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Showing 1 to 12 of 13 entries
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A principle to die for.

BMJ (Clinical research ed.)

Pocklington S.
PMID: 10550117
BMJ. 1999 Nov 06;319(7219):1277. doi: 10.1136/bmj.319.7219.1277.

No abstract available.

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Pocklington S. A principle to die for. BMJ. 1999;319(7219):1277doi: 10.1136/bmj.319.7219.1277.
Pocklington, S. (1999). A principle to die for. BMJ (Clinical research ed.), 319(7219), 1277. https://doi.org/10.1136/bmj.319.7219.1277
Pocklington. "A principle to die for." BMJ (Clinical research ed.) vol. 319,7219 (1999): 1277. doi: https://doi.org/10.1136/bmj.319.7219.1277
Pocklington S. A principle to die for. BMJ. 1999 Nov 06;319(7219):1277. doi: 10.1136/bmj.319.7219.1277. PMID: 10550117; PMCID: PMC1117047.
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Hydrocarbons in waters adjacent to an oil exploratory site in the western North Atlantic Ocean.

Environmental science & technology

Gassmann G, Pocklington R.
PMID: 22283218
Environ Sci Technol. 1984 Nov 01;18(11):869-72. doi: 10.1021/es00129a011.

No abstract available.

Cite
Gassmann G, Pocklington R. Hydrocarbons in waters adjacent to an oil exploratory site in the western North Atlantic Ocean. Environ Sci Technol. 1984;18(11):869-72doi: 10.1021/es00129a011.
Gassmann, G., & Pocklington, R. (1984). Hydrocarbons in waters adjacent to an oil exploratory site in the western North Atlantic Ocean. Environmental science & technology, 18(11), 869-72. https://doi.org/10.1021/es00129a011
Gassmann, G, and Pocklington, R. "Hydrocarbons in waters adjacent to an oil exploratory site in the western North Atlantic Ocean." Environmental science & technology vol. 18,11 (1984): 869-72. doi: https://doi.org/10.1021/es00129a011
Gassmann G, Pocklington R. Hydrocarbons in waters adjacent to an oil exploratory site in the western North Atlantic Ocean. Environ Sci Technol. 1984 Nov 01;18(11):869-72. doi: 10.1021/es00129a011. PMID: 22283218.
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The British Pharmacopœia.

The Hospital

Cockington AJ.
PMID: 29823511
Hospital (Lond 1886). 1914 Oct 03;57(1476):22.

No abstract available.

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Cockington AJ. The British Pharmacopœia. Hospital (Lond 1886). 1914;57(1476):22
Cockington, A. J. (1914). The British Pharmacopœia. The Hospital, 57(1476), 22.
Cockington, A J. "The British Pharmacopœia." The Hospital vol. 57,1476 (1914): 22.
Cockington AJ. The British Pharmacopœia. Hospital (Lond 1886). 1914 Oct 03;57(1476):22. PMID: 29823511; PMCID: PMC5228783.
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Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants.

Nature communications

Sanders B, D'Andrea D, Collins MO, Rees E, Steward TGJ, Zhu Y, Chapman G, Legge SE, Pardiñas AF, Harwood AJ, Gray WP, O'Donovan MC, Owen MJ, Errington AC, Blake DJ, Whitcomb DJ, Pocklington AJ, Shin E.
PMID: 35031607
Nat Commun. 2022 Jan 14;13(1):27. doi: 10.1038/s41467-021-27601-0.

Coordinated programs of gene expression drive brain development. It is unclear which transcriptional programs, in which cell-types, are affected in neuropsychiatric disorders such as schizophrenia. Here we integrate human genetics with transcriptomic data from differentiation of human embryonic stem...

Cite
Sanders B, D'Andrea D, Collins MO, et al. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nat Commun. 2022;13(1):27doi: 10.1038/s41467-021-27601-0.
Sanders, B., D'Andrea, D., Collins, M. O., Rees, E., Steward, T. G. J., Zhu, Y., Chapman, G., Legge, S. E., Pardiñas, A. F., Harwood, A. J., Gray, W. P., O'Donovan, M. C., Owen, M. J., Errington, A. C., Blake, D. J., Whitcomb, D. J., Pocklington, A. J., & Shin, E. (2022). Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature communications, 13(1), 27. https://doi.org/10.1038/s41467-021-27601-0
Sanders, Bret, et al. "Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants." Nature communications vol. 13,1 (2022): 27. doi: https://doi.org/10.1038/s41467-021-27601-0
Sanders B, D'Andrea D, Collins MO, Rees E, Steward TGJ, Zhu Y, Chapman G, Legge SE, Pardiñas AF, Harwood AJ, Gray WP, O'Donovan MC, Owen MJ, Errington AC, Blake DJ, Whitcomb DJ, Pocklington AJ, Shin E. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nat Commun. 2022 Jan 14;13(1):27. doi: 10.1038/s41467-021-27601-0. PMID: 35031607.
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Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

