrane protein Crumbs, a conserved regulator of a

101 way activity is modulated via inter-cellular transmembrane proteins Crumbs and Echinoid that are both

102 The transmembrane protein Cx43 has key roles in fibrogenic p

103 Dendritic cell-specific transmembrane protein (DC-STAMP) plays a key role in the

104 sion required the dendrocyte-expressed seven transmembrane protein (DC-STAMP)-dependent non-apoptotic

105 v14/Cornichon family that mediates export of transmembrane proteins despite the potential for such cl

106 in the study of the intracellular traffic of transmembrane proteins due to its tightly regulated traf

107 ntroduced to represent the behavior of cargo transmembrane proteins during the vesicle fusion to the

108 tochondrial uncoupling protein 1, which is a transmembrane protein essentially lacking extramembraneo

109 or expressed on myeloid cells 2 (TREM2) is a transmembrane protein expressed on microglia within the

110 Binding of this antibody to B7-H6, a transmembrane protein expressed on tumor and other stres

111 nella-containing vacuole where this putative transmembrane protein facilitates intravacuolar iron acq

112 ein-coupled receptors constitute the largest transmembrane protein family involved in cell signaling.

113 ach, we showed that apoptosis-inducing human transmembrane proteins, FasL and TRAIL, synthesized and

114 roaches addressing the kinetic parameters of transmembrane protein flipping.

115 Ameloblasts express transmembrane proteins for transport of mineral ions and

116 ell adhesion, cellular stress responses, and transmembrane protein fragment degradation.

117 The seven-pass transmembrane protein Frizzled (Fz) is a critical compon

118 products but also through direct control of transmembrane protein function.

119 The ClC family of transmembrane proteins functions throughout nature to co

120 NT*-transmembrane protein fusions yield up to eight times mo

121 hether an internal, in-frame truncation of a transmembrane protein gamma-sarcoglycan is functional.

122 nd genomic approach, we identified the TMEM2 transmembrane protein gene as a direct transcriptional t

123 ree recent studies find that the single-pass transmembrane protein HAP2 mediates gamete fusion and is

124 The sperm-restricted single-pass transmembrane protein HAP2-GCS1 has been postulated to f

125 The conserved transmembrane protein, HAP2/GCS1, has been linked to fer

126 Several groups of auxiliary transmembrane proteins have been described that enhance

127 e-1 (PECAM-1, a highly expressed endothelial transmembrane protein) help to achieve specific therapeu

128 CD7 is a transmembrane protein highly expressed in acute T-cell l

129 The interferon-induced transmembrane protein (IFITM) family of proteins inhibit

130 plex with proteins of the interferon-induced transmembrane protein (IFITM) family.

131 ISGs, the genes encoding interferon-induced transmembrane protein (IFITM) have been reported to inhi

132 Interferon-inducible transmembrane proteins (IFITMs) can restrict the entry o

133 Recently, interferon-induced transmembrane proteins (IFITMs) have been identified to

134 Interferon-inducible transmembrane proteins (IFITMs) inhibit a broad spectrum

135 Interferon-induced transmembrane proteins (IFITMs) restrict the entry of di

136 cell-intrinsic factors (interferon-inducible transmembrane proteins, IFITMs), on the pH regulation in

137 gs were: (i) the FL strain encodes 16 virion transmembrane proteins; (ii) eight of these proteins are

138 ple leukocyte lineages, and encodes a type I transmembrane protein (IL12Rbeta1) that associates with

139 an enigmatic endoplasmic-reticulum-resident transmembrane protein implicated in a variety of disorde

140 of an apparently immune-invisible borrelial transmembrane protein in facilitating infection and its

141 mice deficient in NRROS, a myeloid-expressed transmembrane protein in the endoplasmic reticulum, deve

142 PRRT2 is a type II transmembrane protein in which only the second hydrophob

143 powerful force of assembly and mobility for transmembrane proteins in lipid bilayers.

144 he tetraspanins are a superfamily of 33 four-transmembrane proteins in mammals, of which the TspanC8

145 we examined coclustering between Gag and the transmembrane proteins in T and HeLa cells using quantit

146 e gained about the structure and function of transmembrane proteins in their native environment.

147 investigated the role of Tmem231, a two-pass transmembrane protein, in MKS complex formation and func

148 -terminal FAT-like domain, some pre-metazoan transmembrane proteins include several YxxP repeats in t

149 These hybrid vesicles contain transmembrane proteins including a small membrane protei

150 UPR is directed by three ER transmembrane proteins including ATF6, IRE1, and PERK.

151 cell membrane complexity is the assembly of transmembrane proteins into oligomeric structures, with

152 ssfully used to reconstitute three different transmembrane proteins into synthetic membranes.

