1 the structure of the protein as revealed by
molecular cloning.
2 hingosine 1-phosphate have been described by
molecular cloning.
3 lysophosphatidic acid have been described by
molecular cloning.
4 g and microsequencing, which was followed by
molecular cloning.
5 s isolated from a recombinant CHO library by
molecular cloning.
6 ples without separating them by culturing or
molecular cloning.
7 truct high-resolution haplotype maps without
molecular cloning.
8 te, 6 mammalian GRKs have been identified by
molecular cloning.
9 and keratocan) have been characterized using
molecular cloning.
10 d-based affinity purification and subsequent
molecular cloning.
11 xo32) were identified in Xenopus oocytes by
molecular cloning.
12 eptors for taste have been identified yet by
molecular cloning.
13 K isoforms were identified in human brain by
molecular cloning.
14 TCRs from PBMCs without cellular sorting or
molecular cloning.
15 DNA computing, biophysics and even standard
molecular cloning.
16 Here we identify by
molecular cloning a Drosophila cDNA encoding a protein (
17 the discovery of hepatitis C virus (HCV) by
molecular cloning almost a quarter of a century ago, unp
18 Our approach requires no
molecular cloning and allows a large number of cell line
19 Here, we report the
molecular cloning and biochemical characterization of Rh
20 This allowed for the
molecular cloning and biological analysis of transmitted
21 Molecular cloning and cDNA sequencing in human brain rev
22 We report the
molecular cloning and characterization of 4.1N, a novel
23 We report the
molecular cloning and characterization of a Histoplasma
24 Here, we describe the
molecular cloning and characterization of a human gene r
25 In this paper, we present the
molecular cloning and characterization of a murine homol
26 We report here the
molecular cloning and characterization of a new full-len
27 Here, we report the
molecular cloning and characterization of a novel AOS-en
28 Here we describe the
molecular cloning and characterization of a novel family
29 We describe the
molecular cloning and characterization of a novel giant
30 We report the
molecular cloning and characterization of a novel human
31 We describe the
molecular cloning and characterization of a novel myeloi
32 We report here the
molecular cloning and characterization of a recently ide
33 We report here the
molecular cloning and characterization of a t(1;14)(q21;
34 In this report, we describe the
molecular cloning and characterization of a third FOG-re
35 ORL-1) was discovered relatively recently by
molecular cloning and characterization of an orphan GPCR
36 The
molecular cloning and characterization of BUR2 presented
37 The
molecular cloning and characterization of BUR3 and BUR6
38 We report here the
molecular cloning and characterization of chicken and mo
39 Here, we report the
molecular cloning and characterization of hJNKK2 alpha,
40 Here, we describe the
molecular cloning and characterization of HOTHEAD (HTH),
41 We now describe the
molecular cloning and characterization of IKKbeta, a sec
42 We believe that the
molecular cloning and characterization of N-SMase cDNA w
43 Reported here is the
molecular cloning and characterization of rat CDO, a nov
44 We report the
molecular cloning and characterization of SMGC, a major
45 In this study, we report the
molecular cloning and characterization of the human 2B4
46 We report here the
molecular cloning and characterization of the mouse CysL
47 We present here the
molecular cloning and characterization of the mutator2 (
48 We report
molecular cloning and characterization of the rat PSGL-1
49 We describe the
molecular cloning and characterization of the unc-64 loc
50 Here we report the
molecular cloning and characterization of this enzyme.
51 In this study, we describe the
molecular cloning and expression analysis of a mouse pyg
52 In this paper we report
molecular cloning and expression analysis of two cystein
53 Molecular cloning and expression indicated that Joro 177
54 Its suitability for genome-scale
molecular cloning and expression is demonstrated in this
55 We report the
molecular cloning and expression of a phosphatidic acid-
56 Here, we report the
molecular cloning and expression of a third member of th
57 d a development of techniques leading to the
molecular cloning and expression of many hematopoietic g
58 Here, we report the
molecular cloning and expression pattern of a new Paired
59 We describe the
molecular cloning and expression pattern of the CLV1 gen
60 Toward this end, we report here the
molecular cloning and extensive structure-function analy
61 In this paper we document the
molecular cloning and functional analysis of the two uni
62 We report here the
molecular cloning and functional characterization of a n
63 We report here the
molecular cloning and functional characterization of a p
64 Here we describe the
molecular cloning and functional characterization of Ara
65 We now report the
molecular cloning and functional expression of a new Sha
66 Here we describe the
molecular cloning and functional expression of a novel m
67 traightforward approach that resulted in the
molecular cloning and functional expression of CCH1 by e
68 We describe
molecular cloning and functional expression of the calci
69 The present work describes the
molecular cloning and functional identification of a uni
70 d cyclization is followed by a discussion of
molecular cloning and heterologous expression of terpeno
71 The
molecular cloning and identification of DNA-binding prot
72 Based on results of
molecular cloning and immunolocalization, it appears tha
73 Molecular cloning and Northern blot analyses reveal that
74 Here we report the
molecular cloning and nucleotide sequence of one of the
75 We report the
molecular cloning and nucleotide sequence of the mpt63 g
76 these preceding studies, we report here the
molecular cloning and recombinant expression in Escheric
77 Herein, we report the
molecular cloning and recombinant expression of both gen
78 bispecific binding modality was generated by
molecular cloning and recombinant protein expression.
