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pro vyhledávání: '"Kojis, T."'
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Autor:
Valentine Lerious, C. Heinzmann, B. J. Austin, James F. McGinnis, Ivana Klisak, Kojis T, J. B. Bateman, R. S. Sparkes
Publikováno v:
Journal of Neuroscience Research. 40:165-168
The gene for the mouse recoverin protein (23 kDa photoreceptor-specific protein, S-modulin, or the Cancer-Associated Retinopathy protein) was recently assigned to mouse chromosome 11, closely linked to trp53. In this paper, the human gene for recover
Autor:
Carper D, T. K. Mohandas, R. S. Sparkes, C. Heinzmann, Bateman Jb, Nishimura C, Anh Diep, Ivana Klisak, Kojis T
Publikováno v:
Genomics. 17:560-565
Aldose reductase (alditol:NAD(P)+ 1-oxidoreductase; EC 1.1.1.21) (AR) catalyzes the reduction of several aldehydes, including that of glucose, to the corresponding sugar alcohol. Using a complementary DNA clone encoding human AR, we mapped the gene s
Autor:
T. K. Mohandas, Jean C. Shih, Ivana Klisak, Anh Diep, Kojis T, C. Heinzmann, Nancy C. Lan, Robert S. Sparkes
Publikováno v:
Genomics. 9:461-465
A gene for serotonin 5HT-2 receptor (HTR2) is assigned to human chromosome 13 by somatic cell hybrids and to region 13q14-q21 by in situ hybridization. It is assigned to mouse chromosome 14 by somatic cell hybrid analysis.
Autor:
T. K. Mohandas, C. Heinzmann, Kojis T, Ivana Klisak, R. S. Sparkes, Mihael H. Polymeropoulos, Pedro Gonzalez, J. B. Bateman, J. S. Zigler, Ponugoti Vasantha Rao
Publikováno v:
Genomics. 23(2)
ζ-Crystallin is a lens protein that has been associated with autosomal dominant congenital cataracts in guinea pigs and thus is a candidate for human congenital cataracts. We have assigned the ζ-crystallin gene (CRYZ) to human chromosome 1 using a
Autor:
C. Heinzmann, Ivana Klisak, Martin Blum, Douglas Geissert, Kojis T, Edward M. De Robertis, Robert S. Sparkes
Publikováno v:
Genomics. 21(2)
Goosecoid is a homeobox gene first isolated from a Xenopus dorsal lip cDNA library. Homologous genes have been isolated from mouse, zebrafish, and chick. In all species examined, the gene is expressed and plays an important role during the process of
Autor:
J. P. Finn, D. Peter, Robert H. Edwards, Ivana Klisak, C. Heinzmann, R. S. Sparkes, Kojis T, Ali Roghani, Yongjian Liu
Publikováno v:
Genomics. 18(3)
The physiologic and behavioral effects of pharmacologic agents that interfere with the transport of monoamine neurotransmitters into vesicles suggest that vesicular amine transport may contribute to human neuropsychiatric disease. To determine whethe
Autor:
Kojis T, Toshimichi Shinohara, C. Heinzmann, Sparkes Rs, Craft Cm, Ivana Klisak, Bateman Jb, Lee Rh
Publikováno v:
Genomics. 18(2)
Phosducin is a soluble photoreceptor phosphoprotein that probably modulates phototransduction in the retina and thus qualifies as a potential candidate gene for retinitis pigmentosa. Using both human/mouse somatic cell hybrids and in situ hybridizati
Autor:
Kojis T, Bateman Jb, R. S. Sparkes, Tiansen Li, Cathy Bowes, Debora B. Farber, Meredithe L. Applebury, T. K. Mohandas, Ivana Klisak
Publikováno v:
Genomics. 12(3)
The gene encoding the β-subunit of rod photoreceptor cGMP phosphodiesterase (gene symbol PDEB, homolog of the mouse rd gene) is mapped to human chromosome 4 using somatic cell hybrids and further localized to the chromosome band 4q16 using in situ h
Autor:
Robert S. Sparkes, J. Bronwyn Bateman, Steve Goldflam, Kojis T, Ivana Klisak, John W. Crabb, C. Heinzmann, John C. Saari, T. K. Mohandas
Publikováno v:
Genomics. 12(1)
Cellular retinaldehyde-binding protein (CRALBP) has properties that suggest that it is involved in the visual process and, therefore, potentially with retinal diseases. A human cDNA probe has been used to map this gene to human chromosome 15q26 (soma