skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 2,814  for All Library Resources

Results 1 2 3 4 5 next page
Show only
Result Number Material Type Add to My Shelf Action Record Details and Options
1
DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy
Material Type:
Article
Add to My Research

DNA methylation changes and increased mRNA expression of coagulation proteins, factor V and thrombomodulin in Fuchs endothelial corneal dystrophy

Cellular and molecular life sciences : CMLS, 2023, Vol.80 (3) [Peer Reviewed Journal]

ISSN: 1420-9071 ;ISSN: 1420-682X ;EISSN: 1420-9071 ;DOI: 10.21203/rs.3.rs-1758860/v1

Full text available

2
The risk allele A of rs200395694 associated with SLE in Swedish patients affects on MEF2D gene regulation and alternative splicing
Material Type:
Conference Proceeding
Add to My Research

The risk allele A of rs200395694 associated with SLE in Swedish patients affects on MEF2D gene regulation and alternative splicing

Human Gene Therapy, 2018, Vol.29 (12), p.A44 [Peer Reviewed Journal]

ISSN: 1557-7422 ;ISSN: 1043-0342 ;EISSN: 1557-7422

Full text available

3
A consensus molecular classification of muscle-invasive bladder cancer
Material Type:
Article
Add to My Research

A consensus molecular classification of muscle-invasive bladder cancer

European urology, 2020-04, Vol.77 (4), p.420-433 [Peer Reviewed Journal]

info:eu-repo/semantics/openAccess © 2019 The Authors. Published by Elsevier B.V. on behalf of European Association of Urology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) http://creativecommons.org/licenses/by-nc-nd/4.0/ ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0302-2838 ;EISSN: 1873-7560 ;DOI: 10.1016/j.eururo.2019.09.006

Digital Resources/Online E-Resources

4
The Cancer Genome Atlas Pan-Cancer analysis project
Material Type:
Article
Add to My Research

The Cancer Genome Atlas Pan-Cancer analysis project

Nature genetics, 2013-10, Vol.45 (10), p.1113-1120 [Peer Reviewed Journal]

Copyright Nature Publishing Group Oct 2013 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2764 ;PMID: 24071849

Full text available

5
A reference panel of 64,976 haplotypes for genotype imputation
Material Type:
Article
Add to My Research

A reference panel of 64,976 haplotypes for genotype imputation

Nature genetics, 2016-10, Vol.48 (10), p.1279-1283 [Peer Reviewed Journal]

Copyright Nature Publishing Group Oct 2016 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3643 ;PMID: 27548312

Full text available

6
Epigenetics in Human Obesity and Type 2 Diabetes
Material Type:
Article
Add to My Research

Epigenetics in Human Obesity and Type 2 Diabetes

Cell metabolism, 2019-05, Vol.29 (5), p.1028-1044 [Peer Reviewed Journal]

2019 The Authors ;Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved. ;2019 The Authors 2019 ;ISSN: 1550-4131 ;EISSN: 1932-7420 ;DOI: 10.1016/j.cmet.2019.03.009 ;PMID: 30982733

Full text available

7
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
Material Type:
Article
Add to My Research

Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

Genetics in medicine, 2021-08, Vol.23 (8), p.1506-1513 [Peer Reviewed Journal]

2021 The Author(s) ;2021. The Author(s). ;The Author(s) 2021. 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. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2021 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-021-01170-5 ;PMID: 34012067

Full text available

8
The repertoire of mutational signatures in human cancer
Material Type:
Article
Add to My Research

The repertoire of mutational signatures in human cancer

Nature (London), 2020-02, Vol.578 (7793), p.94-101 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Feb 6, 2020 ;The Author(s) 2020 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-1943-3 ;PMID: 32025018

Full text available

9
The mutational constraint spectrum quantified from variation in 141,456 humans
Material Type:
Article
Add to My Research

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature (London), 2020-05, Vol.581 (7809), p.434-443 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group May 28, 2020 ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2020 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-2308-7 ;PMID: 32461654

Full text available

10
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
Material Type:
Article
Add to My Research

