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1 CSPG4-specific chimeric, humanized, or fully human monoclonal antibody.
2 antification of somatropin and a therapeutic human monoclonal antibody.
3 t manner by IVIG, F(ab)2-IVIG and irrelevant human monoclonal antibody.
4 the epitopes of several broadly neutralizing human monoclonal antibodies.
5 epitope sites targeted by virus neutralising human monoclonal antibodies.
6 he isolation and characterization of a fully human monoclonal antibody (1C1) that selectively binds b
7                                              Human monoclonal antibody 2219 is a neutralizing antibod
8 ied as the epitope of the HIV-1 neutralizing human monoclonal antibody 2F5 (MAb 2F5).
9                                          The human monoclonal antibody 2F5 neutralizes primary human
10 om the polyreactive and broadly neutralizing human monoclonal antibody 2F5 was targeted into the mous
11                     The broadly neutralizing human monoclonal antibody 2F5 was used to select for vir
12  with the corresponding broadly neutralizing human monoclonal antibody 2F5, provides a target for str
13 gnition epitope for the broadly neutralizing human monoclonal antibody 2F5.
14 gp41 is a target of two broadly neutralizing human monoclonal antibodies, 2F5 and 4E10, and is an imp
15 lasmablast enrichment technique to isolate a human monoclonal antibody, 46B8 that neutralizes all IBV
16 plasma, HIV immunoglobulin, soluble CD4, and human monoclonal antibodies 4E10, 2F5, and b12.
17 o phosphatidylinositol phosphate (PIP) and a human monoclonal antibody (4E10) that is known to have b
18 ed gp41-specific cross-reactive neutralizing human monoclonal antibodies, 4E10 and 2F5, target linear
19 r actions of two rare, broadly neutralizing, human monoclonal antibodies, 4E10 and 2F5, which target
20          Here we show that the DENV-specific human monoclonal antibody 5J7 is exceptionally potent, n
21                                  We isolated human monoclonal antibody 5J8, which neutralized a broad
22  that the hemagglutinin (HA) stalk-targeting human monoclonal antibody 81.39a effectively neutralized
23 ated a large panel of orthopoxvirus-specific human monoclonal antibodies (Abs) from immune subjects t
24                                              Human monoclonal antibodies (Abs) to the CD4 binding dom
25                             A combination of human monoclonal antibodies, actoxumab and bezlotoxumab,
26                                 Neutralizing human monoclonal antibodies against alpha-toxin (AT) and
27 -controlled study of two neutralizing, fully human monoclonal antibodies against C. difficile toxins
28 , we identified a panel of macropinocytosing human monoclonal antibodies against CD46, a negative reg
29   We have previously identified neutralizing human monoclonal antibodies against Nipah virus (NiV) an
30                                Production of human monoclonal antibodies against Stx, which are highl
31               We also tested the effect of a human monoclonal antibody against ANGPTL4 on lipid level
32     We aimed to compare panitumumab, a fully human monoclonal antibody against EGFR, plus radiotherap
33 Then we report the identification of HS20, a human monoclonal antibody against GPC3, which preferenti
34 trial evaluated the safety and efficacy of a human monoclonal antibody against interleukin-12 (anti-i
35 hn's disease, the efficacy of ustekinumab, a human monoclonal antibody against interleukin-12 and int
36 sed the efficacy and safety of brodalumab, a human monoclonal antibody against interleukin-17 recepto
37  the development of a highly effective fully human monoclonal antibody against Jagged1 (clone 15D11).