153 dentified in mammals as a signal-transducing transmembrane protein involved in cell migration.

154 e that ODZ1 (also known as TENM1), a type II transmembrane protein involved in fetal brain developmen

155 The endoplasmic reticulum (ER) transmembrane protein IRE-1 maintains ER homeostasis by

156 evidence indicates that signaling by the ER transmembrane protein IRE1alpha is critical for this tra

157 The oncogenic MUC1-C transmembrane protein is, like MYC, aberrantly expressed

158 The influence of the membrane on transmembrane proteins is central to a number of biologi

159 /H(+) exchanger type I (chNHE1), a multispan transmembrane protein, is a cellular receptor of the sub

160 Caveolin (Cav)1, a widely expressed transmembrane protein, is involved in the regulation of

161 steine-rich motor neuron 1 (Crim1), a type I transmembrane protein, is strongly expressed in the deve

162 encodes a previously uncharacterized type I transmembrane protein, KIAA0319L (denoted hereafter as A

163 We show that LRP4, a conserved transmembrane protein known for its postsynaptic roles,

164 used to the N terminus of exosome-associated transmembrane protein Lamp2b were cleaved in samples der

165 hybrid SLBs, the role of the PEG-cushion on transmembrane protein lateral mobility was investigated.

166 Otoferlin, a six-C2 domain transmembrane protein linked to deafness in humans, is h

167 Although integrins are known to be transmembrane proteins, little is known about the role o

168 ur work provides a comprehensive analysis of transmembrane protein localization to the INM and paves

169 antiviral factors IFITMs (interferon-induced transmembrane proteins) located in membrane-bound compar

170 Here, we show that the transmembrane protein Lrig2 negatively regulates ADAM-me

171 the highly conserved SYTANLAAF motif in the transmembrane protein M3, and the fifth is in an extra-c

172 Although similar transmembrane proteins mediate self/nonself recognition

173 MDR is typically associated with transmembrane proteins mediating efflux of administered

174 ponents of a cell line while still retaining transmembrane protein mobility and activity.

175 x is responsible for the cleavage of several transmembrane proteins, most notably the amyloid precurs

176 At least six types of transmembrane proteins must be recovered, but the rules

177 hologue, and co-expression of Minion and the transmembrane protein Myomaker is sufficient to induce c

178 ed that myomaker, a skeletal muscle-specific transmembrane protein necessary for myoblast fusion, is

179 blished that tyrosine phosphorylation of the transmembrane protein nephrin promotes recruitment of th

180 connected to the actin cytoskeleton via the transmembrane protein nephrin.

181 The normal distribution of nuclear envelope transmembrane proteins (NETs) is disrupted in several hu

182 tions through targeting the nuclear envelope transmembrane proteins (NETs) that direct their normal r

183 affic, including the poorly understood small transmembrane proteins neural-specific gene 1 and 2 (Nsg

184 VEGF165 binds the transmembrane protein neuropilin 1 (NRP1) and promotes t

185 e-wide haploid genetic screen identified the transmembrane protein neuropilin 2 (NRP2) and tetraspani

186 Here, we show that the transmembrane protein, Nogo-A, inhibits neurite outgrowt

187 Perforin-2 is a transmembrane protein of cytosolic vesicles -derived fro

188 long-standing puzzle and identifies NACHO, a transmembrane protein of neuronal endoplasmic reticulum

189 We show that TMEM230 encodes a transmembrane protein of secretory/recycling vesicles, i

190 data provide genetic evidence that a mutant transmembrane protein of synaptic vesicles in neurons is

191 s otoferlin, a six C2-domain, Ca(2+)-binding transmembrane protein of synaptic vesicles.

192 Dystroglycan, an extracellular and transmembrane protein of the dystrophin-glycoprotein com

193 4) domain of Sun proteins [5-7], a family of transmembrane proteins of the inner nuclear membrane (IN

194 o Alzheimer's disease, but how its action on transmembrane proteins other than the amyloid precursor

195 However, the structural determinants of transmembrane protein partitioning to raft domains are n

196 Transmembrane proteins play crucial role in signaling, i

197 ch on alloherpesvirus VTPs.IMPORTANCE Virion transmembrane proteins play key roles in the biology of

198 Pirt is a transmembrane protein predominantly expressed in periphe

199 mplex, as CRB1 is a structural and signaling transmembrane protein present in three cell classes: Mul

200 oprotein A repetitions predominant (GARP), a transmembrane protein present on stimulated Tregs but no

201 Here we show that VCAM1, a transmembrane protein previously found in quiescent adul

202 colocalizes with a group of uropod-directed transmembrane proteins, PSGL-1, CD43, and CD44, at the p