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article

Nature genetics, 2018-04, Vol.50 (4), p.559 [Peer Reviewed Journal]

ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-018-0084-1

Full text available

11
The evolutionary history of 2,658 cancers
Material Type:
Article
Add to My Research

The evolutionary history of 2,658 cancers

Nature (London), 2020-02, Vol.578 (7793), p.122-128 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Feb 6, 2020 ;The Author(s) 2020 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-019-1907-7 ;PMID: 32025013

Full text available

12
Pan-cancer analysis of whole genomes
Material Type:
Article
Add to My Research

Pan-cancer analysis of whole genomes

Nature (London), 2020-02, Vol.578 (7793), p.82-93 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Feb 6, 2020 ;info:eu-repo/semantics/openAccess ;The Author(s) 2020 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-020-1969-6 ;PMID: 32025007

Full text available

13
Patterns of somatic structural variation in human cancer genomes
Material Type:
Article
Add to My Research

Patterns of somatic structural variation in human cancer genomes

Nature (London), 2020-02, Vol.578 (7793), p.112-121 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Feb 6, 2020 ;The Author(s) 2020 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-019-1913-9 ;PMID: 32025012

Full text available

14
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Material Type:
Article
Add to My Research

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

American journal of human genetics, 2019-01, Vol.104 (1), p.21-34 [Peer Reviewed Journal]

2018 The Authors ;Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved. ;2018 The Authors 2018 ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2018.11.002 ;PMID: 30554720

Full text available

15
Unexplored therapeutic opportunities in the human genome
Material Type:
Article
Add to My Research

Unexplored therapeutic opportunities in the human genome

Nature reviews. Drug discovery, 2018-05, Vol.17 (5), p.317-332 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group May 2018 ;ISSN: 1474-1776 ;EISSN: 1474-1784 ;DOI: 10.1038/nrd.2018.14 ;PMID: 29472638

Full text available

16
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Material Type:
Article
Add to My Research

Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

Nature genetics, 2020-03, Vol.52 (3), p.331-341 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2020 ;The Author(s) 2020 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-019-0576-7 ;PMID: 32025003

Full text available

17
A high-stringency blueprint of the human proteome
Material Type:
Article
Add to My Research

A high-stringency blueprint of the human proteome

Nature communications, 2020-10, Vol.11 (1), p.5301-5301, Article 5301 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2020 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-19045-9 ;PMID: 33067450

Full text available

18
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Material Type:
Article
Add to My Research

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Nature genetics, 2013-10, Vol.45 (10), p.1150-1159 [Peer Reviewed Journal]

COPYRIGHT 2013 Nature Publishing Group ;COPYRIGHT 2013 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2013 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.2742 ;PMID: 23974872

Full text available

19
A multimodal cell census and atlas of the mammalian primary motor cortex
Material Type:
Article
Add to My Research

A multimodal cell census and atlas of the mammalian primary motor cortex

Nature (London), 2021-10, Vol.598 (7879), p.86-102 [Peer Reviewed Journal]

2021. The Author(s). ;Copyright Nature Publishing Group Oct 7, 2021 ;The Author(s) 2021 ;ISSN: 0028-0836 ;ISSN: 1476-4687 ;EISSN: 1476-4687 ;DOI: 10.1038/s41586-021-03950-0 ;PMID: 34616075

Full text available

20
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Material Type:
Article
Add to My Research

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature genetics, 2022-12, Vol.54 (12), p.1803-3 [Peer Reviewed Journal]

2022. The Author(s). ;Copyright Nature Publishing Group Dec 2022 ;The Author(s) 2022 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-022-01233-6 ;PMID: 36474045

Full text available

Results 1 - 20 of 2,814  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (1,897)

Refine My Results

New Records 

  1. New From Last Month  (9)
  2. New From Last 3 Month  (24)
  3. More options open sub menu

Language 

  1. English  (2,779)
  2. Japanese  (423)
  3. Norwegian  (37)
  4. Swedish  (36)
  5. More options open sub menu

Searching Remote Databases, Please Wait