38        We assessed the effects of AMG 145, a human monoclonal antibody against PCSK9, in patients wit
39                          Evolocumab, a fully human monoclonal antibody against proprotein convertase
40                             AMG 145, a fully human monoclonal antibody against proprotein convertase
41 randomized study compared denosumab, a fully human monoclonal antibody against receptor activator of
42 vestigated the effects of denosumab, a fully human monoclonal antibody against receptor activator of
43 vestigated the ability of denosumab, a fully human monoclonal antibody against receptor activator of
44                               We generated a human monoclonal antibody against scavenger receptor cla
45  activity of 80R immunoglobulin G1 (IgG1), a human monoclonal antibody against severe acute respirato
46                              5C12 HuMAb is a human monoclonal antibody against the A subunit of Shiga
47  the safety and efficacy of AMG 334, a fully human monoclonal antibody against the CGRP receptor, for
48 the efficacy and safety of erenumab, a fully human monoclonal antibody against the CGRP receptor, in
49                       Ustekinumab is a fully human monoclonal antibody against the p40 subunit of int
50           Lexatumumab is an agonistic, fully human monoclonal antibody against tumor necrosis factor-
51                         Ganitumab is a fully human monoclonal antibody against type-1 insulin-like gr
52                        Evolocumab is a fully human, monoclonal antibody against PCSK9 that reduces lo
53                             A ligand-mimetic human monoclonal antibody AL-57 (activated LFA-1 clone 5
54 oires offers a novel route to discover fully human monoclonal antibodies and identify antigens of pot
55  sensitivity to neutralizing patient IgG and human monoclonal antibodies AR3A and AR4A and (ii) incre
56 upport further development of m336 and other human monoclonal antibodies as potential therapeutics fo
57 bust system for the discovery of therapeutic human monoclonal antibodies; as a surrogate readout of t
58                    We investigated whether a human monoclonal antibody (AVP-21D9) to protective antig
59 l administration of the broadly neutralizing human monoclonal antibody b12 can protect macaques from
60                                          The human monoclonal antibody b12 recognizes a conserved epi
61                              Bezlotoxumab, a human monoclonal antibody, binds to C. difficile toxin B
62       We have developed a method to generate human monoclonal antibodies by selecting phage antibody
63               We have previously described a human monoclonal antibody called KM33 that blocks these
64                                 Selection of human monoclonal antibodies can identify immunodominant
65                                      Several human monoclonal antibodies can neutralize a range of hu
66                                We describe a human monoclonal antibody, CH65, obtained by isolating r
67 ve immunization with combinations containing human monoclonal antibodies completely prevented infecti
68 port the isolation and characterization of a human monoclonal antibody CR8020 with broad neutralizing
69                              Here, we report human monoclonal antibodies, CR8033, CR8071, and CR9114,
70                                          The human monoclonal antibody, D5, binds to this target and
71 s with a potency that rivals that of several human monoclonal antibodies, demonstrating that computat
72                                    The fully human monoclonal antibody denosumab (formerly known as A
73                         HLA class I-specific human monoclonal antibodies derived from women sensitize
74                   We assessed ustekinumab, a human monoclonal antibody directed against these cytokin
75 S for simultaneous detection of the residual human monoclonal antibody drug and endogenous human IgG
76                                          The human monoclonal antibody Fab X5 neutralizes a broad ran
77    Among a panel of 18 dengue virus-reactive human monoclonal antibodies, four groups of antibodies w
78 isplay to produce a panel of chimeric rabbit/human monoclonal antibody fragments (both Fab and scFv)
79 , we isolated a panel of dengue prM-specific human monoclonal antibodies from individuals after infec
80                                   We derived human monoclonal antibodies from persons who received th
81  agents against ZIKV, we isolated a panel of human monoclonal antibodies from subjects that were prev
82                                   We derived human monoclonal antibodies from the bone marrow of a pa
83               Further, by using TG2-specific human monoclonal antibodies generated from intestinal pl
84                                      A fully human monoclonal antibody has been isolated that binds t
85                                          The human monoclonal antibody HC-1 recognizes a conformation
86                                  Recombinant human monoclonal antibodies (hmAb) against gliadin are p
87 trated that DENV serotype 2 (DENV2)-specific human monoclonal antibody (HMAb) 2D22 is therapeutic in
88                                              Human monoclonal antibody (hMAb) targeting the hemagglut
89 roadly cross-reactive HIV-neutralizing CD4bs human monoclonal antibody (hmAb), m18.
