1,495 research outputs found
A variation in the formation of the median nerve: communicating branch between the musculocutaneous and median nerves in man
We encountered variation in the formation of the median nerve in a 66-year-old male cadaver during dissection of the upper extremity of 20 adult cadavers. The dissections were made at the Department of Cellular Biology and Anatomy, Louisiana State University Medical Center. The median nerve was formed by fusion of four branches, three of them coming from the lateral cord and one from the medial cord. The normal radix from the lateral cord followed a very close oblique course over the axillary artery. The first unusual radix to the median nerve had an anastomoses from the musculocutaneous nerve to the median nerve in the proximal part of the left arm. The second unusual radix also came from the musculocutaneous nerve after it had pierced the coracobrachialis muscle and then joined with the median nerve. These kinds of variations are vulnerable to damage in radical neck dissection and other surgical operations of the axilla and upper arm. The communicating branch can be explained on the basis of its embryologic development and also ought to be distinguished from the other nerve variations in the upper extremity. The aim of this paper is to provide additional information for the classification of previously found communications between the musculocutaneous and median nerves
Effect of Lethally Damaged Tumour Cells upon the Growth of Admixed Viable Cells in Diffusion Chambers
IT has been shown that the proliferation of a small viable tumour graft is stimulated by the presence of irreversibly X-ray damaged tumour cells (Revesz, 1958) or viable but genetically incompatible cells (Klein and Klein, 1956). Histological examination (Ringertz, Klein and Revesz, 1959) showed an enhanced granulation tissue formation in and around the implant. The intensity of this reaction was parallel to the stimulating effect of X-ray damaged, genetically incompatible, and heat-killed cells, respectively. This would indicate that the stimulating function may depend on the formation of a proper tumour bed. In addition, a direct " feeder " effect (Puck, Marcus and Cieciura, 1956) may also play a certain role sinice heavily irradiated cells were stimulatory even in the case of freely suspended ascites tumour cells (Revesz, 1955; Scott, 1957; Mazurek and Duplan, 1959). The diffusion chamber technique of Algire, Weaver and Prehn (1954) permits the isolation of the graft from direct contact with host cells. Filter membraines with adequately small pores permit the diffusion of soluble materials but preven
The anastomotic artery connecting the axillary or brachial artery to one of the forearm arteries
A vessel connecting the axillary or brachial artery to one of the forearm arteries was found in a 65 year old male cadaver, during the gross anatomy dissection of the upper extremity of 20 adult cadavers at the Department of Cellular Biology and Anatomy, Louisiana State University Medical Center. The right radial artery originated from the brachial artery nearly at the usual level and was connected to the axillary or brachial artery by a long slender anastomotic artery (vasa aberrantia). The anastomotic artery coursed under the medial side of the biceps muscle between the median and musculocutaneous nerves, and gave off two muscular branches to the biceps muscle. The anastomotic artery coursed between the median and musculocutaneous nerves in the arm, it passed to the forearm under the bicipital aponeurosis and connected the main radial artery on the radial side of the forearm. The anastomotic artery can be explained on the basis of its embryologic development and also ought to be distinguished from the other common arterial variations in the upper extremity
Scalable, Time-Responsive, Digital, Energy-Efficient Molecular Circuits using DNA Strand Displacement
We propose a novel theoretical biomolecular design to implement any Boolean
circuit using the mechanism of DNA strand displacement. The design is scalable:
all species of DNA strands can in principle be mixed and prepared in a single
test tube, rather than requiring separate purification of each species, which
is a barrier to large-scale synthesis. The design is time-responsive: the
concentration of output species changes in response to the concentration of
input species, so that time-varying inputs may be continuously processed. The
design is digital: Boolean values of wires in the circuit are represented as
high or low concentrations of certain species, and we show how to construct a
single-input, single-output signal restoration gate that amplifies the
difference between high and low, which can be distributed to each wire in the
circuit to overcome signal degradation. This means we can achieve a digital
abstraction of the analog values of concentrations. Finally, the design is
energy-efficient: if input species are specified ideally (meaning absolutely 0
concentration of unwanted species), then output species converge to their ideal
concentrations at steady-state, and the system at steady-state is in (dynamic)
equilibrium, meaning that no energy is consumed by irreversible reactions until
the input again changes.
Drawbacks of our design include the following. If input is provided
non-ideally (small positive concentration of unwanted species), then energy
must be continually expended to maintain correct output concentrations even at
steady-state. In addition, our fuel species - those species that are
permanently consumed in irreversible reactions - are not "generic"; each gate
in the circuit is powered by its own specific type of fuel species. Hence
different circuits must be powered by different types of fuel. Finally, we
require input to be given according to the dual-rail convention, so that an
input of 0 is specified not only by the absence of a certain species, but by
the presence of another. That is, we do not construct a "true NOT gate" that
sets its output to high concentration if and only if its input's concentration
is low. It remains an open problem to design scalable, time-responsive,
digital, energy-efficient molecular circuits that additionally solve one of
these problems, or to prove that some subset of their resolutions are mutually
incompatible.Comment: version 2: the paper itself is unchanged from version 1, but the
arXiv software stripped some asterisk characters out of the abstract whose
purpose was to highlight words. These characters have been replaced with
underscores in version 2. The arXiv software also removed the second
paragraph of the abstract, which has been (attempted to be) re-inserted.
