Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Katie, Carnie"'
1
Akademický článek
Screening for phenotypic outliers identifies an unusually low concentration of a β-lactoglobulin B protein isoform in bovine milk caused by a synonymous SNP
Autor: Stephen R. Davis, Hamish E. Ward, Van Kelly, David Palmer, Alexandra E. Ankersmit-Udy, Thomas J. Lopdell, Sarah D. Berry, Mathew D. Littlejohn, Kathryn Tiplady, Linda F. Adams, Katie Carnie, Alayna Burrett, Natalie Thomas, Russell G. Snell, Richard J. Spelman, Klaus Lehnert
Publikováno v: Genetics Selection Evolution, Vol 54, Iss 1, Pp 1-11 (2022)
Abstract Background Milk samples from 10,641 dairy cattle were screened by a mass spectrometry method for extreme concentrations of the A or B isoforms of the whey protein, β-lactoglobulin (BLG), to identify causative genetic variation driving chang
Externí odkaz: https://doaj.org/article/460d3305b076430b8ce7ce75746098c0
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2
Akademický článek
Non-additive QTL mapping of lactation traits in 124,000 cattle reveals novel recessive loci
Autor: Edwardo G. M. Reynolds, Thomas Lopdell, Yu Wang, Kathryn M. Tiplady, Chad S. Harland, Thomas J. J. Johnson, Catherine Neeley, Katie Carnie, Richard G. Sherlock, Christine Couldrey, Stephen R. Davis, Bevin L. Harris, Richard J. Spelman, Dorian J. Garrick, Mathew D. Littlejohn
Publikováno v: Genetics Selection Evolution, Vol 54, Iss 1, Pp 1-16 (2022)
Abstract Background Deleterious recessive conditions have been primarily studied in the context of Mendelian diseases. Recently, several deleterious recessive mutations with large effects were discovered via non-additive genome-wide association studi
Externí odkaz: https://doaj.org/article/c6d74fe902814b03a9b570eab1034eda
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3
Non-additive association analysis using proxy phenotypes identifies novel cattle syndromes
Autor: Carole Charlier, B.L. Harris, Michael Keehan, Dorian J. Garrick, Kathryn Tiplady, Keren E. Dittmer, Gemma Worth, Katie Carnie, Michel Georges, Chad Harland, Thomas Lopdell, Mathew Littlejohn, Catherine Neeley, Thomas Johnson, Mark Walker, Christine Couldrey, Stephen R. Davis, Richard J. Spelman, Richard G. Sherlock, Edwardo Reynolds
Publikováno v: Nature Genetics. 53:949-954
Mammalian species carry ~100 loss-of-function variants per individual1,2, where ~1-5 of these impact essential genes and cause embryonic lethality or severe disease when homozygous3. The functions of the remainder are more difficult to resolve, altho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::85da76a6dbb7ea65191fc5ed105d1d47
https://doi.org/10.1038/s41588-021-00872-5
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5
Screening for phenotypic outliers identifies an unusually low concentration of a β-lactoglobulin B protein isoform in bovine milk caused by a synonymous SNP
Autor: Stephen R. Davis, Hamish E. Ward, Van Kelly, David Palmer, Alexandra E. Ankersmit-Udy, Thomas J. Lopdell, Sarah D. Berry, Mathew D. Littlejohn, Kathryn Tiplady, Linda F. Adams, Katie Carnie, Alayna Burrett, Natalie Thomas, Russell G. Snell, Richard J. Spelman, Klaus Lehnert
Publikováno v: Genetics, selection, evolution : GSE. 54(1)
Background Milk samples from 10,641 dairy cattle were screened by a mass spectrometry method for extreme concentrations of the A or B isoforms of the whey protein, β-lactoglobulin (BLG), to identify causative genetic variation driving changes in BLG
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9564310f557a9af0f80e19fe33f6ed6a
https://pubmed.ncbi.nlm.nih.gov/35296234
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