90 was reported to resist neutralization by the human monoclonal antibodies (hmAbs) 80R and S3.1, which
91 e identification and characterization of new human monoclonal antibodies (hMAbs) able to neutralize p
92                                         Five human monoclonal antibodies (HMAbs) are described that c
93            In the current study, we obtained human monoclonal antibodies (hMAbs) directly from antibo
94 roduction and analysis of HIV-1 Env-specific human monoclonal antibodies (hMAbs) isolated from vaccin
95 nistic studies with anti-dengue virus (DENV) human monoclonal antibodies (hMAbs) provide a rational a
96 tro against a panel of 12 well-characterized human monoclonal antibodies (HMAbs) targeting diverse E1
97                 Previously, we identified 10 human monoclonal antibodies (HMAbs) that bind E2 glycopr
98                           Epitope mapping of human monoclonal antibodies (HMAbs) that bind to an adja
99 erplay between these antibodies, we isolated human monoclonal antibodies (HMAbs) to aa 412 to 423, de
100 1E2 glycoproteins, as defined in part by HCV human monoclonal antibodies (HMAbs) to conformational ep
101               Characterization of a panel of human monoclonal antibodies (HMAbs) to HCV by competitio
102 omplementary strategy is to use neutralizing human monoclonal antibodies (HMAbs) to prevent acute inf
103                 A panel of immunoglobulin G1 human monoclonal antibodies (HMAbs) to three immunogenic
104                                              Human monoclonal antibodies (HMAbs) with neutralizing ca
105 lobal E2 alanine scanning with a panel of 16 human monoclonal antibodies (hmAbs), resulting in an unp
106 ation by chronic-phase patient sera and lead human monoclonal antibodies (HMAbs).
107 tocol for the production of antigen-specific human monoclonal antibodies (hmAbs).
108 d binding affinity of a panel of anti-HCV E2 human monoclonal antibodies (HMAbs).
109      By using HuMAb-Mouse (Medarex) animals, human monoclonal antibodies (Hu-MAbs) were developed aga
110     We investigated the efficacy of specific human monoclonal antibodies (HuMab) and alpaca polyclona
111 igational product containing a mixture of 26 human monoclonal antibodies (HuMAbs) against mature viri
112 ed with OspA from B. burgdorferi to generate human monoclonal antibodies (HuMabs) against OspA.
113 n and preclinical evaluation of neutralizing human monoclonal antibodies (HuMAbs) against the Shiga t
114 pursue this treatment modality, we developed human monoclonal antibodies (HuMAbs) directed against th
115 to express 3 human rabies virus-neutralizing human monoclonal antibodies (huMAbs) in a rhabdovirus ve
116 administration of Shiga toxin (Stx)-specific human monoclonal antibodies (HuMAbs) is considered a pro
117  We have previously shown that Stx2-specific human monoclonal antibodies (HuMAbs) protect mice and pi
118             In this report we describe fully human monoclonal antibodies (HuMAbs) that neutralize the
119  neutralizing activities; they are the first human monoclonal antibodies identified against these vir
120 fragments of antigen binding (Fabs) from two human monoclonal antibodies, IgG-94 and IgG-RC, isolated
121 uid-liquid phase separation in a solution of human monoclonal antibody, IgG2, and the effects of huma
122 e expression of an EGFP-labeled single-chain human monoclonal antibody, IK17, which binds to MDA-LDL,
123 4 and their sensitivity to neutralization by human monoclonal antibody immunoglobulin G1b12 and, to a
124 e the efficacy and safety of teprotumumab, a human monoclonal antibody inhibitor of IGF-IR, in patien
125                          Characterization of human monoclonal antibodies is providing considerable in
126                             The isolation of human monoclonal antibodies is providing important insig
127                                    CR4354, a human monoclonal antibody isolated from a patient, neutr
128 d to the Fab fragment of 1G2, a neutralizing human monoclonal antibody isolated from a seropositive s
129 n addition, the technological convergence of human monoclonal antibody isolation, structural biology,
130 ve broadly cross-reactive HIV-1-neutralizing human monoclonal antibodies known to date, X5 is the onl
