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1
Correlation between Density of CD8+ T-cell Infiltrate in Microsatellite Unstable Colorectal Cancers and Frameshift Mutations: A Rationale for Personalized Immunotherapy
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Correlation between Density of CD8+ T-cell Infiltrate in Microsatellite Unstable Colorectal Cancers and Frameshift Mutations: A Rationale for Personalized Immunotherapy

Cancer research (Chicago, Ill.), 2015-09, Vol.75 (17), p.3446-3455 [Peer Reviewed Journal]

2015 American Association for Cancer Research. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0008-5472 ;EISSN: 1538-7445 ;DOI: 10.1158/0008-5472.CAN-14-3051 ;PMID: 26060019

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2
Alternative tumour-specific antigens
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Alternative tumour-specific antigens

Nature reviews. Cancer, 2019-08, Vol.19 (8), p.465-478 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Aug 2019 ;ISSN: 1474-175X ;EISSN: 1474-1768 ;DOI: 10.1038/s41568-019-0162-4 ;PMID: 31278396

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3
Precise therapeutic gene correction by a simple nuclease-induced double-stranded break
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Precise therapeutic gene correction by a simple nuclease-induced double-stranded break

Nature (London), 2019-04, Vol.568 (7753), p.561-565 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Apr 25, 2019 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-019-1076-8 ;PMID: 30944467

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4
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
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Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

American journal of human genetics, 2012-03, Vol.90 (3), p.467-477 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Mar 9, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.01.017 ;PMID: 22341971 ;CODEN: AJHGAG

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5
Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing
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Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing

Molecular therapy, 2019-05, Vol.27 (5), p.986-998 [Peer Reviewed Journal]

2019 The Author(s) ;Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved. ;2019. The Author(s) ;2019 The Author(s) 2019 ;ISSN: 1525-0016 ;EISSN: 1525-0024 ;DOI: 10.1016/j.ymthe.2019.03.007 ;PMID: 30930113

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6
Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9
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Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9

Molecular therapy, 2018-06, Vol.26 (6), p.1529-1538 [Peer Reviewed Journal]

2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;2018. The Authors ;2018 The Authors 2018 ;ISSN: 1525-0016 ;EISSN: 1525-0024 ;DOI: 10.1016/j.ymthe.2018.03.018 ;PMID: 29730196

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7
Complex dynamics under tension in a high-efficiency frameshift stimulatory structure
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Complex dynamics under tension in a high-efficiency frameshift stimulatory structure

Proceedings of the National Academy of Sciences - PNAS, 2019-09, Vol.116 (39), p.19500-19505 [Peer Reviewed Journal]

Copyright National Academy of Sciences Sep 24, 2019 ;2019 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1905258116 ;PMID: 31409714

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8
MACSE v2: Toolkit for the Alignment of Coding Sequences Accounting for Frameshifts and Stop Codons
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MACSE v2: Toolkit for the Alignment of Coding Sequences Accounting for Frameshifts and Stop Codons

Molecular biology and evolution, 2018-10, Vol.35 (10), p.2582-2584 [Peer Reviewed Journal]

Attribution - NonCommercial ;The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 2018 ;ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/molbev/msy159 ;PMID: 30165589

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9
Genetic Control of Seed Shattering in Rice by the APETALA2 Transcription Factor SHATTERING ABORTION1
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Genetic Control of Seed Shattering in Rice by the APETALA2 Transcription Factor SHATTERING ABORTION1

The Plant cell, 2012-03, Vol.24 (3), p.1034-1048 [Peer Reviewed Journal]

2012 American Society of Plant Biologists ;Copyright American Society of Plant Biologists Mar 2012 ;2012 American Society of Plant Biologists. All rights reserved. 2012 ;ISSN: 1040-4651 ;EISSN: 1532-298X ;DOI: 10.1105/tpc.111.094383 ;PMID: 22408071

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10
Integrative Analyses of Colorectal Cancer Show Immunoscore Is a Stronger Predictor of Patient Survival Than Microsatellite Instability
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Integrative Analyses of Colorectal Cancer Show Immunoscore Is a Stronger Predictor of Patient Survival Than Microsatellite Instability

Immunity (Cambridge, Mass.), 2016-03, Vol.44 (3), p.698-711 [Peer Reviewed Journal]