Nature genetics

Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR.
PMID: 31160808
Nat Genet. 2019 Jul;51(7):1193. doi: 10.1038/s41588-019-0450-7.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Pardiñas AF, Holmans P, Pocklington AJ, et al. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat Genet. 2019;51(7):1193doi: 10.1038/s41588-019-0450-7.
Pardiñas, A. F., Holmans, P., Pocklington, A. J., Escott-Price, V., Ripke, S., Carrera, N., Legge, S. E., Bishop, S., Cameron, D., Hamshere, M. L., Han, J., Hubbard, L., Lynham, A., Mantripragada, K., Rees, E., MacCabe, J. H., McCarroll, S. A., Baune, B. T., Breen, G., Byrne, E. M., Dannlowski, U., Eley, T. C., Hayward, C., Martin, N. G., McIntosh, A. M., Plomin, R., Porteous, D. J., Wray, N. R., Caballero, A., Geschwind, D. H., Huckins, L. M., Ruderfer, D. M., Santiago, E., Sklar, P., Stahl, E. A., Won, H., Agerbo, E., Als, T. D., Andreassen, O. A., Bækvad-Hansen, M., Mortensen, P. B., Pedersen, C. B., Børglum, A. D., Bybjerg-Grauholm, J., Djurovic, S., Durmishi, N., Pedersen, M. G., Golimbet, V., Grove, J., Hougaard, D. M., Mattheisen, M., Molden, E., Mors, O., Nordentoft, M., Pejovic-Milovancevic, M., Sigurdsson, E., Silagadze, T., Hansen, C. S., Stefansson, K., Stefansson, H., Steinberg, S., Tosato, S., Werge, T., Collier, D. A., Rujescu, D., Kirov, G., Owen, M. J., O'Donovan, M. C., & Walters, J. T. R. (2019). Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature genetics, 51(7), 1193. https://doi.org/10.1038/s41588-019-0450-7
Pardiñas, Antonio F, et al. "Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection." Nature genetics vol. 51,7 (2019): 1193. doi: https://doi.org/10.1038/s41588-019-0450-7
Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat Genet. 2019 Jul;51(7):1193. doi: 10.1038/s41588-019-0450-7. PMID: 31160808.
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Characterization of PKC2, a gene encoding a second protein kinase C isotype of Saccharomyces cerevisiae.

Current biology : CB

Simon AJ, Saville SP, Jamieson L, Pocklington MJ, Donnelly SF, Ron D, Milner Y, Mochly-Rosent D, Orr-Sternlicht E.
PMID: 15335814
Curr Biol. 1993 Dec 01;3(12):813-21. doi: 10.1016/0960-9822(93)90215-a.

BACKGROUND: Protein kinase C (PKC) has attracted considerable attention over the past decade, primarily because of its presumed role in cellular growth control and tumourigenesis. Mammalian cells express at least 10 different isozymes of PKC; it is this complexity...

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Simon AJ, Saville SP, Jamieson L, et al. Characterization of PKC2, a gene encoding a second protein kinase C isotype of Saccharomyces cerevisiae. Curr Biol. 1993;3(12):813-21doi: 10.1016/0960-9822(93)90215-a.
Simon, A. J., Saville, S. P., Jamieson, L., Pocklington, M. J., Donnelly, S. F., Ron, D., Milner, Y., Mochly-Rosent, D., & Orr-Sternlicht, E. (1993). Characterization of PKC2, a gene encoding a second protein kinase C isotype of Saccharomyces cerevisiae. Current biology : CB, 3(12), 813-21. https://doi.org/10.1016/0960-9822(93)90215-a
Simon, A J, et al. "Characterization of PKC2, a gene encoding a second protein kinase C isotype of Saccharomyces cerevisiae." Current biology : CB vol. 3,12 (1993): 813-21. doi: https://doi.org/10.1016/0960-9822(93)90215-a
Simon AJ, Saville SP, Jamieson L, Pocklington MJ, Donnelly SF, Ron D, Milner Y, Mochly-Rosent D, Orr-Sternlicht E. Characterization of PKC2, a gene encoding a second protein kinase C isotype of Saccharomyces cerevisiae. Curr Biol. 1993 Dec 01;3(12):813-21. doi: 10.1016/0960-9822(93)90215-a. PMID: 15335814.
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Air quality legislation and controls--imperfectly conceived solutions to imperfectly understood problems?.