131                               A neutralizing human monoclonal antibody, KZ52, protects guinea pigs fr
132                                            A human monoclonal antibody, LymphoStat-B, specific for hu
133  AGMs showed that the therapeutic window for human monoclonal antibody m102.4, previously shown to re
134                             Here we report a human monoclonal antibody, m826, that binds to H7 hemagg
135           We solved the crystal structure of human monoclonal antibody (MAb) 2158, which targets a co
136  unique epitope for the broadly neutralizing human monoclonal antibody (MAb) 2G12 on the gp120 surfac
137                                          The human monoclonal antibody (MAb) A32 is a nonneutralizing
138                   Competitive binding of the human monoclonal antibody (mAb) LE2E9 revealed overlappi
139 including an A32-like epitope, recognized by human monoclonal antibody (MAb) N60-i3, and a hybrid A32
140                       Ustekinumab is a fully human monoclonal antibody (mAb) that binds specifically
141 first to enter the clinic, ustekinumab, is a human monoclonal antibody (mAb) that binds to the p40 su
142 ve at blocking opsonic killing mediated by a human monoclonal antibody (mAb) to native PNAG than it w
143 evolution, and structure of a broad-spectrum human monoclonal antibody (mAb), MEDI8852, effectively r
144 Further, these viruses were neutralized by a human monoclonal antibody (MAb), S230.15, but the parent
145                                We isolated a human monoclonal antibody (mAb), ZKA190, that potently c
146                                   Use of the human monoclonal antibody, MAB-T88, did not improve the
147                                          Two human monoclonal antibodies, mAb100 and mAb114, in combi
148                                          Two human monoclonal antibodies (MAbs) (2F5 and 4E10) agains
149                     The broadly neutralizing human monoclonal antibodies (MAbs) 2F5 and 4E10, both ta
150                 We isolated a large panel of human monoclonal antibodies (mAbs) against BDBV glycopro
151             We screened a panel of mouse and human monoclonal antibodies (MAbs) against chikungunya v
152 virus-like particles (VLPs) to isolate seven human monoclonal antibodies (MAbs) against the CHIKV env
153                            We tested whether human monoclonal antibodies (MAbs) against the three maj
154 t into dengue immunity, we characterized 145 human monoclonal antibodies (mAbs) and identified a prev
155 1 due to modest potency and breadth of early human monoclonal antibodies (MAbs) and perceived insurmo
156 n-specific sorting, we isolated Env-specific human monoclonal antibodies (MAbs) and studied the clona
157 he genes encoding broadly HIV-1-neutralizing human monoclonal antibodies (MAbs) are highly divergent
158                                              Human monoclonal antibodies (mAbs) are under development
159 To guide vaccine design, we assessed whether human monoclonal antibodies (MAbs) b12 and b6 against th
160  influenza virus hemagglutinin (HA)-reactive human monoclonal antibodies (MAbs) by hybridoma technolo
161                             We characterized human monoclonal antibodies (MAbs) cloned from influenza
162                             RECENT FINDINGS: Human monoclonal antibodies (mAbs) derived from rheumati
163                                        Fully human monoclonal antibodies (mAbs) derived from transgen
164                                              Human monoclonal antibodies (mAbs) designed for immunoth
165    Here we describe the detailed analysis of human monoclonal antibodies (MAbs) directed against HCV
166                                Although rare human monoclonal antibodies (mAbs) exist that broadly ne
167         We report here the identification of human monoclonal antibodies (MAbs) from a large nonimmun
168                               The first uses human monoclonal antibodies (MAbs) generated against the
169        Although highly inhibitory murine and human monoclonal antibodies (mAbs) have been generated,
170 tion of a large panel of naturally occurring human monoclonal antibodies (MAbs) obtained from subject
171                                              Human monoclonal antibodies (MAbs) specific for HIV-2 V3
