Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Iveta Kalcheva"'
Publikováno v:
Pain. 85:395-404
It has been hypothesized that spinal morphine tolerance results from protein kinase C (PKC) mediated phosphorylation. Chronic lumbar intrathecal (i.t.) infusion of morphine (20 nmol/microl/h) was shown to produce antinociception on day 1 (d1) that di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f9a862a27d4ec9aeff62e48688c401
https://doi.org/10.1016/s0304-3959(99)00281-x
https://doi.org/10.1016/s0304-3959(99)00281-x
The spinal biology in humans and animals of pain states generated by persistent small afferent input
Publikováno v:
Proceedings of the National Academy of Sciences. 96:7680-7686
Behavioral models indicate that persistent small afferent input, as generated by tissue injury, results in a hyperalgesia at the site of injury and a tactile allodynia in areas adjacent to the injury site. Hyperalgesia reflects a sensitization of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0283a7e184ff2f98567e56484b753d89
https://doi.org/10.1073/pnas.96.14.7680
https://doi.org/10.1073/pnas.96.14.7680
Autor:
Jihye Park, Fred J. Koehrn, Iveta Kalcheva, Mathias Leinders, Bong-Kiun Kaang, Nam-Kyung Yu, David L. Boyle, Veronica I. Shubayev, Beatrix Bartok, Michael P. Hefferan, Linda S. Sorkin, Gary S. Firestein
Publikováno v:
Pain. 155(6)
PI3-kinases (PI3Ks) participate in nociception within spinal cord, dorsal root ganglion (DRG), and peripheral nerves. To extend our knowledge, we immunohistochemically stained for each of the 4 class I PI3K isoforms along with several cell-specific m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::194303b6e34bddaf955c5e9d6eb27543
https://pubmed.ncbi.nlm.nih.gov/24631588
https://pubmed.ncbi.nlm.nih.gov/24631588
Publikováno v:
Proceedings of the National Academy of Sciences. 92:12352-12356
Representational difference analysis was used to identify strain-specific differences in the pseudoautosomal region (PAR) of mouse X and Y chromosomes. One second generation (C57BL/6 x Mus spretus) x Mus spretus interspecific backcross male carrying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51f35cbed462a4bd588299225d4311ba
https://doi.org/10.1073/pnas.92.26.12352
https://doi.org/10.1073/pnas.92.26.12352
Autor:
Christoph Plass, Verne M. Chapman, Dawn E. Watkins-Chow, Yoshihide Hayashizaki, Sally A. Camper, Roger L. Eddy, Thomas B. Shows, Sheila N.J. Sait, Nobuo Takagi, Hideo Shibata, Iveta Kalcheva, Takayuki Ueda
Publikováno v:
Cytogenetic and Genome Research. 68:19-24
The genetic map location of the recently discovered imprinted gene U2afbpL has been verified and refined in several mouse crosses. RI strain analysis had previously shown that the gene is located on mouse chromosome 11. This assignment has been verif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b66e1e6976f32ce4776e4077783c909
https://doi.org/10.1159/000133881
https://doi.org/10.1159/000133881
Autor:
Dan Mercola, Linda Wasserman, Robert O. Stuart, Charles C. Berry, Igor Klacansky, Karen C. Arden, Steven Goodison, William Wachsman, Yipeng Wang, Anne Sawyers, Daniel R. Masys, Iveta Kalcheva, Jessica Wang-Rodriguez, David Tarin, Michael McClelland
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 101(2)
Prostate tumors are complex entities composed of malignant cells mixed and interacting with nonmalignant cells. However, molecular analyses by standard gene expression profiling are limited because spatial information and nontumor cell types are lost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c96aadd4b9013f5bae0dda54d4e8927
https://pubmed.ncbi.nlm.nih.gov/14722351
https://pubmed.ncbi.nlm.nih.gov/14722351
Autor:
Aldons J. Lusis, Scott Silvey, Olga Iakoubova, Jim Choi, Iveta Kalcheva, Judi Louie, James D. Cavalcoli, Katherine M. Dains, Vitaly Nimon, Kit F. Lau, Ali Andalibi, Madalyne Cunanan, David A. Ross, Christine L. Olsson, David B. West, Migdad Machrus, L. Gordon Bentley, Catherine Beauheim
Publikováno v:
Genomics. 74(1)
An important approach for understanding complex disease risk using the mouse is to map and ultimately identify the genes conferring risk. Genes contributing to complex traits can be mapped to chromosomal regions using genome scans of large mouse cros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08e6e6ca469dafb81bd851e33d8599b
https://pubmed.ncbi.nlm.nih.gov/11374905
https://pubmed.ncbi.nlm.nih.gov/11374905
Autor:
Nandita Quaderi, Orsetta Zuffardi, Huntington F. Willard, Sushma S. Thomas, Rosemary W. Elliott, Laura Carrel, Verne M. Chapman, Elena I. Rugarli, Laura Dal Zotto, Patricia A. Lingerfelter, Andrea Ballabio, Giulia Arrigo, Valentina Valsecchi, Iveta Kalcheva, Chao Huang Yen, Christine M. Disteche, Eugenio Montini
We have recently reported isolation of the gene responsible for X-linked Opitz G/BBB syndrome, a defect of midline development. MID1 is located on the distal short arm of the human X chromosome (Xp22. 3) and encodes a novel member of the B box family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b78715ed5173449d6e09b129b1c40ac9
http://hdl.handle.net/11588/130677
http://hdl.handle.net/11588/130677
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 8(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70aaa5a5f87d9f17a3155bc5210b8314
https://pubmed.ncbi.nlm.nih.gov/9250875
https://pubmed.ncbi.nlm.nih.gov/9250875
Autor:
Hideo Shibata, Nina Kotelevtseva, Hiroyuki Sasaki, Reiko Kato, Iveta Kalcheva, Verne M. Chapman, Linda J. Mullins, Yoshihide Hayashizaki, Yasushi Okazaki, Shinji Hirotsune, William A. Held, John J. Mullins, Christoph Plass
Publikováno v:
Nature genetics. 14(1)
Normal mammalian development requires a diploid combination of both haploid parental genomes. Uniparental disomy for certain segments of specific chromosomes results in aberrant development or prenatal lethality, indicating that the parental genomes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::285e5cb99a04fdef400ae9635b21ac12
https://pubmed.ncbi.nlm.nih.gov/8782830
https://pubmed.ncbi.nlm.nih.gov/8782830