203 ctrochemical methodology for the analysis of transmembrane proteins reconstituted into a liposomal sy

204 Rhomboid family multipass transmembrane proteins regulate diverse cellular process

205 ue to mutations in the NPC1 gene, encoding a transmembrane protein related to the Sonic hedgehog (Shh

206 The artificial transmembrane proteins reported here are the simplest kn

207 ABCD1 encodes a peroxisomal transmembrane protein required for very long chain fatty

208 Endosomal recycling of transmembrane proteins requires sequence-dependent recog

209 The PKR-like ER kinase (PERK), a transmembrane protein, resides in the endoplasmic reticu

210 required for transport (ESCRT) to the seven-transmembrane protein Rim21 in the ambient pH signaling

211 Here we demonstrate that the transmembrane protein RodZ mediates MreB rotation by dir

212 cassette-type ATPases, a substrate-specific transmembrane protein (S component) and a transmembrane

213 The transmembrane proteins semaphorin-1a (Sema-1a) and plexi

214 Here we identify the host transmembrane protein SERINC5, and to a lesser extent SE

215 g prevent the incorporation of the multipass transmembrane proteins serine incorporator 3 (SERINC3) a

216 The lysosomal transmembrane protein, SLC38A9, is required for mTORC1 a

217 ched, induces accumulation of the seven-pass transmembrane protein Smoothened (Smo) within the primar

218 SHH signalling is transduced through the transmembrane protein Smoothened (SMO), which localizes

219 r-like receptor Patched1 regulates the seven-transmembrane protein Smoothened remains mysterious, par

220 the ubiquitin hydrolase that deubiquitinates transmembrane proteins sorted as cargoes into ILVs.

221 termini of NPHP4 and NPHP5 interact with the transmembrane protein SSTR3 and thus spatially map to th

222 embrane phase, and have implications for how transmembrane protein structures respond to their physic

223 KEY POINTS: Small transmembrane proteins such as FXYDs, which interact wit

224 s unknown how exosomes/microvesicles deliver transmembrane proteins such as PMCA4 to sperm.

225 and is regulated by numerous AMPAR accessory transmembrane proteins such as TARPs, cornichons, and CK

226 s to the distribution within synapses of key transmembrane proteins, such as receptors, can dramatica

227 We found that the integral transmembrane proteins SUN1/UNC84A and SUN2/UNC84B are p

228 tion of the atypical AMPA receptor auxiliary transmembrane protein SynDIG1 regulates its stability an

229 ic transmembrane protein (S component) and a transmembrane protein (T component) that physically inte

230 Here we show that type II transmembrane protein tenomodulin (TNMD) is upregulated

231 We show that TMCO1 is an ER transmembrane protein that actively prevents Ca(2+) stor

232 Tregs, TGF-beta1 activation requires GARP, a transmembrane protein that binds and presents latent TGF

233 onventional autophagic activity of TMEM59, a transmembrane protein that contains the WD40 domain-bind

234 Orai1 is a transmembrane protein that forms homomeric, calcium-sele

235 Tril is a transmembrane protein that functions as a co-receptor fo

236 vivirus nonstructural protein 2B (NS2B) is a transmembrane protein that functions as a cofactor for v

237 Together, these studies identify a transmembrane protein that functions to negatively regul

238 how that NRG3, like CRD-NRG1, is a dual-pass transmembrane protein that harbors a second transmembran

239 GDE2, a six-transmembrane protein that induces differentiation by do

240 nd that tetherin, a broad-spectrum antiviral transmembrane protein that inhibits the egress of a vari

241 ion by tetherin (BST-2 or CD317), which is a transmembrane protein that inhibits virus release from i

242 y to amino acid transporters, as a lysosomal transmembrane protein that interacts with the Rag guanos

243 C-terminal subunit (MUC1-C) is an oncogenic transmembrane protein that is aberrantly expressed in MM

244 ceptor is an evolutionarily highly conserved transmembrane protein that is essential to a wide spectr

245 Lrp4 is a transmembrane protein that is mutated in patients with h

246 prostate specific membrane antigen (PSMA), a transmembrane protein that is overexpressed in prostate

247 synthesized as a highly glycosylated type I transmembrane protein that is subsequently cleaved, resu

248 Neuregulin1 (NRG1) is a single transmembrane protein that plays a critical role in neur

249 Dysferlin is a large transmembrane protein that plays a key role in cell memb

250 precursor-like protein 1 (APLP1) is a type I transmembrane protein that plays a role in synaptic adhe

251 as TMEM97, an endoplasmic reticulum-resident transmembrane protein that regulates the sterol transpor