172                             The selection of human monoclonal antibodies (MAbs) specific for human im
173                      Here we have cloned 113 human monoclonal antibodies (mAbs) specific for LASV gly
174 ly-N-acetylated glucosamine (PNAG) by use of human monoclonal antibodies (MAbs) specific for such epi
175                  For Pseudomonas aeruginosa, human monoclonal antibodies (mAbs) targeting the Psl bio
176 d from sorted single ASCs to produce over 50 human monoclonal antibodies (mAbs) that bound to the thr
177                We isolated and characterized human monoclonal antibodies (mAbs) that neutralize CHIKV
178                                We identified human monoclonal antibodies (mAbs) that neutralize genet
179                                              Human monoclonal antibodies (MAbs) that neutralize SARS-
180                                          Two human monoclonal antibodies (MAbs) that neutralized DENV
181 ated from a single donor 13 new neutralizing human monoclonal antibodies (mAbs) that recognize the RS
182                             Using a panel of human monoclonal antibodies (mAbs) to DENV, we showed th
183 tro activities and efficacies in mice of two human monoclonal antibodies (MAbs) to type 8 PS, NAD (Ig
184                   We report 3 LukAB-specific human monoclonal antibodies (mAbs) with distinct mechani
185 d neutralization properties of 15 anti-HIV-2 human monoclonal antibodies (MAbs), 14 of which were new
186 iously characterized a panel of neutralizing human monoclonal antibodies (MAbs), but the majority of
187                         Several neutralizing human monoclonal antibodies (mAbs), including m336, a ge
188                          We identified three human monoclonal antibodies (MAbs), m336, m337, and m338
189 ultaneous quantitation of two coadministered human monoclonal antibodies (mAbs), mAb-A and mAb-B of I
190                                  Using fully human monoclonal antibodies (MAbs), we now have shown th
191 for neutralizing antibodies in studies using human monoclonal antibodies (MAbs).
192                                              Human monoclonal antibodies may be a useful adjunct to f
193              These data suggest that the 80R human monoclonal antibody may be a useful viral entry in
194 r and suggest that inhibition of CTGF with a human monoclonal antibody may control primary and metast
195                    We have developed a fully human monoclonal antibody, MEDI-575, that selectively bi
196                             We show that the human monoclonal antibody, MEDI1912, selected against ne
197 rted the isolation and characterization of 2 human monoclonal antibodies neutralizing CHIKV in vitro:
198 s a neutralizing anti-interleukin-13 (IL-13) human monoclonal antibody obtained from a phage display
199 robust SCID mouse-based method for isolating human monoclonal antibodies of desired specificity from
200 erotypic neutralizing epitopes recognized by human monoclonal antibodies onto the surface of the VP8*
201                                          The human monoclonal antibody opicinumab (BIIB033, anti-LING
202  sensitive PDGF D sandwich ELISA using fully human monoclonal antibodies, PDGF D was detected at elev
203 argeted liposomal nanoprobe by conjugating a human monoclonal antibody, PGN635 that specifically targ
204 ecognized by a recently discovered family of human monoclonal antibodies (PGT151-PGT158).
205   We have previously shown that Stx-specific human monoclonal antibodies protect STEC-infected animal
206                                We found that human monoclonal antibodies recognized the Sa antigenic
207  a single-chain variable fragment of the 17b human monoclonal antibody recognizing a highly conserved
208 lly, neutralizing M-CSF activity via a novel human monoclonal antibody reduced the CD14(+)CD16(+) mon
209 es and provide a better understanding of the human monoclonal antibody response to influenza in the c
210                                          The human monoclonal antibody rHIgM22 enhances remyelination
211  the few known potent broadly cross-reactive human monoclonal antibodies, scFv X5, could be improved
212 -B12, and -B35 expression on platelets using human monoclonal antibodies specific for these antigens.
