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M Vance

Showing results (181-190 of 466) with videos related to

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The Journal of Biological Chemistry|February 26, 2009
The serine protease plasmin cleaves the amino-terminal domain of the NR2A subunit to relieve zinc inhibition of the N-methyl-D-aspartate receptorsHongjie Yuan, Katie M Vance, Candice E Junge, et al.
Plos Neglected Tropical Diseases|August 13, 2013
The schistosome oesophageal gland: initiator of blood processingXiao-Hong Li, William de Castro-Borges, Sophie Parker-Manuel, et al.
The Journal of Physiology|June 20, 2018
A structurally derived model of subunit-dependent NMDA receptor functionAlasdair J Gibb, Kevin K Ogden, Miranda J McDaniel, et al.
American Journal of Human Genetics|June 1, 1992
Recombination of 4p16 DNA markers in an unusual family with Huntington diseaseC Pritchard, N Zhu, J Zuo, et al.
Genomics|July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4AK B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Genomics|March 1, 1990
Confirmation of linkage in von Hippel-Lindau diseaseJ M Vance, K W Small, M A Jones, et al.
American Journal of Human Genetics|July 1, 1996
Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2BJ M Vance, M C Speer, J M Stajich, et al.
American Journal of Human Genetics|August 27, 1998
Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I geneN P Liu, J Baldwin, F Jonasson, et al.
Neurology|March 1, 1992
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entitiesL J Loprest, M A Pericak-Vance, J Stajich, et al.
Pageof 47

Showing results (181-190 of 466) with videos related to

Sort By:
Pageof 47
The Journal of Biological Chemistry|February 26, 2009
The serine protease plasmin cleaves the amino-terminal domain of the NR2A subunit to relieve zinc inhibition of the N-methyl-D-aspartate receptorsHongjie Yuan, Katie M Vance, Candice E Junge, et al.
Plos Neglected Tropical Diseases|August 13, 2013
The schistosome oesophageal gland: initiator of blood processingXiao-Hong Li, William de Castro-Borges, Sophie Parker-Manuel, et al.
The Journal of Physiology|June 20, 2018
A structurally derived model of subunit-dependent NMDA receptor functionAlasdair J Gibb, Kevin K Ogden, Miranda J McDaniel, et al.
American Journal of Human Genetics|June 1, 1992
Recombination of 4p16 DNA markers in an unusual family with Huntington diseaseC Pritchard, N Zhu, J Zuo, et al.
Genomics|July 20, 1995
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4AK B Othmane, D Loeb, R Hayworth-Hodgte, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Genomics|March 1, 1990
Confirmation of linkage in von Hippel-Lindau diseaseJ M Vance, K W Small, M A Jones, et al.
American Journal of Human Genetics|July 1, 1996
Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2BJ M Vance, M C Speer, J M Stajich, et al.
American Journal of Human Genetics|August 27, 1998
Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I geneN P Liu, J Baldwin, F Jonasson, et al.
Neurology|March 1, 1992
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entitiesL J Loprest, M A Pericak-Vance, J Stajich, et al.
Pageof 47