The Science of the total environment

Pocklington D.
PMID: 10535137
Sci Total Environ. 1999 Sep 01;235(1):399-401. doi: 10.1016/s0048-9697(99)00246-6.

The development of legislative controls for the improvement of air quality is reviewed. In particular, the controls relating to motor vehicle emissions are discussed, and the effects of moving from direct measures relating to vehicle construction and manufacture, to...

Cite
Pocklington D. Air quality legislation and controls--imperfectly conceived solutions to imperfectly understood problems?. Sci Total Environ. 1999;235(1):399-401doi: 10.1016/s0048-9697(99)00246-6.
Pocklington, D. (1999). Air quality legislation and controls--imperfectly conceived solutions to imperfectly understood problems?. The Science of the total environment, 235(1), 399-401. https://doi.org/10.1016/s0048-9697(99)00246-6
Pocklington. "Air quality legislation and controls--imperfectly conceived solutions to imperfectly understood problems?." The Science of the total environment vol. 235,1 (1999): 399-401. doi: https://doi.org/10.1016/s0048-9697(99)00246-6
Pocklington D. Air quality legislation and controls--imperfectly conceived solutions to imperfectly understood problems?. Sci Total Environ. 1999 Sep 01;235(1):399-401. doi: 10.1016/s0048-9697(99)00246-6. PMID: 10535137.
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Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin.

Animal : an international journal of animal bioscience

Reynolds CK, Beever DE, Steinberg W, Packington AJ.
PMID: 22444335
Animal. 2007 Mar;1(3):375-80. doi: 10.1017/S1751731107666105.

The effect of feeding supplemental biotin on net absorption and metabolism of nutrients by the portal-drained viscera (PDV; the gut, pancreas, spleen and associated fat) and liver of lactating dairy cows was measured. Three cows in early to mid-lactation...

Cite
Reynolds CK, Beever DE, Steinberg W, et al. Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin. Animal. 2007;1(3):375-80doi: 10.1017/S1751731107666105.
Reynolds, C. K., Beever, D. E., Steinberg, W., & Packington, A. J. (2007). Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin. Animal : an international journal of animal bioscience, 1(3), 375-80. https://doi.org/10.1017/S1751731107666105
Reynolds, C K, et al. "Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin." Animal : an international journal of animal bioscience vol. 1,3 (2007): 375-80. doi: https://doi.org/10.1017/S1751731107666105
Reynolds CK, Beever DE, Steinberg W, Packington AJ. Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin. Animal. 2007 Mar;1(3):375-80. doi: 10.1017/S1751731107666105. PMID: 22444335.
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Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants.

Nature communications

Sanders B, D'Andrea D, Collins MO, Rees E, Steward TGJ, Zhu Y, Chapman G, Legge SE, Pardiñas AF, Harwood AJ, Gray WP, O'Donovan MC, Owen MJ, Errington AC, Blake DJ, Whitcomb DJ, Pocklington AJ, Shin E.
PMID: 35031607
Nat Commun. 2022 Jan 14;13(1):27. doi: 10.1038/s41467-021-27601-0.

Coordinated programs of gene expression drive brain development. It is unclear which transcriptional programs, in which cell-types, are affected in neuropsychiatric disorders such as schizophrenia. Here we integrate human genetics with transcriptomic data from differentiation of human embryonic stem...

Cite
Sanders B, D'Andrea D, Collins MO, et al. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nat Commun. 2022;13(1):27doi: 10.1038/s41467-021-27601-0.
Sanders, B., D'Andrea, D., Collins, M. O., Rees, E., Steward, T. G. J., Zhu, Y., Chapman, G., Legge, S. E., Pardiñas, A. F., Harwood, A. J., Gray, W. P., O'Donovan, M. C., Owen, M. J., Errington, A. C., Blake, D. J., Whitcomb, D. J., Pocklington, A. J., & Shin, E. (2022). Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature communications, 13(1), 27. https://doi.org/10.1038/s41467-021-27601-0
Sanders, Bret, et al. "Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants." Nature communications vol. 13,1 (2022): 27. doi: https://doi.org/10.1038/s41467-021-27601-0
Sanders B, D'Andrea D, Collins MO, Rees E, Steward TGJ, Zhu Y, Chapman G, Legge SE, Pardiñas AF, Harwood AJ, Gray WP, O'Donovan MC, Owen MJ, Errington AC, Blake DJ, Whitcomb DJ, Pocklington AJ, Shin E. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nat Commun. 2022 Jan 14;13(1):27. doi: 10.1038/s41467-021-27601-0. PMID: 35031607.
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Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin.