213  safety of tezepelumab (AMG 157/MEDI9929), a human monoclonal antibody specific for the epithelial-ce
214                                Ipilimumab, a human monoclonal antibody targeted against cytotoxic T-l
215                                        Fully human monoclonal antibodies targeting CTLA-4 have been s
216                   The efficacy of TCN-032, a human monoclonal antibody targeting a conserved epitope
217                 Ofatumumab (HuMax-CD20) is a human monoclonal antibody targeting a distinct small-loo
218                         Panitumumab, a fully human monoclonal antibody targeting the epidermal growth
219                         Panitumumab, a fully human monoclonal antibody targeting the epidermal growth
220  To our knowledge, these are the first fully human monoclonal antibodies that are specific to integri
221             Isolation of these antibodies as human monoclonal antibodies that block virus binding and
222 rated and characterized five different fully human monoclonal antibodies that bound to and neutralize
223  also make possible the rapid development of human monoclonal antibodies that could become a potent i
224           Here we show that a combination of human monoclonal antibodies that cross-react with the gl
225                   Here, we describe a set of human monoclonal antibodies that define what is, to the
226                                         Many human monoclonal antibodies that neutralize multiple cla
227              Here we report the isolation of human monoclonal antibodies that recognize erythrocytes
228                        Ipilimumab is a fully human monoclonal antibody that binds cytotoxic T-lymphoc
229                       Conatumumab is a fully human monoclonal antibody that binds to and activates hu
230               Rituximab is a chimeric murine/human monoclonal antibody that binds to CD20 on B lympho
231                       PF-00547659 is a fully human monoclonal antibody that binds to human mucosal ad
232                               Panitumumab, a human monoclonal antibody that binds to the epidermal gr
233                             Ustekinumab is a human monoclonal antibody that binds to the shared p40 s
234                        Adalimumab is a fully human monoclonal antibody that binds tumor necrosis fact
235 ment after treatment with dupilumab, a fully-human monoclonal antibody that blocks both pathways.
236                              Ipilimumab is a human monoclonal antibody that blocks cytotoxic T-lympho
237                           Dupilumab, a fully human monoclonal antibody that blocks interleukin-4 and
238                             Ustekinumab is a human monoclonal antibody that inhibits receptor-binding
239                  We tested erenumab, a fully human monoclonal antibody that inhibits the calcitonin g
240                               Canakinumab, a human monoclonal antibody that neutralizes interleukin-1
241        This drug, belimumab (Benlysta), is a human monoclonal antibody that neutralizes the B-cell su
242 dy was undertaken to investigate whether the human monoclonal antibody that neutralizes transforming
243 ule (V1V2ZM109-1FD6) in complex with 830A, a human monoclonal antibody that recognizes a V1V2 epitope
244                                 Sirukumab, a human monoclonal antibody that selectively binds to the
245             BACKGROUND & AIMS: MEDI2070 is a human monoclonal antibody that selectively inhibits inte
246 re we report the generation of aducanumab, a human monoclonal antibody that selectively targets aggre
247                       Rilotumumab is a fully human monoclonal antibody that selectively targets the l
248 le-chain variable region construct of 17b, a human monoclonal antibody that targets a conserved CD4-i
249                   MEDI4893 is a neutralizing human monoclonal antibody that targets alpha-toxin (AT)
250 PET/NIRF) imaging agents, using 5B1, a fully human monoclonal antibody that targets CA19.9, a well-es
251                       Panitumumab is a fully human monoclonal antibody that targets EGFR.
252  vascular risk indicates that canakinumab, a human monoclonal antibody that targets IL-1beta, markedl
253                               5B1 is a fully human, monoclonal antibody that has shown promise for th
254                       Rilotumumab is a fully human, monoclonal antibody that neutralises HGF.
255  model in humanized mice and used it to test human monoclonal antibody therapy.
