Relevant bibliographies by topics / Retina cDNA cloning/synthesis

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Retina cDNA cloning/synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Retina cDNA cloning/synthesis"

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Voisin, P., J. Guerlotté, M. Bernard, J. P. Collin, and M. Cogné. "Molecular cloning and nucleotide sequence of a cDNA encoding hydroxyindole O-methyltransferase from chicken pineal gland." Biochemical Journal 282, no. 2 (1992): 571–76. http://dx.doi.org/10.1042/bj2820571.

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Hydroxyindole O-methyltransferase (EC 2.1.1.4) is the enzyme that catalyses the synthesis of melatonin in the pineal gland and in the retina. Polyadenylated RNA from chicken pineal glands was used to prepare a cDNA library in lambda gt11. The library was screened with an antiserum directed against chicken hydroxyindole O-methyltransferase, and one cDNA clone was isolated. The fusion protein expressed by phage lysogens was identified on Western blots as a 165 kDA immunoreactive protein (beta-galactosidase, 110 kDa; hydroxyindole O-methyltransferase, 38 kDa). The fusion protein exhibited hydroxy
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HSU, Lily C., Wen-Chung CHANG, Ines HOFFMANN, and Gregg DUESTER. "Molecular analysis of two closely related mouse aldehyde dehydrogenase genes: identification of a role for Aldh1, but not Aldh-pb, in the biosynthesis of retinoic acid." Biochemical Journal 339, no. 2 (1999): 387–95. http://dx.doi.org/10.1042/bj3390387.

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Mammalian class I aldehyde dehydrogenase (ALDH1) has been implicated as a retinal dehydrogenase in the biosynthesis of retinoic acid, a modulator of gene expression and cell differentiation. As the first step towards studying the regulation of ALDH1 and its physiological role in the biosynthesis of retinoic acid, mouse ALDH1 cDNA and genomic clones have been characterized. During the cloning process, an additional closely related gene was also isolated and named Aldh-pb, owing to its high amino acid sequence identity (92%) with the rat phenobarbitol-inducible ALDH protein (ALDH-PB). Aldh1 span
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Acharya, Harsha R., Constance M. Dooley, Wallace B. Thoreson, and Iqbal Ahmad. "cDNA Cloning and Expression Analysis ofNeuroDmRNA in Human Retina." Biochemical and Biophysical Research Communications 233, no. 2 (1997): 459–63. http://dx.doi.org/10.1006/bbrc.1997.6483.

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Nakagawa, Yuzo, Che-Hui Kuo, Kayoko Ishii, Sadao Shiosaka, Masaya Tohyama, and Naomasa Miki. "Cloning and characterization of a cDNA specific for bovine retina." Neuroscience Research 3, no. 4 (1986): 300–310. http://dx.doi.org/10.1016/0168-0102(86)90022-2.

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Yamaki, Kunihiko, Yoosuke Takahashi, Shozo Sakuragi, and Kenichi Matsubara. "Molecular cloning of the S-antigen cDNA from bovine retina." Biochemical and Biophysical Research Communications 142, no. 3 (1987): 904–10. http://dx.doi.org/10.1016/0006-291x(87)91499-9.

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Hughes, Bret A., Gyanendra Kumar, Yukun Yuan, et al. "Cloning and functional expression of human retinal Kir2.4, a pH-sensitive inwardly rectifying K+ channel." American Journal of Physiology-Cell Physiology 279, no. 3 (2000): C771—C784. http://dx.doi.org/10.1152/ajpcell.2000.279.3.c771.

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To identify novel potassium channel genes expressed in the retina, we screened a human retina cDNA library with an EST sequence showing partial homology to inwardly rectifying potassium (Kir) channel genes. The isolated cDNA yielded a 2,961-base pair sequence with the predicted open reading frame showing strong homology to the rat Kir2.4 (rKir2.4). Northern analysis of mRNA from human and bovine tissues showed preferential expression of Kir2.4 in the neural retina. In situ hybridization to sections of monkey retina detected Kir2.4 transcript in most retinal neurons. Somatic hybridization analy
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O'Brien, John, Harris Ripps, and Muayyad R. Al-Ubaidi. "Molecular cloning of a rod opsin cDNA from the skate retina." Gene 193, no. 2 (1997): 141–50. http://dx.doi.org/10.1016/s0378-1119(97)00079-6.

