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Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans.

Frontiers in genetics

Voruganti VS, Kent JW, Debnath S, Cole SA, Haack K, Göring HH, Carless MA, Curran JE, Johnson MP, Almasy L, Dyer TD, Maccluer JW, Moses EK, Abboud HE, Mahaney MC, Blangero J, Comuzzie AG.
PMID: 24379826
Front Genet. 2013 Dec 16;4:279. doi: 10.3389/fgene.2013.00279. eCollection 2013.

Increased serum uric acid (SUA) is a risk factor for gout and renal and cardiovascular disease (CVD). The purpose of this study was to identify genetic factors that affect the variation in SUA in 632 Mexican Americans participants of...

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Voruganti VS, Kent JW, Debnath S, et al. Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans. Front Genet. 2013;4:279doi: 10.3389/fgene.2013.00279.
Voruganti, V. S., Kent, J. W., Debnath, S., Cole, S. A., Haack, K., Göring, H. H., Carless, M. A., Curran, J. E., Johnson, M. P., Almasy, L., Dyer, T. D., Maccluer, J. W., Moses, E. K., Abboud, H. E., Mahaney, M. C., Blangero, J., & Comuzzie, A. G. (2013). Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans. Frontiers in genetics, 4279. https://doi.org/10.3389/fgene.2013.00279
Voruganti, Venkata Saroja, et al. "Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans." Frontiers in genetics vol. 4 (2013): 279. doi: https://doi.org/10.3389/fgene.2013.00279
Voruganti VS, Kent JW, Debnath S, Cole SA, Haack K, Göring HH, Carless MA, Curran JE, Johnson MP, Almasy L, Dyer TD, Maccluer JW, Moses EK, Abboud HE, Mahaney MC, Blangero J, Comuzzie AG. Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans. Front Genet. 2013 Dec 16;4:279. doi: 10.3389/fgene.2013.00279. eCollection 2013. PMID: 24379826; PMCID: PMC3863993.
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Horse carboxylesterases: evidence for six CES1 and four families of CES genes on chromosome 3.

Comparative biochemistry and physiology. Part D, Genomics & proteomics

Holmes RS, Cox LA, Vandeberg JL.
PMID: 20403742
Comp Biochem Physiol Part D Genomics Proteomics. 2009 Mar;4(1):54-65. doi: 10.1016/j.cbd.2008.10.004. Epub 2008 Nov 05.

Carboxylesterases (CES) are responsible for the detoxification of a wide range of drugs and xenobiotics, and may contribute to cholesterol, fatty acid and lung surfactant metabolism. In this study, in silico methods were used to predict the amino acid...

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Holmes RS, Cox LA, Vandeberg JL. Horse carboxylesterases: evidence for six CES1 and four families of CES genes on chromosome 3. Comp Biochem Physiol Part D Genomics Proteomics. 2008;4(1):54-65doi: 10.1016/j.cbd.2008.10.004.
Holmes, R. S., Cox, L. A., & Vandeberg, J. L. (2009). Horse carboxylesterases: evidence for six CES1 and four families of CES genes on chromosome 3. Comparative biochemistry and physiology. Part D, Genomics & proteomics, 4(1), 54-65. https://doi.org/10.1016/j.cbd.2008.10.004
Holmes, Roger S, et al. "Horse carboxylesterases: evidence for six CES1 and four families of CES genes on chromosome 3." Comparative biochemistry and physiology. Part D, Genomics & proteomics vol. 4,1 (2009): 54-65. doi: https://doi.org/10.1016/j.cbd.2008.10.004
Holmes RS, Cox LA, Vandeberg JL. Horse carboxylesterases: evidence for six CES1 and four families of CES genes on chromosome 3. Comp Biochem Physiol Part D Genomics Proteomics. 2009 Mar;4(1):54-65. doi: 10.1016/j.cbd.2008.10.004. Epub 2008 Nov 05. PMID: 20403742; PMCID: PMC2916739.
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Genomics and proteomics of vertebrate cholesterol ester lipase (LIPA) and cholesterol 25-hydroxylase (CH25H).

3 Biotech

Holmes RS, Vandeberg JL, Cox LA.
PMID: 22582164
3 Biotech. 2011 Sep;1(2):99-109. doi: 10.1007/s13205-011-0013-9. Epub 2011 Aug 03.

