Search

Your search keyword '"Pratt, V."' showing total 155 results
Start Over Author "Pratt, V."
155 results on '"Pratt, V."'

5. von Willebrand disease: proposing definitions for future research

Author

Connell, N.T., James, P.D., Brignardello-Petersen, R., Abdul-Kadir, R., Ameer, B., Arapshian, A., Couper, S., Paola, J. di, Eikenboom, J., Giraud, N., Grow, J.M., Haberichter, S., Jacobs-Pratt, V., Konkle, B.A., Kouides, P., Laffan, M., Lavin, M., Leebeek, F.W.G., McLintock, C., McRae, S., Montgomery, R., O'Brien, S.H., O'Donnell, J.S., Ozelo, M.C., Scappe, N., Sidonio, R., Tosetto, A., Weyand, A.C., Kalot, M.A., Husainat, N., Mustafa, R.A., Flood, V.H., and Hematology

Subjects
von Willebrand Diseases, von Willebrand Factor, Commentary, Humans
Published
2021

9. Two-way channel with disconnect

Author

Pratt, V., Goos, G., editor, Hartmanis, J., editor, Barstow, D., editor, Brauer, W., editor, Brinch Hansen, P., editor, Gries, D., editor, Luckham, D., editor, Moler, C., editor, Pnueli, A., editor, Seegmüller, G., editor, Stoer, J., editor, Wirth, N., editor, Denvir, B. T., editor, Harwood, W. T., editor, Jackson, M. I., editor, and Wray, M. J., editor

Published
1985
Full Text
View/download PDF

10. Using graphs to understand PDL

Author

Pratt, V. R., Goos, G., editor, Hartmanis, J., editor, Brauer, W., editor, Brinch Hansen, P., editor, Gries, D., editor, Moler, C., editor, Seegmüller, G., editor, Stoer, J., editor, Wirth, N., editor, and Kozen, Dexter, editor

Published
1982
Full Text
View/download PDF

11. Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting

Author

Kalman, L. V., Agundez, J. A. G., Lindqvist Appell, Malin, Black, J. L., Bell, G. C., Boukouvala, S., Bruckner, C., Bruford, E., Caudle, K., Coulthard, S. A., Daly, A. K., Del Tredici, A. L., den Dunnen, J. T., Drozda, K., Everts, R. E., Flockhart, D., Freimuth, R. R., Gaedigk, A., Hachad, H., Hartshorne, T., Ingelman-Sundberg, M., Klein, T. E., Lauschke, V. M., Maglott, D. R., McLeod, H. L., McMillin, G. A., Meyer, U. A., Mueller, D. J., Nickerson, D. A., Oetting, W. S., Pacanowski, M., Pratt, V. M., Relling, M. V., Roberts, A., Rubinstein, W. S., Sangkuhl, K., Schwab, M., Scott, S. A., Sim, S. C., Thirumaran, R. K., Toji, L. H., Tyndale, R. F., van Schaik, R. H. N., Whirl-Carrillo, M., Yeo, K. T. J., Zanger, U. M., Kalman, L. V., Agundez, J. A. G., Lindqvist Appell, Malin, Black, J. L., Bell, G. C., Boukouvala, S., Bruckner, C., Bruford, E., Caudle, K., Coulthard, S. A., Daly, A. K., Del Tredici, A. L., den Dunnen, J. T., Drozda, K., Everts, R. E., Flockhart, D., Freimuth, R. R., Gaedigk, A., Hachad, H., Hartshorne, T., Ingelman-Sundberg, M., Klein, T. E., Lauschke, V. M., Maglott, D. R., McLeod, H. L., McMillin, G. A., Meyer, U. A., Mueller, D. J., Nickerson, D. A., Oetting, W. S., Pacanowski, M., Pratt, V. M., Relling, M. V., Roberts, A., Rubinstein, W. S., Sangkuhl, K., Schwab, M., Scott, S. A., Sim, S. C., Thirumaran, R. K., Toji, L. H., Tyndale, R. F., van Schaik, R. H. N., Whirl-Carrillo, M., Yeo, K. T. J., and Zanger, U. M.

Abstract

This article provides nomenclature recommendations developed by an international workgroup to increase transparency and standardization of pharmacogenetic (PGx) result reporting. Presently, sequence variants identified by PGx tests are described using different nomenclature systems. In addition, PGx analysis may detect different sets of variants for each gene, which can affect interpretation of results. This practice has caused confusion and may thereby impede the adoption of clinical PGx testing. Standardization is critical to move PGx forward.

