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1
Correction: Genome-wide association study identifies genetic variants underlying footrot in Portuguese Merino sheep
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Correction: Genome-wide association study identifies genetic variants underlying footrot in Portuguese Merino sheep

BMC genomics, 2024-03, Vol.25 (1), p.241-241 [Peer Reviewed Journal]

COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1471-2164 ;EISSN: 1471-2164 ;DOI: 10.1186/s12864-024-10130-7 ;PMID: 38438869

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2
Serum micro-RNAs with mutation-targeted RNA modification: a potent cancer detection tool constructed using an optimized machine learning workflow
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Serum micro-RNAs with mutation-targeted RNA modification: a potent cancer detection tool constructed using an optimized machine learning workflow

Scientific reports, 2024-04, Vol.14 (1), p.9016-9016 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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. ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-59480-y ;PMID: 38641707

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3
Enhancing missense variant pathogenicity prediction with protein language models using VariPred
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Enhancing missense variant pathogenicity prediction with protein language models using VariPred

Scientific reports, 2024-04, Vol.14 (1), p.8136-8136 [Peer Reviewed Journal]

2024. Crown. ;Crown 2024. 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. ;Crown 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-51489-7 ;PMID: 38584172

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4
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease
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Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease

Nature genetics, 2024-04, Vol.56 (4), p.579-4 [Peer Reviewed Journal]

2024. The Author(s). ;Copyright Nature Publishing Group Apr 2024 ;The Author(s) 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01694-x ;PMID: 38575728

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5
Protein-altering variants at copy number-variable regions influence diverse human phenotypes
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Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Nature genetics, 2024-04, Vol.56 (4), p.569-2 [Peer Reviewed Journal]

2024. The Author(s). ;Copyright Nature Publishing Group Apr 2024 ;The Author(s) 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01684-z ;PMID: 38548989

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6
Exome-wide analysis implicates rare protein-altering variants in human handedness
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Exome-wide analysis implicates rare protein-altering variants in human handedness

Nature communications, 2024-04, Vol.15 (1), p.2632-2632 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-46277-w ;PMID: 38565598

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7
Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levels
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Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levels

Nature communications, 2024-04, Vol.15 (1), p.3352-3352 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-47735-1 ;PMID: 38688933

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8
Genetic control of DNA methylation is largely shared across European and East Asian populations
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Genetic control of DNA methylation is largely shared across European and East Asian populations

Nature communications, 2024-03, Vol.15 (1), p.2713-2713 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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. ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-47005-0 ;PMID: 38548728

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9
Genetic similarity between relatives provides evidence on the presence and history of assortative mating
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Genetic similarity between relatives provides evidence on the presence and history of assortative mating

Nature communications, 2024-03, Vol.15 (1), p.2641-2641 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-46939-9 ;PMID: 38531929

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10
The genetic architecture of multimodal human brain age
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The genetic architecture of multimodal human brain age

Nature communications, 2024-03, Vol.15 (1), p.2604-2604 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-46796-6 ;PMID: 38521789

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11
QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration
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QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration

Nature communications, 2024-03, Vol.15 (1), p.1972-1972 [Peer Reviewed Journal]

2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024. 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. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-46063-8 ;PMID: 38438351

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12
Update in genetic and epigenetic causes of hypertension
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Article
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Update in genetic and epigenetic causes of hypertension

Cellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1) [Peer Reviewed Journal]

The Author(s) 2024 ;ISSN: 1420-682X ;EISSN: 1420-9071 ;DOI: 10.1007/s00018-024-05220-4

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13
Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech
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Article
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Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech

Cellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1) [Peer Reviewed Journal]

The Author(s) 2024 ;ISSN: 1420-682X ;EISSN: 1420-9071 ;DOI: 10.1007/s00018-024-05149-8

Digital Resources/Online E-Resources

14
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
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Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes

Nature communications, 2024, Vol.15 (1), p.3557-3557 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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. ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-47399-x ;PMID: 38670944

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15
Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction
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Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction

Nature genetics, 2024-05, Vol.56 (5), p.819-3 [Peer Reviewed Journal]

2024. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group May 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01736-4 ;PMID: 38741014

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16
Improving gastrointestinal health in children and young people with cystic fibrosis
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Article
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Improving gastrointestinal health in children and young people with cystic fibrosis

Archives of disease in childhood, 2024-05, p.archdischild-2024-326900 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2024-326900 ;PMID: 38724066

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17
Cell-type-specific and disease-associated expression quantitative trait loci in the human lung
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Article
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Cell-type-specific and disease-associated expression quantitative trait loci in the human lung

Nature genetics, 2024-04, Vol.56 (4), p.595-3 [Peer Reviewed Journal]

2024. The Author(s). ;Copyright Nature Publishing Group Apr 2024 ;The Author(s) 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01702-0 ;PMID: 38548990

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18
Species-wide quantitative transcriptomes and proteomes reveal distinct genetic control of gene expression variation in yeast
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Species-wide quantitative transcriptomes and proteomes reveal distinct genetic control of gene expression variation in yeast

Proceedings of the National Academy of Sciences - PNAS, 2024-05, Vol.121 (19), p.e2319211121-e2319211121 [Peer Reviewed Journal]

Copyright National Academy of Sciences May 7, 2024 ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2024 the Author(s). Published by PNAS. 2024 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.2319211121 ;PMID: 38696467

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19
Exploiting meta-analysis of genome-wide interaction with serum 25-hydroxyvitamin D to identify novel genetic loci associated with pulmonary function
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Exploiting meta-analysis of genome-wide interaction with serum 25-hydroxyvitamin D to identify novel genetic loci associated with pulmonary function

The American journal of clinical nutrition, 2024-05, Vol.119 (5), p.1227-1237 [Peer Reviewed Journal]

2024 The Authors ;Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright American Society for Clinical Nutrition, Inc. May 2024 ;2024 The Authors 2024 ;ISSN: 0002-9165 ;EISSN: 1938-3207 ;DOI: 10.1016/j.ajcnut.2024.03.007 ;PMID: 38484975

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20
Improving selection decisions with mating information by accounting for Mendelian sampling variances looking two generations ahead
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Improving selection decisions with mating information by accounting for Mendelian sampling variances looking two generations ahead

Genetics selection evolution (Paris), 2024-05, Vol.56 (1), p.41-41 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024. 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) 2024 ;ISSN: 0999-193X ;EISSN: 1297-9686 ;DOI: 10.1186/s12711-024-00899-2 ;PMID: 38773363

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