Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Louis S. Ramagli"'
Autor:
Yujia Huo, Yue Lu, Jean Pierre J. Issa, David Graber, Steven M. Kornblau, Louis S. Ramagli, Jaroslav Jelinek, Gabriel G. Malouf, Marcos R. Estecio, Jumpei Yamazaki, Shoudan Liang, Hai Long
Publikováno v:
Epigenetics. 8:92-104
Acute myeloid leukemia (AML) is sustained by a population of cancer stem cells (CSCs or cancer-initiating cell). The mechanisms underlying switches from CSCs to non-CSCs in vivo remain to be understood. We address this issue in AML from the aspect of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9468ca4f4fac7fa1a63496cc214247cc
https://doi.org/10.4161/epi.23243
https://doi.org/10.4161/epi.23243
Autor:
Brian C. Ramagli, Louis S. Ramagli, Barry W. Brown, Patrick M. Lynch, Mary Coolbaugh-Murphy, Marsha L. Frazier, Jing Ping Xu, Stanley R. Hamilton, Michael J. Siciliano
Publikováno v:
Human Mutation. 31:317-324
Most hereditary nonpolyposis colorectal cancer (HNPCC) patients inherit a defective allele of a mismatch repair (MMR) gene, usually MLH1 or MSH2, resulting in high levels of microsatellite instability (MSI-H) in the tumors. Presence of MSI in the nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::935609741220361144dd58967fe6a5dd
https://doi.org/10.1002/humu.21190
https://doi.org/10.1002/humu.21190
Autor:
Tiina Suominen, Michael J. Siciliano, Tomasz J. Czernuszewicz, Linda L. Bachinski, Ralf Krahe, Mark D. Shriver, Louis S. Ramagli, B. Udd
Publikováno v:
Neurology. 72:490-497
Background: The myotonic dystrophies (DM1, DM2) are the most common adult muscle diseases and are characterized by multisystem involvement. DM1 has been described in diverse populations, whereas DM2 seems to occur primarily in European Caucasians. Bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::230b88a228e0214e2f507b9d610c336f
https://doi.org/10.1212/01.wnl.0000333665.01888.33
https://doi.org/10.1212/01.wnl.0000333665.01888.33
Publikováno v:
Current Colorectal Cancer Reports. 3:185-190
The contributions and limitations of the traditional method for evaluating microsatellite instability by standard polymerase chain reaction (PCR) in identifying mismatch repair (MMR) gene mutations in the Lynch syndrome form of hereditary nonpolyposi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79395a274d3c625ef06b8c67de887a9b
https://doi.org/10.1007/s11888-007-0029-z
https://doi.org/10.1007/s11888-007-0029-z
Publikováno v:
Mechanisms of Ageing and Development. 126:1051-1059
Small pool PCR (SP-PCR) is a sensitive method for the detection and quantification of microsatellite instability (MSI) in somatic cells. Here we propose that mutant microsatellite fragments accumulate with age in normal somatic cells and that this in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43150e6ffe0a9822b64ac5b8624ab1e2
https://doi.org/10.1016/j.mad.2005.06.005
https://doi.org/10.1016/j.mad.2005.06.005
Autor:
Carolyn A. Peterson, Gunilla Kanter-Smoler, Lei Li, Michael J. Siciliano, Ying Fei Wei, Randy J. Legerski, Louis S. Ramagli, Per Sunnerhagen
Publikováno v:
Oncogene. 18:1689-1699
The RAD17 gene product of S. Pombe is an essential component of the checkpoint control pathway which responds to both DNA damage and disruption of replication. We have identified a human cDNA that encodes a polypeptide which is structurally conserved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15e3d087855271790c92f2b3ce16c086
https://doi.org/10.1038/sj.onc.1202469
https://doi.org/10.1038/sj.onc.1202469
Autor:
Louis S. Ramagli, Evan E. Eichler, Michael J. Siciliano, Harvey W. Mohrenweiser, Thomas C. Wood, Richard M. Weinshilboum, Chengtao Her
Publikováno v:
Genomics. 53:284-295
We have cloned and characterized cDNAs that encode two human hydroxysteroid sulfotransferase (SULT) enzymes, SULT2B1a and SULT2B1b, as well as the single gene that encodes both of these enzymes. The two cDNAs differed at their 5'-termini and had 1050
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14950305109ec46088948f7b50558783
https://doi.org/10.1006/geno.1998.5518
https://doi.org/10.1006/geno.1998.5518
Autor:
Shoudan Liang, Rong He, Jaroslav Jelinek, Jean Pierre J. Issa, Yue Lu, Louis S. Ramagli, Elizabeth J. Shpall, Marcos R. Estecio
Publikováno v:
Epigenetics. 7(12)
Genome wide analysis of DNA methylation provides important information in a variety of diseases, including cancer. Here, we describe a simple method, Digital Restriction Enzyme Analysis of Methylation (DREAM), based on next generation sequencing anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33cea1d24c2f88a46e5b159e8b7f225e
https://pubmed.ncbi.nlm.nih.gov/23075513
https://pubmed.ncbi.nlm.nih.gov/23075513
Autor:
Lisa V. Tsui, Chuan Gao, Tej K. Pandita, Ralph B. Arlinghaus, Louis S. Ramagli, Chau D. Pham, Balraj Singh
Publikováno v:
International journal of oncology. 11(6)
In order to determine the physiological significance of c-mos RNA expression in somatic cells, we introduced antisense c-mos under the control of an inducible promoter. NIH/3T3 cells were stably transfected with antisense mos under the control of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945cc893b973f33ac6dedd603633fb22
https://pubmed.ncbi.nlm.nih.gov/21528318
https://pubmed.ncbi.nlm.nih.gov/21528318
Publikováno v:
Journal of Virology. 64:3093-3096
The v-mos protein, termed p37v-mos, has a closely associated serine/threonine protein kinase activity. To provide further information about its protein kinase activity, we tested the activity of p37v-mos produced in a cell-free translation system fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ddd97d600b7f2eb474ecae8a0b780c9
https://doi.org/10.1128/jvi.64.6.3093-3096.1990
https://doi.org/10.1128/jvi.64.6.3093-3096.1990