79 Molecular cloning and sequence analysis of this genomic
80 Molecular cloning and sequence analysis showed that, rel
81 Molecular cloning and sequence comparison indicate that
82 Molecular cloning and sequence determination for 8822 bp
83 Molecular cloning and sequencing indicate that IKK-gamma
84 ed from purified p30 and p38 facilitated the
molecular cloning and sequencing of cDNAs coding for the
85 Molecular cloning and sequencing of polymerase chain rea
86 onors and 11 NHL biopsy samples by extensive
molecular cloning and sequencing.
87 Here, we used
molecular cloning and site-directed mutagenesis to ident
88 We report here the
molecular cloning and some properties of EI-C.
89 equencing technologies that do not depend on
molecular cloning and that produce very long reads.
90 In this report, we describe the
molecular cloning and the complete nucleotide sequence o
91 Here, we report the
molecular cloning and the functional characterization of
92 We report the
molecular cloning and tissue distribution of zebrafish t
93 ate additional protein methyltransferases by
molecular cloning and to characterize new methyltransfer
94 We report the purification,
molecular cloning,
and characterization of a 40-kDa glyc
95 We report the purification,
molecular cloning,
and expression of a novel cytosolic c
96 Here we describe the purification,
molecular cloning,
and expression of this vitamin D resi
97 We now report the identification,
molecular cloning,
and functional characterization of a
98 Through genetic mapping,
molecular cloning,
and RNA interference, we have demonst
99 using a HOS-CD4+ cell system, biological and
molecular cloning,
and sequencing the envelope gene V3 r
100 Recently, using
molecular cloning approaches, three new neuropeptide Y (
101 iated with a widely diverse microbiota using
molecular cloning approaches.
102 d for this approach require manipulation via
molecular cloning as well as in vitro transcription.
103 tylcholine receptors have been discovered by
molecular cloning,
but their pharmacological similaritie
104 We now describe the
molecular cloning,
characterization and expression of Kr
105 Here, we report on the
molecular cloning,
characterization, and expression of t
106 Molecular cloning,
DNA sequencing and sequence analysis
107 were uncovered, the relatively new field of
molecular cloning enabled us and indeed, the entire comm
108 ptide sequence information which was used in
molecular cloning experiments.
109 In this report, we describe the
molecular cloning,
expression, and characterization of E
110 In this report we describe
molecular cloning,
expression, and characterization of h
111 Here we report the
molecular cloning,
expression, localization, and functio
112 Here we report on the
molecular cloning,
expression, localization, and pharmac
113 Over the last four decades,
molecular cloning has evolved tremendously.
