J. S. Trimmer

Dynamic localization and clustering of dendritic KV2.1 voltage- dependent potassium, channels in developing hippocampal neurons (2001)

Antonucci,D. E., Lim,S. T., Vassanelli,S., Trimmer,J. S.

Dendritic excitability is modulated by the highly variable spatial and temporal expression pattern of voltage-dependent potassium channels. Somatodendritic Kv2.1 channels contribute a major component...

Dynamic localization and clustering of dendritic KV2.1 voltage- dependent potassium, channels in developing hippocampal neurons (2001)

Antonucci, D. E., Lim, S. T., Vassanelli, S., Trimmer, J. S.

Dendritic excitability is modulated by the highly variable spatial and temporal expression pattern of voltage-dependent potassium channels. Somatodendritic Kv2.1 channels contribute a major component...

Immunological identification and characterization of a delayed rectifier K+ channel polypeptide in rat brain.

Trimmer, J S

Antibodies specific for the drk1 polypeptide were used to characterize the corresponding protein in rat brain. Recombinant and synthetic immunogens containing fragments of the drk1 polypeptide were...

Monoclonal antibodies increase intracellular Ca2+ in sea urchin spermatozoa.

Trimmer, J S, Schackmann, R W, Vacquier, V D

Changes in intracellular free Ca2+ ([Ca2+]i) of sea urchin (Strongylocentrotus purpuratus) spermatozoa were measured using the fluorescent Ca2+ indicators fura-2 and indo-1. The intracellular pH...

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M

Paramyotonia congenita (PC), an autosomal dominant muscle disease, shares some clinical and electrophysiological similarities with another myotonic muscle disorder, hyperkalemic periodic paralysis...

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

Ptacek, L J, Tyler, F, Trimmer, J S, Agnew, W S, Leppert, M

Hyperkalemic periodic paralysis (HYPP) is an autosomal dominant muscle disease with electrophysiological abnormalities suggesting a defect in a voltage-gated sodium channel (NaCh) gene. A human NaCh...

Immunological identification and characterization of a delayed rectifier K+ channel polypeptide in rat brain.

Trimmer, J S

Antibodies specific for the drk1 polypeptide were used to characterize the corresponding protein in rat brain. Recombinant and synthetic immunogens containing fragments of the drk1 polypeptide were...

Monoclonal antibodies increase intracellular Ca2+ in sea urchin spermatozoa.

Trimmer, J S, Schackmann, R W, Vacquier, V D

Changes in intracellular free Ca2+ ([Ca2+]i) of sea urchin (Strongylocentrotus purpuratus) spermatozoa were measured using the fluorescent Ca2+ indicators fura-2 and indo-1. The intracellular pH...

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Ptacek, L J, Trimmer, J S, Agnew, W S, Roberts, J W, Petajan, J H, Leppert, M

Paramyotonia congenita (PC), an autosomal dominant muscle disease, shares some clinical and electrophysiological similarities with another myotonic muscle disorder, hyperkalemic periodic paralysis...

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

Ptacek, L J, Tyler, F, Trimmer, J S, Agnew, W S, Leppert, M

Hyperkalemic periodic paralysis (HYPP) is an autosomal dominant muscle disease with electrophysiological abnormalities suggesting a defect in a voltage-gated sodium channel (NaCh) gene. A human NaCh...