Cholesterol ester lipase (LIPA; EC 3.1.1.13) and cholesterol 25-hydroxylase (CH25H; EC 1.14.99.48) play essential role in cholesterol metabolism in the body by hydrolysing cholesteryl esters and triglycerides within lysosomes (LIPA) and catalysing the formation of 25-hydroxycholesterol from cholesterol (CH25H)...

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Holmes RS, Vandeberg JL, Cox LA. Genomics and proteomics of vertebrate cholesterol ester lipase (LIPA) and cholesterol 25-hydroxylase (CH25H). 3 Biotech. 2011;1(2):99-109doi: 10.1007/s13205-011-0013-9.
Holmes, R. S., Vandeberg, J. L., & Cox, L. A. (2011). Genomics and proteomics of vertebrate cholesterol ester lipase (LIPA) and cholesterol 25-hydroxylase (CH25H). 3 Biotech, 1(2), 99-109. https://doi.org/10.1007/s13205-011-0013-9
Holmes, Roger S, et al. "Genomics and proteomics of vertebrate cholesterol ester lipase (LIPA) and cholesterol 25-hydroxylase (CH25H)." 3 Biotech vol. 1,2 (2011): 99-109. doi: https://doi.org/10.1007/s13205-011-0013-9
Holmes RS, Vandeberg JL, Cox LA. Genomics and proteomics of vertebrate cholesterol ester lipase (LIPA) and cholesterol 25-hydroxylase (CH25H). 3 Biotech. 2011 Sep;1(2):99-109. doi: 10.1007/s13205-011-0013-9. Epub 2011 Aug 03. PMID: 22582164; PMCID: PMC3324826.
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A new class of mammalian carboxylesterase CES6.

Comparative biochemistry and physiology. Part D, Genomics & proteomics

Holmes RS, Cox LA, Vandeberg JL.
PMID: 20161041
Comp Biochem Physiol Part D Genomics Proteomics. 2009 Sep;4(3):209-17. doi: 10.1016/j.cbd.2009.03.002.

Mammalian carboxylesterases (CES) exhibit broad substrate specificities, catalyse hydrolytic and transesterification reactions with a wide range of drugs and xenobiotics and are widely distributed in the body. Four CES classes have been previously described, namely CES1 (major liver form);...

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Holmes RS, Cox LA, Vandeberg JL. A new class of mammalian carboxylesterase CES6. Comp Biochem Physiol Part D Genomics Proteomics. 2009;4(3):209-17doi: 10.1016/j.cbd.2009.03.002.
Holmes, R. S., Cox, L. A., & Vandeberg, J. L. (2009). A new class of mammalian carboxylesterase CES6. Comparative biochemistry and physiology. Part D, Genomics & proteomics, 4(3), 209-17. https://doi.org/10.1016/j.cbd.2009.03.002
Holmes, Roger S, et al. "A new class of mammalian carboxylesterase CES6." Comparative biochemistry and physiology. Part D, Genomics & proteomics vol. 4,3 (2009): 209-17. doi: https://doi.org/10.1016/j.cbd.2009.03.002
Holmes RS, Cox LA, Vandeberg JL. A new class of mammalian carboxylesterase CES6. Comp Biochem Physiol Part D Genomics Proteomics. 2009 Sep;4(3):209-17. doi: 10.1016/j.cbd.2009.03.002. PMID: 20161041; PMCID: PMC2753981.
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Mammalian Glutamyl Aminopeptidase Genes (ENPEP) and Proteins: Comparative Studies of a Major Contributor to Arterial Hypertension.

Journal of data mining in genomics & proteomics

Holmes RS, Spradling-Reeves KD, Cox LA.
PMID: 29900035
J Data Mining Genomics Proteomics. 2017;8(2). doi: 10.4172/2153-0602.1000211. Epub 2017 Jun 13.

Glutamyl aminopeptidase (ENPEP) is a member of the M1 family of endopeptidases which are mammalian type II integral membrane zinc-containing endopeptidases. ENPEP is involved in the catabolic pathway of the renin-angiotensin system forming angiotensin III, which participates in blood...