114 Molecular cloning has identified two vesicular monoamine
115 Molecular cloning has isolated two subtypes of Na+-nucle
116 Molecular cloning has recently demonstrated that the ves
117 Molecular cloning has recently identified a vertebrate b
118 Molecular cloning has revealed a diverse family of genes
119 In tomato (Solanum lycopersicum),
molecular cloning has revealed that the underlying genes
120 Molecular cloning has revealed the presence of a large n
121 structural biology, molecular modelling and
molecular cloning have enabled the systematic functional
122 ecombination holds the potential for optimal
molecular cloning,
however, current strategies require s
123 d pXO2 of Bacillus anthracis was isolated by
molecular cloning in Escherichia coli and shown to repli
124 However, this approach relies on
molecular cloning in order to isolate and amplify indivi
125 With the availability of techniques of
molecular cloning in the early 1 980s, the first hematop
126 Enabled by the tools of
molecular cloning,
initial experimental queries into the
127 Molecular cloning is an important procedure in molecular
128 Here we report the
molecular cloning of a cDNA encoding a human homologue o
129 We report here the
molecular cloning of a cDNA encoding MIH of the edible c
130 Here, we report the
molecular cloning of a cDNA encoding this antigen and sh
131 We report the purification and
molecular cloning of a cDNA for a 53-kDa beta1,3-glucan-
132 These results represent the first
molecular cloning of a cDNA for the lysosomal type Ca2+-
133 We report the
molecular cloning of a class of putative human receptors
134 Here, we report the
molecular cloning of a GATA-3 interacting protein, repre
135 We have recently reported the
molecular cloning of a gene, gspK, in Vibrio cholerae th
136 Molecular cloning of a HEV-expressed core1-beta 1,3-N-ac
137 We have recently reported the isolation and
molecular cloning of a human immunodeficiency virus type
138 report the identification, purification, and
molecular cloning of a human protein that promotes the f
139 Here, we report the
molecular cloning of a mouse gene encoding an Lc3 syntha
140 t of a transcription map will facilitate the
molecular cloning of a myeloid leukemia suppressor gene
141 tion of the smallest CDS will facilitate the
molecular cloning of a myeloid leukemia suppressor gene
142 commonly deleted segment will facilitate the
molecular cloning of a myeloid leukemia suppressor gene
143 Molecular cloning of a near full-length cDNA revealed th
144 Here we report the
molecular cloning of a new member of the mammalian MAP k
145 Here, we report the
molecular cloning of a novel human gene that shares sign
146 We report the
molecular cloning of a novel isoform of p38 MAP kinase,
147 We report here the
molecular cloning of a novel member of the triglyceride
148 In this report, we describe the
molecular cloning of a novel, low-molecular-weight antig
149 We describe the first isolation by
molecular cloning of a plant CPSase gene (CPAII) derived
150 This is the first report of the
molecular cloning of a plant LKR-SDH genomic and cDNA se
151 ched for oncogenes and recently reported the
molecular cloning of a potent oncogene (hPTTG) from huma
152 Here we describe the
molecular cloning of a putative molecular scaffold prote
153 mammary carcinoma cell lines resulted in the
molecular cloning of a receptor-like PTP, also known as
154 We report the
molecular cloning of a rice plant homolog of these anima
155 We describe here the mutant phenotype and
molecular cloning of a second maize gene that functions
156 Molecular cloning of a serotonin transporter from the ce
157 This constitutes the first report on the
molecular cloning of a sialic acid-specific O-acetyleste
158 We describe here the isolation and
molecular cloning of Acanthamoeba MBP.
159 Molecular cloning of ADAMTS13 elucidates the structure o
160 soenzymes from Aspergillus fumigatus and the
molecular cloning of amadoriase II.
161 We report here the
molecular cloning of an approximately 1-Mb region of rec
162 The
molecular cloning of AXR5 revealed that the gene encodes
163 Here, we describe the purification and
molecular cloning of CA150, a nuclear protein that is as
164 Like many toxic genes, the
molecular cloning of CCH1 has been a major challenge; co
165 shed the relationship between p36 and p40 by
molecular cloning of cDNAs that encode both proteins and
166 Here we describe the
molecular cloning of CIKS (connection to IKK and SAPK/JN
167 Molecular cloning of corneal epithelial CAP37 indicated
168 Purification and
molecular cloning of ecto-ATPase and other canalicular p
169 Molecular cloning of eer1 reveals that its mutant phenot
170 Here we describe the identification and
molecular cloning of flotillin.
171 Here we report the
molecular cloning of GAI and a closely related gene GRS.
172 Since the
molecular cloning of GCS, much has been learned about th
173 We report here on the
molecular cloning of GLUCOSE INSENSITIVE1 (GIN1) and ABS
174 Molecular cloning of GPVI has revealed the presence of a
175 The
molecular cloning of HCA and the availability of recombi
176 Molecular cloning of hepatobiliary transport systems has
177 Molecular cloning of HIV-1 PCR products which might impr
178 Here we report the
molecular cloning of human and mouse orthologs of the ye
179 Molecular cloning of human RyR2 identified 2 alternative
180 r introgression mapping and, ultimately, for
molecular cloning of interacting genes that contribute t
181 Molecular cloning of low-voltage activated (LVA) T-type
182 Molecular cloning of Lr21 was facilitated by diploid/pol
183 t map provides an important resource for the
molecular cloning of Ltxs1.