2016 Elsevier Inc. ;Copyright © 2016 Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Mar 15, 2016 ;ISSN: 1074-7613 ;EISSN: 1097-4180 ;DOI: 10.1016/j.immuni.2016.02.025 ;PMID: 26982367

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11
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice
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Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice

PLoS genetics, 2019-05, Vol.15 (5), p.e1008130-e1008130 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008130 ;PMID: 31048900

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12
Insertion-and-deletion-derived tumour-specific neoantigens and the immunogenic phenotype: a pan-cancer analysis
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Insertion-and-deletion-derived tumour-specific neoantigens and the immunogenic phenotype: a pan-cancer analysis

The lancet oncology, 2017-08, Vol.18 (8), p.1009-1021 [Peer Reviewed Journal]

2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved. ;Copyright Elsevier Limited Aug 1, 2017 ;ISSN: 1470-2045 ;EISSN: 1474-5488 ;DOI: 10.1016/S1470-2045(17)30516-8 ;PMID: 28694034

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13
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children
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Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children

American journal of human genetics, 2018-03, Vol.102 (3), p.487-493 [Peer Reviewed Journal]

2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;Distributed under a Creative Commons Attribution 4.0 International License ;2018 The Authors 2018 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2018.01.021 ;PMID: 29478779

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14
Truncated FGFR2 is a clinically actionable oncogene in multiple cancers
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Truncated FGFR2 is a clinically actionable oncogene in multiple cancers

Nature (London), 2022-08, Vol.608 (7923), p.609-617 [Peer Reviewed Journal]

Copyright Nature Publishing Group Aug 18, 2022 ;The Authors 2022, corrected publication 2022 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-022-05066-5 ;PMID: 35948633

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15
Shared Immunogenic Poly-Epitope Frameshift Mutations in Microsatellite Unstable Tumors
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Shared Immunogenic Poly-Epitope Frameshift Mutations in Microsatellite Unstable Tumors

Cell, 2020-12, Vol.183 (6), p.1634-1649.e17 [Peer Reviewed Journal]

2020 Elsevier Inc. ;Copyright © 2020 Elsevier Inc. All rights reserved. ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/j.cell.2020.11.004 ;PMID: 33259803

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16
Whole-exome Sequencing Identified a Novel Frameshift Mutation of Neurofibromin 1 in a Chinese Family with Neurofibromatosis Type 1
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Whole-exome Sequencing Identified a Novel Frameshift Mutation of Neurofibromin 1 in a Chinese Family with Neurofibromatosis Type 1

Annals of clinical and laboratory science, 2018-11, Vol.48 (6), p.808 [Peer Reviewed Journal]

EISSN: 1550-8080 ;PMID: 30610056

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17
Knockout of the HMG domain of the porcine SRY gene causes sex reversal in gene-edited pigs
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Knockout of the HMG domain of the porcine SRY gene causes sex reversal in gene-edited pigs

Proceedings of the National Academy of Sciences - PNAS, 2021-01, Vol.118 (2) [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by PNAS. ;Copyright National Academy of Sciences Jan 12, 2021 ;Copyright © 2021 the Author(s). Published by PNAS. 2021 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2008743118 ;PMID: 33443157

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18
Nonsense-mediated RNA decay: an emerging modulator of malignancy
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Nonsense-mediated RNA decay: an emerging modulator of malignancy

Nature reviews. Cancer, 2022-08, Vol.22 (8), p.437-451 [Peer Reviewed Journal]

2022. Springer Nature Limited. ;Springer Nature Limited 2022. ;ISSN: 1474-175X ;EISSN: 1474-1768 ;DOI: 10.1038/s41568-022-00481-2 ;PMID: 35624152

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19
MATRILINEAL, a sperm-specific phospholipase, triggers maize haploid induction
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MATRILINEAL, a sperm-specific phospholipase, triggers maize haploid induction

Nature (London), 2017-02, Vol.542 (7639), p.105-109 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2, 2017 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature20827 ;PMID: 28114299 ;CODEN: NATUAS

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20
OsMATL mutation induces haploid seed formation in indica rice
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OsMATL mutation induces haploid seed formation in indica rice

Nature plants, 2018-08, Vol.4 (8), p.530-533 [Peer Reviewed Journal]

Copyright Nature Publishing Group Aug 2018 ;ISSN: 2055-0278 ;EISSN: 2055-0278 ;DOI: 10.1038/s41477-018-0193-y ;PMID: 29988153

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