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Cauley, K., B. W. Agranoff, and D. Goldman. "Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina." Journal of Cell Biology 108, no. 2 (1989): 637–45. http://dx.doi.org/10.1083/jcb.108.2.637.

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A new non-alpha (n alpha) member of the nicotinic acetylcholine receptor (nAChR) gene family designated GFn alpha-2 has been identified in goldfish retina by cDNA cloning. This cDNA clone encodes a protein with structural features common to all nAChR subunits sequenced to date; however, unlike all known alpha-subunits of the receptor, it lacks the cysteine residues believed to be involved in acetylcholine binding. Northern blot analysis shows multiple transcripts hybridizing to the GFn alpha-2 cDNA in goldfish retina but undetectable levels of hybridizable RNA in brain, muscle, or liver. S1 nu
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Pardhasaradhi, Komanduri, R. Krishnan Kutty, Chang Shin Park, and Gopal Krishna. "Cloning and sequencing of heat shock factor (HSF1) cDNA from human retina." Current Eye Research 13, no. 10 (1994): 739–42. http://dx.doi.org/10.3109/02713689409047008.

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ZOU, Ming-Feng, Lin BAI, Bo KANG, and Xue-Wei LI. "cDNA cloning and expression analysis of Opn4 gene in retina of swines." Hereditas (Beijing) 35, no. 7 (2013): 890–95. http://dx.doi.org/10.3724/sp.j.1005.2013.00890.

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Dissertations / Theses on the topic "Retina cDNA cloning/synthesis"

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Dent, C. L. "cDNA cloning and the retina." Thesis, University of Liverpool, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384395.

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Modesti, Alessandra. "Synthesis, cloning and expression of the cDNA for a bovine liver phosphotyrosine-protein phosphatase." Thesis, Cranfield University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358330.

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Book chapters on the topic "Retina cDNA cloning/synthesis"

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Steinbergs, Juris, and Aleksander Tsimanis. "cDNA Synthesis and Cloning." In Basic Cloning Procedures. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-71965-3_1.

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Bhat, Alangar Ishwara, and Govind Pratap Rao. "cDNA Synthesis and Cloning." In Springer Protocols Handbooks. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0334-5_43.

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Ishibashi, Jun, Hisako Saido-Sakanaka, and Minoru Yamakawa. "Isolation, cDNA Cloning, and Chemical Synthesis of Oryctes rhinoceros Defensin." In Peptides: The Wave of the Future. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_484.

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Selsted, Michael E., Jack N. Levy, Robert J. Van Abel, James S. Cullor, Roger J. Bontems, and George Barany. "Purification, characterization, synthesis and cDNA cloning of indolicidin: A tryptophan-rich microbicidal tridecapeptide from neutrophils." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_367.

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Conference papers on the topic "Retina cDNA cloning/synthesis"

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Uzan, G., A. Lajmanovich, M. H. Prandini, Ph Frachet, A. Duperray, and G. Marguerie. "MOLECULAR CLONING OF PLATELET GPIIb FROM HEL CELLS AND HUMAN MEGAKARYOCYTES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643960.

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Platelet GP IIb-IIIa is an heterodimer which functions as a receptor for fibrinogen, fibronectin and Von Willebrand factor and is implicated in platelet adhesive reactions. To study the structure function relationship of this glycoprotein, a recombinant DNA approach was initiated. cDNA expression libraries were constructed in » gtll vector, from erythro-leukemia cells (HEL) and megakaryocytes mRNA. The human megakaryocytes were isolated from patients with chronic myeloid leukemia. The HEL library was initially screened with polyclonal antibodies anti GPIIb IIIa. One clone, λIIbI, containing a
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Wasley, Louise C., Andrew J. Dorner, and Randal C. Kaufman. "SYNTHESIS. PROCESSING AND SECRETION OF HUMAN FACTOR VIII IN MAMMALIAN CELLS: REQUIREMENT FOR VON WILLEBRAND FACTOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643874.

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In the plasma factor VIII exists as a complex with von Willebrand factor (vWF). The cloning of the cDNA for factor VIII has provided the ability to develop mammalian cell lines which express high levels of factor VIII by using appropriatate expression plasmids and DNA cotransformation with selectable markers. We have studied the synthesis, processing, and secretion of factor VIII expressed in baby hamster kidney cells and in Chinese hamster ovary cells by 35S-methionine pulse and chase labeling and analysis by immunoprecipitation with specific antibodies which recognize the light and heavy cha
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