252 Cytochrome c oxidase (CcO) is a transmembrane protein that uses the free energy of O2 re

253 orobaculum tepidum BchF revealed an integral transmembrane protein that was efficiently isolated by d

254 Claudins are tight-junction transmembrane proteins that act as paracellular ion chan

255 contact sites composed of clustered connexin transmembrane proteins that act in dual capacities as ch

256 is process is the endocytic retrieval of the transmembrane proteins that are enriched in synaptic ves

257 strictly depends on LAP1 and LULL1, type II transmembrane proteins that are integral parts of the To

258 Teneurins are large type II transmembrane proteins that are necessary for the normal

259 Ion channels are transmembrane proteins that are synthesized within the c

260 KEY POINTS: Ion channels are transmembrane proteins that are synthesized within the c

261 rface diffusion of GPI-anchored proteins and transmembrane proteins that associate with actin is driv

262 been limited by lack of knowledge regarding transmembrane proteins that can be used to target and is

263 ngs to an evolutionarily conserved family of transmembrane proteins that can interact with a variety

264 ein S-Acyl Transferases (PATs) are multipass transmembrane proteins that catalyze S-acylation (common

265 ture virions, were severely deficient in the transmembrane proteins that comprise the entry fusion co

266 activated, seven-alpha-helical, retinylidene transmembrane proteins that have been identified in thou

267 A subset of eSTKs are single-pass transmembrane proteins that have extracellular penicilli

268 anins comprise a diverse family of four-pass transmembrane proteins that play critical roles in the i

269 We have constructed 26-amino acid transmembrane proteins that specifically transform cells

270 alytical experiments were performed with two transmembrane proteins; the Na(+)/K(+)ATPase that contai

271 gy-related gene 9 (Atg9) encodes a multipass transmembrane protein thought to act as a membrane carri

272 he Bestrophin1 (BEST1) gene, which encodes a transmembrane protein thought to function as an ion chan

273 We found that the lysosomal transmembrane protein TMEM55B recruits JIP4 to the lysos

274 ected by mutations in the genes encoding the transmembrane proteins TMHS, TMIE, TMC1 and TMC2.

275 ESCRT dysfunction causes ubiquitinated transmembrane proteins to accumulate at endosomes, and w

276 Palmitoylated cysteines typically target transmembrane proteins to domains enriched in cholestero

277 that are necessary and sufficient to target transmembrane proteins to either the axon or the dendrit

278 facilitate fusion of OVS in the delivery of transmembrane proteins to sperm.

279 PTPRB is a transmembrane protein tyrosine phosphatase known to regu

280 isting of vascular endothelial cadherin, the transmembrane protein tyrosine phosphatase LAR, and the

281 ites infecting hepatic cells rely on the PVM transmembrane protein UIS3 to avoid elimination by host-

282 Here, we have reported that the endogenous transmembrane protein upstream-of-mTORC2 (UT2) negativel

283 t of 'core PCP' proteins, which includes the transmembrane proteins Van Gogh-like (Vangl) and Frizzle

284 Virion transmembrane proteins (VTPs) mediate key functions in t

285 tes the intracellular trafficking of several transmembrane proteins, we did not detect any effects of

286 riants in MFSD8, a gene encoding a lysosomal transmembrane protein, were identified in 2 families wit

287 ABCG4 is an ATP-binding cassette transmembrane protein which has been shown, in vitro, to

288 tified PbgA, a periplasmic domain-containing transmembrane protein, which binds cardiolipin glyceroph

289 efficient expression and purification of non-transmembrane proteins, which are otherwise refractory t

290 ing 8A (LRRC8A) is an ubiquitously expressed transmembrane protein with 17 leucine-rich repeats (LRRs

291 1 (ECA11) and encodes a glycosylated, type I transmembrane protein with 247 amino acids.

292 ar compartment, suggesting that L2 becomes a transmembrane protein with a short luminal portion and w

293 und that OIG-8, a previously uncharacterized transmembrane protein with a single immunoglobulin (Ig)

294 beta-Dystroglycan (beta-DG) is a transmembrane protein with critical roles in cell adhesi

295 We found that TMEFF2, a transmembrane protein with EGF-like and two follistatin-

296 CALHM1, a transmembrane protein with shared structural features to

297 HMGIC fusion partner-like 2) encodes a tetra-transmembrane protein with unknown functions.

298 es I and II, which like NRG2 are single-pass transmembrane proteins with an Ig-like domain, share the

299 ACS-array" approach to identify 18 genes for transmembrane proteins with high expression in mDA proge

300 icle adsorption to prevent immobilization of transmembrane proteins with protruding domains.