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Holmes RS, Spradling-Reeves KD, Cox LA. Mammalian Glutamyl Aminopeptidase Genes (ENPEP) and Proteins: Comparative Studies of a Major Contributor to Arterial Hypertension. J Data Mining Genomics Proteomics. 2017;8(2)doi: 10.4172/2153-0602.1000211.
Holmes, R. S., Spradling-Reeves, K. D., & Cox, L. A. (2017). Mammalian Glutamyl Aminopeptidase Genes (ENPEP) and Proteins: Comparative Studies of a Major Contributor to Arterial Hypertension. Journal of data mining in genomics & proteomics, 8(2), . https://doi.org/10.4172/2153-0602.1000211
Holmes, Roger S, et al. "Mammalian Glutamyl Aminopeptidase Genes (ENPEP) and Proteins: Comparative Studies of a Major Contributor to Arterial Hypertension." Journal of data mining in genomics & proteomics vol. 8,2 (2017). doi: https://doi.org/10.4172/2153-0602.1000211
Holmes RS, Spradling-Reeves KD, Cox LA. Mammalian Glutamyl Aminopeptidase Genes (ENPEP) and Proteins: Comparative Studies of a Major Contributor to Arterial Hypertension. J Data Mining Genomics Proteomics. 2017;8(2). doi: 10.4172/2153-0602.1000211. Epub 2017 Jun 13. PMID: 29900035; PMCID: PMC5995572.
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Semiology of spontaneous generalized tonic-clonic seizures in the epileptic baboon.

Epilepsia open

Szabó CÁ, González DA, Koneru S.
PMID: 32524046
Epilepsia Open. 2020 Mar 20;5(2):213-219. doi: 10.1002/epi4.12388. eCollection 2020 Jun.

OBJECTIVE: The epileptic baboon provides an animal model for juvenile myoclonic epilepsy (JME), demonstrating spontaneous generalized tonic-clonic seizures (GTCS) in addition to generalized myoclonic, absence and multifocal seizures. While photoconvulsive responses have been described in this model, spontaneous GTCS...

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Szabó CÁ, González DA, Koneru S. Semiology of spontaneous generalized tonic-clonic seizures in the epileptic baboon. Epilepsia Open. 2020;5(2):213-219doi: 10.1002/epi4.12388.
Szabó, C. �. �., González, D. A., & Koneru, S. (2020). Semiology of spontaneous generalized tonic-clonic seizures in the epileptic baboon. Epilepsia open, 5(2), 213-219. https://doi.org/10.1002/epi4.12388
Szabó, Charles Ákos, et al. "Semiology of spontaneous generalized tonic-clonic seizures in the epileptic baboon." Epilepsia open vol. 5,2 (2020): 213-219. doi: https://doi.org/10.1002/epi4.12388
Szabó CÁ, González DA, Koneru S. Semiology of spontaneous generalized tonic-clonic seizures in the epileptic baboon. Epilepsia Open. 2020 Mar 20;5(2):213-219. doi: 10.1002/epi4.12388. eCollection 2020 Jun. PMID: 32524046; PMCID: PMC7278549.
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Evolution of Vertebrate Solute Carrier Family 9B Genes and Proteins (.

Journal of phylogenetics & evolutionary biology

Holmes RS, Spradling-Reeves KD, Cox LA.
PMID: 28868326
J Phylogenetics Evol Biol. 2016 Aug;4(3). doi: 10.4172/2329-9002.1000167. Epub 2016 Jun 10.

No abstract available.

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Holmes RS, Spradling-Reeves KD, Cox LA. Evolution of Vertebrate Solute Carrier Family 9B Genes and Proteins (. J Phylogenetics Evol Biol. 2016;4(3)doi: 10.4172/2329-9002.1000167.
Holmes, R. S., Spradling-Reeves, K. D., & Cox, L. A. (2016). Evolution of Vertebrate Solute Carrier Family 9B Genes and Proteins (. Journal of phylogenetics & evolutionary biology, 4(3), . https://doi.org/10.4172/2329-9002.1000167
Holmes, Roger S, et al. "Evolution of Vertebrate Solute Carrier Family 9B Genes and Proteins (." Journal of phylogenetics & evolutionary biology vol. 4,3 (2016). doi: https://doi.org/10.4172/2329-9002.1000167
Holmes RS, Spradling-Reeves KD, Cox LA. Evolution of Vertebrate Solute Carrier Family 9B Genes and Proteins (. J Phylogenetics Evol Biol. 2016 Aug;4(3). doi: 10.4172/2329-9002.1000167. Epub 2016 Jun 10. PMID: 28868326; PMCID: PMC5578470.
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Bovine Carboxylesterases: Evidence for Two CES1 and Five Families of CES Genes on Chromosome 18.

