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Promise and pitfalls of the Immunochip.

Arthritis research & therapy

Cortes A, Brown MA.
PMID: 21345260
Arthritis Res Ther. 2011 Feb 01;13(1):101. doi: 10.1186/ar3204.

Genomewide association studies (GWAS) have proven a powerful hypothesis-free method to identify common disease-associated variants. Even quite large GWAS, however, have only at best identified moderate proportions of the genetic variants contributing to disease heritability. To provide cost-effective genotyping...

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Cortes A, Brown MA. Promise and pitfalls of the Immunochip. Arthritis Res Ther. 2011;13(1):101doi: 10.1186/ar3204.
Cortes, A., & Brown, M. A. (2011). Promise and pitfalls of the Immunochip. Arthritis research & therapy, 13(1), 101. https://doi.org/10.1186/ar3204
Cortes, Adrian, and Brown, Matthew A. "Promise and pitfalls of the Immunochip." Arthritis research & therapy vol. 13,1 (2011): 101. doi: https://doi.org/10.1186/ar3204
Cortes A, Brown MA. Promise and pitfalls of the Immunochip. Arthritis Res Ther. 2011 Feb 01;13(1):101. doi: 10.1186/ar3204. PMID: 21345260; PMCID: PMC3157635.
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Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children.

The Journal of pediatrics

Lantos JD.
PMID: 34166672
J Pediatr. 2021 Oct;237:13-15. doi: 10.1016/j.jpeds.2021.06.042. Epub 2021 Jun 21.

No abstract available.

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Lantos JD. Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children. J Pediatr. 2021;237:13-15doi: 10.1016/j.jpeds.2021.06.042.
Lantos, J. D. (2021). Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children. The Journal of pediatrics, 23713-15. https://doi.org/10.1016/j.jpeds.2021.06.042
Lantos, John D. "Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children." The Journal of pediatrics vol. 237 (2021): 13-15. doi: https://doi.org/10.1016/j.jpeds.2021.06.042
Lantos JD. Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children. J Pediatr. 2021 Oct;237:13-15. doi: 10.1016/j.jpeds.2021.06.042. Epub 2021 Jun 21. PMID: 34166672.
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Comparative transcriptome analysis reveals the genes and pathways involved in terminal drought tolerance in pearl millet.

Plant molecular biology

Shivhare R, Asif MH, Lata C.
PMID: 32430635
Plant Mol Biol. 2020 Aug;103(6):639-652. doi: 10.1007/s11103-020-01015-w. Epub 2020 May 19.

Pearl millet is a widely cultivated grain and forage crop in areas frequented with hot and dry weather, and high temperature. Being cultivated in arid and semi-arid regions, the crop often encounters intermittent water stress either at early stages...

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Shivhare R, Asif MH, Lata C. Comparative transcriptome analysis reveals the genes and pathways involved in terminal drought tolerance in pearl millet. Plant Mol Biol. 2020;103(6):639-652doi: 10.1007/s11103-020-01015-w.
Shivhare, R., Asif, M. H., & Lata, C. (2020). Comparative transcriptome analysis reveals the genes and pathways involved in terminal drought tolerance in pearl millet. Plant molecular biology, 103(6), 639-652. https://doi.org/10.1007/s11103-020-01015-w
Shivhare, Radha, et al. "Comparative transcriptome analysis reveals the genes and pathways involved in terminal drought tolerance in pearl millet." Plant molecular biology vol. 103,6 (2020): 639-652. doi: https://doi.org/10.1007/s11103-020-01015-w
Shivhare R, Asif MH, Lata C. Comparative transcriptome analysis reveals the genes and pathways involved in terminal drought tolerance in pearl millet. Plant Mol Biol. 2020 Aug;103(6):639-652. doi: 10.1007/s11103-020-01015-w. Epub 2020 May 19. PMID: 32430635.
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[DNA microarrays].

Zeitschrift fur Rheumatologie

Biesen R, Häupl T.
PMID: 21956826
Z Rheumatol. 2011 Nov;70(9):803-6, 808. doi: 10.1007/s00393-011-0869-4.

Since their development in the 1990s DNA microarrays have advanced to one of the most important technologies for biomedical research. Miniaturization enables up to 1 million different sequence-specific DNA hybridization tests to be performed on an area of less...

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Biesen R, Häupl T. DNA-Microarrays. [DNA microarrays]. Z Rheumatol. 2011;70(9):803-6, 808doi: 10.1007/s00393-011-0869-4.
Biesen, R., & Häupl, T. (2011). DNA-Microarrays. [DNA microarrays]. Zeitschrift fur Rheumatologie, 70(9), 803-6, 808. https://doi.org/10.1007/s00393-011-0869-4
Biesen, R, and Häupl, T. "DNA-Microarrays." [DNA microarrays]. Zeitschrift fur Rheumatologie vol. 70,9 (2011): 803-6, 808. doi: https://doi.org/10.1007/s00393-011-0869-4
Biesen R, Häupl T. DNA-Microarrays. [DNA microarrays]. Z Rheumatol. 2011 Nov;70(9):803-6, 808. doi: 10.1007/s00393-011-0869-4. German. PMID: 21956826.
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Genetic recombination in Escherichia coli. II. Calculation of incorporation frequency and relative map distance by recombinant analysis.