Also, although the secondary subject is "Soft Condensed Matter", this
classification was chosen by the arXiv moderators after submission, not
chosen by the authors. The authors consider this submission to be a
theoretical computer science paper
A Macrophage Phenotype for a Constitutive, Class II Antigen-Expressing, Human Dermal Perivascular Dendritic Cell
A previously uncharacterized population of class II antigen-bearing dendritic cells that are intimately associated with the dermal microvasculature was identified in normal human skin using a double-label, indirect immunofluorescence technique. The only other major HLA-DR positive dermal cell type noted in these studies, the dermal microvascular endothelial cell (DMVEC), appeared to express lesser amounts of HLA-DR region gene product than did this dermal perivascular dendritic cell (DPDC). These DPDC were particularly common around small vessels in the superficial vascular plexus of the papillary dermis and were distinct from the mast cell, another cell type normally seen in a similar location. Phenotypic and ultrastructural studies have determined that the DPDC is more closely related to the monocyte/macro-phage lineage than the dendritic cell lineage. The perivascular location and phenotype of this cell distinguishes it from other previously described constitutive dermal cell types such as the classic “histiocyte,” veiled cell, and dendrocyte. The relatively rich expression of all three major HLA-D region gene products by this dermal perivascular dendritic macro-phage would suggest that it could play a significant role in the immunobiology of the dermal microvascular unit
Electron-phonon scattering in quantum point contacts
We study the negative correction to the quantized value of the
conductance of a quantum point contact due to the backscattering of electrons
by acoustic phonons. The correction shows activated temperature dependence and
also gives rise to a zero-bias anomaly in conductance. Our results are in
qualitative agreement with recent experiments studying the 0.7 feature in the
conductance of quantum point contacts.Comment: 4 pages, no figure
Stub model for dephasing in a quantum dot
As an alternative to Buttiker's dephasing lead model, we examine a dephasing
stub. Both models are phenomenological ways to introduce decoherence in chaotic
scattering by a quantum dot. The difference is that the dephasing lead opens up
the quantum dot by connecting it to an electron reservoir, while the dephasing
stub is closed at one end. Voltage fluctuations in the stub take over the
dephasing role from the reservoir. Because the quantum dot with dephasing lead
is an open system, only expectation values of the current can be forced to
vanish at low frequencies, while the outcome of an individual measurement is
not so constrained. The quantum dot with dephasing stub, in contrast, remains a
closed system with a vanishing low-frequency current at each and every
measurement. This difference is a crucial one in the context of quantum
algorithms, which are based on the outcome of individual measurements rather
than on expectation values. We demonstrate that the dephasing stub model has a
parameter range in which the voltage fluctuations are sufficiently strong to
suppress quantum interference effects, while still being sufficiently weak that
classical current fluctuations can be neglected relative to the nonequilibrium
shot noise.Comment: 8 pages with 1 figure; contribution for the special issue of J.Phys.A
on "Trends in Quantum Chaotic Scattering
Temperature and magnetic-field dependence of the quantum corrections to the conductance of a network of quantum dots
We calculate the magnetic-field and temperature dependence of all quantum
corrections to the ensemble-averaged conductance of a network of quantum dots.
We consider the limit that the dimensionless conductance of the network is
large, so that the quantum corrections are small in comparison to the leading,
classical contribution to the conductance. For a quantum dot network the
conductance and its quantum corrections can be expressed solely in terms of the
conductances and form factors of the contacts and the capacitances of the
quantum dots. In particular, we calculate the temperature dependence of the
weak localization correction and show that it is described by an effective
dephasing rate proportional to temperature.Comment: 24 pages, 14 figure
Experimental Biological Protocols with Formal Semantics
Both experimental and computational biology is becoming increasingly
automated. Laboratory experiments are now performed automatically on
high-throughput machinery, while computational models are synthesized or
inferred automatically from data. However, integration between automated tasks
in the process of biological discovery is still lacking, largely due to
incompatible or missing formal representations. While theories are expressed
formally as computational models, existing languages for encoding and
automating experimental protocols often lack formal semantics. This makes it
challenging to extract novel understanding by identifying when theory and
experimental evidence disagree due to errors in the models or the protocols
used to validate them. To address this, we formalize the syntax of a core
protocol language, which provides a unified description for the models of
biochemical systems being experimented on, together with the discrete events
representing the liquid-handling steps of biological protocols. We present both
a deterministic and a stochastic semantics to this language, both defined in
terms of hybrid processes. In particular, the stochastic semantics captures
uncertainties in equipment tolerances, making it a suitable tool for both
experimental and computational biologists. We illustrate how the proposed
protocol language can be used for automated verification and synthesis of
laboratory experiments on case studies from the fields of chemistry and
molecular programming
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