Animal : an international journal of animal bioscience

Reynolds CK, Beever DE, Steinberg W, Packington AJ.
PMID: 22444335
Animal. 2007 Mar;1(3):375-80. doi: 10.1017/S1751731107666105.

The effect of feeding supplemental biotin on net absorption and metabolism of nutrients by the portal-drained viscera (PDV; the gut, pancreas, spleen and associated fat) and liver of lactating dairy cows was measured. Three cows in early to mid-lactation...

Cite
Reynolds CK, Beever DE, Steinberg W, et al. Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin. Animal. 2007;1(3):375-80doi: 10.1017/S1751731107666105.
Reynolds, C. K., Beever, D. E., Steinberg, W., & Packington, A. J. (2007). Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin. Animal : an international journal of animal bioscience, 1(3), 375-80. https://doi.org/10.1017/S1751731107666105
Reynolds, C K, et al. "Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin." Animal : an international journal of animal bioscience vol. 1,3 (2007): 375-80. doi: https://doi.org/10.1017/S1751731107666105
Reynolds CK, Beever DE, Steinberg W, Packington AJ. Net nutrient absorption and liver metabolism in lactating dairy cows fed supplemental dietary biotin. Animal. 2007 Mar;1(3):375-80. doi: 10.1017/S1751731107666105. PMID: 22444335.
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Genetic association of FMRP targets with psychiatric disorders.

Molecular psychiatry

Clifton NE, Rees E, Holmans PA, Pardiñas AF, Harwood JC, Di Florio A, Kirov G, Walters JTR, O'Donovan MC, Owen MJ, Hall J, Pocklington AJ.
PMID: 33077856
Mol Psychiatry. 2021 Jul;26(7):2977-2990. doi: 10.1038/s41380-020-00912-2. Epub 2020 Oct 19.

Genes encoding the mRNA targets of fragile X mental retardation protein (FMRP) are enriched for genetic association with psychiatric disorders. However, many FMRP targets possess functions that are themselves genetically associated with psychiatric disorders, including synaptic transmission and plasticity,...

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Clifton NE, Rees E, Holmans PA, et al. Genetic association of FMRP targets with psychiatric disorders. Mol Psychiatry. 2020;26(7):2977-2990doi: 10.1038/s41380-020-00912-2.
Clifton, N. E., Rees, E., Holmans, P. A., Pardiñas, A. F., Harwood, J. C., Di Florio, A., Kirov, G., Walters, J. T. R., O'Donovan, M. C., Owen, M. J., Hall, J., & Pocklington, A. J. (2021). Genetic association of FMRP targets with psychiatric disorders. Molecular psychiatry, 26(7), 2977-2990. https://doi.org/10.1038/s41380-020-00912-2
Clifton, Nicholas E, et al. "Genetic association of FMRP targets with psychiatric disorders." Molecular psychiatry vol. 26,7 (2021): 2977-2990. doi: https://doi.org/10.1038/s41380-020-00912-2
Clifton NE, Rees E, Holmans PA, Pardiñas AF, Harwood JC, Di Florio A, Kirov G, Walters JTR, O'Donovan MC, Owen MJ, Hall J, Pocklington AJ. Genetic association of FMRP targets with psychiatric disorders. Mol Psychiatry. 2021 Jul;26(7):2977-2990. doi: 10.1038/s41380-020-00912-2. Epub 2020 Oct 19. PMID: 33077856; PMCID: PMC8505260.
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Man's First Route to America.

Science (New York, N.Y.)

Pocklington R.
PMID: 17729608
Science. 1970 Mar 27;167(3926):1670. doi: 10.1126/science.167.3926.1670.

No abstract available.

Cite
Pocklington R. Man's First Route to America. Science. 1970;167(3926):1670doi: 10.1126/science.167.3926.1670.
Pocklington, R. (1970). Man's First Route to America. Science (New York, N.Y.), 167(3926), 1670. https://doi.org/10.1126/science.167.3926.1670
Pocklington, R. "Man's First Route to America." Science (New York, N.Y.) vol. 167,3926 (1970): 1670. doi: https://doi.org/10.1126/science.167.3926.1670
Pocklington R. Man's First Route to America. Science. 1970 Mar 27;167(3926):1670. doi: 10.1126/science.167.3926.1670. PMID: 17729608.
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Showing 1 to 12 of 13 entries