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Manfred Zimmermann

Researcher at Heidelberg University

Publications -  163
Citations -  14945

Manfred Zimmermann is an academic researcher from Heidelberg University. The author has contributed to research in topics: Spinal cord & Nociception. The author has an hindex of 50, co-authored 163 publications receiving 14516 citations. Previous affiliations of Manfred Zimmermann include University of Siena & Max Planck Society.

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Ethical guidelines for investigations of experimental pain in conscious animals.

Manfred Zimmermann
- 01 Jun 1983 - 
TL;DR: The Committee for Research and Ethical Issues of the International Association for the Study of Pain (IASP®) is concerned with the ethical aspects of studies producing experimental pain and any suffering it may cause in animals.
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Altered expression of Bcl-2, Bcl-X, Bax, and c-Fos colocalizes with DNA fragmentation and ischemic cell damage following middle cerebral artery occlusion in rats

TL;DR: Findings suggest that a shift in the ratio of cell death repressor Bcl-2 to cell death effector Bax and a concomitant activation of c-Fos may contribute to neuronal apoptosis in the infarcted thalamus and cortex.
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The transcription factors c-JUN, JUN D and CREB, but not FOS and KROX-24, are differentially regulated in axotomized neurons following transection of rat sciatic nerve.

TL;DR: In adult rats, expression of c-JUN, Jun B, JUN D, c-FOS, FOS B, KROX-24 and CREB proteins was investigated by immunocytochemistry in L4 and L5 dorsal root ganglia and lumbar spinal cord for up to 300 days following transection of the left sciatic nerve.
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Block of c-Fos and JunB expression by antisense oligonucleotides inhibits light-induced-phase shifts of the mammalian circadian clock

TL;DR: It is demonstrated for the first time that inducible transcription factors such as c‐Fos and JunB are an essential part of fundamental biological processes in the adult mammalian nervous system, e.g. of light‐induced phase shifts of the circadian pacemaker.
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Basal expression of the inducible transcription factors c-Jun, JunB, JunD, c-Fos, FosB, and Krox-24 in the adult rat brain.

TL;DR: Investigation of the expression of c‐Jun, JunB, JunD, c‐Fos, FosB, and Krox proteins in the brain of untreated male Sprague‐Dawley and female BDIX rats by immunocytochemistry using specific antibodies provides new insights into the ability of neurons to react with changes of gene expression to external stimulation under physiological or pathological conditions.