Mutation research

de Haan PG, Verhoef C.
PMID: 5333389
Mutat Res. 1966 Apr;3(2):111-7. doi: 10.1016/0027-5107(66)90024-8.

No abstract available.

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de Haan PG, Verhoef C. Genetic recombination in Escherichia coli. II. Calculation of incorporation frequency and relative map distance by recombinant analysis. Mutat Res. 1966;3(2):111-7doi: 10.1016/0027-5107(66)90024-8.
de Haan, P. G., & Verhoef, C. (1966). Genetic recombination in Escherichia coli. II. Calculation of incorporation frequency and relative map distance by recombinant analysis. Mutation research, 3(2), 111-7. https://doi.org/10.1016/0027-5107(66)90024-8
de Haan, P G, and Verhoef, C. "Genetic recombination in Escherichia coli. II. Calculation of incorporation frequency and relative map distance by recombinant analysis." Mutation research vol. 3,2 (1966): 111-7. doi: https://doi.org/10.1016/0027-5107(66)90024-8
de Haan PG, Verhoef C. Genetic recombination in Escherichia coli. II. Calculation of incorporation frequency and relative map distance by recombinant analysis. Mutat Res. 1966 Apr;3(2):111-7. doi: 10.1016/0027-5107(66)90024-8. PMID: 5333389.
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Bioinformatics and biomedical informatics.

TheScientificWorldJournal

Najarian K, Deriche R, Kon MA, Hirata NS.
PMID: 23818827
ScientificWorldJournal. 2013 May 29;2013:591976. doi: 10.1155/2013/591976. Print 2013.

No abstract available.

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Najarian K, Deriche R, Kon MA, et al. Bioinformatics and biomedical informatics. ScientificWorldJournal. 2013;2013:591976doi: 10.1155/2013/591976.
Najarian, K., Deriche, R., Kon, M. A., & Hirata, N. S. (2013). Bioinformatics and biomedical informatics. TheScientificWorldJournal, 2013591976. https://doi.org/10.1155/2013/591976
Najarian, Kayvan, et al. "Bioinformatics and biomedical informatics." TheScientificWorldJournal vol. 2013 (2013): 591976. doi: https://doi.org/10.1155/2013/591976
Najarian K, Deriche R, Kon MA, Hirata NS. Bioinformatics and biomedical informatics. ScientificWorldJournal. 2013 May 29;2013:591976. doi: 10.1155/2013/591976. Print 2013. PMID: 23818827; PMCID: PMC3681308.
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So many needles, so much hay.

Human molecular genetics

Brennan MB, Hochgeschwender U.
PMID: 7757061
Hum Mol Genet. 1995 Feb;4(2):153-6. doi: 10.1093/hmg/4.2.153.

No abstract available.

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Brennan MB, Hochgeschwender U. So many needles, so much hay. Hum Mol Genet. 1995;4(2):153-6doi: 10.1093/hmg/4.2.153.
Brennan, M. B., & Hochgeschwender, U. (1995). So many needles, so much hay. Human molecular genetics, 4(2), 153-6. https://doi.org/10.1093/hmg/4.2.153
Brennan, M B, and Hochgeschwender, U. "So many needles, so much hay." Human molecular genetics vol. 4,2 (1995): 153-6. doi: https://doi.org/10.1093/hmg/4.2.153
Brennan MB, Hochgeschwender U. So many needles, so much hay. Hum Mol Genet. 1995 Feb;4(2):153-6. doi: 10.1093/hmg/4.2.153. PMID: 7757061.
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Statement on bioinformatics and capturing the benefits of genome sequencing for society.

Human genomics

Capps B, Chadwick R, Joly Y, Lysaght T, Mills C, Mulvihill JJ, Zwart H.
PMID: 31142362
Hum Genomics. 2019 May 29;13(1):24. doi: 10.1186/s40246-019-0208-4.

The HUGO Committee on Ethics, Law and Society (CELS) undertook a Working Group exploration of the key ethical issues arising from genome sequencing in 2013. The Imagined Futures paper the group subsequently published proposed points to consider when applying...

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Capps B, Chadwick R, Joly Y, et al. Statement on bioinformatics and capturing the benefits of genome sequencing for society. Hum Genomics. 2019;13(1):24doi: 10.1186/s40246-019-0208-4.
Capps, B., Chadwick, R., Joly, Y., Lysaght, T., Mills, C., Mulvihill, J. J., & Zwart, H. (2019). Statement on bioinformatics and capturing the benefits of genome sequencing for society. Human genomics, 13(1), 24. https://doi.org/10.1186/s40246-019-0208-4
Capps, Benjamin, et al. "Statement on bioinformatics and capturing the benefits of genome sequencing for society." Human genomics vol. 13,1 (2019): 24. doi: https://doi.org/10.1186/s40246-019-0208-4
Capps B, Chadwick R, Joly Y, Lysaght T, Mills C, Mulvihill JJ, Zwart H. Statement on bioinformatics and capturing the benefits of genome sequencing for society. Hum Genomics. 2019 May 29;13(1):24. doi: 10.1186/s40246-019-0208-4. PMID: 31142362; PMCID: PMC6542037.
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AMBER: Assessment of Metagenome BinnERs.

