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1
Recognition of the antigen-presenting molecule MR1 by a Vδ3 + γδ T cell receptor
Recognition of the antigen-presenting molecule MR1 by a Vδ3 + γδ T cell receptor
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Recognition of the antigen-presenting molecule MR1 by a Vδ3 + γδ T cell receptor

Proceedings of the National Academy of Sciences - PNAS, 2021-12, Vol.118 (49) [Peer Reviewed Journal]

Copyright National Academy of Sciences Dec 7, 2021 ;2021 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2110288118 ;PMID: 34845016

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2
CD32 expression is associated to T-cell activation and is not a marker of the HIV-1 reservoir
CD32 expression is associated to T-cell activation and is not a marker of the HIV-1 reservoir
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CD32 expression is associated to T-cell activation and is not a marker of the HIV-1 reservoir

Nature communications, 2018-07, Vol.9 (1), p.2739-10, Article 2739 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-05157-w ;PMID: 30013105

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3
New B7 Family Checkpoints in Human Cancers
New B7 Family Checkpoints in Human Cancers
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New B7 Family Checkpoints in Human Cancers

Molecular cancer therapeutics, 2017-07, Vol.16 (7), p.1203-1211 [Peer Reviewed Journal]

2017 American Association for Cancer Research. ;Copyright American Association for Cancer Research Inc Jul 2017 ;ISSN: 1535-7163 ;EISSN: 1538-8514 ;DOI: 10.1158/1535-7163.mct-16-0761 ;PMID: 28679835

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4
Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy
Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy
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Chimeric antigen receptor-engineered natural killer cells for cancer immunotherapy

Journal of hematology and oncology, 2020-12, Vol.13 (1), p.168-168, Article 168 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1756-8722 ;EISSN: 1756-8722 ;DOI: 10.1186/s13045-020-00998-9 ;PMID: 33287875

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5
Blocking expression of inhibitory receptor NKG2A overcomes tumor resistance to NK cells
Blocking expression of inhibitory receptor NKG2A overcomes tumor resistance to NK cells
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Blocking expression of inhibitory receptor NKG2A overcomes tumor resistance to NK cells

The Journal of clinical investigation, 2019-05, Vol.129 (5), p.2094-2106 [Peer Reviewed Journal]

COPYRIGHT 2019 American Society for Clinical Investigation ;COPYRIGHT 2019 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation May 2019 ;2019 American Society for Clinical Investigation 2019 American Society for Clinical Investigation ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/jci123955 ;PMID: 30860984

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6
What to do with HLA-DO/H-2O two decades later?
What to do with HLA-DO/H-2O two decades later?
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What to do with HLA-DO/H-2O two decades later?

Immunogenetics (New York), 2019-03, Vol.71 (3), p.189-196 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2019 ;Immunogenetics is a copyright of Springer, (2019). All Rights Reserved. ;ISSN: 0093-7711 ;EISSN: 1432-1211 ;DOI: 10.1007/s00251-018-01097-3 ;PMID: 30683973

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7
Risk of Pediatric Celiac Disease According to HLA Haplotype and Country
Risk of Pediatric Celiac Disease According to HLA Haplotype and Country
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Risk of Pediatric Celiac Disease According to HLA Haplotype and Country

The New England journal of medicine, 2014-07, Vol.371 (1), p.42-49 [Peer Reviewed Journal]

Copyright © 2014 Massachusetts Medical Society. All rights reserved. ;2015 INIST-CNRS ;Copyright © 2014 Massachusetts Medical Society. 2014 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1313977 ;PMID: 24988556 ;CODEN: NEJMAG

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8
Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians
Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians
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Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians

PLoS genetics, 2019-04, Vol.15 (4), p.e1008092 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Molineros et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Molineros et al 2019 Molineros et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008092 ;PMID: 31022184

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9
Phenotyping and Target Expression Profiling of CD34+/CD38− and CD34+/CD38+ Stem- and Progenitor cells in Acute Lymphoblastic Leukemia
Phenotyping and Target Expression Profiling of CD34+/CD38− and CD34+/CD38+ Stem- and Progenitor cells in Acute Lymphoblastic Leukemia
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Phenotyping and Target Expression Profiling of CD34+/CD38− and CD34+/CD38+ Stem- and Progenitor cells in Acute Lymphoblastic Leukemia

Neoplasia (New York, N.Y.), 2018-06, Vol.20 (6), p.632-642 [Peer Reviewed Journal]

2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Neoplasia Press Jun 2018 ;2018 The Authors 2018 ;ISSN: 1476-5586 ;ISSN: 1522-8002 ;EISSN: 1476-5586 ;DOI: 10.1016/j.neo.2018.04.004 ;PMID: 29772458

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10
PD-1/PD-L1 complex resembles the antigen-binding Fv domains of antibodies and T cell receptors
PD-1/PD-L1 complex resembles the antigen-binding Fv domains of antibodies and T cell receptors
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PD-1/PD-L1 complex resembles the antigen-binding Fv domains of antibodies and T cell receptors

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (8), p.3011-3016 [Peer Reviewed Journal]

Copyright 2008 The National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Feb 26, 2008 ;2008 by The National Academy of Sciences of the USA ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.0712278105 ;PMID: 18287011

