Manuel de dissection ou Éléments d'anatomie générale, descriptive et topographique /

Mode of access: Internet.

A correct statement of the circumstances that attended the last illness and death of Mrs. Southcott : with an account of the appearances exhibited on dissection : and the artifices that were employed to deceive her medical attendants /

Caption title: A statement of the circumstances attending the last illness of Joanna Southcott.

Holden's manual of the dissection of the human body,

Mode of access: Internet.

Manuel d'anatomie et de dissection du cheval : ostéologie /

Mode of access: Internet.

Guide to the dissection of the horse;

Mode of access: Internet.

Laboratory guide to the dissection and study of the anatomy of the domestic ruminants (ox, sheep, goat) by Duane Russell Peterson.

Mode of access: Internet.

Dissection guide for veterinary anatomy /

Mode of access: Internet.

Guide to the dissection of the horse,

Spiral binding.

Guide to the dissection of the dog.

"Third edition, reprinted 1955, 1958, 1962."

Manuel des amphitryons : contenant un traité de la dissection des viandes à table, la nomenclature des menus les plus nouveaux pour chaque saison, et des élémens de politesse gourmande : ouvrage indispensable à tous ceux qui sont jaloux de faire bonne chère, et de la faire faire aux autres /

Includes bibliographical references and index.

Female students in dissection room

Dissection room for female students, called hen medics, first floor of the Anatomical Laboratory. The women had separate dissection rooms until 1908 (source: Not Just Any Medical School by Horace W. Davenport.)

Female students in dissection room

Dissection room for female students, called hen medics, first floor of the Anatomical Laboratory. The women had separate dissection rooms until 1908 (source: Not Just Any Medical School by Horace W. Davenport.)

A laboratory guide for the dissection of the cat

Mode of access: Internet.

Functional dissection of the Suppressor of UnderReplication protein of Drosophila melanogaster: identification of domains influencing chromosome binding and DNA replication

The Suppressor of UnderReplication (SuUR) gene controls the DNA underreplication in intercalary and pericentric heterochromatin of Drosophila melanogaster salivary gland polytene chromosomes. In the present work, we investigate the functional importance of different regions of the SUUR protein by expressing truncations of the protein in an UAS-GAL4 system. We find that SUUR has at least two separate chromosome-binding regions that are able to recognize intercalary and pericentric heterochromatin specifically. The C-terminal part controls DNA underreplication in intercalary heterochromatin and partially in pericentric heterochromatin regions. The C-terminal half of SUUR suppresses endoreplication when ectopically expressed in the salivary gland. Ectopic expression of the N-terminal fragments of SUUR depletes endogenous SUUR from polytene chromosomes, causes the SuUR(-) stopphenotype and induces specific swellings in heterochromatin.

Dissection of peripheral and central endogenous opioid modulation of systemic interleukin-1 beta responses using c-fos expression in the rat brain

In opiate addicts or patients receiving morphine treatment, it has been reported that the immune system is often compromised. The mechanisms responsible for the adverse effects of opioids on responses to infection are not clear but it is possible that central and/or peripheral opioid receptors may be important. We have utilised an experimental immune challenge model in rats, the systemic administration of the human pro-inflammatory cytokine interleukin-1 beta (IL-1 beta) to study the effects of selectively blocking peripheral opioid receptors only (using naloxone methiodide) or after blocking both central and peripheral opioid receptors (using naloxone). Pre-treatment with naloxone methiodide decreased (15%) IL-1 beta-induced Fos-immunoreactivity (Fos-IR) in medial parvocellular paraventricular nucleus (mPVN) corticotropin-releasing hormone (CRH) neurons but increased responses in the ventrolateral medulla (VLM) C1 (65%) and nucleus tractus solitarius (NTS) A2 (110%) catecholamine cell groups and area postrema (136%). However no effect of blocking peripheral opioid receptors was detected in the central nucleus of the amygdala (CeA) or dorsal bed nucleus of the stria terminalis (BNST). We next determined the effect of blocking both central and peripheral opioid receptors with naloxone and, when compared to the naloxone methiodide pre-treated group, a further 60% decrease in Fos-IR mPVN CRH neurons induced by IL-1 beta was detected, which was attributed to block of central opioid receptors. Similar comparisons also detected decreases in Fos-IR neurons induced by IL-1 beta in the VLM A1, VLM C1 and NTS A2 catecholamine cell groups, area postrema, and parabrachial nucleus. In contrast, pre-treatment with naloxone increased Fos-IR neurons in CeA (98%) and dorsal BNST (72%). These results provide novel evidence that endogenous opioids can influence central neural responses to systemic IL-1 beta and also suggest that the differential patterns of activation may arise because of actions at central and/or peripheral opioid receptors that might be important in regulating behavioural, hypothalamic-pituitary-adrenal axis and sympathetic nervous system responses during an immune challenge. (c) 2005 Elsevier Ltd. All rights reserved.