Published
2016
Full Text
View/download PDF

15. A standardized framework for the validation and verification of clinical molecular genetic tests.

Author

Mattocks, C.J., Morris, M.A., Matthijs, G., Swinnen, E., Corveleyn, A., Dequeker, E., Muller, C.R., Pratt, V., Wallace, A., Mattocks, C.J., Morris, M.A., Matthijs, G., Swinnen, E., Corveleyn, A., Dequeker, E., Muller, C.R., Pratt, V., and Wallace, A.

Abstract

01 december 2010, Item does not contain fulltext, The validation and verification of laboratory methods and procedures before their use in clinical testing is essential for providing a safe and useful service to clinicians and patients. This paper outlines the principles of validation and verification in the context of clinical human molecular genetic testing. We describe implementation processes, types of tests and their key validation components, and suggest some relevant statistical approaches that can be used by individual laboratories to ensure that tests are conducted to defined standards.

Published
2010

45. Southern Michigan trout streams. (Fisheries research report: 1242)

Author

Pratt, V. S., Pratt, V. S., Pratt, V. S., and Pratt, V. S.

Abstract

v. Irregular no. 1- 1930, Some volumes issued in revised editions, Nos. for 1930- issued by the Institute for Fisheries Research; by the Michigan Fisheries Division., Electronic serial mode of access: World Wide Web via the Michigan DNR, Institute for Fisheries Research site., Microfiche copy: Microfiche. Washington, D.C. : U.S. Govt. Print. Off. microfiches : negative ; 11 x 15 cm., (dlps) AAG2862.1242.001, http://name.umdl.umich.edu/AAG2862.1242.001, http://quod.lib.umich.edu/t/text/accesspolicy.html

Published
1950

46. Populations, ecology, and management of marginal trout streams in southern Michigan. (Ph.D thesis) (Fisheries research report: 1383)

Author

Pratt, V. S., Pratt, V. S., Pratt, V. S., and Pratt, V. S.

Abstract

v. Irregular no. 1- 1930, Some volumes issued in revised editions, Nos. for 1930- issued by the Institute for Fisheries Research; by the Michigan Fisheries Division., Electronic serial mode of access: World Wide Web via the Michigan DNR, Institute for Fisheries Research site., Microfiche copy: Microfiche. Washington, D.C. : U.S. Govt. Print. Off. microfiches : negative ; 11 x 15 cm., (dlps) AAG2862.1383.001, http://name.umdl.umich.edu/AAG2862.1383.001, http://quod.lib.umich.edu/t/text/accesspolicy.html

Published
1953

48. Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study

Author

Monaghan, K G, Highsmith, W E, Amos, J, Pratt, V M, Roa, B, Friez, M, Pike-Buchanan, L L, Buyse, I M, Redman, J B, Strom, C M, Young, A L, and Sun, W

Abstract

Purpose: We expect that the mutation panel currently recommended for preconception/prenatal CF carrier screening will be modified as new information is learned regarding the phenotype associated with specific mutations and allele frequencies in various populations. One such example is the I148T mutation, originally described as a severe CF mutation. After implementation of CF population-based carrier screening, we learned that I148T exists as a complex allele with 3199del6 in patients with clinical CF, whereas asymptomatic compound heterozygotes for I148T and a second severe CF mutation were negative for 3199del6.Methods: We performed reflex testing for 3199del6 on 663 unrelated specimens, including I148T heterozygotes, compound heterozygotes, and a homozygous individual.Results: Less than 1% of I148T carriers were also positive for 3199del6. Excluding subjects tested because of a suspected or known CF diagnosis or positive family history, 0.6% of I148T-positive individuals were also positive for 3199del6. We identified 1 I148T homozygote and 6 unrelated compound heterozygous individuals with I148T and a second CF variant (2 of whom also carried 3199del6). In addition, one fetus with echogenic bowel and one infertile male were heterozygous for I148T (3199del6 negative).Conclusions: Reflex testing for 3199del6 should be considered whenever I148T is identified. Reflex testing is of particular importance for any symptomatic patient or whenever one member of a couple carries a deleterious CF mutation and the other member is an I148T heterozygote. Further population data are required to determine if I148T, in the absence of 3199del6, is associated with mild or atypical CF or male infertility.

Published
2004
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results