Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Narayan K, Bhat"'
Autor:
Jon M. Wigginton, Robin Winkler-Pickett, Narayan K. Bhat, Michael Sanford, Anna T. Mason, Meagan Horner, Earl W. Bere, John R. Ortaldo, James Cherry, Howard A. Young, Deborah L. Hodge
Publikováno v:
Blood. 107:1468-1475
Our previous studies have identified mechanisms by which cytokine production, blocked by Ly49G2 receptor cross-linking, can be overridden. In this study we analyzed the regulation of other ITAM-positive receptor signaling on NK, NKT, and T cells and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9be2574a3953a1b34d45f135edbabe1
https://doi.org/10.1182/blood-2005-04-1579
https://doi.org/10.1182/blood-2005-04-1579
Autor:
Takis S. Papas, Dennis K. Watson, Nicoletta Sacchi, Shigeyoshi Fujiwara, Arun K. Seth, Robert J. Fisher, Narayan K. Bhat, George Mavrothalassitis, Shigeki Koizumi, Cheryl L. Jorcyk, Clifford W. Schweinfest, Stavros D. Kottaridis, Richard Ascione
Publikováno v:
American Journal of Medical Genetics. 37:251-261
The human ETS2 and ERG genes are members of the ETS gene family, with sequence homology to the viral ets gene of the avian erythroblastosis retrovirus, E26. These genes are located on chromosome 21 and molecular genetic analysis of Down syndrome (DS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df9ccb62558ea04e226c7093d9193c58
https://doi.org/10.1002/ajmg.1320370751
https://doi.org/10.1002/ajmg.1320370751
Autor:
Garrison A. Owens, David J. Munroe, James Cherry, Casey Frankenberger, Kelly Martin, Narayan K. Bhat, Claudia Stewart, Gabriela Tudor
Publikováno v:
JALA: Journal of the Association for Laboratory Automation. 9:128-134
PCR-based fluorescent detection assays for the relative and quantitative measurement of gene expression, such as Taq Man™, LUX™, and SYBR Green™, are currently in wide spread use due to their general applicability, low cost, reproducibility, ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8402a860e8198af70ff4cc480e17d8af
https://doi.org/10.1016/j.jala.2004.04.011
https://doi.org/10.1016/j.jala.2004.04.011
Loss of a-Type Lamin Expression Compromises Nuclear Envelope Integrity Leading to Muscular Dystrophy
Autor:
Colin L. Stewart, Teresa Sullivan, Miriam R. Anver, Kunio Nagashima, Diana Escalante-Alcalde, Narayan K. Bhat, Harshida Bhatt, Brian Burke
Publikováno v:
The Journal of Cell Biology
The nuclear lamina is a protein meshwork lining the nucleoplasmic face of the inner nuclear membrane and represents an important determinant of interphase nuclear architecture. Its major components are the A- and B-type lamins. Whereas B-type lamins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02f5f2202b7dbc01a714c8d4088aba4d
http://europepmc.org/articles/PMC2169344
http://europepmc.org/articles/PMC2169344
Publikováno v:
Journal of Neuro-Oncology. 31:09-16
Ewing's sarcoma family of tumors (EFT) contain reciprocal translocations, of which approximately 90% occur between the long arm of chromosomes 11 and 22, t(11;22)(q24;q12), resulting in the formation of chimeric proteins generated by a fusion of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3fbc8fc4cd447438c6d1e427ad49dd0
https://doi.org/10.1023/a:1005716926800
https://doi.org/10.1023/a:1005716926800
Publikováno v:
Proceedings of the National Academy of Sciences. 92:4442-4446
We have ectopically expressed transcription factor ETS1 in two different highly tumorigenic human colon cancer cell lines, DLD-1 and HCT116, that do not express endogenous ETS1 protein and have obtained several independent clones. The expression of w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3abfba61de64cdd8d2ef4f67f78410a8
https://doi.org/10.1073/pnas.92.10.4442
https://doi.org/10.1073/pnas.92.10.4442
Autor:
Narayan K. Bhat, Vincenzo Romano-Spica, Panagiotis Georgiou, Hiroaki Suzuki, Pei Guo Kui, Shin-Lin Chen
Publikováno v:
Hybridoma. 13:1-8
The epitope for E44 monoclonal antibody (mAb) was mapped using mutated ETS1 proteins lacking different carboxy-terminal regions and by the employment of synthetic oligopeptides spanning the epitope region. This epitope lies around Arg211 of the human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fbe4ac8a61bae16a833cd3ea49f65ce
https://doi.org/10.1089/hyb.1994.13.1
https://doi.org/10.1089/hyb.1994.13.1
Publikováno v:
Virology. 196:15-24
We have examined human T-lymphotropic virus type I (HTLV-I) gene expression in the human T-cell line, C8166-45 (C81), as a model to define the gene products expressed from defective proviruses. C81 cells contain one complete and two different deleted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::741543fd41e048616c9787d85893012c
https://doi.org/10.1006/viro.1993.1450
https://doi.org/10.1006/viro.1993.1450
Autor:
Shigeki Koizumi, J M Mariano, George Mavrothalassitis, Narayan K. Bhat, Takis S. Papas, Robert J. Fisher, A Kondoh
Publikováno v:
Journal of Biological Chemistry. 267:17957-17965
The human ETS1 proto-oncogene proteins have been isolated from the T-cell leukemia line, CEM, by immunoaffinity chromatography and their identity confirmed by NH2-terminal amino acid sequencing. Incubation of CEM cells with N alpha-p-tosyl-L-lysine c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::558ad340a24f1ad5c1e92909b4cea208
https://doi.org/10.1016/s0021-9258(19)37136-4
https://doi.org/10.1016/s0021-9258(19)37136-4
Autor:
Takis S. Papas, Narayan K. Bhat
Publikováno v:
Hybridoma. 11:277-294
A monoclonal antibody recognizing ets proteins from a variety of species has been developed. This antibody recognizes ets1, ets2, erg, and other related proteins. It has a high affinity for the ets1 protein. The epitope for the pan ets mAb consists o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55963f8c0e25f43fcaf26162015f9eeb
https://doi.org/10.1089/hyb.1992.11.277
https://doi.org/10.1089/hyb.1992.11.277