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Results of search for 'au:"HAYDEN, M"', page 14 of 32
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Authors
Bertsche, W
Bloch, M
Brunzell, J D
Cesar, C L
Charlton, M
Fajans, J
Fujiwara, M C
Gill, D R
Goldberg, Y P
Hangst, J S
Hardy, W N
Hayden, M
Hayden, M E
Hayden, M J
Hayden, M K
Hayden, M L
Hayden, M R
Kastelein, J J
Madsen, N
Nasir, J
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Adolescent
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Amino Acid Sequence
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Base Sequence
Female
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Huntington Disease
Lipoprotein Lipase
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Molecular Sequence Data
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261.
Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneity.
[electronic resource]
by
Greenberg, L J
Martell, R W
Theilman, J
Hayden, M R
Joubert, J
Producer:
19911203
In:
Human genetics
vol. 87
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262.
Plasmid vectors useful in the study of translation initiation signals.
[electronic resource]
by
Wyckoff, E
Sampson, L
Hayden, M
Parr, R
Huang, W M
Casjens, S
Producer:
19861023
In:
Gene
vol. 43
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263.
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease.
[electronic resource]
by
Riess, O
Noerremoelle, A
Collins, C
Mah, D
Weber, B
Hayden, M R
Producer:
19930610
In:
Nature genetics
vol. 1
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264.
Pathological association and dissociation of functional systems in multiple sclerosis and Huntington's disease.
[electronic resource]
by
Clark, C M
Jacova, C
Klonoff, H
Kremer, B
Hayden, M
Paty, D
Producer:
19970627
In:
Journal of clinical and experimental neuropsychology
vol. 19
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265.
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.
[electronic resource]
by
Brinkman, R R
Mezei, M M
Theilmann, J
Almqvist, E
Hayden, M R
Producer:
19970603
In:
American journal of human genetics
vol. 60
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266.
Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana.
[electronic resource]
by
Tuzgöl, S
Bijvoet, S M
Bruin, T
Kastelein, J J
Hayden, M R
Producer:
19950209
In:
Journal of medical genetics
vol. 31
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267.
Onset and pre-onset studies to define the Huntington's disease natural history.
[electronic resource]
by
Squitieri, F
Cannella, M
Giallonardo, P
Maglione, V
Mariotti, C
Hayden, M R
Producer:
20020207
In:
Brain research bulletin
vol. 56
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268.
Intrinsic cleavage of receptor-interacting protein kinase-1 by caspase-6.
[electronic resource]
by
van Raam, B J
Ehrnhoefer, D E
Hayden, M R
Salvesen, G S
Producer:
20130815
In:
Cell death and differentiation
vol. 20
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269.
Phosphate Metabolism in Cardiorenal Metabolic Disease.
[electronic resource]
by
Gupta, Deepashree
Brietzke, Stephen
Hayden, M R
Kurukulasuriya, L Romayne
Sowers, James R
Publication details:
Cardiorenal medicine
2011
In:
Cardiorenal medicine
vol. 1
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270.
Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3.
[electronic resource]
by
Andrew, S
Theilmann, J
Hedrick, A
Mah, D
Weber, B
Hayden, M R
Producer:
19920730
In:
Genomics
vol. 13
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271.
Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency.
[electronic resource]
by
Henderson, H E
Devlin, R
Peterson, J
Brunzell, J D
Hayden, M R
Producer:
19910419
In:
Molecular biology & medicine
vol. 7
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272.
A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing.
[electronic resource]
by
Andrew, S E
Goldberg, Y P
Theilmann, J
Zeisler, J
Hayden, M R
Producer:
19940523
In:
Human molecular genetics
vol. 3
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273.
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease.
[electronic resource]
by
Clee, S M
Loubser, O
Collins, J
Kastelein, J J
Hayden, M R
Producer:
20020109
In:
Clinical genetics
vol. 60
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274.
The FDG/PET methodology for early detection of disease onset: a statistical model.
[electronic resource]
by
Clark, C M
Ammann, W
Martin, W R
Ty, P
Hayden, M R
Producer:
19910401
In:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
vol. 11
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275.
A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency.
[electronic resource]
by
Langlois, S
Deeb, S
Brunzell, J D
Kastelein, J J
Hayden, M R
Producer:
19890316
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 86
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276.
Adverse psychological events occurring in the first year after predictive testing for Huntington's disease. The Canadian Collaborative Study Predictive Testing.
[electronic resource]
by
Lawson, K
Wiggins, S
Green, T
Adam, S
Bloch, M
Hayden, M R
Producer:
19970221
In:
Journal of medical genetics
vol. 33
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277.
Phenotypic variation of mutations in the human lipoprotein-lipase gene.
[electronic resource]
by
Hayden, M R
Kastelein, J J
Funke, H
Brunzell, J D
Ma, Y
Producer:
19930930
In:
Biochemical Society transactions
vol. 21
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278.
Thatcher wheat line RL6149 carries Lr64 and a second leaf rust resistance gene on chromosome 1DS.
[electronic resource]
by
Kolmer, J A
Bernardo, A
Bai, G
Hayden, M J
Anderson, J A
Producer:
20200226
In:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik
vol. 132
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279.
The genetics and molecular biology of apolipoprotein CII.
[electronic resource]
by
Hayden, M R
Vergani, C
Humphries, S E
Kirby, L
Shukin, R
McLeod, R
Producer:
19870205
In:
Advances in experimental medicine and biology
vol. 201
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280.
Cloning, overexpression, and purification of cytosine deaminase from Saccharomyces cerevisiae.
[electronic resource]
by
Hayden, M S
Linsley, P S
Wallace, A R
Marquardt, H
Kerr, D E
Producer:
19980526
In:
Protein expression and purification
vol. 12
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