Comparative biochemistry and physiology. Part D, Genomics & proteomics

Holmes RS, Cox LA, Vandeberg JL.
PMID: 20161341
Comp Biochem Physiol Part D Genomics Proteomics. 2009 Mar 01;4(1):11-20. doi: 10.1016/j.cbd.2008.09.002.

Predicted bovine carboxylesterase (CES) protein and gene sequences were derived from bovine (Bos taurus) genomic sequence data. Two bovine CES1 genes (CES1.1 and CES1.2) were located on chromosome 18 encoding amino acid sequences that were 81% identical. Two forms...

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Holmes RS, Cox LA, Vandeberg JL. Bovine Carboxylesterases: Evidence for Two CES1 and Five Families of CES Genes on Chromosome 18. Comp Biochem Physiol Part D Genomics Proteomics. 2009;4(1):11-20doi: 10.1016/j.cbd.2008.09.002.
Holmes, R. S., Cox, L. A., & Vandeberg, J. L. (2009). Bovine Carboxylesterases: Evidence for Two CES1 and Five Families of CES Genes on Chromosome 18. Comparative biochemistry and physiology. Part D, Genomics & proteomics, 4(1), 11-20. https://doi.org/10.1016/j.cbd.2008.09.002
Holmes, Roger S, et al. "Bovine Carboxylesterases: Evidence for Two CES1 and Five Families of CES Genes on Chromosome 18." Comparative biochemistry and physiology. Part D, Genomics & proteomics vol. 4,1 (2009): 11-20. doi: https://doi.org/10.1016/j.cbd.2008.09.002
Holmes RS, Cox LA, Vandeberg JL. Bovine Carboxylesterases: Evidence for Two CES1 and Five Families of CES Genes on Chromosome 18. Comp Biochem Physiol Part D Genomics Proteomics. 2009 Mar 01;4(1):11-20. doi: 10.1016/j.cbd.2008.09.002. PMID: 20161341; PMCID: PMC2680296.
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A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study.

International journal of vascular medicine

Diego VP, Almasy L, Rainwater DL, Mahaney MC, Comuzzie AG, Cole SA, Tracy RP, Stern MP, Maccluer JW, Blangero J.
PMID: 21151504
Int J Vasc Med. 2010;2010:490241. doi: 10.1155/2010/490241. Epub 2010 Jun 27.

Background. D-dimer is associated with increasing severity of atherosclerosis and with increased risk of a cardiovascular disease (CVD). Methods and Results. To better understand this risk factor, we performed a genome scan on 803 (301 males and 502 females)...

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Diego VP, Almasy L, Rainwater DL, et al. A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study. Int J Vasc Med. 2010;2010:490241doi: 10.1155/2010/490241.
Diego, V. P., Almasy, L., Rainwater, D. L., Mahaney, M. C., Comuzzie, A. G., Cole, S. A., Tracy, R. P., Stern, M. P., Maccluer, J. W., & Blangero, J. (2010). A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study. International journal of vascular medicine, 2010490241. https://doi.org/10.1155/2010/490241
Diego, V P, et al. "A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study." International journal of vascular medicine vol. 2010 (2010): 490241. doi: https://doi.org/10.1155/2010/490241
Diego VP, Almasy L, Rainwater DL, Mahaney MC, Comuzzie AG, Cole SA, Tracy RP, Stern MP, Maccluer JW, Blangero J. A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study. Int J Vasc Med. 2010;2010:490241. doi: 10.1155/2010/490241. Epub 2010 Jun 27. PMID: 21151504; PMCID: PMC2989697.
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Genetic architecture of transmission stage production and virulence in schistosome parasites.

Virulence

Le Clec'h W, Chevalier FD, McDew-White M, Menon V, Arya GA, Anderson TJC.
PMID: 34167443
Virulence. 2021 Dec;12(1):1508-1526. doi: 10.1080/21505594.2021.1932183.