184 With the
molecular cloning of many of the proteins and regulatory
185 The
molecular cloning of many of the transporter and regulat
186 Molecular cloning of membrane-spanning mammalian adenyly
187 Molecular cloning of mouse ADAMTS13 identified 2 truncat
188 Coincident with the
molecular cloning of NF-kappaB/RelA and identification o
189 ce in the study of axon regeneration was the
molecular cloning of Nogo.
190 We report the purification and
molecular cloning of NPA-binding PM APs and associated p
191 The
molecular cloning of nuclear genes that restore fertilit
192 Molecular cloning of p205 cDNA reveals a bipartite struc
193 Here we describe the
molecular cloning of p64H1, a p64 homolog, from both hum
194 Here we report the
molecular cloning of par-6 and the immunolocalization of
195 We report the
molecular cloning of PPcK from the facultative Crassulac
196 The
molecular cloning of Rgh3 suggests that alternative RNA
197 Molecular cloning of RRP6 revealed its homology to a 100
198 Molecular cloning of SGL1 revealed that it encodes the M
199 Here we describe the
molecular cloning of SLAP-130, a SLP-76-associated phosp
200 Molecular cloning of slp1+ revealed that slp1+ encodes a
201 dure we utilized shortens and simplifies the
molecular cloning of small double-stranded DNA viruses a
202 Molecular cloning of subunit 4 of the complex revealed t
203 We report here the identification and
molecular cloning of such a porin.
204 The
molecular cloning of tapasin revealed it to be a transme
205 Here we report the
molecular cloning of TGP3, an additional G-DNA-binding p
206 In this study, we likewise report the
molecular cloning of the 2-O-sulfatase from the same bac
207 Molecular cloning of the AVR-Pita and Pi-ta genes will a
208 We report the
molecular cloning of the binding protein that recognizes
209 Molecular cloning of the breakpoints of a t(1;10)(p22q21
210 Molecular cloning of the C3aR has facilitated studies to
211 The
molecular cloning of the CA125 antigen will lead to a be
212 Here we report the
molecular cloning of the cadherin-associated tyrosine ph
213 However,
molecular cloning of the cDNA encoding this protein (p22
214 We report the
molecular cloning of the complete ancestral TPC gene fam
215 al analysis of single and double mutants and
molecular cloning of the corresponding SEC genes, we est
216 We report here the
molecular cloning of the Delta4,5 glycuronidase gene fro
217 Recent
molecular cloning of the epithelial sodium channel (ENaC
218 ean (Glycine max) nodules, we now report the
molecular cloning of the first legume PpcK from a soybea
219 Molecular cloning of the full-length Stramonita NOS (Sh-
220 Molecular cloning of the gene encoding pp36 should facil
221 Molecular cloning of the gene shows that the inferred HI
222 We report here the
molecular cloning of the gene that encodes MKK7 and demo
223 (QTL) mapping is still too coarse to permit
molecular cloning of the genetic determinants.
224 ningoencephalitis in horses and sheep led to
molecular cloning of the genome of a novel, negative-str
225 of cis-IPTase activity 40 years ago and the
molecular cloning of the human cDNA encoding the mammali
226 In this study we describe the
molecular cloning of the mRNA sequence encoding the chic
227 actor, followed by amino acid sequencing and
molecular cloning of the murine cDNA, the orthologue of
228 In the present study, we report the
molecular cloning of the myeloid DAP12-associating lecti
229 Recently, two groups have reported the
molecular cloning of the putative catalytic subunit (hES
230 Molecular cloning of the SCCA genomic region revealed th
231 Molecular cloning of the SPA1 gene indicates that SPA1 i
232 The
molecular cloning of the t(5;10)(q33;q22) associated wit
233 Before the
molecular cloning of the T1rs, it had been proposed that
234 sms of taste sensation have been gained from
molecular cloning of the transduction elements, biochemi
235 sients are absent in tre cardiomyocytes, and
molecular cloning of the tre mutation revealed that the
236 This study reports the
molecular cloning of the two Ppc genes in C. reinhardtii
237 The
molecular cloning of these genes allowed us to examine t
238 The
molecular cloning of these novel WT-sensitive type III P
239 The purification and
molecular cloning of this cell surface receptor were fin
240 The
molecular cloning of this gene may lead to a better unde
241 The
molecular cloning of this region provides a valuable too
242 Here, we report the
molecular cloning of three Bla g 1 cDNA clones, which sh
243 The
molecular cloning of three high-affinity lysophosphatidi
244 We describe here the
molecular cloning of TTN5 using a T-DNA-tagged allele.
