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A E Mackenzie

Showing results (41-50 of 56) with videos related to

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Human Heredity|January 1, 1991
DNA polymorphism and linkage disequilibrium within the apolipoprotein CII locus on human chromosome 19A E MacKenzie, H L MacLeod, S C Leblond, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2000
The hippocampal neurons of neuronal apoptosis inhibitory protein 1 (NAIP1)-deleted mice display increased vulnerability to kainic acid-induced injuryM Holcik, C S Thompson, Z Yaraghi, et al.
Journal of Neural Transmission. Supplementum|February 10, 2000
Neuronal apoptosis inhibitory protein (NAIP)-like immunoreactivity in brains of adult patients with Down syndromeR Seidl, M Bajo, K Böhm, et al.
American Journal of Medical Genetics|March 17, 1997
Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genesM J Somerville, A G Hunter, H L Aubry, et al.
Endocrinology|March 10, 1998
Expression of inhibitor of apoptosis proteins (IAPs) in rat granulosa cells during ovarian follicular development and atresiaJ Li, J M Kim, P Liston, et al.
Genomics|March 1, 1991
Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophyG Shutler, A E MacKenzie, H Brunner, et al.
Anesthesiology|July 1, 1991
A comparison of the caffeine halothane muscle contracture test with the molecular genetic diagnosis of malignant hyperthermiaA E MacKenzie, G Allen, D Lahey, et al.
American Journal of Human Genetics|November 1, 1991
D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19qC Tsilfidis, A E MacKenzie, G Shutler, et al.
Human Molecular Genetics|November 1, 1994
Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophyM D McLean, N Roy, A E MacKenzie, et al.
American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Human Heredity|January 1, 1991
DNA polymorphism and linkage disequilibrium within the apolipoprotein CII locus on human chromosome 19A E MacKenzie, H L MacLeod, S C Leblond, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2000
The hippocampal neurons of neuronal apoptosis inhibitory protein 1 (NAIP1)-deleted mice display increased vulnerability to kainic acid-induced injuryM Holcik, C S Thompson, Z Yaraghi, et al.
Journal of Neural Transmission. Supplementum|February 10, 2000
Neuronal apoptosis inhibitory protein (NAIP)-like immunoreactivity in brains of adult patients with Down syndromeR Seidl, M Bajo, K Böhm, et al.
American Journal of Medical Genetics|March 17, 1997
Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genesM J Somerville, A G Hunter, H L Aubry, et al.
Endocrinology|March 10, 1998
Expression of inhibitor of apoptosis proteins (IAPs) in rat granulosa cells during ovarian follicular development and atresiaJ Li, J M Kim, P Liston, et al.
Genomics|March 1, 1991
Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophyG Shutler, A E MacKenzie, H Brunner, et al.
Anesthesiology|July 1, 1991
A comparison of the caffeine halothane muscle contracture test with the molecular genetic diagnosis of malignant hyperthermiaA E MacKenzie, G Allen, D Lahey, et al.
American Journal of Human Genetics|November 1, 1991
D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19qC Tsilfidis, A E MacKenzie, G Shutler, et al.
Human Molecular Genetics|November 1, 1994
Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophyM D McLean, N Roy, A E MacKenzie, et al.
American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
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