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11
Sortase-mediated modification of αDEC205 affords optimization of antigen presentation and immunization against a set of viral epitopes
Sortase-mediated modification of αDEC205 affords optimization of antigen presentation and immunization against a set of viral epitopes
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Sortase-mediated modification of αDEC205 affords optimization of antigen presentation and immunization against a set of viral epitopes

Proceedings of the National Academy of Sciences - PNAS, 2013-01, Vol.110 (4), p.1428-1433 [Peer Reviewed Journal]

copyright © 1993-2008 National Academy of Sciences of the United States of America ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1214994110 ;PMID: 23297227

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12
Unregulated antigen-presenting cell activation by T cells breaks self tolerance
Unregulated antigen-presenting cell activation by T cells breaks self tolerance
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Unregulated antigen-presenting cell activation by T cells breaks self tolerance

Proceedings of the National Academy of Sciences - PNAS, 2019-01, Vol.116 (3), p.1007-1016 [Peer Reviewed Journal]

Volumes 1–89 and 106–116, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright National Academy of Sciences Jan 15, 2019 ;2019 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1818624116 ;PMID: 30598454

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13
Bi- and trispecific immune cell engagers for immunotherapy of hematological malignancies
Bi- and trispecific immune cell engagers for immunotherapy of hematological malignancies
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Bi- and trispecific immune cell engagers for immunotherapy of hematological malignancies

Journal of hematology and oncology, 2023-07, Vol.16 (1), p.83-83 [Peer Reviewed Journal]

2023. The Author(s). ;COPYRIGHT 2023 BioMed Central Ltd. ;2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 1756-8722 ;EISSN: 1756-8722 ;DOI: 10.1186/s13045-023-01482-w ;PMID: 37501154

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14
NKG2A‐checkpoint inhibition and its blockade critically depends on peptides presented by its ligand HLA‐E
NKG2A‐checkpoint inhibition and its blockade critically depends on peptides presented by its ligand HLA‐E
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NKG2A‐checkpoint inhibition and its blockade critically depends on peptides presented by its ligand HLA‐E

Immunology, 2022-08, Vol.166 (4), p.507-521 [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd. ;2022 The Authors. Immunology published by John Wiley & Sons Ltd. ;2022. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0019-2805 ;EISSN: 1365-2567 ;DOI: 10.1111/imm.13515 ;PMID: 35596615

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15
CAR‐NK cell in cancer immunotherapy; A promising frontier
CAR‐NK cell in cancer immunotherapy; A promising frontier
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CAR‐NK cell in cancer immunotherapy; A promising frontier

Cancer science, 2021-09, Vol.112 (9), p.3427-3436 [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. ;COPYRIGHT 2021 John Wiley & Sons, Inc. ;2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/cas.14993 ;PMID: 34050690

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16
Multimodal pooled Perturb-CITE-seq screens in patient models define mechanisms of cancer immune evasion
Multimodal pooled Perturb-CITE-seq screens in patient models define mechanisms of cancer immune evasion
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Multimodal pooled Perturb-CITE-seq screens in patient models define mechanisms of cancer immune evasion

Nature genetics, 2021-03, Vol.53 (3), p.332-341 [Peer Reviewed Journal]

COPYRIGHT 2021 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2021 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-021-00779-1 ;PMID: 33649592

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17
A Review of Clinical Outcomes of CAR T-Cell Therapies for B-Acute Lymphoblastic Leukemia
A Review of Clinical Outcomes of CAR T-Cell Therapies for B-Acute Lymphoblastic Leukemia
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A Review of Clinical Outcomes of CAR T-Cell Therapies for B-Acute Lymphoblastic Leukemia

International journal of molecular sciences, 2021-02, Vol.22 (4), p.2150 [Peer Reviewed Journal]

2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms22042150 ;PMID: 33670075

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18
Characterisation of the Immunomodulatory Effects of Meningococcal Opa Proteins on Human Peripheral Blood Mononuclear Cells and CD4+ T Cells
Characterisation of the Immunomodulatory Effects of Meningococcal Opa Proteins on Human Peripheral Blood Mononuclear Cells and CD4+ T Cells
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Characterisation of the Immunomodulatory Effects of Meningococcal Opa Proteins on Human Peripheral Blood Mononuclear Cells and CD4+ T Cells

PloS one, 2016-04, Vol.11 (4), p.e0154153-e0154153 [Peer Reviewed Journal]

2016 Jones et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Jones et al 2016 Jones et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0154153 ;PMID: 27111850

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19
T cell costimulation, checkpoint inhibitors and anti-tumor therapy
T cell costimulation, checkpoint inhibitors and anti-tumor therapy
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T cell costimulation, checkpoint inhibitors and anti-tumor therapy

Journal of biosciences, 2020-12, Vol.45 (1), Article 50 [Peer Reviewed Journal]

Indian Academy of Sciences 2020 ;Journal of Biosciences is a copyright of Springer, (2020). All Rights Reserved. ;Indian Academy of Sciences 2020. ;ISSN: 0250-5991 ;EISSN: 0973-7138 ;DOI: 10.1007/s12038-020-0020-2 ;PMID: 32345776

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20
Pathogenesis and transmission of SARS-CoV-2 in golden hamsters
Pathogenesis and transmission of SARS-CoV-2 in golden hamsters
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Pathogenesis and transmission of SARS-CoV-2 in golden hamsters

Nature (London), 2020-07, Vol.583 (7818), p.834-838 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 30, 2020 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-2342-5 ;PMID: 32408338

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