245 In this paper, we describe the
molecular cloning of two new protein components of CFP a
246 Here, we report
molecular cloning of two TRPV1 cDNA variants from dorsal
247 Molecular cloning of vesicular monoamine transporters sh
248 ture high-resolution mapping and ultimately,
molecular cloning,
of the interacting genes that contrib
249 eosporus was analyzed by Tn5099 mutagenesis,
molecular cloning,
partial DNA sequencing, and insertion
250 native plant membranes, we describe here the
molecular cloning,
physical mapping, and heterologous ex
251 need for enzymatic assembly and reduces all
molecular cloning procedures to a single-tube, single-st
252 In this study, we report the
molecular cloning,
promoter characterization, developmen
253 In the previous paper, we described the
molecular cloning,
recombinant expression, and prelimina
254 Molecular cloning results revealed that ovochymase is tr
255 From peptide sequence,
molecular cloning revealed a cDNA encoding a novel prote
256 Molecular cloning revealed four isoforms of the protein.
257 Molecular cloning revealed that LC1 is a member of the S
258 Molecular cloning revealed that teleosts have eight SCNA
259 Molecular cloning revealed that this phenotype is caused
260 Molecular cloning revealed the similarity of gephyrin to
261 Molecular cloning revealed the unique serpin endopin 2C
262 specifically to methylated DNA in vitro and
molecular cloning reveals a similarity to a known methyl
263 Molecular cloning reveals that dak and box encode ext2 a
264 Molecular cloning reveals that the heart and mind lesion
265 Using
molecular cloning,
RT-PCR, Western blotting, immunolocal
266 A more exact characterization through
molecular cloning showed that 97.7% of replicons contain
267 PKA assays and
molecular cloning showed that one suppressor mutation (s
268 Molecular cloning shows that she-1 encodes a novel F box
269 receptors of medical interest, it has eluded
molecular cloning since its discovery, and the gene that
270 cription-polymerase chain reaction (RT-PCR),
molecular cloning,
Southern hybridization, nucleotide se
271 posite nucleotide sequence, thereby forgoing
molecular cloning steps and the use of restriction enzym
272 A complete circumvention of
molecular cloning steps qualifies this method for sequen
273 Recent
molecular cloning studies have found several families of
274 Recent fluorescent in situ hybridization and
molecular cloning studies have identified several novel
275 Molecular cloning studies have identified three differen
276 Pharmacological and
molecular cloning studies have identified three opioid-r
277 Molecular cloning studies have revealed a large family o
278 Molecular cloning studies have revealed the existence of
279 Molecular cloning studies have shown that GPCRs form one
280 Evidence from pharmacological and
molecular cloning studies indicates the presence of mult
281 The emergence of
molecular cloning techniques and identification of fluor
282 re, we use biochemical, ultrastructural, and
molecular cloning techniques to obtain a comprehensive p
283 In addition,
molecular cloning techniques were used to clone and expr
284 Using standard
molecular cloning techniques, we identified and isolated
285 p through in vivo replication using standard
molecular cloning techniques.
286 Here we show by
molecular cloning that each catalytic subunit in amphibi
287 of Ramon y Cajal to the current advances in
molecular cloning,
the retina has served as an ideal mod
288 n, the discovery of oncogenes, the advent of
molecular cloning,
the search for human cancer viruses,
289 or function and that this method requires no
molecular cloning,
this method should be applicable for
290 alterations of the genome requires extensive
molecular cloning to build targeting vectors and DNA-bas
291 We employed
molecular cloning to examine how PTEN's stability, subce
292 boratory-based selection, the application of
molecular cloning to insecticide targets and to the meta
293 mass spectrometry sequencing techniques and
molecular cloning to isolate a unique melanoma Ag recogn
294 Evidence of emp4
molecular cloning was provided by the isolation of four
295 Molecular cloning was used to identify four novel mu-con
296 Using
molecular cloning,
we describe a family of potent small
297 Using
molecular cloning,
we have identified three separate dom
298 uorescence in situ hybridization (FISH), and
molecular cloning,
we show that 5 CEBP gene family membe
299 Using
molecular cloning,
we systematically studied the impact
300 After biologic and
molecular cloning,
we were able to identify a single fra