256 ires can be mined for the discovery of fully human monoclonal antibodies to B-CLL cell-surface antige
257               We generated a total of 63 new human monoclonal antibodies to compare the B-cell respon
258  In this study, we have generated a panel of human monoclonal antibodies to dengue virus.
259     We evaluated the therapeutic activity of human monoclonal antibodies to DENV EDE for their abilit
260 readth of the recently isolated neutralizing human monoclonal antibodies to HIV-1 have stimulated int
261                                  We identify human monoclonal antibodies to O-antigens that are highl
262 blished phase I and II trials with two fully human monoclonal antibodies to PCSK9 have provided compr
263 o review the phase 1 and 2 trials with fully human monoclonal antibodies to proprotein convertase sub
264                      CBH-2 is a neutralizing human monoclonal antibody to a domain B epitope that is
265 ite the clinical validation of this model, a human monoclonal antibody to CA19.9 (a highly visible bu
266            Lumiliximab is a chimeric macaque-human monoclonal antibody to CD23, a protein expressed o
267                In addition, treatment with a human monoclonal antibody to HCMV glycoprotein B rescues
268  maturation, and characterization of a fully human monoclonal antibody to human NKG2D.
269                           We have isolated a human monoclonal antibody to IL-17A (CAT-2200) that can
270                          Evolocumab, a fully human monoclonal antibody to PCSK9 (proprotein convertas
271                        In phase 1 studies, a human monoclonal antibody to PCSK9, AMG145, was well tol
272  assessed the effects of evolocumab, a fully human monoclonal antibody to PCSK9, on Lp(a), the relati
273                             AMG 145, a fully human monoclonal antibody to PCSK9, prevents PCSK9/LDL-R
274      In phase 2 studies, evolocumab, a fully human monoclonal antibody to PCSK9, reduced LDL-C levels
275                         SAR236553 is a fully human monoclonal antibody to PCSK9.
276          A second monoclonal antibody [PRM1 (human monoclonal antibody to PR)], which recognizes part
277                          Evolocumab, a fully human monoclonal antibody to proprotein convertase subti
278 ts were passively immunized with AVP-21D9, a human monoclonal antibody to protective antigen (PA), at
279                 Denosumab (AMG 162), a fully human monoclonal antibody to RANKL, shares the pharmacol
280        Denosumab is an investigational fully human monoclonal antibody to receptor activator of nucle
281                           Denosumab, a fully human monoclonal antibody to receptor activator of nucle
282                                          The human monoclonal antibody to serotype 8 pneumococcal cap
283 ty of dupilumab (SAR231893/REGN668), a fully human monoclonal antibody to the alpha subunit of the in
284      The potential therapeutic activity of a human monoclonal antibody to the human interleukin-12 p4
285                         Denosumab is a fully human monoclonal antibody to the receptor activator of n
286              Subcutaneous golimumab, a fully human monoclonal antibody to tumor necrosis factor-alpha
287 activity as an immunogen, we generated fully human monoclonal antibodies using the XenoMouse(TM) plat
288                                    The fully human monoclonal antibody ustekinumab is an efficacious
289 t of cell culture-grown HCV infectivity by a human monoclonal antibody was also observed.
290               By screening a large number of human monoclonal antibodies, we have found that IgM anti
291  of several neutralizing and nonneutralizing human monoclonal antibodies were also determined, which
292 tralize inhibitory RGMa, clinically relevant human monoclonal antibodies were systemically administer
293                     Purified HCV E2-specific human monoclonal antibodies were used to further verify
294         Cross-reactivity was studied using a human monoclonal antibody which inhibits allergic patien
295  ZIKV nonstructural protein 1 (NS1)-specific human monoclonal antibody, which we used to develop an N
296 lated and characterized two protective fully human monoclonal antibodies with specificity for protect
297 ration-dependent self-interactions for three human monoclonal antibodies with unique solution behavio
298       Here we present a broadly neutralizing human monoclonal antibody with an unusual binding modali
299  and identified a high affinity, allosteric, human monoclonal antibody, XMetA, which mimicked the glu
300 ent of a highly therapeutic and neutralizing human monoclonal antibody, ZIKV-117.

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