GigaScience

Meyer F, Hofmann P, Belmann P, Garrido-Oter R, Fritz A, Sczyrba A, McHardy AC.
PMID: 29893851
Gigascience. 2018 Jun 01;7(6). doi: 10.1093/gigascience/giy069.

Reconstructing the genomes of microbial community members is key to the interpretation of shotgun metagenome samples. Genome binning programs deconvolute reads or assembled contigs of such samples into individual bins. However, assessing their quality is difficult due to the...

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Meyer F, Hofmann P, Belmann P, et al. AMBER: Assessment of Metagenome BinnERs. Gigascience. 2018;7(6)doi: 10.1093/gigascience/giy069.
Meyer, F., Hofmann, P., Belmann, P., Garrido-Oter, R., Fritz, A., Sczyrba, A., & McHardy, A. C. (2018). AMBER: Assessment of Metagenome BinnERs. GigaScience, 7(6), . https://doi.org/10.1093/gigascience/giy069
Meyer, Fernando, et al. "AMBER: Assessment of Metagenome BinnERs." GigaScience vol. 7,6 (2018). doi: https://doi.org/10.1093/gigascience/giy069
Meyer F, Hofmann P, Belmann P, Garrido-Oter R, Fritz A, Sczyrba A, McHardy AC. AMBER: Assessment of Metagenome BinnERs. Gigascience. 2018 Jun 01;7(6). doi: 10.1093/gigascience/giy069. PMID: 29893851; PMCID: PMC6022608.
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Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis.

Genetics in medicine : official journal of the American College of Medical Genetics

Mighton C, Shickh S, Uleryk E, Pechlivanoglou P, Bombard Y.
PMID: 32921787
Genet Med. 2021 Jan;23(1):22-33. doi: 10.1038/s41436-020-00957-2. Epub 2020 Sep 14.

This study systematically reviewed and synthesized the literature on psychological and clinical outcomes of receiving a variant of uncertain significance (VUS) from multigene panel testing or genomic sequencing. MEDLINE and EMBASE were searched. Two reviewers screened studies and extracted...

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Mighton C, Shickh S, Uleryk E, et al. Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis. Genet Med. 2020;23(1):22-33doi: 10.1038/s41436-020-00957-2.
Mighton, C., Shickh, S., Uleryk, E., Pechlivanoglou, P., & Bombard, Y. (2021). Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis. Genetics in medicine : official journal of the American College of Medical Genetics, 23(1), 22-33. https://doi.org/10.1038/s41436-020-00957-2
Mighton, Chloe, et al. "Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis." Genetics in medicine : official journal of the American College of Medical Genetics vol. 23,1 (2021): 22-33. doi: https://doi.org/10.1038/s41436-020-00957-2
Mighton C, Shickh S, Uleryk E, Pechlivanoglou P, Bombard Y. Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis. Genet Med. 2021 Jan;23(1):22-33. doi: 10.1038/s41436-020-00957-2. Epub 2020 Sep 14. PMID: 32921787.
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Circular genetic maps.

Journal of cellular physiology

Stahl FW.
PMID: 5582805
J Cell Physiol. 1967 Oct;70(2):Suppl:1-4. doi: 10.1002/jcp.1040700403.

No abstract available.

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Stahl FW. Circular genetic maps. J Cell Physiol. 1967;70(2):Suppl:1-4doi: 10.1002/jcp.1040700403.
Stahl, F. W. (1967). Circular genetic maps. Journal of cellular physiology, 70(2), Suppl:1-4. https://doi.org/10.1002/jcp.1040700403
Stahl, F W. "Circular genetic maps." Journal of cellular physiology vol. 70,2 (1967): Suppl:1-4. doi: https://doi.org/10.1002/jcp.1040700403
Stahl FW. Circular genetic maps. J Cell Physiol. 1967 Oct;70(2):Suppl:1-4. doi: 10.1002/jcp.1040700403. PMID: 5582805.
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Funding needed for private enterprise in genome sequencing.

Nature

Shulman S.
PMID: 3352738
Nature. 1988 Mar 31;332(6163):387. doi: 10.1038/332387a0.

No abstract available.

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Shulman S. Funding needed for private enterprise in genome sequencing. Nature. 1988;332(6163):387doi: 10.1038/332387a0.
Shulman, S. (1988). Funding needed for private enterprise in genome sequencing. Nature, 332(6163), 387. https://doi.org/10.1038/332387a0
Shulman, S. "Funding needed for private enterprise in genome sequencing." Nature vol. 332,6163 (1988): 387. doi: https://doi.org/10.1038/332387a0
Shulman S. Funding needed for private enterprise in genome sequencing. Nature. 1988 Mar 31;332(6163):387. doi: 10.1038/332387a0. PMID: 3352738.
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Showing 49 to 60 of 64 entries