Both theory and experimental data from pathogens suggest that the production of transmission stages should be strongly associated with virulence, but the genetic bases of parasite transmission/virulence traits are poorly understood. The blood fluke

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Le Clec'h W, Chevalier FD, McDew-White M, et al. Genetic architecture of transmission stage production and virulence in schistosome parasites. Virulence. 2021;12(1):1508-1526doi: 10.1080/21505594.2021.1932183.
Le Clec'h, W., Chevalier, F. D., McDew-White, M., Menon, V., Arya, G. A., & Anderson, T. J. C. (2021). Genetic architecture of transmission stage production and virulence in schistosome parasites. Virulence, 12(1), 1508-1526. https://doi.org/10.1080/21505594.2021.1932183
Le Clec'h, Winka, et al. "Genetic architecture of transmission stage production and virulence in schistosome parasites." Virulence vol. 12,1 (2021): 1508-1526. doi: https://doi.org/10.1080/21505594.2021.1932183
Le Clec'h W, Chevalier FD, McDew-White M, Menon V, Arya GA, Anderson TJC. Genetic architecture of transmission stage production and virulence in schistosome parasites. Virulence. 2021 Dec;12(1):1508-1526. doi: 10.1080/21505594.2021.1932183. PMID: 34167443; PMCID: PMC8237990.
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Cerebrospinal Fluid Levels of Monoamine Metabolites in the Epileptic Baboon.

Journal of primatology

Szabó CÁ, Patel M, Uteshev VV.
PMID: 26924854
J Primatol. 2015 Dec;4(2). doi: 10.4172/2167-6801.1000129. Epub 2015 Oct 14.

The baboon represents a natural model for genetic generalized epilepsy and sudden unexpected death in epilepsy (SUDEP). In this retrospective study, cerebrospinal fluid (CSF) monoamine metabolites and scalp electroencephalography (EEG) were evaluated in 263 baboons of a pedigreed colony....

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Szabó CÁ, Patel M, Uteshev VV. Cerebrospinal Fluid Levels of Monoamine Metabolites in the Epileptic Baboon. J Primatol. 2015;4(2)doi: 10.4172/2167-6801.1000129.
Szabó, C. �. �., Patel, M., & Uteshev, V. V. (2015). Cerebrospinal Fluid Levels of Monoamine Metabolites in the Epileptic Baboon. Journal of primatology, 4(2), . https://doi.org/10.4172/2167-6801.1000129
Szabó, C Ákos, et al. "Cerebrospinal Fluid Levels of Monoamine Metabolites in the Epileptic Baboon." Journal of primatology vol. 4,2 (2015). doi: https://doi.org/10.4172/2167-6801.1000129
Szabó CÁ, Patel M, Uteshev VV. Cerebrospinal Fluid Levels of Monoamine Metabolites in the Epileptic Baboon. J Primatol. 2015 Dec;4(2). doi: 10.4172/2167-6801.1000129. Epub 2015 Oct 14. PMID: 26924854; PMCID: PMC4765963.
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Mammalian carboxylesterase 5: comparative biochemistry and genomics.

Comparative biochemistry and physiology. Part D, Genomics & proteomics

Holmes RS, Cox LA, Vandeberg JL.
PMID: 19727319
Comp Biochem Physiol Part D Genomics Proteomics. 2008 Sep;3(3):195-204. doi: 10.1016/j.cbd.2008.05.002.

Carboxylesterase 5 (CES5) (also called cauxin or CES7) is one of at least five mammalian CES gene families encoding enzymes of broad substrate specificity and catalysing hydrolytic and transesterification reactions. In silico methods were used to predict the amino...

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Holmes RS, Cox LA, Vandeberg JL. Mammalian carboxylesterase 5: comparative biochemistry and genomics. Comp Biochem Physiol Part D Genomics Proteomics. 2008;3(3):195-204doi: 10.1016/j.cbd.2008.05.002.
Holmes, R. S., Cox, L. A., & Vandeberg, J. L. (2008). Mammalian carboxylesterase 5: comparative biochemistry and genomics. Comparative biochemistry and physiology. Part D, Genomics & proteomics, 3(3), 195-204. https://doi.org/10.1016/j.cbd.2008.05.002
Holmes, Roger S, et al. "Mammalian carboxylesterase 5: comparative biochemistry and genomics." Comparative biochemistry and physiology. Part D, Genomics & proteomics vol. 3,3 (2008): 195-204. doi: https://doi.org/10.1016/j.cbd.2008.05.002
Holmes RS, Cox LA, Vandeberg JL. Mammalian carboxylesterase 5: comparative biochemistry and genomics. Comp Biochem Physiol Part D Genomics Proteomics. 2008 Sep;3(3):195-204. doi: 10.1016/j.cbd.2008.05.002. PMID: 19727319; PMCID: PMC2583452.
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Showing 1 to 12 of 17 entries