Gary V. Allen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Gary V. Allen has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
D Gerami
1 shared publicationDavid A. Hopkins
Department of Anatomy and Neurobiology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada, B3H 4H7
1 shared publicationLaura P. R. Reynolds
Dalhousie University
1 shared publicationM.J Esser
1 shared publicationM.J. Esser
Dalhousie University, Faculty of Medicine, Department of Anatomy and Neurobiology, Halifax, Nova Scotia, Canada
1 shared publicationS.P Pronych
1 shared publication
Latest Publications
- 1 September 2003
- Published by Springer Nature in The Cerebellum
- Vol. 2 (3) , 171-177
A review of heat shock protein induction following cerebellar injury
Exposure of cells to stressful environments such as heat shock, ischemia, trauma and disease, induces the cellular expression of heat shock proteins (Hsps). Since the discovery of heat shock proteins...
- 1 September 2003
- Published by Springer Nature in The Cerebellum
- Vol. 2 (3) , 171-177
A review of heat shock protein induction following cerebellar injury
Exposure of cells to stressful environments such as heat shock, ischemia, trauma and disease, induces the cellular expression of heat shock proteins (Hsps). Since the discovery of heat shock proteins...
- 20 February 2001
- Published by Elsevier in Neuroscience
- Vol. 102 (3) , 603-614
Induction of heat shock proteins and motor function deficits after focal cerebellar injury
- 20 February 2001
- Published by Elsevier in Neuroscience
- Vol. 102 (3) , 603-614
Induction of heat shock proteins and motor function deficits after focal cerebellar injury
- 1 July 2000
- Published by Elsevier in Neuroscience
- Vol. 99 (1) , 93-105
Conditioning effects of repetitive mild neurotrauma on motor function in an animal model of focal brain injury
- 1 July 2000
- Published by Elsevier in Neuroscience
- Vol. 99 (1) , 93-105
Conditioning effects of repetitive mild neurotrauma on motor function in an animal model of focal brain injury
- 31 August 1998
- Published by Wiley in Journal of Comparative Neurology
- Vol. 398 (3) , 347-358
Convergent prefrontal cortex and mamillary body projections to the medial pontine nuclei: A light and electron microscopic study in the rat
To study the convergence of medial prefrontal cortex and mamillary body projections to the medial pontine nuclei, light and electron microscopic, neuroanatomical, tract-tracing experiments were performed. Injections of horseradish peroxidase conjugated to wheat germ agglutinin (WGA-HRP), biotin conjugated to dextran (BD), or rhodamine conjugated to dextran (RD) were made individually or in combinations into the cerebral cortex, hypothalamus, or pons. In addition, injections of WGA-HRP into the medial prefrontal cortex and electrolytic lesions of the mamillary body were made to study the synaptology of afferent projections to the pontine nuclei. In the light microscopic studies, injections of WGA-HRP into the rostromedial pontine nuclei produced dense, retrograde labeling both in the dorsal peduncular area of the medial prefrontal cortex and in the medial mamillary nucleus, pars medialis. Injections of the anterograde tracers BD and RD into the medial prefrontal cortex and the medial mamillary nuclei, respectively, resulted in partially overlapping terminal fields in the rostromedial pontine nuclei. In the electron microscopic studies, injections of WGA-HRP into the dorsal peduncular area and electrolytic lesions of the mamillary body produced anterogradely labeled axon terminals and degenerating axon terminals that synapsed on the same dendrites or neuronal somata in the rostromedial pontine nuclei. The results demonstrate that the medial prefrontal cortex and the medial mamillary nuclei have partially overlapping projections to the rostromedial pontine nuclei and implicate precerebellar relay nuclei in the integration of limbic and/or autonomic functions mediated by convergent projections from the cerebral cortex and the hypothalamus.
- 31 August 1998
- Published by Wiley in Journal of Comparative Neurology
- Vol. 398 (3) , 347-358
Convergent prefrontal cortex and mamillary body projections to the medial pontine nuclei: A light and electron microscopic study in the rat
To study the convergence of medial prefrontal cortex and mamillary body projections to the medial pontine nuclei, light and electron microscopic, neuroanatomical, tract-tracing experiments were performed. Injections of horseradish peroxidase conjugated to wheat germ agglutinin (WGA-HRP), biotin conjugated to dextran (BD), or rhodamine conjugated to dextran (RD) were made individually or in combinations into the cerebral cortex, hypothalamus, or pons. In addition, injections of WGA-HRP into the medial prefrontal cortex and electrolytic lesions of the mamillary body were made to study the synaptology of afferent projections to the pontine nuclei. In the light microscopic studies, injections of WGA-HRP into the rostromedial pontine nuclei produced dense, retrograde labeling both in the dorsal peduncular area of the medial prefrontal cortex and in the medial mamillary nucleus, pars medialis. Injections of the anterograde tracers BD and RD into the medial prefrontal cortex and the medial mamillary nuclei, respectively, resulted in partially overlapping terminal fields in the rostromedial pontine nuclei. In the electron microscopic studies, injections of WGA-HRP into the dorsal peduncular area and electrolytic lesions of the mamillary body produced anterogradely labeled axon terminals and degenerating axon terminals that synapsed on the same dendrites or neuronal somata in the rostromedial pontine nuclei. The results demonstrate that the medial prefrontal cortex and the medial mamillary nuclei have partially overlapping projections to the rostromedial pontine nuclei and implicate precerebellar relay nuclei in the integration of limbic and/or autonomic functions mediated by convergent projections from the cerebral cortex and the hypothalamus.
- 22 February 1998
- Published by Wiley in Journal of Comparative Neurology
- Vol. 391 (4) , 526-544
Trigeminal-reticular connections: Possible pathways for nociception-induced cardiovascular reflex responses in the rat
- 22 February 1998
- Published by Wiley in Journal of Comparative Neurology
- Vol. 391 (4) , 526-544
Trigeminal-reticular connections: Possible pathways for nociception-induced cardiovascular reflex responses in the rat
- 1 April 1997
- Published by Elsevier in Brain Research
- Vol. 754 (1-2) , 269-278
Trigeminal autonomic pathways involved in nociception-induced reflex cardiovascular responses
- 1 April 1997
- Published by Elsevier in Brain Research
- Vol. 754 (1-2) , 269-278
Trigeminal autonomic pathways involved in nociception-induced reflex cardiovascular responses