Paired cell aligament using a jagged microarray electrode

1994 ◽  
Vol 34 (2) ◽  
pp. 199-202 ◽  
Author(s):  
Norio Matsumoto ◽  
Tomokazu Matsue ◽  
Isamu Uchida
Keyword(s):  
2018 ◽  
Vol 71 (11) ◽  
pp. A158
Author(s):  
Kathryn Arnold ◽  
John Blair ◽  
Jonathan Paul ◽  
Atman Shah ◽  
Sandeep Nathan ◽  
...  

2008 ◽  
Vol E91-C (5) ◽  
pp. 731-735 ◽  
Author(s):  
S. CHO ◽  
I. H. PARK ◽  
J. H. LEE ◽  
J.-G. YUN ◽  
D.-H. KIM ◽  
...  

2019 ◽  
Vol 7 (3) ◽  
pp. 938-950 ◽  
Author(s):  
Chang Yang ◽  
Yun Wang ◽  
Ming Hua Ge ◽  
Yu Jie Fu ◽  
Rui Hao ◽  
...  

Aptamer S30 selected using modified paired cell-based approach can precisely target CD33-positive cancer cells and deliver anticancer drugs.


2018 ◽  
Vol 68 ◽  
pp. S613-S614
Author(s):  
K.B. Halpern ◽  
S. Itzkovitz ◽  
R. Shenhav
Keyword(s):  

Endocrinology ◽  
2008 ◽  
Vol 149 (9) ◽  
pp. 4638-4646 ◽  
Author(s):  
Jean-Paul Paluzzi ◽  
William K. Russell ◽  
Ronald J. Nachman ◽  
Ian Orchard

After a blood meal, Rhodnius prolixus undergoes a rapid diuresis to eliminate excess water and salts. During the voiding of this primary urine, R. prolixus acts as a vector of Chagas’ disease, with the causative agent, Trypanosoma cruzi, infecting the human host via the urine. Diuresis in R. prolixus is under the neurohormonal control of serotonin and peptidergic diuretic hormones, and thus, diuretic hormones play an important role in the transmission of Chagas’ disease. Although diuretic hormones may be degraded or excreted, resulting in the termination of diuresis, it would also seem appropriate, given the high rates of secretion, that a potent antidiuretic factor could be present and act to prevent excessive loss of water and salts after the postgorging diuresis. Despite the medical importance of R. prolixus, no genes for any neuropeptides have been cloned, including obviously, those that control diuresis. Here, using molecular biology in combination with matrix-assisted laser desorption ionization-time of flight-tandem mass spectrometry, we determined the sequence of the CAPA gene and CAPA-related peptides in R. prolixus, which includes a peptide with anti-diuretic activity. We have characterized the expression of mRNA encoding these peptides in various developmental stage and also examined the tissue-specific distribution in fifth-instars. The expression is localized to numerous bilaterally paired cell bodies within the central nervous system. In addition, our results show that RhoprCAPA gene expression is also associated with the testes, suggesting a novel role for this family of peptides in reproduction.


1987 ◽  
Vol 127 (1) ◽  
pp. 249-277
Author(s):  
J. P. C. DUMONT ◽  
J. J. WINE

1. We describe the phasic neuromuscular system of the crayfish telson and establish its homology with the abdominal flexor system that provides the powerstroke for tailflip escape responses. 2. Three paired phasic telson muscles are innervated by 11 paired neurones which have somata in the terminal (sixth) ganglion and axons in the sixth nerve. These are the posterior and ventral telson flexors and the anterior telson muscle. 3. Studies of embryonic ganglia provide evidence that the sixth ganglion is a fusion product of two ancestral ganglia, plus a partial ganglion that is not homologous with the segmental ganglia. 4. Two of the telson flexor motor neurones are homologues of the single motor giant found in each anterior hemiganglion. Among the shared features which led to this conclusion are: size, soma position, distribution of terminals to the muscles, dendrite morphology, pattern of direct inputs from the giant axons, and the marked tendency for low-frequency depression of the neuromuscular synapse. 5. Two of the telson flexor neurones are homologues of the single flexor inhibitor found in each anterior hemiganglion. In addition to numerous morphological similarities, these two cells produce IPSPs in the telson flexor muscles. 6. Six of the seven remaining motor neurones were identified as homologues of the non-giant fast flexor excitors of anterior ganglia. These can be divided into two uneven groups according to their ganglia of origin. The sixth segmental group of fast flexor motor neurones consists of four neurones (one less than expected) and the seventh segmental group consists of two neurones (three less than expected). 7. The remaining neurone provides the sole innervation of the anterior telson muscle. Although previously classified as a telson flexor muscle, we found that the anterior telson muscle moves the uropod but not the telson. The innervation of this muscle and the pattern of inputs to the anterior telson motor neurone from identified interneurones are unlike that of any fast flexor muscle or motor neurone. We conclude that the anterior telson muscle and its motor neurone are not homologues of anterior components of the fast flexor system. 8. In anterior ganglia, a prominent premotor neurone known as the segmental giant is presynaptic to all fast flexor motor neurones except the motor giants and flexor inhibitors. We identified a single paired cell in the sixth ganglion which appears to be the segmental giant homologue.


2014 ◽  
Vol 30 (7) ◽  
pp. 711-716 ◽  
Author(s):  
Luana Portes Ozório Coelho ◽  
João Leandro de Paula Ferreira ◽  
Gabriela Bastos Cabral ◽  
Paula Morena de Souza Guimarães ◽  
Luis Fernando de Macedo Brigido

2013 ◽  
Vol 539 ◽  
pp. 255-258
Author(s):  
Miao Miao Cui ◽  
Xiu Chun Yang ◽  
Jun Wei Hou

Firstly, porous anodic aluminum oxide template was prepared by a two-step anodization process, then AgBr nanowire arrays were successfully synthesized by paired cell deposition. X-ray diffraction (XRD) indicates that the as-synthesized samples are composed of face-centered AgBr. Field-emission scanning electron microscopy (FESEM) shows that the average diameter of the nanowire arrays is about 70nm.


2018 ◽  
Vol 36 (10) ◽  
pp. 962-970 ◽  
Author(s):  
Keren Bahar Halpern ◽  
Rom Shenhav ◽  
Hassan Massalha ◽  
Beata Toth ◽  
Adi Egozi ◽  
...  

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